Applications are invited for the post of Junior Research Fellowship (JRF) in a time bound research

project under ANRF/ARG program for a temporary period, purely on contractual basis as per the

following details.

Position Junior Research Fellowship

Number of Vacancy 01

Project Title

Development and commercialization of CRISPR-CAS/Fluorescence based dual electrochemical sensor for the instant and affordable diagnosis of Scrub Typhus Department of Bio-Sciences and Technology, MMEC, MM(DU)

Project Tenure 3 Years

Job Description

The selected candidate will work on the development of a CRISPR-Cas and fluorescence-based dual electrochemical sensor for rapid and affordable diagnosis of Scrub Typhus.

Responsibilities include biosensor fabrication, electrode modification, assay optimization,

analytical validation, data analysis, and assistance in prototype development, reporting, and research publications.

Essential Qualification

M. Sc. Biotechnology/Microbiology/Biomedical Technology with at least 60% marks and should be NET qualified or M. Tech inBiotechnology/Microbiology/Biomedical Technology with at least 60% marks.Age Limit As per GOI rulesAge Relaxation As per GOI rulesFellowship Rs. 37,000 per month +8% HRA

Principle Investigator (PI)

Co- Principle Investigator

(Co-PI)

Dr. Ankur Kaushal, Sr. Associate Professor, Deptt. of Bio-Sciences and Technology, MMEC, Maharishi Markandeshwar (Deemed to be University) Mullana-Ambala

Dr. Shagun Gupta, Associate Professor, Deptt. of Bio-Sciences and Technology, MMEC, Maharishi Markandeshwar (Deemed to be University) Mullana-Ambala

How to Apply

Interested candidates may submit their application and bio-data through email to

,

.

Candidates will be called for a personal interview in the seminar room Central Research Cell, Maharishi Markandeshwar (Deemed to be University), Mullana

Date and time of interview: 31/03/2026, 10:00AM

Read Less

Applications are invited for the post of Junior Research Fellowship (JRF) in a time bound research

project under ANRF/ARG program for a temporary period, purely on contractual basis as per the

following details.

Position Junior Research Fellowship

Number of Vacancy 01

Project Title

Development and commercialization of CRISPR-CAS/Fluorescence based dual electrochemical sensor for the instant and affordable diagnosis of Scrub Typhus Department of Bio-Sciences and Technology, MMEC, MM(DU)

Project Tenure 3 Years

Job Description

The selected candidate will work on the development of a CRISPR-Cas and fluorescence-based dual electrochemical sensor for rapid and affordable diagnosis of Scrub Typhus.

Responsibilities include biosensor fabrication, electrode modification, assay optimization,

analytical validation, data analysis, and assistance in prototype development, reporting, and research publications.

Essential Qualification

M. Sc. Biotechnology/Microbiology/Biomedical Technology with at least 60% marks and should be NET qualified or M. Tech inBiotechnology/Microbiology/Biomedical Technology with at least 60% marks.Age Limit As per GOI rulesAge Relaxation As per GOI rulesFellowship Rs. 37,000 per month +8% HRA

Principle Investigator (PI)

Co- Principle Investigator

(Co-PI)

Dr. Ankur Kaushal, Sr. Associate Professor, Deptt. of Bio-Sciences and Technology, MMEC, Maharishi Markandeshwar (Deemed to be University) Mullana-Ambala

Dr. Shagun Gupta, Associate Professor, Deptt. of Bio-Sciences and Technology, MMEC, Maharishi Markandeshwar (Deemed to be University) Mullana-Ambala

How to Apply

Interested candidates may submit their application and bio-data through email to

,

.

Candidates will be called for a personal interview in the seminar room Central Research Cell, Maharishi Markandeshwar (Deemed to be University), Mullana

Date and time of interview: 31/03/2026, 10:00AM

Read Less

Job description

We are recruiting Laboratory Assistant

Qualified, experienced and passionate Teachers from Gurugram may apply.

Experience: Min. 2-4 years

Location: MatriKiran, Sector 83, Vatika India Next, Gurugram

Job Responsibilities:

Maintaining laboratories (Physics, Chemistry, Biology) and stock registers.Prepare the laboratory for practical classes.Assist teachers during practical sessions and demonstrations.Ensure safe handling and storage of apparatus.Follow School guidelines, policies and safety standards.Perform any other duty assigned by the School management.

Qualifications & Eligibility Criteria:

Should have Bachelors Degree in Science.Should have completed the Certified Program in Laboratory Techniques (CPLT)Computer knowledge is mandatory.Excellent verbal and written communication skills. Read Less

Job description

We are recruiting Laboratory Assistant

Qualified, experienced and passionate Teachers from Gurugram may apply.

Experience: Min. 2-4 years

Location: MatriKiran, Sector 83, Vatika India Next, Gurugram

Job Responsibilities:

Maintaining laboratories (Physics, Chemistry, Biology) and stock registers.Prepare the laboratory for practical classes.Assist teachers during practical sessions and demonstrations.Ensure safe handling and storage of apparatus.Follow School guidelines, policies and safety standards.Perform any other duty assigned by the School management.

Qualifications & Eligibility Criteria:

Should have Bachelors Degree in Science.Should have completed the Certified Program in Laboratory Techniques (CPLT)Computer knowledge is mandatory.Excellent verbal and written communication skills. Read Less

About the Role

We are seeking a self-driven Scientist to lead and deliver end-to-end molecular biology projects in our NBE Services portfolio. You will design and execute strategies for engineered antibodies, enzymes, structural proteins, and mutant strains - supporting global drug discovery programs in a fast-paced CRO environment.

Key Responsibilities

Design and execute molecular biology workflows for production of engineered antibodies, enzymes, structural/reagent proteins, and mutant strainsLead gene synthesis, cloning, vector design/swapping, antibody gene sequencing, and site-directed mutagenesis projectsGenerate CRISPR-based mutants in prokaryotic systems; perform sequence data analysis and validationExecute mRNA isolation, cDNA synthesis, and gene expression analysis using Real-Time PCRSupport HCP/HCD estimation, data analysis, and protein engineering initiativesOversee plasmid production and chromatographic purification (affinity, IEX, SEC)Manage microbial, yeast, and fungal strain engineering, including cell bank preparation and characterizationOperate and optimize automation/high-throughput platforms (liquid handlers, robotic systems)Mentor and lead the molecular biology team; drive project planning, execution, and client communicationPrepare technical reports, presentations, project proposals, and SOPs with minimal reviewEnsure 100% compliance with GLP/GMP, ALCOA+ data integrity, and lab safety standards

Must-Have Qualifications

6-10 years of hands-on industrial or advanced academic experience in molecular biology R&DExpertise in:

• Cloning (In-Fusion, Gibson, TOPO, ligation-based)

• Vector design, gene synthesis, mutagenesis, antibody sequencing

• CRISPR-based editing in prokaryotes

• RT-qPCR, mRNA/cDNA workflows, sequence analysis

• Mammalian/microbial cell culture and strain engineering

• SnapGene, Sequencher, Benchling, or equivalent bioinformatics tools

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Mandatory skill - Python + ML (Machine Learning) - Data Science

Experience: 5-12 Years only

Results-driven Data Scientist with hands-on experience in data analysis, data wrangling, and business insights generation using Python and SQL. Adept at translating complex datasets into actionable recommendations. Possesses a solid foundation in statistics and machine learning, with emerging exposure to large language models (LLMs) and OpenAI technologies.

