PHARMA STUFF

Author: Sudheer vanguri

  • Soterius Senior Drug Safety Associate – Pharmacovigilance

    Soterius Senior Drug Safety Associate Recruitment 2026

    Soterius is hiring a Senior Drug Safety Associate for its Clinical Safety and Pharmacovigilance function in Noida.
    The role is suitable for professionals with 2–4 years of experience in Drug Safety and Pharmacovigilance activities.
    The position involves ICSR case processing, adverse event review, safety database activities, compliance, quality management, documentation, and client requirements.
    The selected professional will also support technology solutions, audits and inspections, SOP development, training, and assigned Pharmacovigilance projects.

    Senior Drug Safety Associate – Clinical Safety & Pharmacovigilance

    Job Overview

    The Senior Drug Safety Associate will support Clinical Safety and Pharmacovigilance activities as requested by management and will be responsible for assigned projects, tasks, quality, compliance, and documentation.

    The role includes activities related to post-marketing and clinical trial safety reports, ICSR case processing, regulatory compliance, safety databases, technology solutions, and stakeholder coordination.

    Job Role & Responsibilities

    The Senior Drug Safety Associate will be responsible for:

    • Support Drug Safety and Pharmacovigilance activities as requested by management.

    • Record and review Adverse Drug Reactions (ADRs) in the safety database or other relevant databases.

    • Process post-marketing and clinical trial reports in accordance with applicable regulatory standards and Soterius client procedures.

    • Ensure high levels of accuracy and quality during safety case processing.

    • Support the development and deployment of assigned technology solutions.

    • Provide administrative support for technology solutions, including:

      • Implementation

      • Validation

      • Upgrades

      • Bug fixes

      • Change requests

      • Product lifecycle support

    • Communicate with required stakeholders as necessary.

    • Carry out administrative duties required for the role.

    • Ensure effective functioning of assigned projects, including ICSR case processing.

    • Ensure compliance with client agreements, applicable regulations, and guidelines.

    • Take ownership of assigned projects and tasks.

    • Ensure adherence to defined timelines and quality requirements.

    • Manage quality, compliance, and documentation across assigned projects.

    • Alert the functional head or designated person regarding concerns or issues relating to personnel management that may affect work quality and functioning.

    • Work continuously with internal and external stakeholders to ensure compliance with agreements, regulations, and applicable guidance.

    • Train and mentor personnel as required.

    • Identify new training and development requirements relevant to the function.

    • Respond to or represent the department/function during audits and inspections, as required.

    • Author and review SOPs and other relevant departmental documents.

    • Perform other responsibilities assigned by management.

    Eligibility & Qualifications

    Experience

    2–4 years of experience

    The supplied job description specifically focuses on experience in Clinical Safety and Pharmacovigilance, including ICSR case processing, safety database activities, quality, compliance, and regulatory requirements.

    Educational Qualification

    The supplied job description does not state a specific educational qualification.

    For a Pharmacovigilance role of this nature, relevant Pharmacy, Life Sciences, or healthcare qualifications may be applicable, but the source does not specify a mandatory degree.

    Eligible Qualification Courses

    B.Pharm | M.Pharm | Pharm.D | B.Sc. Life Sciences | M.Sc. Life Sciences

    The above course list is role-aligned; the supplied job description itself does not specify mandatory educational qualifications.

    Pharmacovigilance & Drug Safety Skills

    The role involves experience or exposure to:

    • Clinical Safety

    • Pharmacovigilance

    • ICSR Case Processing

    • Adverse Drug Reactions

    • Safety Database Management

    • Post-Marketing Safety Reports

    • Clinical Trial Safety Reports

    • Regulatory Compliance

    • Client Procedures

    • Quality Management

    • Compliance Management

    • Safety Documentation

    • SOP Authoring and Review

    • Audit and Inspection Support

    • Training and Mentoring

    • Pharmacovigilance Technology Solutions

    Quality & Compliance Responsibilities

    The position requires maintaining quality and compliance across assigned projects, including:

    • Compliance with client agreements

    • Applicable regulations and guidelines

    • Quality requirements

    • Documentation requirements

    • Project timelines

    • SOP compliance

    • Audit and inspection readiness

    Job Location & Details

    Company: Soterius

    Job Title: Senior Drug Safety Associate

    Function: Clinical Safety and Pharmacovigilance

    Location: Noida, Uttar Pradesh

    Employment Type: Full Time

    Experience: 2–4 years

    How to Apply

    Interested and eligible candidates can apply online through the official Soterius careers portal.

