Category: Featured

Indero Recruitment – Senior Clinical Data Coder

Indero is inviting applications for the Senior Clinical Data Coder – India position on a permanent, full-time basis. This home-based opportunity is suitable for experienced professionals in clinical data coding, clinical trials, and pharmaceutical or contract research organization (CRO) environments. Candidates with at least five years of relevant experience, knowledge of MedDRA and WHO Drug dictionaries, and expertise in coding module setup can apply. The role involves clinical data coding, coding convention management, data review, query resolution, and coordination of coding activities across multiple studies.

Company Overview

Indero is a global contract research organization specializing in dermatology and rheumatology clinical research. Formerly known as Innovaderm, the company has more than two decades of clinical research experience and supports pharmaceutical and biotechnology sponsors through services spanning protocol design, patient recruitment, trial monitoring, and biometrics.

Indero emphasizes collaboration, innovation, reliability, and responsiveness, with opportunities for professional development and advancement.

Job Details

Job Role & Responsibilities

The Senior Clinical Data Coder will lead and oversee clinical data coding activities across multiple ongoing studies, ensuring coding accuracy, regulatory compliance, and timely delivery of study requirements.

Key responsibilities include:

• Code medical terms and medications accurately using MedDRA, WHO Drug, and internal coding conventions.

• Oversee coding module setup for assigned studies and ensure appropriate configurations and workflows.

• Define, document, and manage coding conventions to maintain consistency across studies.

• Coordinate coding activities as the Lead Coder across multiple studies simultaneously.

• Validate sponsor coding licenses.

• Prioritize coding deliverables and balance workloads across studies and timelines.

• Contribute to the coding sections of Data Management Plans.

• Oversee and perform dictionary version upgrades and related activities.

• Validate and test coding setups, coding report programming, and associated database checks.

• Support clinical data review and resolve data clarifications within required timelines.

• Mentor and guide junior or backup coders.

• Contribute to process optimization, SOP development, and coding best practices.

• Maintain effective communication with Data Management Leads, Clinical Research Associates (CRAs), and other stakeholders.

Eligibility & Qualifications

Candidates should possess a Bachelor’s degree or equivalent in Pharmacy, Life Sciences, or a related field. Medical or Nursing backgrounds are also acceptable.

Experience Requirements

• Minimum 5 years of relevant clinical data coding experience in clinical trials or the pharmaceutical/CRO environment.

• Demonstrated experience in coding module setup and coding convention management.

• Experience prioritizing coding tasks across multiple clinical studies.

• Experience in clinical data review and query management.

Required Skills & Competencies

Applicants should demonstrate the following skills and knowledge:

• Thorough knowledge of medical terminology.

• Working knowledge of MedDRA and WHO Drug medical dictionaries.

• Experience with coding module configuration, validation, and dictionary upgrades.

• Understanding of clinical data management workflows and coding-related database checks.

• Strong organizational, analytical, and problem-solving skills.

• High attention to detail and commitment to data accuracy.

• Excellent written and verbal English communication skills.

• Ability to lead and support colleagues in a global team environment.

• Good knowledge of Good Clinical Practice (GCP).

• Familiarity with applicable Health Canada, US FDA, and European Medicines Agency (EMA) regulations and guidelines.

Work Location & Benefits

This is a home-based position in India. Candidates should be legally eligible to work in India and willing to attend some meetings outside regular working hours, primarily in the evening.

Indero lists the following benefits:

• Flexible work schedule.

• Permanent, full-time employment.

• Ongoing learning and development opportunities.

• Opportunities for professional growth and advancement.

How to Apply

Interested and eligible candidates can submit their applications through the official Indero careers website.

Apply for Senior Clinical Data Coder – India

Applicants should review the official requirements and ensure they have the relevant clinical data coding experience, medical dictionary knowledge, and coding leadership capabilities.

Job Summary

Vantive Recruitment – Executive, Post Market Surveillance

Vantive is inviting applications for the Executive – Post Market Surveillance position in Gurgaon, Haryana. This opportunity falls under the Quality Product Surveillance category and focuses on medical device complaint handling, regulatory reporting, and post-market product monitoring. The role involves reviewing customer complaints, assessing reportability, preparing Medical Device Reports (MDRs), coordinating investigations, and ensuring timely complaint closure. Candidates interested in quality assurance, medical device safety, complaint management, and regulatory compliance can review the official job listing for eligibility details.

Company Overview

Vantive is a vital organ therapy company focused on extending lives and expanding possibilities for patients and healthcare teams. With a 70-year legacy in kidney care, the company is advancing dialysis services through digital solutions and advanced therapies while investing in the development of vital organ treatments.

Job Details

Job Role & Responsibilities

The Executive – Post Market Surveillance will manage and process product complaints and Medical Device Reports across multiple product lines, following applicable procedures and regulatory requirements.