Key Skill Areas:

Programming & Tools: Python (Pandas, NumPy, Matplotlib, Seaborn, Scikit-learn), SQL (complex queries, joins, CTEs, window functions), Git

Data Analysis & Visualization: Exploratory Data Analysis (EDA), trend and correlation analysis, hypothesis testing, dashboards (Power BI/Tableau), storytelling with data

Databases & Data Handling: SQL Server, MySQL, basic knowledge of Spark/BigQuery/Hive is a plus

Statistics & ML (Foundational): Descriptive and inferential statistics, regression, classification, clustering (K-Means), model evaluation metrics (accuracy, precision, recall, AUC), overfitting/underfitting, cross-validation

LLM/AI Exposure: Familiarity with prompt engineering, OpenAI APIs, basic usage of GPT models for data/text automation, awareness of LLM limitations and applications in analytics

Soft Skills: Strong problem-solving ability, attention to detail, stakeholder communication, ability to translate business problems into data solutions

Experience Highlights:

Conducted in-depth data analysis to uncover trends, patterns, and anomalies that informed strategic decisions across product, marketing, and operations teams

Designed and implemented scalable data pipelines and automated data workflows using Python and SQL

Developed and maintained analytical models and dashboards to track key business metrics and performance indicators

Applied statistical methods and machine learning techniques to solve real-world business problems such as forecasting, segmentation, and performance optimization

Collaborated with stakeholders to gather requirements, translate business questions into analytical approaches, and communicate findings with clarity

Explored the use of LLMs (e.g., OpenAI GPT) for enhancing internal workflows and accelerating data-driven tasks such as querying, summarization, and content generation

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BIOINFORMATICS INTERN

Hyperworks Imaging is a cutting-edge technology company based out of Bengaluru, India since 2016. We are building disruptive and transformative products and solutions in diverse verticals ranging from Finance, Energy to Materials.

We are a rapidly growing company, working with multiple companies around the world. We also support their needs for strong technical professionals to help build and maintain their proprietary platforms.

The following position is for our affiliated company NuMarg Inc () working to accelerate AI based bioleaching processes. This is a full time position to support R&D teams inhouse, external universities in India and abroad and requires immediate joining.

JOB OVERVIEW

We're looking for a bioinformatics intern to work on metabolic models of Gluconobacter oxydans (and other acidophilic microbes) and use them to generate testable hypotheses for bioleaching applications - recovering metals from ores and waste materials using microbial processes.

The intern will be based in Bangalore, working closely with a strong in-house Machine Learning team. The role also involves active collaboration with academic experts in biology, chemical engineering, and materials science across leading universities in India - making it a rare opportunity to work at the interface of computation, ML, and experimental science within a rich, cross-disciplinary network.

Day-to-day work involves building and refining genome-scale metabolic models (GEMs), running simulations to identify promising metabolic strategies for bioleaching, and translating those findings into experimental designs for collaborating wet-lab teams.

MUST HAVE

Hands-on familiarity with Genome-Scale Metabolic Models (GEMs) - building, curating, and validating themPractical experience with Flux Balance Analysis (FBA) and related methods (FVA - Flux Variability Analysis and its variations)Proficiency in Python for data analysis and scriptingWorking experience with COBRApy - loading SBML models, running FBA simulations, interpreting flux results

GOOD TO HAVE:

Familiarity with neural networks applied in synthetic biology - e.g. predicting promoter/enzyme strength, flux estimation, or gene circuit designComfort working alongside ML engineers and translating biological problems into ML-tractable formulationsKnowledge of G. oxydans or other acidophilic bacteriaBackground in bioleaching, biomining, or metal recovery processesExperience integrating omics data (transcriptomics, metabolomics) into metabolic modelsWet-lab or bioreactor exposure

QUALIFICATIONS: Masters in Bioinformatics, Computational Biology, Microbiology, or Biochemical Engineering.

SALARY DETAILS: Commensurate with experience

JOINING DATE : Immediate

CONTACT:

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India (Remote + Mumbai Lab Setup) Full-Time Supporting U.S. Operations IST - EST Overlap Required Reporting to: Director of Technical & Analytical Sciences - Hubot CDMO, South Bend, Indiana, USA

Build the science. Own the methods. Shape a lab from the ground up.

Hubot, Inc. is a U.S.-based CDMO serving Fortune 500 pharmaceutical and personal care brands across North America and globally. Through Hubot India Private Limited, we are building a world-class analytical function that operates in direct partnership with our U.S. Quality and Technical teams.

This is a dual-mandate role unlike most analytical positions in the market. You will simultaneously support U.S. lab operations remotely - overseeing method development, transfer, verification, and release data review - while also building and operationalizing Hubot India's analytical and testing laboratory in Mumbai from the ground up.

If you are a seasoned analytical chemist who wants to do more than run methods - this is your platform.

Why Hubot India ?

Lab Builder Opportunity Lead the physical and operational setup of a new analytical lab in Mumbai

Global Technical Exposure Direct collaboration with U.S. Analytical, Quality, and Regulatory teams

Growth-Stage Platform 25-30% YoY revenue growth forecast through 2030

Method Ownership Full lifecycle responsibility: development, transfer, validation, verification

Career Path Clear progression to Principal Scientist or Analytical Sciences Lead (India)

Role Overview:

This role has two equally important dimensions:

1 U.S. Operations Support (Remote) Serve as the analytical backbone for Hubot's U.S. lab reviewing testing and release data, owning method development and transfer activities, and providing expert troubleshooting support across chromatographic and spectrophotometric platforms.

2 Mumbai Lab Establishment Lead the planning, setup, qualification, and operationalization of Hubot India's analytical and testing laboratory including instrument procurement, SOP development, personnel hiring, and regulatory readiness.

This role requires 4 - 5 hours of daily overlap with U.S. Eastern Time ( 5:00-10:00 PM IST) as and when required.

Key Responsibilities

Method Development & Analytical Sciences

Independently perform method development, method transfer, method verification, and method validation for chromatographic and spectrophotometric techniques HPLC, UPLC, GC, TOC, UV/Vis, FTIR, and titrationServe as the primary method troubleshooting resource identify, document, and resolve critical factors affecting method performance across all platformsLead Cleaning Validation method development including swab and rinse sample method development and testing, MACO/limit calculations, TOC-based and HPLC/UPLC-based verification, and protocol and report authoringSupport Cleaning Validation sample testing and ensure alignment with FDA Cleaning Validation guidanceInterpret analytical data, compare results against specifications, and prepare trend reports and deviation assessmentsAuthor SOPs, analytical testing procedures, batch release testing forms, and document templatesAssist with laboratory investigations, deviations, and CAPA preparation and executionBecome the resident LIMS expert perform supervisory sign-off for electronic reports and oversee data integrity compliance

U.S. Lab Data Review & Release Support

Review routine and complex laboratory testing data for accuracy, GLP compliance, and specification conformanceReview and approve batch release testing data generated by U.S. lab team membersProvide guidance and mentorship to junior U.S. team members on method execution and complianceServe as point of contact for analytical project updates to U.S. laboratory supervision and clientsSupport scheduling and planning of internal and external client project work

Mumbai Lab Setup & Operationalization

Lead site selection, layout planning, and fit-out coordination for the Mumbai analytical laboratoryDefine instrument procurement list HPLC, UPLC, GC, TOC analyzer, FTIR, UV/Vis, and ancillary equipmentDevelop lab-specific SOPs, safety protocols, and quality systems aligned with GMP/GLP standardsOversee instrument qualification (IQ/OQ/PQ) and method transfer from U.S. to India labRecruit, onboard, and train analytical laboratory staff in MumbaiEstablish regulatory readiness for future customer audits and Indian regulatory requirements (CDSCO, BIS as applicable)

What You Bring

Core Instrumentation Expert Level Required

Demonstrated expert-level proficiency in HPLC, UPLC, GC, and TOC - including independent method development, validation, troubleshooting, and data interpretation on all four platformsHands-on experience with FTIR/ATR-FTIR, UV/Vis spectrophotometry, Karl Fischer titration, and dissolution testing