    Apply Now – Soterius Senior Drug Safety Associate

    Job Summary

    Category Details
    Company Soterius
    Vacancies Senior Drug Safety Associate
    Required Education Relevant Pharmacy, Life Sciences or Healthcare qualification; specific qualification not stated in the source
    Experience 2–4 years

  • Syneos Health Medical Writer I / Medical Writer II – CSR Narratives

    Syneos Health Medical Writer I / Medical Writer II – CSR Narratives

    Syneos Health is hiring Medical Writer I / Medical Writer II – CSR Narratives for its Clinical Solutions team in India.
    The role focuses on clinical and medical writing, particularly drafting and reviewing patient narratives and Clinical Study Reports (CSRs).
    Medical writers will prepare and edit clinical documents, review statistical analysis plans and data specifications, and collaborate with Data Management, Biostatistics, Regulatory Affairs, and Medical Affairs teams.
    Candidates with a Master’s/M.Pharm or Bachelor’s degree and relevant experience in narrative writing can apply for this remote or hybrid opportunity.

    Medical Writer I / Medical Writer II – CSR Narratives

    Job Overview

    The position is part of Syneos Health’s Clinical Solutions team and involves preparing medical writing deliverables with minimal supervision.

    The role particularly requires experience in drafting and reviewing narratives, along with knowledge of clinical research, regulatory guidelines, and medical writing standards.

    Job Requisition ID: 25111845
    Work Location: India – Remote / Gurugram – Hybrid
    Employment Type: Full Time

    Job Role & Responsibilities

    The Medical Writer will be responsible for compiling, writing, editing, and reviewing medical writing deliverables.

    Key responsibilities include:

    • Mentor less experienced medical writers on projects, as necessary.

    • Compile, write, and edit medical writing deliverables.

    • Serve as a medical writer within and across departments with minimal supervision.

    • Develop or support various clinical documents, including:

      • Clinical Study Protocols

      • Clinical Study Protocol Amendments

      • Clinical Study Reports (CSRs)

      • Patient Narratives

      • Annual Reports

      • Investigator Brochures

    • Review Statistical Analysis Plans (SAPs) and table, figure, and listing specifications for appropriate content, grammar, format, and consistency.

    • Interact with department heads and staff members in:

      • Data Management

      • Biostatistics

      • Regulatory Affairs

      • Medical Affairs

    • Serve as a peer reviewer on the internal review team.

    • Address team comments accurately to ensure scientific content, clarity, overall consistency, and proper document format.

    • Follow established regulatory standards, including ICH-E3 guidelines, Company SOPs, client standards, and approved templates.

    • Complete medical writing projects on time and within budget.

    • Perform online clinical literature searches, as applicable.

    • Apply working knowledge of the drug development process and regulatory guidelines.

    • Continue professional development to remain current with regulatory guidance and client expectations in medical writing.

    • Stay aware of budget specifications for assigned projects and work within budgeted hours.

    • Communicate changes to medical writing leadership.

    • Complete required administrative tasks within specified timeframes.

    • Perform other work-related duties as assigned.

    • Minimal travel may be required, less than 25%.

    Eligibility & Qualifications

    Educational Qualification

    The job posting states that candidates should have:

    • Postgraduate qualification – Master’s / M.Pharm

    • Bachelor’s degree

    Experience

    The source specifies:

    • Minimum 1 year of experience working in narratives with a Master’s qualification

    • 2 years of experience with a Graduation qualification

    • Good experience in drafting and reviewing narratives

    Eligible Qualification Courses

    M.Pharm | Master’s Degree in Relevant Field | Bachelor’s Degree in Relevant Field

    Required Skills

    Candidates should have:

    • Extensive knowledge of English grammar.

    • Knowledge of FDA regulations and guidelines.

    • Knowledge of ICH regulations and guidelines.

    • Familiarity with the AMA Style Guide.

    • Strong presentation skills.

    • Strong proofreading skills.

    • Strong interpersonal skills.

    • Leadership skills.

    • Ability to work effectively as part of a team.

    • High degree of independence.

    • Strong proficiency in:

      • MS Word

      • MS Excel

      • PowerPoint

      • Email

      • Internet

    • Familiarity with principles of clinical research.

    • Ability to interpret and present clinical data and other complex information.

    Medical Writing & Clinical Research Areas

    The role provides exposure to:

    • Clinical Study Reports

    • Patient Narratives

    • Clinical Study Protocols

    • Protocol Amendments

    • Annual Reports

    • Investigator Brochures

    • Medical Writing

    • Clinical Research

    • Clinical Data Interpretation

    • Statistical Analysis Plans

    • Table, Figure and Listing Specifications

    • Clinical Literature Searches

    • ICH-E3 Guidelines

    • FDA Regulations

    • Regulatory Documentation

    Job Location & Work Mode

    Company: Syneos Health

    Job Title: Medical Writer I / Medical Writer II – CSR Narratives

    Location: India – Remote / Gurugram – Hybrid

    Job Type: Full Time

    Job Requisition ID: 25111845

    Work Mode: Remote (Pre-Approved) / Gurugram Hybrid

    Travel: Less than 25% may be required

    How to Apply

    Interested and eligible candidates can apply online through the official Syneos Health Careers portal.