Key responsibilities include:

• Open complaint records and collect the information required for complaint processing.

• Conduct written and verbal follow-ups with customers to obtain additional complaint details.

• Determine whether complaints meet regulatory reporting requirements.

• Prepare associated regulatory reports, including Medical Device Reports (MDRs), in accordance with applicable regulations.

• Evaluate complaints to determine whether an investigation is required.

• Coordinate the retrieval of product samples when necessary for investigations.

• Respond to customer complaints through written and verbal communication.

• Ensure timely closure of complaints in accordance with established procedures.

• Manage complaint-related workflows and identify issues requiring escalation.

• Triage internal and external communications related to product complaints.

• Participate in continuous improvement initiatives and assigned projects.

Eligibility & Qualifications

Pharmacy, Biomedical Engineering, Biotechnology, Life Sciences, and medical device quality or regulatory affairs.

Key Skills & Competencies

The responsibilities described in the listing indicate the importance of the following skills:

• Product complaint handling and documentation.

• Complaint reportability assessment.

• Medical Device Reporting (MDR) and regulatory documentation.

• Customer communication and follow-up.

• Complaint investigation coordination and sample retrieval.

• Workflow management and issue escalation.

• Compliance with established procedures.

• Quality improvement and cross-functional coordination.

Job Location

The position is based in Gurgaon, Haryana, India. The listing identifies the role under Quality Product Surveillance.

How to Apply

Interested candidates can review the official job description and submit their application through Vantive’s careers portal.

Apply for Executive – Post Market Surveillance

Applicants should verify the educational requirements, experience criteria, and other application details on the official portal.

Job Summary

Patanjali Research Foundation Recruitment – Scientific/Medical Writer

Patanjali Research Foundation is inviting applications for the Scientific/Medical Writer position in its Drug Discovery and Development Division. This opportunity is suitable for postgraduate and PhD candidates in Life Sciences, Biology, Chemistry, Pharmacy, Biotechnology, and related disciplines. Candidates with 2–4 years of experience in scientific manuscript writing, medical writing, or publication support are preferred, while freshers with strong subject knowledge may also be considered. The role involves scientific manuscript development, literature reviews, clinical research documentation, regulatory writing, and preparation of publication-ready research content.

Company Overview

Patanjali Research Foundation works in research and development across scientific disciplines. Its Drug Discovery and Development Division is seeking a scientific writing professional to support the Biology, Chemistry, and Clinical Research departments through scientific manuscripts, research documentation, and regulatory writing.

Job Details

Job Role & Responsibilities

The selected candidate will support scientific manuscript writing and documentation for Biology, Chemistry, and Clinical Research teams.

Key responsibilities include:

• Write, review, and edit scientific manuscripts for peer-reviewed journals in Biology, Chemistry, and Clinical Research.

• Develop review articles, research manuscripts, abstracts, posters, and conference presentations.

• Ensure manuscripts comply with journal-specific author guidelines and publication standards.

• Prepare literature reviews, study protocols, clinical study reports, regulatory documents, and project proposals.

• Collaborate with researchers to convert experimental, preclinical, and clinical data into publication-ready content.

• Conduct systematic literature reviews using recognized scientific databases.

• Analyze and interpret biological, chemical, and clinical datasets for accurate scientific representation.

• Perform quality checks for scientific accuracy, grammar, references, and formatting.

• Work with Biology, Chemistry, and Clinical Research teams, as well as project managers.

• Coordinate with internal and external stakeholders to support timely manuscript submission.

• Present complex experimental and clinical findings in clear, concise, scientifically accurate language.

• Adapt scientific content for researchers, clinicians, regulatory authorities, and peer reviewers.

• Use manuscript submission systems, reference management tools, and documentation software.

• Recommend improvements to scientific documentation quality and workflow efficiency.

Eligibility & Qualifications

Candidates should possess a Master’s degree or PhD in Life Sciences, Biology, Chemistry, Pharmacy, Biotechnology, or a related discipline.

Experience Requirements

• Preferred experience: 2–4 years.

• Freshers with strong subject knowledge may also be considered.

• Proven experience in manuscript writing or scientific/medical writing.

• Experience supporting publications in Biology, Chemistry, or Clinical Research is preferred.

Required Skills

Applicants should have the ability to:

• Write and edit scientific manuscripts with accuracy and clarity.

• Interpret scientific literature and research data.

• Prepare publication-ready documents in accordance with journal requirements.

• Conduct literature searches and systematic reviews.

• Manage references, citations, formatting, and manuscript submissions.

• Collaborate with multidisciplinary research teams.

• Communicate scientific findings effectively to different audiences.

• Maintain high standards of scientific accuracy and documentation quality.

Benefits

Patanjali Research Foundation lists the following benefits for this position:

• Competitive salary and benefits package.

