About Lluminae

Lluminae is a premier integrative skin and hair aesthetics clinic located in WTC Kharadi, Pune.

Designed as a 'Sanctuary in the Chaos,' it blends advanced clinical science with holistic, root-cause therapies.

Focuses on delivering a premium, calming, and results-driven client experience.

Role Overview

Deliver exceptional in-room client experiences through advanced aesthetic treatments.

Operate and master laser technologies while maintaining a calming, luxury environment.

Serve as a key touchpoint in defining the client's physical and emotional experience.

Core Competencies & Attributes

Bring a calm, grounded presence into every treatment session.

Maintain impeccable hygiene and room standards at all times.

Demonstrate emotional intelligence in adapting communication style to client needs.

Continuously evolve skills across both holistic and clinical treatments.

Technical Responsibilities

Operate Laser Hair Removal systems (Diode, Nd:YAG) with precision and safety.

Perform facials, extractions, and massages with high manual dexterity.

Handle devices such as HydraFacial, microneedling, LED therapy, and Q-switch prep.

Recommend skincare and treatment packages in a consultative, non-salesy manner.

Qualifications & Requirements

Diploma in Beauty Therapy, Cosmetology, or Medical Aesthetics.

CIDESCO or CIBTAC certification preferred.

Strong understanding of laser physics, Fitzpatrick scale, and safety protocols.

Knowledge of skincare ingredients and post-treatment care.

Basic understanding of facial anatomy and lymphatic system.

What Lluminae Offers

Access to world-class lasers and premium infrastructure.

Opportunity to work with a high-value corporate clientele.

Continuous training on global protocols and new technologies.

Clear growth path toward senior leadership roles.

To Apply:

Please send your CV along with a short cover letter explaining your philosophy on "Integrative Aesthetics" and why you are ready to transition into a premium luxury clinic environment to .

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ABOUT QI SPINE :

Founded when surgery was the only mainstream solution to back pain, QI Spine emerged with a simple idea: non-surgical recovery should be the first option, not the last resort. Since then, we've built India's only spine-focused medical system - combining the expertise of 250+ specialists with cutting-edge AI tools like Doctor QI, our proprietary diagnostic engine. With 22 clinics across major cities, we've:

Consulted over 2.5 lakh patients

Prevented 15,000+ unnecessary spine surgeries

Achieved a 95% recovery rate - among the best in the world

Our Mission :

To redefine spine care by blending clinical excellence, intelligent systems, and strong operational discipline.

Role requirement - Freshers

Post Training - Job Responibilities

Doing a comprehensive first consultation with patients arriving at the accurate final diagnosis of his/ her conditionExplaining the diagnosis, the treatment approach and outcomes to be expected post treatment to the patient and convincing them to start treatment with us. Ensuring complete case hand-overs to the Patient Counsellors or other Doctors when needed to ensure smooth patient handling journey Administering treatment to the patients as per the defined Plan of Care.Tracking progress of the patient throughout the treatment journey to ensure outcomes are achieved in a timely mannerContinuous expectation setting with patients on the importance of being compliant with the treatment and home exercise programs to ensure treatment of the root cause for full recovery and not just pain reductionRecommending the supoort needed by patients to maintain their posture while doing their daily activities Maintaining all records of patients diagnosis, treatment and outcomes on the app and keeping it updated real timeCoordinating with the central escalations team or with other internal medical specialists (ortho, neuro) to ensure the right medical intervention for the patient ensuring holistic patient careCollaborating with the virtual team and ensuring complete case overs to ensure that patients who are unable to travel regularly for their treatment to the clinic are getting the desired treatment virtually.

Expected Skills & Behaviour

Work collaboratively with the clinic team and cross functional teams ensuring excellent patient treatment and experience in the clinic at all times. Highest levels of patient ownership and ownership for the organisation when representing it in front of the patientContinuous learning to excel clinically and as a Doctor overall

Qualifications :

Min BPTh

Shift Timings:

Shift 1 - 7am to 3pmShift 2 - 1pm to 9pm.It is pre-requisite for interested applicants to be open to working in either shifts.

Working days

6 days working with 1 weekly off (Our clinics are open on all days of the week and hence Sundays is a working day for the Doctors. They will however receive their weekly off during one of the weekdays)

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Company Description

docfliq is a medical knowledge and medico-marketing company partnering with global pharma medical affairs teams across MEA, Europe, APAC, and LatAm. We design and deliver Delphi consensus programs, KAP studies, real-world evidence, accredited HCP education, and capacity-building suites across therapy areas including vaccines, cardiovascular rare disease, hematology, neurology, oncology, IBD, and infectious disease. Our clients are leading global innovative pharma companies. With offices in Dubai, Singapore, and India, docfliq sits at the intersection of scientific rigor, editorial craft, and AI-enabled HCP engagement.