    Apply Now – Syneos Health Medical Writer I / II

    Job Summary

    Category Details
    Company Syneos Health
    Vacancies Medical Writer I / Medical Writer II – CSR Narratives
    Required Education Master’s / M.Pharm or Bachelor’s degree
    Experience Minimum 1 year with Master’s qualification; 2 years with Bachelor’s qualification; narrative writing experience required

  • Pharmacovigilance Associate Jobs at Apcer Life Sciences

    Apcer Life Sciences Pharmacovigilance Associate Recruitment 2026

    Apcer Life Sciences is hiring a Pharmacovigilance Associate for its healthcare and life sciences team in Noida and Ahmedabad.
    The position is suitable for professionals with 2–3 years of experience in Pharmacovigilance and ICSR case processing.
    The role involves ICSR data entry, case triage, coding, narrative writing, follow-up letters, literature review, quality checks, and safety reporting support.
    Candidates with B.Pharm or M.Pharm in any specialization can apply for this full-time, permanent opportunity.

    Pharmacovigilance Associate – ICSR Case Processing

    Job Role & Responsibilities

    The Pharmacovigilance Associate will support Pharmacovigilance activities involving Individual Case Safety Reports (ICSRs), safety databases, literature review, and regulatory compliance.

    Key responsibilities include:

    • Perform data entry of ICSRs in the Pharmacovigilance database.

    • Enter source data into the database.

    • Perform case coding.

    • Prepare narratives.

    • Generate follow-up letters.

    • Perform book-in and triaging of ICSRs.

    • Review literature articles and assess them for identifying valid ICSRs, where applicable.

    • Perform quality checks of ICSRs in the database, where applicable.

    • Support preparation of aggregate reports, where applicable.

    • Support signal detection of adverse drug reactions (ADRs) using cases received for client products, where applicable.

    • Ensure compliance with project guidelines.

    • Execute company Standard Operating Procedures (SOPs).

    • Build and maintain good relationships across functional units and company affiliates.

    • Maintain awareness of changes to or new regulations affecting Pharmacovigilance activities.

    • Carry out necessary administrative duties required for the role.

    • Perform other duties assigned by management.

    Eligibility & Qualifications

    Educational Qualification

    B.Pharm in Any Specialization – Required

    M.Pharm in Any Specialization – Required/Listed

    Experience

    2–3 years of experience

    The role is particularly relevant for candidates with experience in:

    • Pharmacovigilance

    • ICSR Case Processing

    • Safety Database Activities

    • Case Coding

    • Narrative Writing

    • Literature Review

    Eligible Qualification Courses

    B.Pharm | M.Pharm

    Required Pharmacovigilance Skills

    Candidates should have experience or knowledge in:

    • ICSR Case Processing

    • Pharmacovigilance Database

    • ICSR Data Entry

    • Case Book-In

    • ICSR Triage

    • MedDRA Coding

    • Narrative Writing

    • Follow-Up Letter Generation

    • Literature Review

    • ICSR Quality Check

    • Aggregate Safety Reports

    • Signal Detection

    • ADR Assessment

    • Pharmacovigilance SOPs

    • Regulatory Compliance

    Pharmacovigilance & Safety Operations

    The position provides exposure to several important Pharmacovigilance activities, including:

    ICSR Processing

    • Source data entry

    • Case coding

    • Narrative writing

    • Follow-up activities

    • Case book-in and triage

    Literature & Safety Review

    • Literature article review

    • Identification of valid ICSRs

    • ADR assessment

    • Signal detection

    Quality & Compliance

    • ICSR quality checks

    • Project guideline compliance

    • Company SOP execution

    • Pharmacovigilance regulatory updates

    • Aggregate report support

    Job Location & Details

    Company: Apcer Life Sciences

    Job Title: Pharmacovigilance Associate

    Location: Noida, Uttar Pradesh / Ahmedabad, Gujarat

    Job Type: Full Time, Permanent

    Department: Healthcare & Life Sciences

    Industry: Pharmaceutical & Life Sciences

    Experience: 2–3 years

    Vacancies: 1

    How to Apply

    Interested and eligible candidates can apply online through the job posting provided by Apcer Life Sciences on Naukri.

    Apply Now – Apcer Life Sciences Pharmacovigilance Associate

    Job Summary

    Category Details
    Company Apcer Life Sciences
    Vacancies Pharmacovigilance Associate – 1 Position
    Required Education B.Pharm in Any Specialization, M.Pharm in Any Specialization
    Experience 2–3 years

  • Indoco Remedies Walk-In Interview | B.Pharm, M.Pharm, B.Sc

    Indoco Remedies Limited is conducting a Walk-In Interview for multiple positions across Production, Quality Control and Quality Assurance departments. The recruitment includes opportunities for Sr. Officers, Officers, Sr. Operators, Operators, Apprentices and Executives. Candidates with B.Pharm, M.Pharm, B.Sc, M.Sc, 10+2, ITI and Diploma qualifications can apply for the respective positions. The openings require experience ranging from freshers to 10 years, depending on the role.