• Opportunity to work in a collaborative research environment.

• Potential for professional growth and career advancement.

How to Apply

Interested candidates should apply by email with the required documents.

1. Prepare your detailed resume and cover letter, including your career aspirations.

2. Include three professional references who are not friends or family members.

3. Send your application to jobs@patanjali.res.in.

4. Mention Scientific/Medical Writing in the email subject line.

Application deadline: 28 February 2027

Official application details: Patanjali Research Foundation – Scientific/Medical Writer

Patanjali Research Foundation states that it is an equal opportunity employer and does not discriminate against applicants based on race, colour, religion, gender, national origin, age, or physical disability.

Job Summary

Worldwide Clinical Trials Recruitment – Senior Clinical Data Co-ordinator

Worldwide Clinical Trials is hiring a Senior Clinical Data Co-ordinator for its Clinical Data Management team in India. The full-time, on-site opportunity is available in Kochi and Trivandrum, Kerala. Candidates with at least five years of experience in data management systems and software, knowledge of CDISC SDTM standards, and SAS programming experience can apply. The role involves clinical database configuration, validation, SAS programming, data reconciliation, and coordination with sponsors and clinical data management teams.

Company Overview

Worldwide Clinical Trials is a global contract research organization (CRO) with more than 3,500 professionals working to support clinical research and improve patient outcomes. The company focuses on delivering clinical trial services through quality, innovation, collaboration, and scientific expertise.

Job Details

Job Role & Responsibilities

The Senior Clinical Data Co-ordinator will coordinate and perform activities related to the configuration, maintenance, and validation of clinical databases, database systems, and associated applications.

Key responsibilities include:

• Coordinate with relevant staff to allocate tasks, establish timelines, report progress, and communicate outstanding issues.

• Assist in training and mentoring Clinical Database Programmers in database configuration and SAS program development, testing, and execution.

• Support Data Management staff in preparing database and SAS program specifications.

• Review specifications for setting up and modifying project-specific data entry software, including edit checks.

• Review validation plans for edit checks and reconciliation checks.

• Develop, test, and run SAS programs for clinical data management, including data validation, reconciliation checks, data listings, and data transfers.

• Configure internal and third-party electronic data capture (eDC) and database software for Data Management teams, sponsors, and clinical sites.

• Test databases and related applications according to IT and Data Management departmental standard operating procedures (SOPs).

• Execute database upload programs and process error reports.

• Coordinate with third-party vendors to resolve issues and implement software changes.

• Communicate with sponsors or their representatives regarding electronic data transfers.

• Support the preparation and maintenance of system procedures and documentation in accordance with applicable SOPs.

• Assist with quality assurance activities and audit requirements.

• Perform other duties as assigned.

Eligibility & Qualifications

Candidates should meet the following requirements:

• Education: Degree-level education or relevant experience.

• Experience: At least 5 years of experience working with data management systems and software.

• Clinical Data Standards: Understanding of CDISC SDTM standards.

• Programming Skills: Experience with the SAS programming language.

Required Skills & Competencies

Applicants should demonstrate the following skills:

• Good written and verbal communication skills.

• A methodical and logical approach to problem-solving.

• Ability to learn new tasks quickly and adapt to different computer systems.

• Strong attention to detail and a questioning approach to data validity.

• Good numerical and computer literacy.

• Ability to work efficiently and collaboratively.

• Customer focus and commitment to delivering on responsibilities.

• Relationship-building, communication, and influencing skills.

• Willingness to embrace innovation and organizational change.

Work Location

The position is listed as on-site and is available in:

• Kochi, Kerala

• Trivandrum, Kerala

This is a full-time opportunity with Worldwide Clinical Trials.

How to Apply

Interested and eligible candidates can apply through the official Worldwide Clinical Trials careers portal.

Apply for Senior Clinical Data Co-ordinator – Worldwide Clinical Trials

Applicants should review the official job description and ensure they meet the experience, CDISC SDTM, and SAS programming requirements before submitting their application.

Job Summary

NIPER Kolkata Recruitment – Junior Research Fellow (JRF)

The National Institute of Pharmaceutical Education and Research (NIPER), Kolkata, is inviting applications for one Junior Research Fellow (JRF) position under an Indian Council of Medical Research (ICMR)-sponsored research project. The opportunity is available in the Department of Medical Devices for research on bio-absorbable and antibiotic surgical staples used for wound closure. Candidates with an M.Pharm, M.S. (Pharm), M.Tech, M.Sc. in relevant scientific disciplines, or equivalent qualifications and at least 60% marks can apply. Applicants with experience in biomaterials development and a valid GPAT, NET, or GATE qualification will be preferred.