Role Description

This is a senior, full-time role based in Dubai (UAE residents) or Mumbai, hybrid with 2 to 3 days in office. Fully remote considered for exceptional candidates.

The Senior Manager, Medical Affairs will lead scientific strategy and narrative across 4 to 6 concurrent client programs. Responsibilities include shaping the scientific story arc for Delphi consensus programs, KAP studies, advisory boards, and accredited HCP certification programs. The role involves writing and owning HCP-grade content end to end, including scientific decks, accredited learning modules, expert briefing documents, and manuscript-style deliverables.

The candidate will partner directly with pharma medical affairs counterparts at affiliate, regional, and global level, and will hold scientific discussions with KOLs and internal medical leads. They will translate clinical evidence into stories that move HCPs, working alongside the design team to ensure the science survives the journey from manuscript to slide.

This is a peer seat on a senior team. Work ships under the candidate's name.

The candidate will also help shape the scientific layer of docfliq 2.0, our next-generation AI-enabled platform for HCP medical education, currently in build.

Qualifications

Clinical or life sciences foundation (MD, MBBS, PharmD, PhD, or equivalent depth)

5+ years in pharma medical affairs, MSL leadership, or a tier-1 medical communications agency working on global or regional pharma accounts. Years flexible for exceptional candidates

Genuine command of at least one major therapy area, with the ability to debate trial design, not just summarise it

Proven portfolio of scientific narrative work, including decks, advisory board reports, accredited modules, or publications

Excellent written English. This role is approximately 60 percent writing

Comfort working with global pharma stakeholders across time zones

Maturity to navigate sensitive client conversations

Good to have

HEOR or evidence generation exposure (burden of disease, value dossiers, RWE protocols)

Slide craft and visual storytelling instincts

Experience with accredited learning frameworks (CME, CPD, SCFHS, EACCME, RCP, UCL, or similar)

Working knowledge of MEA, Europe, APAC, or LatAm pharma markets

Seniority Level

Head level. Open to Director for exceptional candidates.

How to Apply

Send your CV along with 2 to 3 work samples (decks, modules, advisory board reports, or publications you led the scientific narrative on) to , with and in copy.

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At Continental Hospitals, we are committed to delivering world-class, patient-centric healthcare driven by clinical excellence, innovation, and compassion. As one of the leading tertiary care hospitals, we bring together cutting-edge technology, advanced infrastructure, and a highly accomplished multidisciplinary team to provide superior outcomes across specialties. Our culture fosters continuous learning, collaboration, and ethical medical practice, empowering consultants to thrive in a dynamic and progressive environment. Joining Continental Hospitals means being part of a vision that is redefining healthcare standards while making a meaningful difference in patients' lives every day.

Job Summary

We are seeking a skilled and compassionate Rheumatologist to join our clinical team. The ideal candidate will be responsible for diagnosing and managing a wide range of autoimmune and musculoskeletal disorders, delivering high-quality patient care, and contributing to multidisciplinary treatment approaches within the hospital.

Key Responsibilities

Diagnose and manage conditions such as:Rheumatoid Arthritis, Gout, Psoriatic ArthritisSystemic Lupus Erythematosus (SLE)Systemic Sclerosis (Scleroderma)Myositis, Sarcoidosis, Childhood ArthritisProvide specialized services including:IVIG (Intravenous Immunoglobulin) therapyArthritis and pain managementTreatment of inflammatory eye diseases related to rheumatologic conditionsDevelop and implement individualized treatment plansMonitor patient progress and adjust therapies accordinglyCollaborate with orthopedics, dermatology, ophthalmology, and other specialtiesConduct OPD and IPD consultationsEnsure accurate clinical documentation and adherence to hospital protocolsEducate patients and families on disease management and lifestyle modifications

Required Qualifications

MBBS MD - General Medicine DM - Rheumatology

Skills & Competencies

Strong clinical expertise in autoimmune and inflammatory disordersExperience in advanced therapies (IVIG, immunosuppressants, biologics)Excellent diagnostic and decision-making skillsStrong communication and patient counseling abilitiesAbility to work effectively in a multidisciplinary hospital environmentPatient-centric, empathetic, and ethical approach

Key Attributes

Detail-oriented and process-drivenStrong collaboration and coordination skillsCommitment to continuous learning and clinical excellence

What We Offer

Opportunity to work in a tertiary care hospital setupAccess to advanced diagnostics and multidisciplinary teamsCompetitive compensation and career growth opportunities

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Company Description

Brain Bristle is a not-for-profit foundation for autism and inclusion, currently based in Mumbai. The organization works with low-income schools across the city to build high-quality education, exposure, and inclusion for students on the autism spectrum and other high learning needs. Brain Bristle focuses on building inclusive school environments from the ground-up, strengthening advocacy for autism, and conducting workshops and awareness programs to expand the reach and impact of its work.