Method & Validation Expertise

8+ years of hands-on analytical chemistry experience in a GMP/GLP-regulated environment - pharmaceutical, OTC, personal care, or medical deviceDemonstrated experience in method development, method transfer, method validation per ICH Q2(R1), and method verification per USPProven expertise in Cleaning Validation - method development, swab/rinse sample testing, MACO limit calculations, TOC and HPLC/UPLC-based verification, and full protocol and report authoringFamiliarity with USP General Chapters, ICH Q2(R1), FDA 21 CFR 211 laboratory controls, and FDA Cleaning Validation guidance

Systems & Compliance

Experience with LIMS platforms and electronic data review systemsFamiliarity with 21 CFR Part 11 electronic records and data integrity requirementsProficiency in chromatography data systems -Agilent, Shimadzu and Thermo preferred

Lab Establishment

Prior experience in lab setup, instrument qualification (IQ/OQ/PQ), or greenfield laboratory establishment strongly preferredFamiliarity with CDSCO or Indian Pharmacopoeia (IP) requirements a plus for Mumbai lab regulatory readiness

Communication & Collaboration

Strong written English communication skills for cross-functional collaboration with U.S. teamsSelf-directed, detail-oriented, and capable of managing multiple priorities across time zonesBA/BS required, M.S. or Ph.D. in Analytical Chemistry, Pharmaceutical Sciences, or related field preferred

How We Measure Success

Method transfer and verification timelines met 95% on time U.S. batch release data review turnaround within defined SLA Cleaning Validation methods developed and approved per project timelines Mumbai lab operational milestone achieved Month 9-12 OOS/deviation rate on transferred methods LIMS supervisory sign-off compliance 100%

About Hubot India Private Limited

Hubot India is a wholly owned subsidiary of Hubot, Inc. (South Bend, Indiana, USA) established to build a world-class technical support function for our U.S. CDMO operations. This is a strategic scientific role with real ownership, real visibility, and a long-term career home.

Apply via LinkedIn or message for a confidential conversation

Read Less

India (Remote + Mumbai Lab Setup) Full-Time Supporting U.S. Operations IST - EST Overlap Required Reporting to: Director of Technical & Analytical Sciences - Hubot CDMO, South Bend, Indiana, USA

Build the science. Own the methods. Shape a lab from the ground up.

Hubot, Inc. is a U.S.-based CDMO serving Fortune 500 pharmaceutical and personal care brands across North America and globally. Through Hubot India Private Limited, we are building a world-class analytical function that operates in direct partnership with our U.S. Quality and Technical teams.

This is a dual-mandate role unlike most analytical positions in the market. You will simultaneously support U.S. lab operations remotely - overseeing method development, transfer, verification, and release data review - while also building and operationalizing Hubot India's analytical and testing laboratory in Mumbai from the ground up.

If you are a seasoned analytical chemist who wants to do more than run methods - this is your platform.

Why Hubot India ?

Lab Builder Opportunity Lead the physical and operational setup of a new analytical lab in Mumbai

Global Technical Exposure Direct collaboration with U.S. Analytical, Quality, and Regulatory teams

Growth-Stage Platform 25-30% YoY revenue growth forecast through 2030

Method Ownership Full lifecycle responsibility: development, transfer, validation, verification

Career Path Clear progression to Principal Scientist or Analytical Sciences Lead (India)

Role Overview:

This role has two equally important dimensions:

1 U.S. Operations Support (Remote) Serve as the analytical backbone for Hubot's U.S. lab reviewing testing and release data, owning method development and transfer activities, and providing expert troubleshooting support across chromatographic and spectrophotometric platforms.

2 Mumbai Lab Establishment Lead the planning, setup, qualification, and operationalization of Hubot India's analytical and testing laboratory including instrument procurement, SOP development, personnel hiring, and regulatory readiness.

This role requires 4 - 5 hours of daily overlap with U.S. Eastern Time ( 5:00-10:00 PM IST) as and when required.

Key Responsibilities

Method Development & Analytical Sciences

Independently perform method development, method transfer, method verification, and method validation for chromatographic and spectrophotometric techniques HPLC, UPLC, GC, TOC, UV/Vis, FTIR, and titrationServe as the primary method troubleshooting resource identify, document, and resolve critical factors affecting method performance across all platformsLead Cleaning Validation method development including swab and rinse sample method development and testing, MACO/limit calculations, TOC-based and HPLC/UPLC-based verification, and protocol and report authoringSupport Cleaning Validation sample testing and ensure alignment with FDA Cleaning Validation guidanceInterpret analytical data, compare results against specifications, and prepare trend reports and deviation assessmentsAuthor SOPs, analytical testing procedures, batch release testing forms, and document templatesAssist with laboratory investigations, deviations, and CAPA preparation and executionBecome the resident LIMS expert perform supervisory sign-off for electronic reports and oversee data integrity compliance

U.S. Lab Data Review & Release Support

Review routine and complex laboratory testing data for accuracy, GLP compliance, and specification conformanceReview and approve batch release testing data generated by U.S. lab team membersProvide guidance and mentorship to junior U.S. team members on method execution and complianceServe as point of contact for analytical project updates to U.S. laboratory supervision and clientsSupport scheduling and planning of internal and external client project work

Mumbai Lab Setup & Operationalization

Lead site selection, layout planning, and fit-out coordination for the Mumbai analytical laboratoryDefine instrument procurement list HPLC, UPLC, GC, TOC analyzer, FTIR, UV/Vis, and ancillary equipmentDevelop lab-specific SOPs, safety protocols, and quality systems aligned with GMP/GLP standardsOversee instrument qualification (IQ/OQ/PQ) and method transfer from U.S. to India labRecruit, onboard, and train analytical laboratory staff in MumbaiEstablish regulatory readiness for future customer audits and Indian regulatory requirements (CDSCO, BIS as applicable)

What You Bring

Core Instrumentation Expert Level Required

Demonstrated expert-level proficiency in HPLC, UPLC, GC, and TOC - including independent method development, validation, troubleshooting, and data interpretation on all four platformsHands-on experience with FTIR/ATR-FTIR, UV/Vis spectrophotometry, Karl Fischer titration, and dissolution testing

Method & Validation Expertise

8+ years of hands-on analytical chemistry experience in a GMP/GLP-regulated environment - pharmaceutical, OTC, personal care, or medical deviceDemonstrated experience in method development, method transfer, method validation per ICH Q2(R1), and method verification per USPProven expertise in Cleaning Validation - method development, swab/rinse sample testing, MACO limit calculations, TOC and HPLC/UPLC-based verification, and full protocol and report authoringFamiliarity with USP General Chapters, ICH Q2(R1), FDA 21 CFR 211 laboratory controls, and FDA Cleaning Validation guidance

Systems & Compliance

Experience with LIMS platforms and electronic data review systemsFamiliarity with 21 CFR Part 11 electronic records and data integrity requirementsProficiency in chromatography data systems -Agilent, Shimadzu and Thermo preferred

Lab Establishment

Prior experience in lab setup, instrument qualification (IQ/OQ/PQ), or greenfield laboratory establishment strongly preferredFamiliarity with CDSCO or Indian Pharmacopoeia (IP) requirements a plus for Mumbai lab regulatory readiness

Communication & Collaboration

Strong written English communication skills for cross-functional collaboration with U.S. teamsSelf-directed, detail-oriented, and capable of managing multiple priorities across time zonesBA/BS required, M.S. or Ph.D. in Analytical Chemistry, Pharmaceutical Sciences, or related field preferred

How We Measure Success

Method transfer and verification timelines met 95% on time U.S. batch release data review turnaround within defined SLA Cleaning Validation methods developed and approved per project timelines Mumbai lab operational milestone achieved Month 9-12 OOS/deviation rate on transferred methods LIMS supervisory sign-off compliance 100%

About Hubot India Private Limited

Hubot India is a wholly owned subsidiary of Hubot, Inc. (South Bend, Indiana, USA) established to build a world-class technical support function for our U.S. CDMO operations. This is a strategic scientific role with real ownership, real visibility, and a long-term career home.