Organization Overview

The National Institute of Pharmaceutical Education and Research (NIPER), Kolkata, operates under the Department of Pharmaceuticals, Ministry of Chemicals and Fertilizers, Government of India.

The institute is recruiting a Junior Research Fellow for a time-bound research project sponsored by the Indian Council of Medical Research (ICMR).

Project Title: Fiber Reinforced Poly (L–lactic acid) for Fabrication of Bio-absorbable and Antibiotic Surgical Staples for Wound Closing.

Job Details

Project Overview

The research project focuses on developing fiber-reinforced poly(L-lactic acid) materials for fabricating bio-absorbable and antibiotic surgical staples for wound closure.

The selected fellow will work within the Department of Medical Devices at NIPER Kolkata. Candidates with experience in biomaterials development are specifically sought for this research opportunity.

Eligibility & Qualifications

Candidates must possess one of the following qualifications, with a minimum of 60% marks in the degree:

M.Tech, M.S. (Pharm), M.Pharm, M.Sc. in Pharmacy, Biomedical Engineering, Biotechnology, M.Sc. in Chemistry, M.Sc. in Material Science, or an equivalent qualification.

The advertisement specifies that experience in biomaterials development is required.

Preferred Qualifications

• Valid GPAT, NET, or GATE qualification.

• Previous experience working on a funded research project.

Age Limit

The upper age limit is 28 years. Age relaxation for SC, ST, OBC, women, and persons with disabilities will be applicable according to Government of India rules.

Job Responsibilities & Research Focus

The project advertisement identifies biomaterials development as a key experience requirement. The research focuses on fiber-reinforced poly(L-lactic acid) for bio-absorbable and antibiotic surgical staples.

Specific day-to-day duties are not separately detailed in the supplied advertisement.

Fellowship & Contract Duration

The selected candidate will not be entitled to claim regular appointment or absorption at NIPER Kolkata on the basis of this fellowship.

Selection Process

• Applications will be reviewed, and candidates will be shortlisted.

• Shortlisted candidates will receive the interview date and time by email.

• No travel or daily allowance (TA/DA) will be paid for attending the interview.

The advertisement does not specify a separate written examination.

How to Apply

Eligible Indian citizens should submit their application by email with the required documents combined into a single PDF file.

Email: nipercontrectt@niperkolkata.ac.in

CC: govinda@niperkolkata.ac.in

Email subject: Application for the post of JRF in Trachea Project

Documents Required

• Updated CV or resume.

• Attested copies of relevant educational certificates and mark sheets.

• Experience certificates, if applicable.

• Supporting documents relevant to the application.

Last date to apply: 17 October 2026. Applications received after the specified deadline may not be considered.

Official Links

• Download the official NIPER Kolkata JRF advertisement (PDF)

• Visit the NIPER Kolkata website

Important Instructions

• The position is purely contractual and time-bound.

• Fellowship continuation depends on satisfactory performance.

• Preference will be given to candidates with valid GPAT, NET, or GATE qualifications.

• Previous experience in a funded project is preferred.

• Canvassing in any form will result in disqualification.

• No TA/DA will be provided for the interview.

Job Summary

Indian Pharmacopoeia Commission Recruitment – Editorial Assistant

The Indian Pharmacopoeia Commission (IPC), under the Ministry of Health and Family Welfare, Government of India, is conducting a walk-in interview cum written test for the Editorial Assistant post at its Ghaziabad office. This opportunity is suitable for candidates with a postgraduate degree in Pharmacy, Chemistry, Biochemistry, Biotechnology, Microbiology, Life Sciences, or a related scientific discipline. Applicants must have at least two years of relevant editorial experience, preferably in scientific, academic, pharmaceutical, or regulatory publications. The selected candidate will work on editing and proofreading Indian Pharmacopoeia monographs and related scientific publications under a one-year contract.

Organization Overview

The Indian Pharmacopoeia Commission is an autonomous organization under the Ministry of Health and Family Welfare, Government of India. It is responsible for publishing the Indian Pharmacopoeia and related publications.

The Editorial Assistant will support scientific publication quality through editing, proofreading, reference verification, documentation management, and coordination with authors, reviewers, and subject experts.

Job Details

Eligibility & Qualifications

Candidates must possess a master’s degree from a recognized university in one of the following disciplines:

M.Pharm, M.Sc. Chemistry, M.Sc. Biochemistry, M.Sc. Biotechnology, M.Sc. Microbiology, M.Sc. Life Sciences, or a related scientific discipline.

Experience Requirements

A minimum of 2 years of relevant experience is required in areas such as:

• Editorial work, preferably involving scientific, academic, pharmaceutical, or regulatory publications.

• Manuscript editing, proofreading, copyediting, and content review.

• Checking references, citations, bibliographies, appendices, addenda, and errata.

• Maintaining publisher-specific style guides and editorial standards.

• Publication workflows, documentation management, and version control.