Role Description

This role is for a Special Education Team Lead at Brain Bristle in Mumbai. The Team Lead will be responsible for supervising and supporting our social work team's work across the schools we work at in Mumbai. This will include working with our team on pedagogy, planning & organization, lesson planning, streamlining processes and accelerating impact across schools and helping plan team trainings.

Qualifications

3+ years experience working with students with autism and other learning disabilities.Teaching experience, particularly in a low income school settingSpecial education and autism education and expertiseStrong impact reporting, data management and communication skillsBachelor's degree in Special Education, Autism or related fieldKnowledge of autism and other developmental disordersUnderstanding of inclusive education practices Read Less

Company Description

Opal Dentistry is a specialist-driven dental clinic renowned for cosmetic dental services, including smile design with veneers and Invisalign, holding the prestigious Black Diamond Invisalign status. Located in Bengaluru, the clinic offers a range of services, from general dental check-ups to full-mouth rehabilitation, all within a sterile and advanced environment. Equipped with the latest technology, Opal Dentistry boasts a team of highly trained specialists. Led by Dr. Kirubaharan MDS, Chief Doctor and Orthodontist, the clinic has transformed over 16,000 smiles successfully.

Role Description

This is a full-time on-site role for a Dentist, based in Bengaluru. The Dentist will be responsible for providing patient care, including routine check-ups, treatment planning, dental procedures, and patient education. Additional responsibilities include identifying dental health problems, recommending therapeutic or corrective procedures, and maintaining accurate patient records. Collaboration with a team of specialists and staying updated with advancements in dental treatments and techniques are integral to this position.

Qualifications

Proficiency in General Dentistry procedures and advanced treatments, including veneers and InvisalignStrong patient care abilities, including communication, consultation, and educationFamiliarity with the latest dental technology and equipmentAttention to detail and precision in diagnosing and performing treatmentsAbility to work collaboratively in a specialist-driven team environmentBDSCommitment to maintaining a sterile, safe, and patient-friendly environment Read Less

Job Description:

Chandigarh University is seeking a dedicated and knowledgeable Assistant Professor in the Pharmacy department. The ideal candidate will contribute to the academic growth of the institution by engaging in teaching, research, and community service. The individual will be responsible for delivering high-quality instruction, developing curriculum, and mentoring students to ensure their academic and professional success. Additionally, the Assistant Professor will engage in scholarly research activities and publish findings in reputable journals.

Key Responsibilities:

- Teach undergraduate and/or graduate courses in Pharmacy.

- Prepare course materials such as syllabi, lectures, assignments, and assessments.

- Assess students' progress and provide constructive feedback.

- Mentor and advise students on their academic and career pathways.

- Conduct and publish original research.

- Participate in departmental, university, and community service activities.

- Stay updated with advancements in the field of Pharmacy.

Skills and Tools Required:

- Strong knowledge of pharmacy practice, pharmaceutical sciences, and relevant technologies.

- Excellent communication and interpersonal skills.

- Proficiency in curriculum development and instructional strategies.

- Familiarity with research methodologies and data analysis tools.

- Ability to work collaboratively in a multidisciplinary team.

- Strong organizational skills and attention to detail.

- Proficiency in using educational tools and software for instruction and assessment.

Required Qualifications:

- Pharm D/Ph.D. in Pharmacy ( Pharmaceutics/Pharmaceutical Chemistry)

- Prior teaching experience at the university level is preferred.

- A track record of research publications in peer-reviewed journals.

- Commitment to continuous professional development and staying abreast of industry trends.

Candidates who meet the above qualifications are encouraged to apply and join a dynamic team dedicated to advancing health education and research at Chandigarh University.

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Medtek Dot AI Pvt limited is a data science consulting company supporting global Pharma and Biotech companies.

Our mission is to help "Unlock insights and drive innovations" using the data collected. We are a team of Biostatistician, Data Managers, Programmer s, Engineers and AI developers.

Job Summary

We are seeking an experienced and detail-oriented Lead Clinical Data Manager to oversee data management activities across clinical trials for pharmaceutical and biotech clients. The ideal candidate will ensure high-quality clinical data is collected, processed, and delivered in compliance with regulatory standards and timelines.