Apply via LinkedIn or message for a confidential conversation

Read Less

India (Remote + Mumbai Lab Setup) Full-Time Supporting U.S. Operations IST - EST Overlap Required Reporting to: Director of Technical & Analytical Sciences - Hubot CDMO, South Bend, Indiana, USA

Build the science. Own the methods. Shape a lab from the ground up.

Hubot, Inc. is a U.S.-based CDMO serving Fortune 500 pharmaceutical and personal care brands across North America and globally. Through Hubot India Private Limited, we are building a world-class analytical function that operates in direct partnership with our U.S. Quality and Technical teams.

This is a dual-mandate role unlike most analytical positions in the market. You will simultaneously support U.S. lab operations remotely - overseeing method development, transfer, verification, and release data review - while also building and operationalizing Hubot India's analytical and testing laboratory in Mumbai from the ground up.

If you are a seasoned analytical chemist who wants to do more than run methods - this is your platform.

Why Hubot India ?

Lab Builder Opportunity Lead the physical and operational setup of a new analytical lab in Mumbai

Global Technical Exposure Direct collaboration with U.S. Analytical, Quality, and Regulatory teams

Growth-Stage Platform 25-30% YoY revenue growth forecast through 2030

Method Ownership Full lifecycle responsibility: development, transfer, validation, verification

Career Path Clear progression to Principal Scientist or Analytical Sciences Lead (India)

Role Overview:

This role has two equally important dimensions:

1 U.S. Operations Support (Remote) Serve as the analytical backbone for Hubot's U.S. lab reviewing testing and release data, owning method development and transfer activities, and providing expert troubleshooting support across chromatographic and spectrophotometric platforms.

2 Mumbai Lab Establishment Lead the planning, setup, qualification, and operationalization of Hubot India's analytical and testing laboratory including instrument procurement, SOP development, personnel hiring, and regulatory readiness.

This role requires 4 - 5 hours of daily overlap with U.S. Eastern Time ( 5:00-10:00 PM IST) as and when required.

Key Responsibilities

Method Development & Analytical Sciences

Independently perform method development, method transfer, method verification, and method validation for chromatographic and spectrophotometric techniques HPLC, UPLC, GC, TOC, UV/Vis, FTIR, and titrationServe as the primary method troubleshooting resource identify, document, and resolve critical factors affecting method performance across all platformsLead Cleaning Validation method development including swab and rinse sample method development and testing, MACO/limit calculations, TOC-based and HPLC/UPLC-based verification, and protocol and report authoringSupport Cleaning Validation sample testing and ensure alignment with FDA Cleaning Validation guidanceInterpret analytical data, compare results against specifications, and prepare trend reports and deviation assessmentsAuthor SOPs, analytical testing procedures, batch release testing forms, and document templatesAssist with laboratory investigations, deviations, and CAPA preparation and executionBecome the resident LIMS expert perform supervisory sign-off for electronic reports and oversee data integrity compliance

U.S. Lab Data Review & Release Support

Review routine and complex laboratory testing data for accuracy, GLP compliance, and specification conformanceReview and approve batch release testing data generated by U.S. lab team membersProvide guidance and mentorship to junior U.S. team members on method execution and complianceServe as point of contact for analytical project updates to U.S. laboratory supervision and clientsSupport scheduling and planning of internal and external client project work

Mumbai Lab Setup & Operationalization

Lead site selection, layout planning, and fit-out coordination for the Mumbai analytical laboratoryDefine instrument procurement list HPLC, UPLC, GC, TOC analyzer, FTIR, UV/Vis, and ancillary equipmentDevelop lab-specific SOPs, safety protocols, and quality systems aligned with GMP/GLP standardsOversee instrument qualification (IQ/OQ/PQ) and method transfer from U.S. to India labRecruit, onboard, and train analytical laboratory staff in MumbaiEstablish regulatory readiness for future customer audits and Indian regulatory requirements (CDSCO, BIS as applicable)

What You Bring

Core Instrumentation Expert Level Required

Demonstrated expert-level proficiency in HPLC, UPLC, GC, and TOC - including independent method development, validation, troubleshooting, and data interpretation on all four platformsHands-on experience with FTIR/ATR-FTIR, UV/Vis spectrophotometry, Karl Fischer titration, and dissolution testing

Method & Validation Expertise

8+ years of hands-on analytical chemistry experience in a GMP/GLP-regulated environment - pharmaceutical, OTC, personal care, or medical deviceDemonstrated experience in method development, method transfer, method validation per ICH Q2(R1), and method verification per USPProven expertise in Cleaning Validation - method development, swab/rinse sample testing, MACO limit calculations, TOC and HPLC/UPLC-based verification, and full protocol and report authoringFamiliarity with USP General Chapters, ICH Q2(R1), FDA 21 CFR 211 laboratory controls, and FDA Cleaning Validation guidance

Systems & Compliance

Experience with LIMS platforms and electronic data review systemsFamiliarity with 21 CFR Part 11 electronic records and data integrity requirementsProficiency in chromatography data systems -Agilent, Shimadzu and Thermo preferred

Lab Establishment

Prior experience in lab setup, instrument qualification (IQ/OQ/PQ), or greenfield laboratory establishment strongly preferredFamiliarity with CDSCO or Indian Pharmacopoeia (IP) requirements a plus for Mumbai lab regulatory readiness

Communication & Collaboration

Strong written English communication skills for cross-functional collaboration with U.S. teamsSelf-directed, detail-oriented, and capable of managing multiple priorities across time zonesBA/BS required, M.S. or Ph.D. in Analytical Chemistry, Pharmaceutical Sciences, or related field preferred

How We Measure Success

Method transfer and verification timelines met 95% on time U.S. batch release data review turnaround within defined SLA Cleaning Validation methods developed and approved per project timelines Mumbai lab operational milestone achieved Month 9-12 OOS/deviation rate on transferred methods LIMS supervisory sign-off compliance 100%

About Hubot India Private Limited

Hubot India is a wholly owned subsidiary of Hubot, Inc. (South Bend, Indiana, USA) established to build a world-class technical support function for our U.S. CDMO operations. This is a strategic scientific role with real ownership, real visibility, and a long-term career home.

Apply via LinkedIn or message for a confidential conversation

Read Less

India (Remote + Mumbai Lab Setup) Full-Time Supporting U.S. Operations IST - EST Overlap Required Reporting to: Director of Technical & Analytical Sciences - Hubot CDMO, South Bend, Indiana, USA

Build the science. Own the methods. Shape a lab from the ground up.

Hubot, Inc. is a U.S.-based CDMO serving Fortune 500 pharmaceutical and personal care brands across North America and globally. Through Hubot India Private Limited, we are building a world-class analytical function that operates in direct partnership with our U.S. Quality and Technical teams.

This is a dual-mandate role unlike most analytical positions in the market. You will simultaneously support U.S. lab operations remotely - overseeing method development, transfer, verification, and release data review - while also building and operationalizing Hubot India's analytical and testing laboratory in Mumbai from the ground up.

If you are a seasoned analytical chemist who wants to do more than run methods - this is your platform.

Why Hubot India ?

