Category: Featured

Fortrea Fresher Clinical Research Professionals 🔥Start-up Associate

B.Sc/M.Sc Life Sciences | Nursing | Medical Technology
0–2+ Years

Apply Here  https://pharmastuff.org/job/fortrea-start-up-associate

Oscar Medicare Pvt. Ltd. is hiring B.Sc. and M.Sc. Biochemistry freshers for its Biochemistry Department in New Delhi. The opportunity is suitable for candidates who have completed their graduation or postgraduation in Biochemistry. The position is within the In-Vitro Diagnostics (IVD) industry. Interested candidates can apply by sharing their updated CV with the recruitment team.

Oscar Medicare Pvt. Ltd. – Biochemistry

Job Position

Department: Biochemistry
Experience: Fresher
Qualification: B.Sc. / M.Sc. in Biochemistry
Location: New Delhi
Industry: In-Vitro Diagnostics (IVD)

Biochemistry Department – Fresher

B.Sc. / M.Sc. Biochemistry

Oscar Medicare Pvt. Ltd. is looking for enthusiastic and motivated B.Sc. / M.Sc. Biochemistry freshers to join its team.

Candidates with a background in Biochemistry can apply for the available opportunity in the company’s In-Vitro Diagnostics (IVD) industry.

Eligibility & Qualifications

Candidates with the following qualifications are eligible to apply:

B.Sc. Biochemistry | M.Sc. Biochemistry

B.Sc. Biochemistry

Candidates who have completed B.Sc. in Biochemistry can apply.

M.Sc. Biochemistry

Candidates who have completed M.Sc. in Biochemistry can apply.

Experience Required

Biochemistry Fresher

Experience: Fresher

The recruitment opportunity is specifically for freshers. Prior work experience is not mentioned in the recruitment announcement.

Department & Industry

Biochemistry Department

The opening is available in the Biochemistry Department.

In-Vitro Diagnostics (IVD)

The position is associated with the In-Vitro Diagnostics (IVD) industry.

Job Location

Oscar Medicare Pvt. Ltd.

New Delhi

Candidates interested in Biochemistry jobs in the IVD industry can apply for this opportunity.

How to Apply

Interested candidates can share their updated CV with Oscar Medicare Pvt. Ltd.

CV Submission

Email: rashi.uppal@oscarbio.com

Candidates should attach their updated CV while applying for the Biochemistry opportunity.

Job Summary

MSN Laboratories is conducting a Walk-In Drive for its Formulation Division at Chinna Chilkamarrri, Telangana. The opening is for the Production Injectables department and is suitable for freshers. Candidates with SSC, ITI or Intermediate qualifications can apply for the available opportunity. The walk-in interview is scheduled for Saturday, 26 September 2026, from 9:00 AM to 4:00 PM.

MSN Laboratories – Production Injectables

Walk-In Interview Details

Date: Saturday, 26 September 2026
Time: 9:00 AM to 4:00 PM

Work Location:
Unit V, Chinna Chilkamarrri

Interview Location:
Unit-5 Chinna Chilkamarrri,
25GX+XHX, Solipur,
Chinna Chilkamarrri, Telangana – 509216

Production Department – Injectables

Production Injectables – Fresher

Department: Production Injectables
Qualification: SSC / ITI / Intermediate
Skill: Freshers
Experience: Freshers

The opening is intended for freshers interested in starting their career in pharmaceutical injectable production.

Eligibility & Qualifications

Candidates with the following educational qualifications can apply:

SSC | ITI | Intermediate

Production Injectables

SSC | ITI | Intermediate

The recruitment notification specifically lists these qualifications for the Production Injectables opportunity.

Experience Required

Production Injectables

Experience: Fresher

Freshers can apply for this opportunity. No prior pharmaceutical industry experience is specified in the recruitment notification.

Job Location

MSN Laboratories – Formulation Division

Work Location: Unit V, Chinna Chilkamarrri, Telangana

Interview Location

Unit-5 Chinna Chilkamarrri
25GX+XHX, Solipur,
Chinna Chilkamarrri, Telangana – 509216

Documents Required

Candidates attending the walk-in interview are requested to bring:

• Updated Resume
• Photocopy of Educational Certificates
• Latest Increment Letter
• Last 3 Months’ Payslips
• Last 6 Months’ Bank Statements
• Passport Size Photographs
• Aadhaar Card Copy

How to Apply

Interested candidates can attend the MSN Laboratories Walk-In Drive on Saturday, 26 September 2026, between 9:00 AM and 4:00 PM.

Walk-In Venue

Unit-5 Chinna Chilkamarrri
25GX+XHX, Solipur,
Chinna Chilkamarrri, Telangana – 509216

Candidates can scan the QR code provided in the recruitment notification for the location and should carry all the required documents to the interview.

Job Summary

Lupin Limited is conducting a Walk-In Interview for experienced professionals in the Quality Control and Quality Assurance departments. The openings are available for Officer / Executive and Officer positions across formulation, API and QA functions. Candidates with B.Pharm or M.Sc qualifications and relevant pharmaceutical industry experience can apply. USFDA and MHRA regulatory exposure is mandatory for the available positions.