• Coordinating with authors, reviewers, subject experts, and publishing teams.

Experience in government organizations, research institutions, pharmacopoeial bodies, scientific publishing houses, or scientific communication companies is desirable.

Job Role & Responsibilities

The selected candidate will support the editing, review, and publication of Indian Pharmacopoeia monographs and related publications.

Key responsibilities include:

1. Edit, proofread, and copyedit Indian Pharmacopoeia (IP) monographs, drafts, errata, addenda, IP Online content, and related publications.

2. Verify references, hyperlinks, citations, bibliographies, and appendices while maintaining IPC-specific editorial standards.

3. Manage documentation, version control, review tracking, and editorial records throughout publication workflows.

4. Coordinate with subject experts and reviewers to ensure timely content review, revision, and finalization.

5. Use MS Word, Excel, PowerPoint, PDF editing tools, AI tools, and editorial management systems to support editorial and publication-related activities.

Salary & Contract Details

The engagement is contractual. According to the vacancy circular, services may be terminated during the contract period if work or conduct is unsatisfactory.

Written Test Syllabus

Candidates should prepare the following subjects for the written test:

• English language: Grammar, comprehension, editing, proofreading, and copyediting.

• Scientific writing and publishing: Editorial practices, style guides, references, citations, bibliographies, appendices, errata, addenda, and publication ethics.

• Scientific knowledge: Basic pharmaceutical, chemical, biological, and life sciences concepts relevant to scientific and pharmacopoeial publications.

• Documentation and quality assurance: Documentation management, version control, editorial workflows, and quality assurance.

• Computer applications: MS Office, PDF editing tools, AI-assisted editing tools, and editorial management systems.

• Analytical ability: Scientific aptitude and analytical reasoning.

Walk-in Interview Details

Important: The walk-in interview cum written test will be conducted in physical mode only. No TA/DA will be paid for attending the selection process.

Documents Required

Candidates must bring the originals and self-attested photocopies of the required documents:

• Educational qualification certificates.

• Experience certificates.

• Updated resume.

• Two passport-size photographs.

• Aadhaar card (original).

• One set of photocopies of all original documents.

• Date of birth certificate.

Candidates should carry all relevant supporting documents for verification at the venue.

How to Apply

Eligible candidates should attend the walk-in interview cum written test at IPC, Ghaziabad, on 28 October 2026, reporting between 9:00 AM and 10:00 AM.

Read the official vacancy circular carefully before attending.

• Download the official IPC Editorial Assistant vacancy circular (PDF)

• Visit the official IPC Careers page

The selected candidate will be informed by the IPC-authorized manpower-providing agency. Candidates are responsible for ensuring that the information and documents submitted are correct.

Job Summary

DDReg Pharma Recruitment – Regulatory Affairs (Biologicals & Vaccines)

DDReg Pharma is hiring for the Senior Associate / Assistant Manager – Regulatory Affairs (Biologicals & Vaccines) position in Gurgaon, India. This opportunity is suitable for regulatory affairs professionals with 3–6 years of relevant experience in pharmaceutical regulatory submissions. The role focuses on preparing CTD/eCTD dossiers, managing CDSCO submissions, handling SUGAM portal activities, and supporting regulatory approvals for biological products and vaccines. Candidates with qualifications in Pharmacy, Life Sciences, Biotechnology, or related disciplines and hands-on regulatory submission experience can apply.

Company Overview

DDReg Pharma provides regulatory and pharmaceutical consulting services supporting regulatory projects across global markets. This position focuses on regulatory affairs activities related to biological products and vaccines, including dossier preparation, submission management, and regulatory compliance.

Job Details

Job Role & Responsibilities

The selected candidate will support regulatory submissions and compliance activities for biological products and vaccines in accordance with applicable Indian regulatory requirements.

Key responsibilities include:

• Prepare and submit Common Technical Document (CTD) and electronic Common Technical Document (eCTD) regulatory dossiers to the Central Drugs Standard Control Organisation (CDSCO).

• Manage clinical trial applications, licences, marketing authorisations, variations, and renewals.

• Handle submissions through the SUGAM portal and respond to regulatory queries.

• Ensure compliance with applicable CDSCO regulations, New Drugs and Clinical Trials Rules (NDCTR), and biologics guidelines.

• Coordinate regulatory activities with clients, internal teams, and regulatory authorities.

• Support documentation and submission processes to facilitate regulatory review and approvals.

Eligibility & Qualifications

Candidates should have a bachelor’s or master’s degree in Pharmacy, Life Sciences, Biotechnology, or a related field.

Relevant qualifications include B.Pharm, M.Pharm, Pharm.D, B.Sc. Life Sciences, M.Sc. Life Sciences, B.Sc. Biotechnology, M.Sc. Biotechnology, or related scientific qualifications aligned with the employer’s stated requirements.