Key Responsibilities

Lead and Manage the assigned Phase1/2/3 Clinical study/studies and makes expert recommendations and/or decisions that assure timelines, deliverables and data quality.

Review EDC design, UAT, study metrics and data quality report

End-to-End CDM expertise

Strong knowledge of Rave EDC

Project Management (Min 5 yrs)

Vendor & Stakeholder Management

Develop and review data management plans (DMP), CRFs/eCRFs, edit checks, and database specifications.

Coordinate with cross-functional teams including Biostatistics, Clinical Operations, Medical Writing, and Regulatory Affairs.

Oversee database design, testing, and validation in EDC systems (e.g., Medidata Rave, Oracle InForm, or similar).

Perform ongoing data review, discrepancy management, query generation and resolution.

Ensure timely database lock, database freeze, and quality deliverables in accordance with project timelines.

Monitor compliance with ICH-GCP, CDISC, FDA, EMA, and other regulatory guidelines.

Act as primary point of contact for clients regarding data management activities.

Reconcile Safety and Efficacy Data

Qualifications

Education & Experience:

Bachelor's or Master's degree in Life Sciences, Pharmacy, Health Informatics, or related field.10+years of clinical data management experience in CRO, pharmaceutical, or biotech industry.Experience with EDC systems (e.g., Medidata Rave, Oracle InForm).

Skills:

Strong understanding of clinical trial processes and GCP.Knowledge of CDISC standards (SDTM), MedDRA, and WHO Drug dictionaries.Excellent attention to detail and problem-solving skills.Strong communication, organizational, and project management skills.Ability to work independently and in a fast-paced, team-oriented environment.

Preferred Qualifications

Experience with oncology, rare disease, or other complex therapeutic areas.Familiarity with programming languages such as SAS or SQL is a plus.CDM certification (e.g., CCDM from SCDM) is an advantage. Read Less

Senior Regulatory Affairs Specialist

Experience: 6-8 Years

Domain: Medical Devices / Combination Products

Role Overview

We are looking for an experienced Regulatory Affairs Specialist with strong expertise in combination products and medical device regulatory submissions. The role involves supporting client engagements focused on preparation, review, maintenance, and lifecycle management of regulatory dossiers and technical documentation for combination products across global markets.

The ideal candidate will work closely with cross-functional client teams including Regulatory Affairs, R&D, Quality, and Clinical functions to ensure submissions are compliant, submission-ready, and aligned with evolving regulatory requirements.

Key Responsibilities

Regulatory Dossier & Technical Documentation

Prepare, compile, review, and maintain regulatory dossiers and technical files for combination products in accordance with applicable global regulations.Support submission activities for drug-device and biologic-device combination products across markets including EU and US.Maintain and update technical documentation throughout the product lifecycle, ensuring ongoing compliance and audit readiness.Review product labeling, IFUs, clinical documentation, risk management files, and supporting technical data for regulatory adequacy.

Client & Cross-Functional Collaboration

Partner directly with client stakeholders, including Regulatory, Quality, R&D, Clinical, and Manufacturing teams, to collect and validate submission documentation.Participate in regulatory strategy discussions and provide recommendations to address submission gaps or compliance risks.Coordinate document reviews, approvals, and submission deliverables within defined timelines.

Compliance & Regulatory Support

Assess regulatory changes and industry standards impacting combination products and provide guidance on implementation.Support gap assessments, remediation activities, and submission readiness reviews.Ensure documentation aligns with applicable standards including EU MDR, FDA regulations, ISO standards, and ICH guidelines.Track submission milestones, regulatory commitments, and documentation status to support timely execution.

Required Qualifications

Bachelor's or Master's degree in Life Sciences, Pharmacy, Biomedical Engineering, Regulatory Affairs, or a related discipline.6-8 years of hands-on regulatory affairs experience within the medical devices or combination products domain.Proven experience preparing and managing combination product dossiers and technical files for global regulatory submissions.Strong understanding of regulatory frameworks including:EU MDR 2017/745FDA 21 CFRICH GuidelinesISO 14971 and related standardsExperience working with:Design DossiersTechnical FilesDesign History Files (DHF)Risk Management DocumentationClinical Evaluation Reports (CER)Labeling and IFU documentationStrong stakeholder management and client communication skills with the ability to work in a collaborative, fast-paced environment.Excellent documentation, analytical, and problem-solving capabilities. Read Less

Senior Regulatory Affairs Specialist

Experience: 6-8 Years

Domain: Medical Devices / Combination Products

Role Overview

We are looking for an experienced Regulatory Affairs Specialist with strong expertise in combination products and medical device regulatory submissions. The role involves supporting client engagements focused on preparation, review, maintenance, and lifecycle management of regulatory dossiers and technical documentation for combination products across global markets.