Lab Builder Opportunity Lead the physical and operational setup of a new analytical lab in Mumbai

Global Technical Exposure Direct collaboration with U.S. Analytical, Quality, and Regulatory teams

Growth-Stage Platform 25-30% YoY revenue growth forecast through 2030

Method Ownership Full lifecycle responsibility: development, transfer, validation, verification

Career Path Clear progression to Principal Scientist or Analytical Sciences Lead (India)

Role Overview:

This role has two equally important dimensions:

1 U.S. Operations Support (Remote) Serve as the analytical backbone for Hubot's U.S. lab reviewing testing and release data, owning method development and transfer activities, and providing expert troubleshooting support across chromatographic and spectrophotometric platforms.

2 Mumbai Lab Establishment Lead the planning, setup, qualification, and operationalization of Hubot India's analytical and testing laboratory including instrument procurement, SOP development, personnel hiring, and regulatory readiness.

This role requires 4 - 5 hours of daily overlap with U.S. Eastern Time ( 5:00-10:00 PM IST) as and when required.

Key Responsibilities

Method Development & Analytical Sciences

Independently perform method development, method transfer, method verification, and method validation for chromatographic and spectrophotometric techniques HPLC, UPLC, GC, TOC, UV/Vis, FTIR, and titrationServe as the primary method troubleshooting resource identify, document, and resolve critical factors affecting method performance across all platformsLead Cleaning Validation method development including swab and rinse sample method development and testing, MACO/limit calculations, TOC-based and HPLC/UPLC-based verification, and protocol and report authoringSupport Cleaning Validation sample testing and ensure alignment with FDA Cleaning Validation guidanceInterpret analytical data, compare results against specifications, and prepare trend reports and deviation assessmentsAuthor SOPs, analytical testing procedures, batch release testing forms, and document templatesAssist with laboratory investigations, deviations, and CAPA preparation and executionBecome the resident LIMS expert perform supervisory sign-off for electronic reports and oversee data integrity compliance

U.S. Lab Data Review & Release Support

Review routine and complex laboratory testing data for accuracy, GLP compliance, and specification conformanceReview and approve batch release testing data generated by U.S. lab team membersProvide guidance and mentorship to junior U.S. team members on method execution and complianceServe as point of contact for analytical project updates to U.S. laboratory supervision and clientsSupport scheduling and planning of internal and external client project work

Mumbai Lab Setup & Operationalization

Lead site selection, layout planning, and fit-out coordination for the Mumbai analytical laboratoryDefine instrument procurement list HPLC, UPLC, GC, TOC analyzer, FTIR, UV/Vis, and ancillary equipmentDevelop lab-specific SOPs, safety protocols, and quality systems aligned with GMP/GLP standardsOversee instrument qualification (IQ/OQ/PQ) and method transfer from U.S. to India labRecruit, onboard, and train analytical laboratory staff in MumbaiEstablish regulatory readiness for future customer audits and Indian regulatory requirements (CDSCO, BIS as applicable)

What You Bring

Core Instrumentation Expert Level Required

Demonstrated expert-level proficiency in HPLC, UPLC, GC, and TOC - including independent method development, validation, troubleshooting, and data interpretation on all four platformsHands-on experience with FTIR/ATR-FTIR, UV/Vis spectrophotometry, Karl Fischer titration, and dissolution testing

Method & Validation Expertise

8+ years of hands-on analytical chemistry experience in a GMP/GLP-regulated environment - pharmaceutical, OTC, personal care, or medical deviceDemonstrated experience in method development, method transfer, method validation per ICH Q2(R1), and method verification per USPProven expertise in Cleaning Validation - method development, swab/rinse sample testing, MACO limit calculations, TOC and HPLC/UPLC-based verification, and full protocol and report authoringFamiliarity with USP General Chapters, ICH Q2(R1), FDA 21 CFR 211 laboratory controls, and FDA Cleaning Validation guidance

Systems & Compliance

Experience with LIMS platforms and electronic data review systemsFamiliarity with 21 CFR Part 11 electronic records and data integrity requirementsProficiency in chromatography data systems -Agilent, Shimadzu and Thermo preferred

Lab Establishment

Prior experience in lab setup, instrument qualification (IQ/OQ/PQ), or greenfield laboratory establishment strongly preferredFamiliarity with CDSCO or Indian Pharmacopoeia (IP) requirements a plus for Mumbai lab regulatory readiness

Communication & Collaboration

Strong written English communication skills for cross-functional collaboration with U.S. teamsSelf-directed, detail-oriented, and capable of managing multiple priorities across time zonesBA/BS required, M.S. or Ph.D. in Analytical Chemistry, Pharmaceutical Sciences, or related field preferred

How We Measure Success

Method transfer and verification timelines met 95% on time U.S. batch release data review turnaround within defined SLA Cleaning Validation methods developed and approved per project timelines Mumbai lab operational milestone achieved Month 9-12 OOS/deviation rate on transferred methods LIMS supervisory sign-off compliance 100%

About Hubot India Private Limited

Hubot India is a wholly owned subsidiary of Hubot, Inc. (South Bend, Indiana, USA) established to build a world-class technical support function for our U.S. CDMO operations. This is a strategic scientific role with real ownership, real visibility, and a long-term career home.

Apply via LinkedIn or message for a confidential conversation

Read Less

India (Remote + Mumbai Lab Setup) Full-Time Supporting U.S. Operations IST - EST Overlap Required Reporting to: Director of Technical & Analytical Sciences - Hubot CDMO, South Bend, Indiana, USA

Build the science. Own the methods. Shape a lab from the ground up.

Hubot, Inc. is a U.S.-based CDMO serving Fortune 500 pharmaceutical and personal care brands across North America and globally. Through Hubot India Private Limited, we are building a world-class analytical function that operates in direct partnership with our U.S. Quality and Technical teams.

This is a dual-mandate role unlike most analytical positions in the market. You will simultaneously support U.S. lab operations remotely - overseeing method development, transfer, verification, and release data review - while also building and operationalizing Hubot India's analytical and testing laboratory in Mumbai from the ground up.

If you are a seasoned analytical chemist who wants to do more than run methods - this is your platform.

Why Hubot India ?

Lab Builder Opportunity Lead the physical and operational setup of a new analytical lab in Mumbai

Global Technical Exposure Direct collaboration with U.S. Analytical, Quality, and Regulatory teams

Growth-Stage Platform 25-30% YoY revenue growth forecast through 2030

Method Ownership Full lifecycle responsibility: development, transfer, validation, verification

Career Path Clear progression to Principal Scientist or Analytical Sciences Lead (India)

Role Overview:

This role has two equally important dimensions:

1 U.S. Operations Support (Remote) Serve as the analytical backbone for Hubot's U.S. lab reviewing testing and release data, owning method development and transfer activities, and providing expert troubleshooting support across chromatographic and spectrophotometric platforms.

2 Mumbai Lab Establishment Lead the planning, setup, qualification, and operationalization of Hubot India's analytical and testing laboratory including instrument procurement, SOP development, personnel hiring, and regulatory readiness.

This role requires 4 - 5 hours of daily overlap with U.S. Eastern Time ( 5:00-10:00 PM IST) as and when required.