Experience Requirements

• 3–6 years of relevant Regulatory Affairs experience.

• Hands-on experience with CDSCO regulatory submissions.

• Practical experience preparing CTD/eCTD dossiers.

• Experience using the SUGAM portal for regulatory submissions.

• Understanding of applicable regulatory requirements for biological products and vaccines.

Required Skills

• Regulatory documentation and dossier preparation.

• Knowledge of CDSCO submission procedures and regulatory requirements.

• Familiarity with NDCTR and applicable biologics guidelines.

• Strong written and verbal communication skills.

• Stakeholder coordination and client communication.

• Ability to manage regulatory submissions and related documentation accurately.

Job Location & Work Environment

The position is based in Gurgaon, Haryana, and follows an office-based working arrangement. The role involves coordination with clients, internal departments, and regulatory authorities to support biologicals and vaccine regulatory projects.

How to Apply

Interested candidates can apply through the DDReg Pharma careers page or submit their CV directly by email.

• Careers page: Senior Associate / Assistant Manager – Regulatory Affairs

• Email: career@ddreg.in

• Company website: DDReg Pharma

Candidates should highlight their CDSCO submission experience, CTD/eCTD dossier preparation, and SUGAM portal expertise in their applications.

Job Summary

ALS Recruitment – Junior Chemist, HPLC Team

ALS Testing Services India Pvt. Ltd. is inviting applications for the Junior Chemist – HPLC Team position in Bengaluru, India. This opportunity is suitable for freshers and candidates with up to one year of testing laboratory experience. The role involves sample preparation, High-Performance Liquid Chromatography (HPLC) analysis, chromatogram review, quality control, and laboratory documentation. Candidates with a B.Sc. or M.Sc. in Chemistry, Analytical Chemistry, Food Technology, Biotechnology, or a related scientific discipline can apply.

Company Overview

ALS is a global scientific testing company that provides laboratory testing services and data-driven insights across multiple industries. Its laboratory teams work to deliver reliable analytical results while maintaining quality, safety, and regulatory compliance.

Job Details

Job Role & Responsibilities

The selected candidate will perform sample preparation, chemical analysis, data processing, and documentation using HPLC and related analytical techniques.

Key responsibilities include:

• Prepare and analyse food, feed, water, environmental, and related samples using HPLC and associated techniques.

• Operate, calibrate, and maintain HPLC systems and supporting laboratory equipment according to approved procedures.

• Analyse vitamins, preservatives, sugars, organic acids, sweeteners, caffeine, colourants, and other chemical parameters within the laboratory’s testing scope.

• Review chromatograms, integration, calibration curves, and quality control data to verify the technical validity of results.

• Prepare and maintain analytical worksheets, test records, instrument logbooks, and laboratory documentation.

• Perform routine instrument suitability checks, preventive maintenance, and troubleshooting.

• Follow approved test methods, standard operating procedures (SOPs), ISO/IEC 17025 requirements, and ALS quality procedures.

• Meet sample throughput targets and agreed laboratory turnaround times.

• Participate in method verification, validation, measurement uncertainty studies, and proficiency testing programmes.

• Assist in investigating analytical deviations, out-of-specification results, and quality incidents under the guidance of the Team Leader.

• Maintain laboratory housekeeping, reagent preparation records, chemical inventory, and safety requirements.

• Support internal audits, NABL assessments, customer audits, and continuous improvement initiatives.

Eligibility & Qualifications

Candidates should have a B.Sc. or M.Sc. in Chemistry, Analytical Chemistry, Food Technology, Biotechnology, or a related scientific discipline.

Relevant courses include B.Sc. Chemistry, M.Sc. Chemistry, B.Sc. Analytical Chemistry, M.Sc. Analytical Chemistry, B.Sc. Food Technology, M.Sc. Food Technology, B.Sc. Biotechnology, and M.Sc. Biotechnology, subject to the employer’s stated qualification criteria.

Experience Requirements

• 0–1 year of experience in a testing laboratory.

• Freshers with academic or internship experience in HPLC techniques may also be considered.

• Experience in food testing laboratories is an added advantage.

Technical Skills & Knowledge

Candidates interested in this position should be familiar with or willing to develop skills in:

• High-Performance Liquid Chromatography (HPLC).

• Sample preparation and analytical testing.

• Chromatogram interpretation and calibration curves.

• Laboratory quality control and analytical documentation.

• Instrument calibration, maintenance, and troubleshooting.

• Standard operating procedures and laboratory safety.

• ISO/IEC 17025 laboratory quality requirements.

Work Location

The position is based at ALS Testing Services India Pvt. Ltd., Bengaluru, Karnataka. The role involves laboratory-based chemical testing and requires compliance with laboratory procedures, quality systems, safety requirements, and turnaround time commitments.