The ideal candidate will work closely with cross-functional client teams including Regulatory Affairs, R&D, Quality, and Clinical functions to ensure submissions are compliant, submission-ready, and aligned with evolving regulatory requirements.

Key Responsibilities

Regulatory Dossier & Technical Documentation

Prepare, compile, review, and maintain regulatory dossiers and technical files for combination products in accordance with applicable global regulations.Support submission activities for drug-device and biologic-device combination products across markets including EU and US.Maintain and update technical documentation throughout the product lifecycle, ensuring ongoing compliance and audit readiness.Review product labeling, IFUs, clinical documentation, risk management files, and supporting technical data for regulatory adequacy.

Client & Cross-Functional Collaboration

Partner directly with client stakeholders, including Regulatory, Quality, R&D, Clinical, and Manufacturing teams, to collect and validate submission documentation.Participate in regulatory strategy discussions and provide recommendations to address submission gaps or compliance risks.Coordinate document reviews, approvals, and submission deliverables within defined timelines.

Compliance & Regulatory Support

Assess regulatory changes and industry standards impacting combination products and provide guidance on implementation.Support gap assessments, remediation activities, and submission readiness reviews.Ensure documentation aligns with applicable standards including EU MDR, FDA regulations, ISO standards, and ICH guidelines.Track submission milestones, regulatory commitments, and documentation status to support timely execution.

Required Qualifications

Bachelor's or Master's degree in Life Sciences, Pharmacy, Biomedical Engineering, Regulatory Affairs, or a related discipline.6-8 years of hands-on regulatory affairs experience within the medical devices or combination products domain.Proven experience preparing and managing combination product dossiers and technical files for global regulatory submissions.Strong understanding of regulatory frameworks including:EU MDR 2017/745FDA 21 CFRICH GuidelinesISO 14971 and related standardsExperience working with:Design DossiersTechnical FilesDesign History Files (DHF)Risk Management DocumentationClinical Evaluation Reports (CER)Labeling and IFU documentationStrong stakeholder management and client communication skills with the ability to work in a collaborative, fast-paced environment.Excellent documentation, analytical, and problem-solving capabilities. Read Less

Senior Regulatory Affairs Specialist

Experience: 6-8 Years

Domain: Medical Devices / Combination Products

Role Overview

We are looking for an experienced Regulatory Affairs Specialist with strong expertise in combination products and medical device regulatory submissions. The role involves supporting client engagements focused on preparation, review, maintenance, and lifecycle management of regulatory dossiers and technical documentation for combination products across global markets.

The ideal candidate will work closely with cross-functional client teams including Regulatory Affairs, R&D, Quality, and Clinical functions to ensure submissions are compliant, submission-ready, and aligned with evolving regulatory requirements.

Key Responsibilities

Regulatory Dossier & Technical Documentation

Prepare, compile, review, and maintain regulatory dossiers and technical files for combination products in accordance with applicable global regulations.Support submission activities for drug-device and biologic-device combination products across markets including EU and US.Maintain and update technical documentation throughout the product lifecycle, ensuring ongoing compliance and audit readiness.Review product labeling, IFUs, clinical documentation, risk management files, and supporting technical data for regulatory adequacy.

Client & Cross-Functional Collaboration

Partner directly with client stakeholders, including Regulatory, Quality, R&D, Clinical, and Manufacturing teams, to collect and validate submission documentation.Participate in regulatory strategy discussions and provide recommendations to address submission gaps or compliance risks.Coordinate document reviews, approvals, and submission deliverables within defined timelines.

Compliance & Regulatory Support

Assess regulatory changes and industry standards impacting combination products and provide guidance on implementation.Support gap assessments, remediation activities, and submission readiness reviews.Ensure documentation aligns with applicable standards including EU MDR, FDA regulations, ISO standards, and ICH guidelines.Track submission milestones, regulatory commitments, and documentation status to support timely execution.

Required Qualifications

Bachelor's or Master's degree in Life Sciences, Pharmacy, Biomedical Engineering, Regulatory Affairs, or a related discipline.6-8 years of hands-on regulatory affairs experience within the medical devices or combination products domain.Proven experience preparing and managing combination product dossiers and technical files for global regulatory submissions.Strong understanding of regulatory frameworks including:EU MDR 2017/745FDA 21 CFRICH GuidelinesISO 14971 and related standardsExperience working with:Design DossiersTechnical FilesDesign History Files (DHF)Risk Management DocumentationClinical Evaluation Reports (CER)Labeling and IFU documentationStrong stakeholder management and client communication skills with the ability to work in a collaborative, fast-paced environment.Excellent documentation, analytical, and problem-solving capabilities. Read Less

Senior Regulatory Affairs Specialist

Experience: 6-8 Years

Domain: Medical Devices / Combination Products

Role Overview

We are looking for an experienced Regulatory Affairs Specialist with strong expertise in combination products and medical device regulatory submissions. The role involves supporting client engagements focused on preparation, review, maintenance, and lifecycle management of regulatory dossiers and technical documentation for combination products across global markets.