Key Responsibilities

Method Development & Analytical Sciences

Independently perform method development, method transfer, method verification, and method validation for chromatographic and spectrophotometric techniques HPLC, UPLC, GC, TOC, UV/Vis, FTIR, and titrationServe as the primary method troubleshooting resource identify, document, and resolve critical factors affecting method performance across all platformsLead Cleaning Validation method development including swab and rinse sample method development and testing, MACO/limit calculations, TOC-based and HPLC/UPLC-based verification, and protocol and report authoringSupport Cleaning Validation sample testing and ensure alignment with FDA Cleaning Validation guidanceInterpret analytical data, compare results against specifications, and prepare trend reports and deviation assessmentsAuthor SOPs, analytical testing procedures, batch release testing forms, and document templatesAssist with laboratory investigations, deviations, and CAPA preparation and executionBecome the resident LIMS expert perform supervisory sign-off for electronic reports and oversee data integrity compliance

U.S. Lab Data Review & Release Support

Review routine and complex laboratory testing data for accuracy, GLP compliance, and specification conformanceReview and approve batch release testing data generated by U.S. lab team membersProvide guidance and mentorship to junior U.S. team members on method execution and complianceServe as point of contact for analytical project updates to U.S. laboratory supervision and clientsSupport scheduling and planning of internal and external client project work

Mumbai Lab Setup & Operationalization

Lead site selection, layout planning, and fit-out coordination for the Mumbai analytical laboratoryDefine instrument procurement list HPLC, UPLC, GC, TOC analyzer, FTIR, UV/Vis, and ancillary equipmentDevelop lab-specific SOPs, safety protocols, and quality systems aligned with GMP/GLP standardsOversee instrument qualification (IQ/OQ/PQ) and method transfer from U.S. to India labRecruit, onboard, and train analytical laboratory staff in MumbaiEstablish regulatory readiness for future customer audits and Indian regulatory requirements (CDSCO, BIS as applicable)

What You Bring

Core Instrumentation Expert Level Required

Demonstrated expert-level proficiency in HPLC, UPLC, GC, and TOC - including independent method development, validation, troubleshooting, and data interpretation on all four platformsHands-on experience with FTIR/ATR-FTIR, UV/Vis spectrophotometry, Karl Fischer titration, and dissolution testing

Method & Validation Expertise

8+ years of hands-on analytical chemistry experience in a GMP/GLP-regulated environment - pharmaceutical, OTC, personal care, or medical deviceDemonstrated experience in method development, method transfer, method validation per ICH Q2(R1), and method verification per USPProven expertise in Cleaning Validation - method development, swab/rinse sample testing, MACO limit calculations, TOC and HPLC/UPLC-based verification, and full protocol and report authoringFamiliarity with USP General Chapters, ICH Q2(R1), FDA 21 CFR 211 laboratory controls, and FDA Cleaning Validation guidance

Systems & Compliance

Experience with LIMS platforms and electronic data review systemsFamiliarity with 21 CFR Part 11 electronic records and data integrity requirementsProficiency in chromatography data systems -Agilent, Shimadzu and Thermo preferred

Lab Establishment

Prior experience in lab setup, instrument qualification (IQ/OQ/PQ), or greenfield laboratory establishment strongly preferredFamiliarity with CDSCO or Indian Pharmacopoeia (IP) requirements a plus for Mumbai lab regulatory readiness

Communication & Collaboration

Strong written English communication skills for cross-functional collaboration with U.S. teamsSelf-directed, detail-oriented, and capable of managing multiple priorities across time zonesBA/BS required, M.S. or Ph.D. in Analytical Chemistry, Pharmaceutical Sciences, or related field preferred

How We Measure Success

Method transfer and verification timelines met 95% on time U.S. batch release data review turnaround within defined SLA Cleaning Validation methods developed and approved per project timelines Mumbai lab operational milestone achieved Month 9-12 OOS/deviation rate on transferred methods LIMS supervisory sign-off compliance 100%

About Hubot India Private Limited

Hubot India is a wholly owned subsidiary of Hubot, Inc. (South Bend, Indiana, USA) established to build a world-class technical support function for our U.S. CDMO operations. This is a strategic scientific role with real ownership, real visibility, and a long-term career home.

Apply via LinkedIn or message for a confidential conversation

Read Less

India (Remote + Mumbai Lab Setup) Full-Time Supporting U.S. Operations IST - EST Overlap Required Reporting to: Director of Technical & Analytical Sciences - Hubot CDMO, South Bend, Indiana, USA

Build the science. Own the methods. Shape a lab from the ground up.

Hubot, Inc. is a U.S.-based CDMO serving Fortune 500 pharmaceutical and personal care brands across North America and globally. Through Hubot India Private Limited, we are building a world-class analytical function that operates in direct partnership with our U.S. Quality and Technical teams.

This is a dual-mandate role unlike most analytical positions in the market. You will simultaneously support U.S. lab operations remotely - overseeing method development, transfer, verification, and release data review - while also building and operationalizing Hubot India's analytical and testing laboratory in Mumbai from the ground up.

If you are a seasoned analytical chemist who wants to do more than run methods - this is your platform.

Why Hubot India ?

Lab Builder Opportunity Lead the physical and operational setup of a new analytical lab in Mumbai

Global Technical Exposure Direct collaboration with U.S. Analytical, Quality, and Regulatory teams

Growth-Stage Platform 25-30% YoY revenue growth forecast through 2030

Method Ownership Full lifecycle responsibility: development, transfer, validation, verification

Career Path Clear progression to Principal Scientist or Analytical Sciences Lead (India)

Role Overview:

This role has two equally important dimensions:

1 U.S. Operations Support (Remote) Serve as the analytical backbone for Hubot's U.S. lab reviewing testing and release data, owning method development and transfer activities, and providing expert troubleshooting support across chromatographic and spectrophotometric platforms.

2 Mumbai Lab Establishment Lead the planning, setup, qualification, and operationalization of Hubot India's analytical and testing laboratory including instrument procurement, SOP development, personnel hiring, and regulatory readiness.

This role requires 4 - 5 hours of daily overlap with U.S. Eastern Time ( 5:00-10:00 PM IST) as and when required.

Key Responsibilities

Method Development & Analytical Sciences

Independently perform method development, method transfer, method verification, and method validation for chromatographic and spectrophotometric techniques HPLC, UPLC, GC, TOC, UV/Vis, FTIR, and titrationServe as the primary method troubleshooting resource identify, document, and resolve critical factors affecting method performance across all platformsLead Cleaning Validation method development including swab and rinse sample method development and testing, MACO/limit calculations, TOC-based and HPLC/UPLC-based verification, and protocol and report authoringSupport Cleaning Validation sample testing and ensure alignment with FDA Cleaning Validation guidanceInterpret analytical data, compare results against specifications, and prepare trend reports and deviation assessmentsAuthor SOPs, analytical testing procedures, batch release testing forms, and document templatesAssist with laboratory investigations, deviations, and CAPA preparation and executionBecome the resident LIMS expert perform supervisory sign-off for electronic reports and oversee data integrity compliance

U.S. Lab Data Review & Release Support

Review routine and complex laboratory testing data for accuracy, GLP compliance, and specification conformanceReview and approve batch release testing data generated by U.S. lab team membersProvide guidance and mentorship to junior U.S. team members on method execution and complianceServe as point of contact for analytical project updates to U.S. laboratory supervision and clientsSupport scheduling and planning of internal and external client project work

Mumbai Lab Setup & Operationalization

Lead site selection, layout planning, and fit-out coordination for the Mumbai analytical laboratoryDefine instrument procurement list HPLC, UPLC, GC, TOC analyzer, FTIR, UV/Vis, and ancillary equipmentDevelop lab-specific SOPs, safety protocols, and quality systems aligned with GMP/GLP standardsOversee instrument qualification (IQ/OQ/PQ) and method transfer from U.S. to India labRecruit, onboard, and train analytical laboratory staff in MumbaiEstablish regulatory readiness for future customer audits and Indian regulatory requirements (CDSCO, BIS as applicable)

What You Bring

Core Instrumentation Expert Level Required

Demonstrated expert-level proficiency in HPLC, UPLC, GC, and TOC - including independent method development, validation, troubleshooting, and data interpretation on all four platformsHands-on experience with FTIR/ATR-FTIR, UV/Vis spectrophotometry, Karl Fischer titration, and dissolution testing