 

How to Apply

Interested candidates should apply online through the official ALS careers portal. Applicants should submit a resume and cover letter demonstrating their motivation and suitability for the position.

Apply here: Junior Chemist – HPLC Team | ALS Official Careers

Review the official job listing for the latest application status and eligibility requirements.

Job Summary

Johnson & Johnson Recruitment – Scientist Pharmacometrics Support

Johnson & Johnson (J&J) is hiring a Scientist Pharmacometrics Support professional for its Clinical Pharmacology & Pharmacometrics (CPP) team in Hyderabad, India. This opportunity is suitable for candidates with a scientific degree and 1–3 years of pharmaceutical industry experience. The role focuses on pharmacokinetic (PK) and pharmacodynamic (PD) data preparation, dataset quality control, modelling support, and regulatory e-submission activities. Candidates with basic R programming skills and an understanding of clinical pharmacology, SDTM, ADaM, and clinical drug development can explore this opportunity.

Company Overview

Johnson & Johnson is a global healthcare company operating across Innovative Medicine and MedTech. Its research and development teams work to discover and develop treatments, improve patient outcomes, and advance healthcare innovation.

The Clinical Pharmacology & Pharmacometrics team supports drug development through pharmacokinetic and pharmacodynamic modelling, simulation, data analysis, and regulatory submission activities.

Job Details

Job Role & Responsibilities

The selected candidate will provide technical and operational support to Clinical Pharmacology and Pharmacometrics leaders across therapeutic areas. The role involves preparing analysis-ready datasets, performing quality checks, and supporting global regulatory submissions under the oversight of a senior Pharmacometrics Support Programmer.

Key responsibilities include:

• Prepare analysis-ready datasets for pharmacokinetic (PK) and/or pharmacodynamic (PD) analyses following interim and final database releases.

• Support datasets used for ADNCA and NONMEM analyses.

• Perform basic pharmacometrics analysis quality control (QC) activities.

• Document QC checks, findings, and follow-up actions.

• Support global regulatory submissions by preparing population PK/PD and Exposure-Response e-submission packages.

• Prepare datasets, control files, outputs, tables, and supporting documentation for regulatory submissions.

• Assist with process improvement initiatives, software validation, and technology enhancements.

• Follow applicable standard operating procedures (SOPs), regulatory requirements, and Johnson & Johnson Credo principles.

• Collaborate with CPP scientists, clinical pharmacology leaders, data management, clinical and statistical programming, bioanalysis, regulatory, and publishing teams.

• Coordinate with external stakeholders and pharmacokinetics office vendors when required.

Eligibility & Qualifications

Candidates must have a bachelor’s degree or equivalent qualification in a scientific discipline.

Relevant qualifications may include B.Pharm, M.Pharm, Pharm.D, B.Sc. Life Sciences, M.Sc. Life Sciences, B.Sc. Biotechnology, M.Sc. Biotechnology, B.Sc. Chemistry, M.Sc. Chemistry, or related scientific qualifications. These are examples of potentially relevant courses; the official posting does not provide an exhaustive list of accepted degrees.

Experience Requirements

• 1–3 years of pharmaceutical industry experience.

• Experience in clinical pharmacology, pharmacometrics, or data analysis support roles is preferred.

• Understanding of clinical drug development processes.

• Familiarity with clinical data structures and pharmacokinetic analysis requirements.

Technical Skills Required

• R programming: Basic proficiency in R for data manipulation.

• Clinical data standards: Basic understanding of SDTM and ADaM data structures.

• Pharmacokinetic analysis: Basic understanding of ADNCA and NONMEM input dataset requirements.

• Pharmacometric modelling: Understanding of non-linear mixed-effects modelling.

• Clinical pharmacology: Knowledge of clinical PK and PK/PD concepts.

• Regulatory submissions: Ability to support preparation of datasets and documentation for global e-submissions.

Non-Technical Skills

• Clear written and verbal communication skills.

• Strong attention to detail and a quality-focused mindset.

• Ability to work effectively with cross-functional teams.

• Good planning, prioritization, and multitasking skills.

• Accountability for timely completion of assigned tasks.

• Willingness to learn and contribute to process improvement.

• Cultural awareness and the ability to collaborate with global teams.

• Ability to work independently under appropriate oversight.

• Fluency in English; local language requirements may apply.

Work Location & Arrangement

The position is based in Hyderabad, India, and is listed as a hybrid-work opportunity. The role involves collaboration with local and global teams and may require approximately 5% travel.

Career Opportunity in Pharmacometrics

This position provides an opportunity to develop expertise in clinical pharmacology, pharmacokinetic and pharmacodynamic data analysis, and regulatory submission support. It may suit early-career professionals interested in pharmacometrics, clinical data programming, pharmacokinetic modelling, and pharmaceutical research and development.