The ideal candidate will work closely with cross-functional client teams including Regulatory Affairs, R&D, Quality, and Clinical functions to ensure submissions are compliant, submission-ready, and aligned with evolving regulatory requirements.

Key Responsibilities

Regulatory Dossier & Technical Documentation

Prepare, compile, review, and maintain regulatory dossiers and technical files for combination products in accordance with applicable global regulations.Support submission activities for drug-device and biologic-device combination products across markets including EU and US.Maintain and update technical documentation throughout the product lifecycle, ensuring ongoing compliance and audit readiness.Review product labeling, IFUs, clinical documentation, risk management files, and supporting technical data for regulatory adequacy.

Client & Cross-Functional Collaboration

Partner directly with client stakeholders, including Regulatory, Quality, R&D, Clinical, and Manufacturing teams, to collect and validate submission documentation.Participate in regulatory strategy discussions and provide recommendations to address submission gaps or compliance risks.Coordinate document reviews, approvals, and submission deliverables within defined timelines.

Compliance & Regulatory Support

Assess regulatory changes and industry standards impacting combination products and provide guidance on implementation.Support gap assessments, remediation activities, and submission readiness reviews.Ensure documentation aligns with applicable standards including EU MDR, FDA regulations, ISO standards, and ICH guidelines.Track submission milestones, regulatory commitments, and documentation status to support timely execution.

Required Qualifications

Bachelor's or Master's degree in Life Sciences, Pharmacy, Biomedical Engineering, Regulatory Affairs, or a related discipline.6-8 years of hands-on regulatory affairs experience within the medical devices or combination products domain.Proven experience preparing and managing combination product dossiers and technical files for global regulatory submissions.Strong understanding of regulatory frameworks including:EU MDR 2017/745FDA 21 CFRICH GuidelinesISO 14971 and related standardsExperience working with:Design DossiersTechnical FilesDesign History Files (DHF)Risk Management DocumentationClinical Evaluation Reports (CER)Labeling and IFU documentationStrong stakeholder management and client communication skills with the ability to work in a collaborative, fast-paced environment.Excellent documentation, analytical, and problem-solving capabilities. Read Less

Job Title: Dialysis Technician

Location: Ireland

Salary: €3000 per month

Job Type: Full-time

Experience Required: 1-3 years (preferred)

Job Description:

We are looking for a skilled and dedicated Dialysis Technician to join our healthcare team in Ireland. The ideal candidate will be responsible for operating dialysis machines, monitoring patients during treatment, and ensuring a safe and hygienic clinical environment.

Key Responsibilities:

Prepare and operate dialysis machines for patient treatment Monitor patients before, during, and after dialysis procedures Maintain accurate treatment records and patient data Ensure proper sterilization and maintenance of equipment Assist medical staff in patient care and emergency situations

Requirements:

Diploma or certification in Dialysis Technology or related field Prior experience in dialysis procedures preferred Good communication and patient care skills Knowledge of safety and infection control protocols

Benefits:

Competitive salary (€3000/month) Opportunity to work in an international healthcare environment Professional growth and training opportunities

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Job Title: Dialysis Technician

Location: Ireland

Salary: €3000 per month

Job Type: Full-time

Experience Required: 1-3 years (preferred)

Job Description:

We are looking for a skilled and dedicated Dialysis Technician to join our healthcare team in Ireland. The ideal candidate will be responsible for operating dialysis machines, monitoring patients during treatment, and ensuring a safe and hygienic clinical environment.

Key Responsibilities:

Prepare and operate dialysis machines for patient treatment Monitor patients before, during, and after dialysis procedures Maintain accurate treatment records and patient data Ensure proper sterilization and maintenance of equipment Assist medical staff in patient care and emergency situations

Requirements:

Diploma or certification in Dialysis Technology or related field Prior experience in dialysis procedures preferred Good communication and patient care skills Knowledge of safety and infection control protocols

Benefits:

Competitive salary (€3000/month) Opportunity to work in an international healthcare environment Professional growth and training opportunities

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Job Title: Dialysis Technician

Location: Ireland

Salary: €3000 per month

Job Type: Full-time

Experience Required: 1-3 years (preferred)

Job Description:

We are looking for a skilled and dedicated Dialysis Technician to join our healthcare team in Ireland. The ideal candidate will be responsible for operating dialysis machines, monitoring patients during treatment, and ensuring a safe and hygienic clinical environment.