Method & Validation Expertise

8+ years of hands-on analytical chemistry experience in a GMP/GLP-regulated environment - pharmaceutical, OTC, personal care, or medical deviceDemonstrated experience in method development, method transfer, method validation per ICH Q2(R1), and method verification per USPProven expertise in Cleaning Validation - method development, swab/rinse sample testing, MACO limit calculations, TOC and HPLC/UPLC-based verification, and full protocol and report authoringFamiliarity with USP General Chapters, ICH Q2(R1), FDA 21 CFR 211 laboratory controls, and FDA Cleaning Validation guidance

Systems & Compliance

Experience with LIMS platforms and electronic data review systemsFamiliarity with 21 CFR Part 11 electronic records and data integrity requirementsProficiency in chromatography data systems -Agilent, Shimadzu and Thermo preferred

Lab Establishment

Prior experience in lab setup, instrument qualification (IQ/OQ/PQ), or greenfield laboratory establishment strongly preferredFamiliarity with CDSCO or Indian Pharmacopoeia (IP) requirements a plus for Mumbai lab regulatory readiness

Communication & Collaboration

Strong written English communication skills for cross-functional collaboration with U.S. teamsSelf-directed, detail-oriented, and capable of managing multiple priorities across time zonesBA/BS required, M.S. or Ph.D. in Analytical Chemistry, Pharmaceutical Sciences, or related field preferred

How We Measure Success

Method transfer and verification timelines met 95% on time U.S. batch release data review turnaround within defined SLA Cleaning Validation methods developed and approved per project timelines Mumbai lab operational milestone achieved Month 9-12 OOS/deviation rate on transferred methods LIMS supervisory sign-off compliance 100%

About Hubot India Private Limited

Hubot India is a wholly owned subsidiary of Hubot, Inc. (South Bend, Indiana, USA) established to build a world-class technical support function for our U.S. CDMO operations. This is a strategic scientific role with real ownership, real visibility, and a long-term career home.

Apply via LinkedIn or message for a confidential conversation

Read Less

India (Remote + Mumbai Lab Setup) Full-Time Supporting U.S. Operations IST - EST Overlap Required Reporting to: Director of Technical & Analytical Sciences - Hubot CDMO, South Bend, Indiana, USA

Build the science. Own the methods. Shape a lab from the ground up.

Hubot, Inc. is a U.S.-based CDMO serving Fortune 500 pharmaceutical and personal care brands across North America and globally. Through Hubot India Private Limited, we are building a world-class analytical function that operates in direct partnership with our U.S. Quality and Technical teams.

This is a dual-mandate role unlike most analytical positions in the market. You will simultaneously support U.S. lab operations remotely - overseeing method development, transfer, verification, and release data review - while also building and operationalizing Hubot India's analytical and testing laboratory in Mumbai from the ground up.

If you are a seasoned analytical chemist who wants to do more than run methods - this is your platform.

Why Hubot India ?

Lab Builder Opportunity Lead the physical and operational setup of a new analytical lab in Mumbai

Global Technical Exposure Direct collaboration with U.S. Analytical, Quality, and Regulatory teams

Growth-Stage Platform 25-30% YoY revenue growth forecast through 2030

Method Ownership Full lifecycle responsibility: development, transfer, validation, verification

Career Path Clear progression to Principal Scientist or Analytical Sciences Lead (India)

Role Overview:

This role has two equally important dimensions:

1 U.S. Operations Support (Remote) Serve as the analytical backbone for Hubot's U.S. lab reviewing testing and release data, owning method development and transfer activities, and providing expert troubleshooting support across chromatographic and spectrophotometric platforms.

2 Mumbai Lab Establishment Lead the planning, setup, qualification, and operationalization of Hubot India's analytical and testing laboratory including instrument procurement, SOP development, personnel hiring, and regulatory readiness.

This role requires 4 - 5 hours of daily overlap with U.S. Eastern Time ( 5:00-10:00 PM IST) as and when required.

Key Responsibilities

Method Development & Analytical Sciences

Independently perform method development, method transfer, method verification, and method validation for chromatographic and spectrophotometric techniques HPLC, UPLC, GC, TOC, UV/Vis, FTIR, and titrationServe as the primary method troubleshooting resource identify, document, and resolve critical factors affecting method performance across all platformsLead Cleaning Validation method development including swab and rinse sample method development and testing, MACO/limit calculations, TOC-based and HPLC/UPLC-based verification, and protocol and report authoringSupport Cleaning Validation sample testing and ensure alignment with FDA Cleaning Validation guidanceInterpret analytical data, compare results against specifications, and prepare trend reports and deviation assessmentsAuthor SOPs, analytical testing procedures, batch release testing forms, and document templatesAssist with laboratory investigations, deviations, and CAPA preparation and executionBecome the resident LIMS expert perform supervisory sign-off for electronic reports and oversee data integrity compliance

U.S. Lab Data Review & Release Support

Review routine and complex laboratory testing data for accuracy, GLP compliance, and specification conformanceReview and approve batch release testing data generated by U.S. lab team membersProvide guidance and mentorship to junior U.S. team members on method execution and complianceServe as point of contact for analytical project updates to U.S. laboratory supervision and clientsSupport scheduling and planning of internal and external client project work

Mumbai Lab Setup & Operationalization

Lead site selection, layout planning, and fit-out coordination for the Mumbai analytical laboratoryDefine instrument procurement list HPLC, UPLC, GC, TOC analyzer, FTIR, UV/Vis, and ancillary equipmentDevelop lab-specific SOPs, safety protocols, and quality systems aligned with GMP/GLP standardsOversee instrument qualification (IQ/OQ/PQ) and method transfer from U.S. to India labRecruit, onboard, and train analytical laboratory staff in MumbaiEstablish regulatory readiness for future customer audits and Indian regulatory requirements (CDSCO, BIS as applicable)

What You Bring

Core Instrumentation Expert Level Required

Demonstrated expert-level proficiency in HPLC, UPLC, GC, and TOC - including independent method development, validation, troubleshooting, and data interpretation on all four platformsHands-on experience with FTIR/ATR-FTIR, UV/Vis spectrophotometry, Karl Fischer titration, and dissolution testing

Method & Validation Expertise

8+ years of hands-on analytical chemistry experience in a GMP/GLP-regulated environment - pharmaceutical, OTC, personal care, or medical deviceDemonstrated experience in method development, method transfer, method validation per ICH Q2(R1), and method verification per USPProven expertise in Cleaning Validation - method development, swab/rinse sample testing, MACO limit calculations, TOC and HPLC/UPLC-based verification, and full protocol and report authoringFamiliarity with USP General Chapters, ICH Q2(R1), FDA 21 CFR 211 laboratory controls, and FDA Cleaning Validation guidance

Systems & Compliance

Experience with LIMS platforms and electronic data review systemsFamiliarity with 21 CFR Part 11 electronic records and data integrity requirementsProficiency in chromatography data systems -Agilent, Shimadzu and Thermo preferred

Lab Establishment

Prior experience in lab setup, instrument qualification (IQ/OQ/PQ), or greenfield laboratory establishment strongly preferredFamiliarity with CDSCO or Indian Pharmacopoeia (IP) requirements a plus for Mumbai lab regulatory readiness

Communication & Collaboration

Strong written English communication skills for cross-functional collaboration with U.S. teamsSelf-directed, detail-oriented, and capable of managing multiple priorities across time zonesBA/BS required, M.S. or Ph.D. in Analytical Chemistry, Pharmaceutical Sciences, or related field preferred

How We Measure Success

Method transfer and verification timelines met 95% on time U.S. batch release data review turnaround within defined SLA Cleaning Validation methods developed and approved per project timelines Mumbai lab operational milestone achieved Month 9-12 OOS/deviation rate on transferred methods LIMS supervisory sign-off compliance 100%

About Hubot India Private Limited

Hubot India is a wholly owned subsidiary of Hubot, Inc. (South Bend, Indiana, USA) established to build a world-class technical support function for our U.S. CDMO operations. This is a strategic scientific role with real ownership, real visibility, and a long-term career home.