How to Apply

Interested candidates can review the full job description and submit their applications through the official Johnson & Johnson careers portal.

Apply here: Scientist Pharmacometrics Support – Hyderabad | Johnson & Johnson

Review the official listing for the latest application status and requirements before applying.

Job Summary

Parexel Recruitment – Senior Data Surveillance Analyst

Parexel is hiring a Senior Data Surveillance Analyst for its Clinical Trials team in India, with Hyderabad as the primary location and Bengaluru as an additional location. This opportunity is suitable for experienced professionals in clinical research, clinical data analytics, and risk-based quality management (RBQM). The role involves centralized monitoring of clinical trials, analysis of Key Risk Indicators (KRIs) and Key Performance Indicators (KPIs), and the use of programming tools to improve data analysis and reporting. Candidates with at least 4 years of biotechnology or pharmaceutical industry experience and 2 years of RBQM experience can review the eligibility requirements.

Company Overview

Parexel is a global clinical development partner providing clinical research and consulting solutions to the life sciences industry. The company collaborates with biopharmaceutical companies and research sites to design and deliver clinical trials, with a focus on patient safety, research quality, and the development of new therapies.

Job Details

Job Role & Responsibilities

The Senior Data Surveillance Analyst will lead centralized monitoring activities for global and complex clinical trials. The role involves configuring and maintaining Risk-Based Quality Management (RBQM) systems, analyzing clinical trial data, and supporting regulatory compliance.

Key responsibilities include:

• Act as a subject matter expert in the configuration, implementation, and execution of centralized monitoring RBQM systems across studies.

• Maintain Key Risk Indicator (KRI) and Quality Tolerance Limit (QTL) libraries within the RBQM platform.

• Coordinate with functional and cross-functional stakeholders to develop centralized monitoring configuration specifications.

• Provide operational expertise, training, and guidance on RBQM systems and serve as an escalation point for centralized monitoring issues.

• Conduct centralized monitoring reviews and interpret KRI and KPI data to provide actionable insights.

• Use programming languages such as R, SQL, or SAS to develop custom analyses, automate workflows, and integrate data systems.

• Support improvements to technologies, systems, processes, and training materials used in centralized monitoring and RBQM.

• Participate in process improvement initiatives and contribute to innovation in centralized monitoring.

• Help improve study execution, data accuracy, patient safety, and clinical trial performance.

Eligibility & Qualifications

Candidates should have a bachelor’s degree or equivalent experience in a related field.

Relevant qualifications may include B.Pharm, M.Pharm, Pharm.D, B.Sc. Life Sciences, M.Sc. Life Sciences, B.Sc. Biotechnology, M.Sc. Biotechnology, Statistics, Biostatistics, Data Science, Clinical Research, or related scientific and analytical disciplines. These are examples of potentially relevant qualifications; the official posting does not provide an exhaustive list of accepted degrees.

Experience Requirements

Applicants must meet the following requirements:

• At least 4 years of relevant biotechnology or pharmaceutical industry experience.

• A minimum of 2 years of direct experience with RBQM systems or similar centralized monitoring platforms.

• Knowledge of ICH-GCP guidelines, regulatory requirements, and clinical trial processes.

• Advanced proficiency in Microsoft Excel for data manipulation and reporting.

Preferred Qualifications

• A master’s degree in a related field, such as Data Science, Biostatistics, or Clinical Research.

• Experience with CluePoints or similar centralized monitoring and RBQM solutions.

• Experience in site monitoring, clinical data management, or clinical operations.

• Ability to identify and interpret business trends and apply findings to centralized monitoring practices.

Required Technical Skills

• Programming: Python, R, SQL, or SAS.

• Data analytics: Clinical trial data analysis, reporting, and interpretation of KRIs and KPIs.

• RBQM systems: System configuration, implementation, execution, and troubleshooting.

• Database management: Database design, clinical databases, and system integration.

• Automation: Developing scripts to automate analytical workflows.

• Clinical research compliance: Knowledge of ICH-GCP, regulatory requirements, and clinical trial processes.

• Communication: Ability to collaborate with cross-functional teams and present findings clearly.

• Problem-solving: Critical thinking, attention to detail, and troubleshooting data refreshes and execution errors.

Career Opportunity in Clinical Data Analytics

This position is suited to experienced professionals looking to advance their careers in centralized monitoring, clinical data surveillance, and risk-based quality management. It combines clinical research knowledge with programming, analytical problem-solving, and system configuration to support data-driven decisions throughout clinical trials.

How to Apply

Interested candidates can review the complete job description and apply through Parexel’s recruitment portal.

Apply here: Senior Data Surveillance Analyst – Parexel Official Careers

Candidates should verify the current application status and location-specific requirements on the official careers page before applying.

Job Summary