Key Responsibilities:

Prepare and operate dialysis machines for patient treatment Monitor patients before, during, and after dialysis procedures Maintain accurate treatment records and patient data Ensure proper sterilization and maintenance of equipment Assist medical staff in patient care and emergency situations

Requirements:

Diploma or certification in Dialysis Technology or related field Prior experience in dialysis procedures preferred Good communication and patient care skills Knowledge of safety and infection control protocols

Benefits:

Competitive salary (€3000/month) Opportunity to work in an international healthcare environment Professional growth and training opportunities

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About Us

Based in San Francisco, California, Turing is the world's leading research accelerator for frontier AI labs and a trusted partner for global enterprises deploying advanced AI systems. Turing supports customers in two ways: first, by accelerating frontier research with high-quality data, advanced training pipelines, plus top AI researchers who specialize in coding, reasoning, STEM, multilinguality, multimodality, and agents; and second, by applying that expertise to help enterprises transform AI from proof of concept into proprietary intelligence with systems that perform reliably, deliver measurable impact, and drive lasting results on the P&L.

What does day-to-day look like:

As a medical specialist, you will bring your subject-matter knowledge to help train and evaluate frontier AI systems. Work might include:

Design and solve advanced medical problems, ranging from diagnostic scenarios to complex clinical case reviewsReview AI-generated answers, assessing their accuracy, depth of reasoning, and claritySpot knowledge gaps and edge cases, and propose improvements to strengthen model performanceCollaborate with AI researchers and fellow medical experts to shape training methods, evaluation strategies, and benchmarksProvide structured feedback and insights that guide the development of next-generation AI for medicine and science

Candidate Requirements:

Attending physicians are welcome to applyMinimum 1 year of clinical practice experience in any countryBackground in any of the following areas is preferred: Internal Medicine, Primary Care, Pediatrics, Surgery, Anesthesia, or Diagnostic SpecialtiesStrong communication skills and ability to collaborate effectively with technical research teams

Engagement details:

Commitment: flexible engagement, remote working, up to 30 hrs/weekDuration: 1 month, with potential extensions based on performance and fit

After applying, you will receive an email with a login link. Please use that link to access the portal and complete your profile.

Know amazing talent? Refer them at and earn money from your network.

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About Us

Based in San Francisco, California, Turing is the world's leading research accelerator for frontier AI labs and a trusted partner for global enterprises deploying advanced AI systems. Turing supports customers in two ways: first, by accelerating frontier research with high-quality data, advanced training pipelines, plus top AI researchers who specialize in coding, reasoning, STEM, multilinguality, multimodality, and agents; and second, by applying that expertise to help enterprises transform AI from proof of concept into proprietary intelligence with systems that perform reliably, deliver measurable impact, and drive lasting results on the P&L.

What does day-to-day look like:

As a medical specialist, you will bring your subject-matter knowledge to help train and evaluate frontier AI systems. Work might include:

Design and solve advanced medical problems, ranging from diagnostic scenarios to complex clinical case reviewsReview AI-generated answers, assessing their accuracy, depth of reasoning, and claritySpot knowledge gaps and edge cases, and propose improvements to strengthen model performanceCollaborate with AI researchers and fellow medical experts to shape training methods, evaluation strategies, and benchmarksProvide structured feedback and insights that guide the development of next-generation AI for medicine and science

Candidate Requirements:

Attending physicians are welcome to applyMinimum 1 year of clinical practice experience in any countryBackground in any of the following areas is preferred: Internal Medicine, Primary Care, Pediatrics, Surgery, Anesthesia, or Diagnostic SpecialtiesStrong communication skills and ability to collaborate effectively with technical research teams

Engagement details:

Commitment: flexible engagement, remote working, up to 30 hrs/weekDuration: 1 month, with potential extensions based on performance and fit

After applying, you will receive an email with a login link. Please use that link to access the portal and complete your profile.

Know amazing talent? Refer them at and earn money from your network.

Read Less

About Us

Based in San Francisco, California, Turing is the world's leading research accelerator for frontier AI labs and a trusted partner for global enterprises deploying advanced AI systems. Turing supports customers in two ways: first, by accelerating frontier research with high-quality data, advanced training pipelines, plus top AI researchers who specialize in coding, reasoning, STEM, multilinguality, multimodality, and agents; and second, by applying that expertise to help enterprises transform AI from proof of concept into proprietary intelligence with systems that perform reliably, deliver measurable impact, and drive lasting results on the P&L.