Apply via LinkedIn or message for a confidential conversation

Read Less

About Iba Cosmetics:

Iba Cosmetics is India's first Halal Certified & Vegan cosmetics brand with a portfolio of 100+ SKUs across skincare, haircare and makeup that deliver proven results along with being completely free of animal-derived ingredients, alcohol, sulphates, and parabens. Our unique differentiator along with excellent product reviews, wide availability pan-India - both online across all major portals and offline across many retail counters and high brand loyalty and repeat purchase rates makes us one of the fastest growing beauty and cosmetics brand in India.

Iba was launched in 2014 and since then has received three rounds of funding from well-known VCs and MNCs to further accelerate its growth.

Job Tile - Cosmetics Production Chemist

Qualifications - B.Sc Chemistry/B.Tech Cosmetology or Higher

Should have min. 2 - 3 years prior experience in cosmetics / personal care production of products such as creams, lotions, shampoo, hair oil, lipsticks, etc.

Job location - Vatva

(candidate should be able to commute to the location using his/her own vehicle)

Expected CTC range - 30 k - 50 k per month (depending on experience)

Job Description -

Documentation Management: Creating and maintaining accurate and comprehensive Product Information Files (PIF), batch manufacturing records, ingredient lists, safety data sheets (MSDS), and technical reports for all products. Liaison with Loan License Manufacturing Partner: Collaborating closely with the technical staff and quality control teams at the third-party (licensed) manufacturing facility to ensure all processes align with the agreed-upon specifications and quality standards.Production Supervision - Supervise all bulk manufacturing happening at the loan license location, ensure proper dispensation, batch manufacturing, filling and packaging. Fill the BMRs online with the requisite details. Auditing and Inspection Readiness: Supporting regulatory authority inspections and audits of the manufacturing facility by providing necessary documentation and technical expertise.Labeling and Packaging Review: Ensuring product labeling, and packaging is carried out by the manufacturing partner as per internal quality and visual standards. Quality Control Oversight: Working with the manufacturing partner's QC team to establish and monitor quality control checks for raw materials, in-process samples, and finished products.Collaboration: Working with the manufacturing partner and Ecotrail's supply chain, warehouse teams to ensure production stays on track at the loan license facility and be the one point contact for all production related matters for Ecotrail at the loan license partner's facility. Innovation: Staying updated on industry trends, new ingredients, and technologies to drive continuous improvement and innovation. In essence, the cosmetic chemist with loan license responsibilities acts as a bridge between the product concept and compliant, high-quality mass production via a third party, while holding accountability for the product's quality, effectiveness, and safety under that licensing arrangement.

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Key Responsibilities:

Providing scientific and regulatory expertise in ecotoxicology to support the development, registration, and lifecycle management of crop protection products.Ensures that ecotoxicological risk assessments comply with global regulatory requirements.Provide scientific input to product stewardship strategies and sustainability initiatives.Support internal and external scientific discussions, including meetings with regulatory authorities and contract research organizations (CROs).Monitor and interpret changes in international ecotoxicology regulations and guidance documents.Monitoring and constant improvement of collaboration with CROs concerning quality and timeline.The interaction with the respective regulatory authorities, pre- and post-submission.Consulting of Research for Phase 1 and Phase 2 chemistry projects concerning regulatory requirements and constraints for upcoming pipeline candidates.Support of the preparation of Phase 3 decisions. Read Less

Key Responsibilities:

Providing scientific and regulatory expertise in ecotoxicology to support the development, registration, and lifecycle management of crop protection products.Ensures that ecotoxicological risk assessments comply with global regulatory requirements.Provide scientific input to product stewardship strategies and sustainability initiatives.Support internal and external scientific discussions, including meetings with regulatory authorities and contract research organizations (CROs).Monitor and interpret changes in international ecotoxicology regulations and guidance documents.Monitoring and constant improvement of collaboration with CROs concerning quality and timeline.The interaction with the respective regulatory authorities, pre- and post-submission.Consulting of Research for Phase 1 and Phase 2 chemistry projects concerning regulatory requirements and constraints for upcoming pipeline candidates.Support of the preparation of Phase 3 decisions. Read Less

We are Hiring: Bioinformatics Trainer

Organization: Cliniwave Institute LLP

Location: Remote

Type: Freelance / Part-time

Role Overview

Cliniwave is looking for a passionate Bioinformatics Trainer to deliver industry-oriented training to students and professionals aspiring to build careers in bioinformatics, genomics, and computational biology.

Key ResponsibilitiesDeliver live, interactive training sessions in BioinformaticsTeach foundational to advanced bioinformatics conceptsTrain learners in sequence analysis, genomics, and NGS workflowsProvide hands-on training using real biological datasetsGuide students on tools, pipelines, and research workflowsSupport assignments, projects, and capstone mentoringContribute to curriculum design and learning materials

Required Skills & ExpertiseStrong knowledge of Bioinformatics and Computational BiologyHands-on experience with sequence analysis & genomics dataFamiliarity with NGS data analysis workflowsProficiency in Python and/or R for biological data analysisExperience with Linux/Unix environmentsFamiliarity with tools like BLAST, Clustal, and bioinformatics databasesUnderstanding of statistics and biological data interpretationPrior teaching or corporate training experience preferred

EligibilityBioinformatics ProfessionalsComputational BiologistsGenomics/NGS Data AnalystsResearchers and Industry ExpertsFreelance Trainers welcome

What We OfferFlexible engagement modelsOpportunity to train future bioinformatics professionalsCompetitive session-based compensationAcademic & industry exposure

How to Apply

Send your CV to:

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Design, select, and oversee environmental fate and degradation studies in accordance with international guidelines (e.g. OECD, EPA, IBAMA).Provide expert interpretation of laboratory and field studies, including Soil degradation OECD 307); Aquatic sediment studies (OECD 308); Anaerobic soil metabolism (OECD 311); Adsorption/desorption (OECD 106), Hydrolysis (OECD 111), Photolysis in water and soil (OECD 316), Volatilization and dissipation studies.Evaluate degradation kinetics (DT50, DT90), metabolite profiles, mass balance, and pathway elucidation.Support higher-tier studies and risk refinement when required (e.g. field dissipation, modelling).Monitoring and constant improvement of collaboration with CROs concerning quality and timeline.The interaction with the respective regulatory authorities, pre- and post-submission.Consulting of Research for Phase 1 and Phase 2 chemistry projects concerning regulatory requirements and constraints for upcoming pipeline candidates.Support of the preparation of Phase 3 decisions. Read Less

Design, select, and oversee environmental fate and degradation studies in accordance with international guidelines (e.g. OECD, EPA, IBAMA).Provide expert interpretation of laboratory and field studies, including Soil degradation OECD 307); Aquatic sediment studies (OECD 308); Anaerobic soil metabolism (OECD 311); Adsorption/desorption (OECD 106), Hydrolysis (OECD 111), Photolysis in water and soil (OECD 316), Volatilization and dissipation studies.Evaluate degradation kinetics (DT50, DT90), metabolite profiles, mass balance, and pathway elucidation.Support higher-tier studies and risk refinement when required (e.g. field dissipation, modelling).Monitoring and constant improvement of collaboration with CROs concerning quality and timeline.The interaction with the respective regulatory authorities, pre- and post-submission.Consulting of Research for Phase 1 and Phase 2 chemistry projects concerning regulatory requirements and constraints for upcoming pipeline candidates.Support of the preparation of Phase 3 decisions. Read Less