    Indoco Remedies Limited – Walk-In Interview

    Walk-In Interview Details

    Date: 26.09.2026, Saturday
    Time: 09:00 AM to 02:00 PM

    Venue

    Indoco Remedies Limited
    Unit-III, Katha, Baddi (H.P.)

    Interested candidates can also send their updated CV to Avinash.kumar@indoco.com.

    Production Department – OSD

    Sr. Officer / Officer – Production OSD

    Area: Production – OSD (Tablet Packing & Manufacturing)
    Qualification: B.Pharmacy / M.Pharmacy
    Experience: 03 to 08 Years

    Sr. Operators / Operators – Production OSD

    Area: Production – OSD (Tablet Packing & Manufacturing) – Hi-cart, Autocartonator and Granulation & Compression Operators
    Qualification: 10+2 / ITI / Diploma
    Experience: 02 to 10 Years

    Apprentice – Production

    Area: Production (Tablet Packing)
    Qualification: ITI / Diploma
    Experience: Fresher

    Quality Control Department

    Sr. Officer / Officer – Quality Control

    Area: Quality Control – HPLC / GLP / RM
    Qualification: B.Sc. / M.Sc.
    Experience: 03 to 08 Years

    Quality Assurance Department – IPQA

    Executive – Quality Assurance

    Area: Quality Assurance – IPQA
    Qualification: B.Pharmacy / M.Pharmacy
    Experience: 06 to 10 Years

    Quality Assurance Department – Qualification, Cleaning & Validation

    Sr. Officer / Officer – QA

    Area: Quality Assurance – Qualification and Cleaning & Validation
    Qualification: B.Pharmacy / M.Pharmacy
    Experience: 03 to 08 Years

    Quality Assurance Department – AQA

    Sr. Officer / Officer – AQA

    Area: Quality Assurance – AQA
    Qualification: B.Pharmacy / M.Pharmacy
    Experience: 03 to 08 Years

    Eligibility & Qualifications

    Candidates with the following qualifications are eligible for the respective positions:

    B.Pharm | M.Pharm | B.Sc | M.Sc | 10+2 | ITI | Diploma

    Production – OSD

    Sr. Officer / Officer: B.Pharmacy / M.Pharmacy

    Sr. Operators / Operators: 10+2 / ITI / Diploma

    Apprentice: ITI / Diploma

    Quality Control

    Sr. Officer / Officer: B.Sc. / M.Sc.

    Quality Assurance – IPQA

    Executive: B.Pharmacy / M.Pharmacy

    Quality Assurance – Qualification, Cleaning & Validation

    Sr. Officer / Officer: B.Pharmacy / M.Pharmacy

    Quality Assurance – AQA

    Sr. Officer / Officer: B.Pharmacy / M.Pharmacy

    Experience Required

    • Production OSD – Sr. Officer / Officer: 03 – 08 Years

    • Production OSD – Sr. Operators / Operators: 02 – 10 Years

    • Production – Apprentice: Fresher

    • Quality Control – Sr. Officer / Officer: 03 – 08 Years

    • Quality Assurance – Executive, IPQA: 06 – 10 Years

    • Quality Assurance – Sr. Officer / Officer: 03 – 08 Years

    • Quality Assurance – AQA Sr. Officer / Officer: 03 – 08 Years

    Key Experience Areas

    Production – OSD

    The available Production positions cover:

    • Tablet Packing

    • Manufacturing

    • Hi-cart

    • Autocartonator

    • Granulation

    • Compression

    Quality Control – OSD

    The Quality Control opening is for candidates with experience in:

    • HPLC

    • GLP

    • RM

    Quality Assurance

    The QA positions cover:

    • IPQA

    • Qualification

    • Cleaning

    • Validation

    • AQA

    How to Apply

    Interested candidates can attend the Indoco Remedies Limited Walk-In Interview on 26 September 2026, between 09:00 AM and 02:00 PM.

    Walk-In Venue

    Indoco Remedies Limited
    Unit-III, Katha, Baddi (H.P.)

    CV Submission

    Candidates can also send their updated CV to:

    Email: Avinash.kumar@indoco.com

    Candidates should mention the relevant position and department when submitting their CV.

    Job Summary

    Company Indoco Remedies Limited
    Vacancies Sr. Officer / Officer – Production OSD; Sr. Operators / Operators – Production OSD; Apprentice – Production; Sr. Officer / Officer – Quality Control; Executive – Quality Assurance IPQA; Sr. Officer / Officer – QA Qualification, Cleaning & Validation; Sr. Officer / Officer – AQA
    Required Education B.Pharm; M.Pharm; B.Sc; M.Sc; 10+2; ITI; Diploma
    Experience Fresher to 10 Years, depending on the position

  • Pharmacovigilance Hiring – Apotex Senior Analyst – Drug Information & Risk Management

    Apotex Senior Analyst – Drug Information & Risk Management

    Apotex is hiring a Senior Analyst – Drug Information & Risk Management in Mumbai, Maharashtra to support its multidisciplinary healthcare team.
    The role focuses on providing professional, unbiased, clinically relevant, and timely medical information regarding Apotex products to internal and external customers.
    The position also involves Risk Management Plans, medical inquiry responses, medical literature research, safety information, medical documentation, and pharmacovigilance compliance.
    Candidates with B.Pharm, M.Pharm, B.Sc., BDS, or a Diploma in Health/Science-related discipline and 1–3 years of Pharmacovigilance experience can apply.