What does day-to-day look like:

As a medical specialist, you will bring your subject-matter knowledge to help train and evaluate frontier AI systems. Work might include:

Design and solve advanced medical problems, ranging from diagnostic scenarios to complex clinical case reviewsReview AI-generated answers, assessing their accuracy, depth of reasoning, and claritySpot knowledge gaps and edge cases, and propose improvements to strengthen model performanceCollaborate with AI researchers and fellow medical experts to shape training methods, evaluation strategies, and benchmarksProvide structured feedback and insights that guide the development of next-generation AI for medicine and science

Candidate Requirements:

Attending physicians are welcome to applyMinimum 1 year of clinical practice experience in any countryBackground in any of the following areas is preferred: Internal Medicine, Primary Care, Pediatrics, Surgery, Anesthesia, or Diagnostic SpecialtiesStrong communication skills and ability to collaborate effectively with technical research teams

Engagement details:

Commitment: flexible engagement, remote working, up to 30 hrs/weekDuration: 1 month, with potential extensions based on performance and fit

After applying, you will receive an email with a login link. Please use that link to access the portal and complete your profile.

Know amazing talent? Refer them at and earn money from your network.

Read Less

About Us

Based in San Francisco, California, Turing is the world's leading research accelerator for frontier AI labs and a trusted partner for global enterprises deploying advanced AI systems. Turing supports customers in two ways: first, by accelerating frontier research with high-quality data, advanced training pipelines, plus top AI researchers who specialize in coding, reasoning, STEM, multilinguality, multimodality, and agents; and second, by applying that expertise to help enterprises transform AI from proof of concept into proprietary intelligence with systems that perform reliably, deliver measurable impact, and drive lasting results on the P&L.

What does day-to-day look like:

As a medical specialist, you will bring your subject-matter knowledge to help train and evaluate frontier AI systems. Work might include:

Design and solve advanced medical problems, ranging from diagnostic scenarios to complex clinical case reviewsReview AI-generated answers, assessing their accuracy, depth of reasoning, and claritySpot knowledge gaps and edge cases, and propose improvements to strengthen model performanceCollaborate with AI researchers and fellow medical experts to shape training methods, evaluation strategies, and benchmarksProvide structured feedback and insights that guide the development of next-generation AI for medicine and science

Candidate Requirements:

Attending physicians are welcome to applyMinimum 1 year of clinical practice experience in any countryBackground in any of the following areas is preferred: Internal Medicine, Primary Care, Pediatrics, Surgery, Anesthesia, or Diagnostic SpecialtiesStrong communication skills and ability to collaborate effectively with technical research teams

Engagement details:

Commitment: flexible engagement, remote working, up to 30 hrs/weekDuration: 1 month, with potential extensions based on performance and fit

After applying, you will receive an email with a login link. Please use that link to access the portal and complete your profile.

Know amazing talent? Refer them at and earn money from your network.

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About Us

Based in San Francisco, California, Turing is the world's leading research accelerator for frontier AI labs and a trusted partner for global enterprises deploying advanced AI systems. Turing supports customers in two ways: first, by accelerating frontier research with high-quality data, advanced training pipelines, plus top AI researchers who specialize in coding, reasoning, STEM, multilinguality, multimodality, and agents; and second, by applying that expertise to help enterprises transform AI from proof of concept into proprietary intelligence with systems that perform reliably, deliver measurable impact, and drive lasting results on the P&L.

What does day-to-day look like:

As a medical specialist, you will bring your subject-matter knowledge to help train and evaluate frontier AI systems. Work might include:

Design and solve advanced medical problems, ranging from diagnostic scenarios to complex clinical case reviewsReview AI-generated answers, assessing their accuracy, depth of reasoning, and claritySpot knowledge gaps and edge cases, and propose improvements to strengthen model performanceCollaborate with AI researchers and fellow medical experts to shape training methods, evaluation strategies, and benchmarksProvide structured feedback and insights that guide the development of next-generation AI for medicine and science

Candidate Requirements:

Attending physicians are welcome to applyMinimum 1 year of clinical practice experience in any countryBackground in any of the following areas is preferred: Internal Medicine, Primary Care, Pediatrics, Surgery, Anesthesia, or Diagnostic SpecialtiesStrong communication skills and ability to collaborate effectively with technical research teams

Engagement details:

Commitment: flexible engagement, remote working, up to 30 hrs/weekDuration: 1 month, with potential extensions based on performance and fit

After applying, you will receive an email with a login link. Please use that link to access the portal and complete your profile.

Know amazing talent? Refer them at and earn money from your network.

Read Less