Lupin Limited Walk-In Interview

Walk-In Interview Details

Date: 26 & 27 September 2026
Day: Saturday & Sunday
Time: 9:00 AM – 6:00 PM

Interview Venue:
Hotel KC Cross Road
Panchkula

Job Location: Pithampur, Indore

Quality Control Department – Lupin Limited

Officer / Executive – QC Formulation

Area: FG / In-Process (Nasal / Derma / MDI & DPI)
Experience: Minimum 2 to 10 Years
Qualification: B.Pharm / M.Sc

Job Profile

• Analyze finished products such as Nasal, Derma and MDI/DPI using tests including Assay, RS, SCU, Spray Pattern, APSD (NGI), DDU and FPM.
• Perform physical tests.
• Operate and maintain instruments including HPLC/GC (Chromeleon), UV, pH meter and Spray View.
• Ensure compliance with GMP, data integrity and 21 CFR Part 11.
• Maintain accurate QC documentation.

Quality Control Department – API

Officer / Executive – QC API

Experience: Minimum 2 to 10 Years
Qualification: B.Pharm / M.Sc

Job Profile

• Perform in-process, HT and stability testing of API products using HPLC, UV, GC, IR and Polarimeter.
• Maintain laboratory documentation as per cGMP, GLP and data integrity requirements.
• Support OOS / OOT investigations.

Quality Control Department – OSD Stability

Officer / Executive – QC Formulation OSD

Area: Stability Section
Experience: Minimum 2 to 10 Years
Qualification: B.Pharm / M.Sc

Job Profile

• Perform stability testing of formulation products as per approved protocols.
• Conduct analysis using HPLC, UV, Dissolution and other analytical instruments.
• Maintain laboratory documentation in compliance with cGMP, GLP and Data Integrity requirements.
• Ensure timely completion of stability studies and reporting.

Quality Control Department – OSD FG / In-Process

Officer / Executive – QC Formulation OSD

Area: FG / In-Process
Experience: Minimum 2 to 10 Years
Qualification: B.Pharm / M.Sc

Job Profile

• Perform analysis of finished products (FG) using HPLC, GC, UV and other analytical instruments in OSD formulations.
• Expertise in pharmaceutical quality systems such as LIMS, QAMS and SAP.
• Handle OOS / OOT and laboratory deviations.

Quality Assurance Department – API

Officer – QA API

Experience: Minimum 3 to 5 Years
Qualification: B.Pharm / M.Sc

Job Profile

• Handle QMS and QRM activities.
• Perform IPQA checks and Line Clearance.
• Execute Process Validation and Cleaning Sampling.
• Review BPR, BMR and Cleaning Records.
• Verify CSV (Computer System Validation) activities.
• Ensure cGMP compliance and documentation accuracy.

Eligibility & Qualifications

Candidates with the following qualifications can apply for the available positions:

B.Pharm | M.Sc

Quality Control – Formulation

B.Pharm | M.Sc

Relevant areas include:

• FG / In-Process
• Nasal
• Derma
• MDI / DPI
• OSD

Quality Control – API

B.Pharm | M.Sc

Quality Assurance – API

B.Pharm | M.Sc

Experience Required

• QC Formulation – FG / In-Process: Minimum 2 – 10 Years
• QC API: Minimum 2 – 10 Years
• QC Formulation OSD – Stability: Minimum 2 – 10 Years
• QC Formulation OSD – FG / In-Process: Minimum 2 – 10 Years
• QA API: Minimum 3 – 5 Years

Key Skills & Experience Areas

Quality Control

Candidates should have relevant experience in:

• HPLC
• GC
• UV
• IR
• Polarimeter
• Dissolution
• Stability Testing
• In-Process Testing
• Finished Product Analysis
• OOS / OOT Investigation
• Laboratory Deviations
• LIMS
• QAMS
• SAP

Quality Assurance

Candidates should have experience in:

• QMS
• QRM
• IPQA
• Line Clearance
• Process Validation
• Cleaning Sampling
• BPR / BMR Review
• Cleaning Records
• CSV
• cGMP Compliance
• Documentation

Mandatory Requirement

USFDA & MHRA Regulatory Exposure

USFDA and MHRA regulatory exposure is mandatory.

Candidates without regulated-market exposure will not be considered.

Marks Requirement

Candidates with less than 5 years of experience must have 60% marks as specified in the recruitment notification.

Previous Interview Eligibility

Candidates who have been interviewed by Lupin in the last 6 months are not eligible to apply.

Documents Required

Candidates attending the walk-in interview should carry:

• Latest Resume
• Last 3 Salary Slips
• Revision / Increment Letter
• Relieving Letters from all previous organizations

Candidates should carry the required documents to the interview venue.

How to Apply

Interested candidates meeting the eligibility criteria can attend the Lupin Limited Walk-In Interview on 26 & 27 September 2026, between 9:00 AM and 6:00 PM.