    Senior Analyst – Drug Information & Risk Management

    Job Summary

    The Senior Analyst will work as part of a multidisciplinary team of healthcare professionals supporting Apotex products in domestic and international markets.

    The role involves coordinating the development of medical documents such as Risk Management Plans and Risk Evaluation Mitigation Plans, while providing medical information related to the safe and effective use of drugs manufactured and marketed by Apotex Inc. and its affiliates and distributors worldwide.

    Job Role & Responsibilities

    The selected candidate will be responsible for:

    • Provide verbal and written responses to medical inquiries from healthcare professionals, sales representatives, and other internal customers regarding Apotex products.

    • Evaluate, analyze, and respond to medical inquiries accurately, objectively, and in a timely manner.

    • Coordinate the preparation and updating of Risk Management & Risk Evaluation Mitigation Plans globally.

    • Provide input into the medical sections of these plans using relevant regional templates.

    • Apply technical and scientific skills to research and interpret medical information.

    • Create and peer review new and revised medical information documents, including:

      • Response documents

      • Recall Q&As

      • Bulletins

      • Other medical information documents

    • Participate in departmental and cross-functional business teams.

    • Support team initiatives and contribute to team goals and projects according to business priorities.

    • Ensure compliance with SOPs relating to adverse event and quality complaint reporting.

    • Maintain awareness of current therapeutics and industry-based medical information regulations.

    • Provide on-call coverage as per the assigned schedule.

    • Assist in the preparation of reports.

    • Update and maintain product databases and files as required.

    • Work as a member of a team to achieve assigned outcomes.

    • Perform work in accordance with established regulatory, compliance, and safety requirements.

    • Perform other duties and special projects, including after-hours coverage of the DISPedia unit, as assigned.

    • Work safely and collaborate with team members to achieve business outcomes.

    • Demonstrate organizational values of Collaboration, Courage, Perseverance, and Passion.

    • Maintain personal adherence to applicable compliance programs, including Global Business Ethics and Compliance, Global Quality, Safety and Environment, and HR policies.

    • Perform other relevant duties as assigned.

    Eligibility & Qualifications

    Educational Qualification

    The job posting lists the following qualifications:

    • Bachelor of Pharmacy (B.Pharm)

    • B.Sc. or Diploma in Health/Science-related discipline

    • Master of Pharmacy (M.Pharm)

    • Bachelor of Dental Surgery (BDS)

    Experience

    1–3 years of experience in Pharmacovigilance

    Eligible Qualification Courses

    B.Pharm | M.Pharm | B.Sc. | BDS | Diploma in Health/Science-related Discipline

    Required Knowledge & Skills

    Candidates should have:

    • Excellent oral and written communication skills.

    • Knowledge of Microsoft Office software, including:

      • Excel

      • PowerPoint

      • Word

      • Outlook

    • Knowledge of Arisg Safety Database

    • Knowledge of MedDRA

    • Knowledge of Argus

    • Knowledge of Embase

    • Knowledge of MLM database

    • Knowledge of online literature searching and review.

    Pharmacovigilance & Medical Information

    The position involves activities related to:

    • Pharmacovigilance

    • Medical Information

    • Medical Inquiry Management

    • Risk Management Plans

    • Risk Evaluation Mitigation Plans

    • Adverse Event Reporting

    • Quality Complaint Reporting

    • Medical Literature Searching

    • MedDRA

    • Argus

    • Arisg Safety Database

    • Embase

    • Safety Information

    • Regulatory and Compliance Requirements

    Job Location & Details

    Company: Apotex

    Job Title: Senior Analyst – Drug Information & Risk Management

    Location: Mumbai, Maharashtra – 400079

    Date: 23 September 2026

    Experience: 1–3 years in Pharmacovigilance

    Job Type: Full Time

    How to Apply

    Interested and eligible candidates can apply online through the official Apotex Careers portal.

    Apply Now – Apotex Senior Analyst, Drug Information & Risk Management

    For inquiries regarding the job posting:

    Email: rpalkar@apotex.co.in

    Job Summary

    Category Details
    Company Apotex
    Vacancies Senior Analyst – Drug Information & Risk Management
    Required Education B.Pharm, M.Pharm, B.Sc., BDS, Diploma in Health/Science-related Discipline
    Experience 1–3 years in Pharmacovigilance

  • Omega Healthcare Medical Data Abstractor | Pharm D, MBBS

    Omega Healthcare is hiring Medical Data Abstractors for candidates with 0–5 years of experience in clinical or non-clinical fields. The role is suitable for professionals with qualifications including BHMS, BAMS, BUMS, BDS, MDS, BPT, MPT, MBBS and Pharm D. Candidates should have knowledge of medical terminology, clinical concepts, human anatomy and physiology, along with strong communication and time management skills.

    Omega Healthcare – Medical Data Abstractor

    Job Position

    Designation: Medical Data Abstractor
    Job Code: OMH/MDA/1857354
    Experience: 0 – 5 Years
    Interview Mode: Virtual / Walk-in

    Medical Data Abstractor – Key Requirements

    Medical Terminology & Clinical Concepts

    Candidates should have expertise in medical terminology and clinical concepts relevant to medical data abstraction activities.

    Human Anatomy & Physiology

    Sound knowledge of human anatomy and physiology is required for the position.

    Communication & Time Management

    Candidates should have strong communication and time management abilities.

    Multitasking

    The role requires candidates to be skilled at multitasking in fast-paced environments while meeting deadlines.

    Eligibility & Qualifications

    Candidates with the following qualifications are eligible to apply:

    BHMS | BAMS | BUMS | BDS | MDS | BPT | MPT | MBBS | Pharm D

    Medical & Healthcare Qualifications

    • BHMS

    • BAMS

    • BUMS

    • BDS

    • MDS

    • BPT

    • MPT

    • MBBS

    • Pharm D

    Experience Required

    Medical Data Abstractor

    Experience: 0 – 5 Years

    Candidates with 0–5 years of experience in a clinical or non-clinical field can apply.

    Skills Required

    Medical Knowledge

    • Medical terminology

    • Clinical concepts

    • Human anatomy

    • Human physiology

    Professional Skills

    • Strong communication skills

    • Time management

    • Multitasking

    • Ability to work in a fast-paced environment

    • Ability to meet deadlines

    Interview Mode

    Virtual / Walk-In Interview

    The recruitment notification specifies Virtual / Walk-in as the interview mode.

    How to Apply

    Interested candidates can send their updated CV to the recruitment team.

    CV Submission

    Email: Ahmedbilal.Mohamedali@omegaHMS.com

    Contact: 9025128400

    Candidates should mention the Medical Data Abstractor position and Job Code: OMH/MDA/1857354 when applying.

    Job Summary

    Company Omega Healthcare
    Vacancies Medical Data Abstractor
    Required Education BHMS; BAMS; BUMS; BDS; MDS; BPT; MPT; MBBS; Pharm D
    Experience 0 – 5 Years

  • Gufic Biosciences Apprentice Jobs | Microbiology, Biotechnology

    Gufic Biosciences Limited is hiring Apprentices for its Quality Control (Micro) department. The opportunity is specifically available for freshers with qualifications in M.Sc. Microbiology, M.Sc. Biotechnology, B.Sc. Microbiology or B.Sc. Biotechnology. The position is associated with the company’s injectable facility in Navsari, Gujarat.

    Gufic Biosciences Limited – Quality Control (Micro)

    Job Position

    Designation: Apprentice
    Department: Quality Control (Micro)
    Experience: Only for Freshers
    Job Location: Navsari, Gujarat

    Quality Control (Micro) Department – Apprentice

    Apprentice

    Gufic Biosciences Limited is looking for freshers to join its Quality Control (Micro) department as Apprentices.

    The recruitment is intended for candidates with a background in Microbiology or Biotechnology.

    Eligibility & Qualifications

    Candidates with the following qualifications are eligible to apply:

    M.Sc. Microbiology | M.Sc. Biotechnology | B.Sc. Microbiology | B.Sc. Biotechnology

    M.Sc. Candidates

    • M.Sc. Microbiology

    • M.Sc. Biotechnology

    B.Sc. Candidates

    • B.Sc. Microbiology

    • B.Sc. Biotechnology

    Experience Required

    Only freshers can apply.

    The recruitment notification specifically states that the Quality Control (Micro) opportunity is for freshers.

    Department & Work Area

    Quality Control – Microbiology

    The position is within the Quality Control (Micro) department at Gufic Biosciences Limited’s injectable facility.

    Candidates with an academic background in Microbiology or Biotechnology are eligible for the Apprentice position.

    Job Location

    Gufic Biosciences Limited – Injectable Facility

    Navsari, Gujarat

    Gufic Biosciences Limited’s recruitment announcement states that the opportunity is for its injectable facility located at Navsari, Gujarat.

    How to Apply

    Interested candidates can send their updated CV to the recruitment team.

    CV Submission

    Email: binal.kapadia@guficbio.com

    Candidates should attach their updated CV when applying for the Quality Control (Micro) Apprentice position.

    Job Summary

    Company Gufic Biosciences Limited
    Vacancies Apprentice – Quality Control (Micro)
    Required Education M.Sc. Microbiology; M.Sc. Biotechnology; B.Sc. Microbiology; B.Sc. Biotechnology
    Experience Only for Freshers

  • DSK InnoSciences Executive Jobs | M.Sc Chemistry

    DSK InnoSciences is hiring an Executive – Project Management for candidates with an M.Sc. in Chemistry qualification. Both freshers and experienced candidates can apply for this opportunity. The position involves working in an office setup while applying chemistry knowledge and does not require candidates to work in a chemistry laboratory. Candidates with strong communication, written and teamwork skills can apply.

    DSK InnoSciences – Executive, Project Management

    Job Position

    Designation: Executive – Project Management
    Department: Project Management
    Qualification: M.Sc. Chemistry
    Experience: Freshers and experienced candidates can apply.

    Project Management Department – Executive

    Executive – Project Management

    DSK InnoSciences is looking for candidates who can leverage their chemistry knowledge in an office-based work environment.

    The position does not require candidates to work in the chemistry laboratory.

    Requirements

    Educational Qualification

    M.Sc. Chemistry

    Experience

    • Freshers can apply.

    • Experienced candidates can also apply.

    Candidate Requirements

    • Female candidates are preferable.

    • Selected candidates will work in an office setup by leveraging their chemistry knowledge.

    • The position does not require candidates to work in the chemistry lab.

    • Should possess excellent communication and written skills.

    • Ability to work independently and as part of a team.

    Eligibility & Qualifications

    Candidates with the following qualification are eligible to apply:

    M.Sc. Chemistry

    Project Management – Executive

    Qualification: M.Sc. Chemistry

    Experience: Freshers and experienced candidates can apply.

    Skills Required

    Communication & Written Skills

    Candidates should possess excellent communication and written skills.

    Teamwork & Independent Working

    Candidates should have the ability to work independently and as part of a team.

    Chemistry Knowledge

    The selected candidates will leverage their chemistry knowledge while working in an office setup. The role does not require laboratory-based chemistry work.

    Job Location

    DSK InnoSciences

    Bithireddi, Kelamangalam
    Hosur – 635113
    Greater Bangalore

    How to Apply

    Interested candidates can share their updated CV with DSK InnoSciences.

    Contact Details

    Email: hr@dskinnosciences.com

    Phone: 8220008266

    Website: www.dskinnosciences.com

    Candidates interested in the Executive – Project Management position can contact the company through the above-mentioned email address or phone number.

    Job Summary

    Company DSK InnoSciences
    Vacancies Executive – Project Management
    Required Education M.Sc. Chemistry
    Experience Freshers and experienced candidates can apply

  • VerGo Pharma Trainee Jobs | M.Sc, B.Pharm, B.Sc

    VerGo Pharma Research Laboratories Pvt. Ltd. is hiring Trainees / Apprentices for multiple departments at its facility in Verna, Goa. The current openings are available in Analytical Development, Production and Quality Control departments. Candidates with M.Sc. in Analytical Chemistry, B.Pharm and B.Sc. in Chemistry qualifications can apply for the respective positions. Interested candidates can submit their CV directly to the company’s recruitment email address.

    VerGo Pharma Research Laboratories – Trainee / Apprentice

    Job Location

    Verna, Goa

    Positions

    Trainee / Apprentice

    VerGo Pharma Research Laboratories has openings across the following departments.

    Analytical Development Department – Trainee / Apprentice

    Trainee / Apprentice

    Qualification: M.Sc. in Analytical Chemistry

    Candidates with an M.Sc. in Analytical Chemistry qualification can apply for the Trainee / Apprentice opportunity in the Analytical Development Department.

    Production Department – Trainee / Apprentice

    Trainee / Apprentice

    Qualification: B.Pharm

    Candidates with a B.Pharm qualification can apply for the Trainee / Apprentice position in the Production Department.

    Quality Control Department – Trainee / Apprentice

    Trainee / Apprentice

    Qualification: B.Sc. in Chemistry

    Candidates with a B.Sc. in Chemistry qualification can apply for the Trainee / Apprentice opportunity in the Quality Control Department.

    Eligibility & Qualifications

    Candidates with the following qualifications are eligible for the respective departments:

    M.Sc. Analytical Chemistry | B.Pharm | B.Sc. Chemistry

    Analytical Development Department

    M.Sc. in Analytical Chemistry

    Production Department

    B.Pharm

    Quality Control Department

    B.Sc. in Chemistry

    Experience Required

    The recruitment notification does not specify prior work experience for these Trainee / Apprentice positions. Fresh graduates / eligible candidates can apply based on the specified educational qualifications.

    How to Apply

    Interested candidates are requested to email their updated CV to the recruitment team.

    CV Submission

    Email: hra1@vergolabs.com

    Candidates should mention the department and position applied for in their email and attach their updated CV.

    Job Summary

    Company VerGo Pharma Research Laboratories Pvt. Ltd.
    Vacancies Trainee / Apprentice – Analytical Development; Trainee / Apprentice – Production; Trainee / Apprentice – Quality Control
    Required Education M.Sc. in Analytical Chemistry; B.Pharm; B.Sc. in Chemistry
    Experience Not specified; Freshers / eligible candidates can apply

  • Zydus Lifesciences Walk-In Interview | ITI, B.Pharm, M.Pharm

    Zydus Lifesciences Limited is conducting a Walk-In Interview for multiple positions at its Animal Health Unit in Ahmedabad. The recruitment drive includes openings in Production, Packing, Quality Assurance and Quality Control departments. Candidates with ITI, Diploma, B.Sc, B.Pharm, M.Pharm and M.Sc qualifications can apply for the available positions. Opportunities are available for both experienced professionals and freshers, depending on the role.

    Zydus Lifesciences Limited – Walk-In Interview

    Walk-In Interview Details

    Date: 26 September 2026
    Time: 9:00 AM – 3:00 PM
    Job Location: Ahmedabad

    Venue:
    Zydus Animal Health and Investments Limited
    Plot No. 12 & 13, Pharmez-SEZ,
    Sarkhej Bavla NH, BA, Matoda,
    Ahmedabad – 382213

    Production Department – OSD

    Plant Operator / Technical Assistant – Production

    Qualifications: ITI / Diploma / B.Sc
    Experience: 3 – 7 Years

    Required Experience: Compression and Granulation.

    Packing Department – OSD

    Plant Operator / Technical Assistant – Packing

    Qualifications: ITI / Diploma / B.Sc
    Experience: 3 – 8 Years

    Required Experience: Blister (BQS) and Bottle Primary Packing.

    Executive / Sr. Executive – Packing

    Qualifications: B.Pharm / M.Pharm / M.Sc
    Experience: 4 – 8 Years

    Required Experience: Bottle & Blister Packing (Primary & Secondary) and Equipment Qualification.

    FTE / Trainee – Packing

    Qualifications: ITI / Diploma
    Experience: Freshers can apply.

    Quality Assurance Department – OSD

    Senior Executive / Assistant Manager – QA

    Qualifications: B.Pharm / M.Pharm
    Experience: 5 – 10 Years

    Required Experience: Equipment Qualification.

    Officer / Assistant Manager – QA

    Qualifications: B.Pharm / M.Pharm
    Experience: 3 – 12 Years

    Required Experience: IPQA, Line Clearance, Sampling, In-Process Check and Team Lead activities.

    Quality Control Department – OSD

    Officer / Executive – QC

    Qualifications: B.Pharm / M.Pharm / M.Sc
    Experience: 3 – 7 Years

    Required Experience: GLP Analyst.

    Eligibility & Qualifications

    Candidates with the following qualifications are eligible for the respective positions:

    ITI | Diploma | B.Sc | B.Pharm | M.Pharm | M.Sc

    Production – OSD

    Plant Operator / Technical Assistant: ITI / Diploma / B.Sc

    Packing – OSD

    Plant Operator / Technical Assistant: ITI / Diploma / B.Sc

    Executive / Sr. Executive: B.Pharm / M.Pharm / M.Sc

    FTE / Trainee: ITI / Diploma

    Quality Assurance – OSD

    Senior Executive / Assistant Manager: B.Pharm / M.Pharm

    Officer / Assistant Manager: B.Pharm / M.Pharm

    Quality Control – OSD

    Officer / Executive: B.Pharm / M.Pharm / M.Sc

    Experience Required

    • Production – Plant Operator / Technical Assistant: 3 – 7 Years

    • Packing – Plant Operator / Technical Assistant: 3 – 8 Years

    • Packing – Executive / Sr. Executive: 4 – 8 Years

    • Packing – FTE / Trainee: Freshers can apply

    • QA – Senior Executive / Assistant Manager: 5 – 10 Years

    • QA – Officer / Assistant Manager: 3 – 12 Years

    • QC – Officer / Executive: 3 – 7 Years

    Key Experience Areas

    Production – OSD

    Candidates should have experience in:

    • Compression

    • Granulation

    Packing – OSD

    Candidates should have experience in:

    Quality Assurance – OSD

    Relevant experience includes:

    • Equipment Qualification

    • IPQA

    • Line Clearance

    • Sampling

    • In-Process Check

    • Team Lead activities

    Quality Control – OSD

    Candidates should have experience as a GLP Analyst.

    How to Apply

    Interested candidates can attend the Zydus Lifesciences Limited Walk-In Interview on 26 September 2026, between 9:00 AM and 3:00 PM.

    Walk-In Venue

    Zydus Animal Health and Investments Limited
    Plot No. 12 & 13, Pharmez-SEZ,
    Sarkhej Bavla NH, BA, Matoda,
    Ahmedabad – 382213

    Candidates should use the Scan to Apply option provided in the official recruitment notification for registration/application.

    Job Summary

    Company Zydus Lifesciences Limited
    Vacancies Plant Operator / Technical Assistant – Production; Plant Operator / Technical Assistant – Packing; Executive / Sr. Executive – Packing; FTE / Trainee – Packing; Senior Executive / Assistant Manager – QA; Officer / Assistant Manager – QA; Officer / Executive – QC
    Required Education ITI; Diploma; B.Sc; B.Pharm; M.Pharm; M.Sc
    Experience Freshers to 12 Years, depending on the position