Interview Venue

Hotel KC Cross Road
Panchkula

Contact Details

Email: suhailkhanl@lupin.com
Phone: 9617733913

Candidates should carry their latest resume and required salary and employment documents.

Job Summary

Intas Pharmaceuticals Ltd. is conducting a Walk-In Drive for SEZ for multiple positions across Injectable Manufacturing, OSD Packing, Quality Control and Quality Assurance. The recruitment includes Senior Officer, Officer, Executive and Technician positions for candidates with relevant pharmaceutical industry experience. Candidates with B.Pharm, M.Pharm, B.Sc, M.Sc, Diploma and ITI qualifications can apply for the respective roles. The walk-in drive is scheduled from 30 September 2026 to 3 October 2026 at Intas Pharmze, Ahmedabad.

Intas Pharmaceuticals – Walk-In Drive for SEZ

Walk-In Interview Details

Date: 30th September 2026 to 3rd October 2026
Time: 09:00 AM to 04:00 PM

Venue:
Intas Pharmaceutical Ltd. (Pharmez)
Plot No. 5 to 14, Pharmez, Near Village: Matoda,
Sarkhej – Bavla National Highway No. 8-A,
Taluka: Sanand, Dist: Ahmedabad – 382213

Injectable Manufacturing Department – Intas Pharmaceuticals

Senior Officer / Officer / Technician

Qualification: B.Pharm / Diploma / ITI / B.Sc
Experience: 03 to 08 Years

Candidates with relevant experience in injectable manufacturing can apply for the available Senior Officer, Officer and Technician positions.

OSD Packing Department – Intas Pharmaceuticals

Senior Officer / Officer / Technician

Qualification: B.Pharm / B.Sc / Diploma / ITI
Experience: 03 to 10 Years

The position is available for candidates with relevant OSD packing experience.

Quality Control Department – HPLC / FP / AMV / Stability

Executive / Senior Officer

Qualification: B.Pharm / M.Sc
Experience: 04 to 09 Years
Shift: Shift Working

Relevant experience in HPLC, FP, AMV and Stability is applicable to this position.

Quality Control Department – Microbiology

Executive / Senior Officer

Area: Environmental Monitoring
Qualification: M.Sc / B.Pharm
Experience: 04 to 09 Years

Candidates with relevant Quality Control Microbiology and Environmental Monitoring experience can apply.

Quality Assurance Department – IPQA

Executive / Senior Officer / Officer

Area: Injectable / OSD
Qualification: B.Pharm / M.Pharm
Experience: 03 to 08 Years
Shift: Shift Working

Candidates with relevant IPQA experience in Injectable or OSD manufacturing can apply.

Quality Assurance Department – Qualification

Executive / Senior Officer / Officer

Qualification: B.Pharm / M.Sc
Experience: 03 to 08 Years
Shift: Shift Working

Candidates with relevant experience in qualification activities can apply.

Quality Assurance Department – QMS

Sr. Officer / Executive

Area: QMS (Injectable)
Qualification: M.Pharm / B.Pharm
Experience: 04 to 08 Years
Shift: Shift Working

Candidates with relevant experience in Quality Management Systems for injectable operations can apply.

Eligibility & Qualifications

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

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

Injectable Manufacturing

B.Pharm | Diploma | ITI | B.Sc

OSD Packing

B.Pharm | B.Sc | Diploma | ITI

Quality Control – HPLC / FP / AMV / Stability

B.Pharm | M.Sc

Quality Control – Microbiology

M.Sc | B.Pharm

Quality Assurance – IPQA

B.Pharm | M.Pharm

Quality Assurance – Qualification

B.Pharm | M.Sc

Quality Assurance – QMS

M.Pharm | B.Pharm

Experience Required

• Injectable Manufacturing: 03 – 08 Years
• OSD Packing: 03 – 10 Years
• QC – HPLC / FP / AMV / Stability: 04 – 09 Years
• QC – Micro / Environmental Monitoring: 04 – 09 Years
• QA – IPQA: 03 – 08 Years
• QA – Qualification: 03 – 08 Years
• QA – QMS (Injectable): 04 – 08 Years

Key Experience Areas

Injectable Manufacturing

Relevant experience in injectable manufacturing is required for the respective position.

OSD Packing

Candidates applying for the OSD Packing positions should have relevant pharmaceutical packing experience.

Quality Control

The available QC positions cover:

• HPLC
• FP
• AMV
• Stability
• Microbiology
• Environmental Monitoring

Quality Assurance

The QA positions cover:

• IPQA
• Injectable / OSD operations
• Qualification
• QMS
• Injectable Quality Management Systems

Important Requirements

Pharmaceutical Manufacturing Experience

Formulation pharmaceutical experience is required for all vacant positions, particularly experience in a regulated manufacturing plant such as USFDA, MHRA or EU-regulated facilities.

Shift Working

Several positions specifically require candidates to be comfortable with shift working.

Previous Interview Candidates

Candidates who have appeared for an interview at Intas within the last six months are requested not to apply.

Shift Duties

Candidates must be open to working in shift duties and should have relevant pharmaceutical industry experience.

Documents Required

Candidates attending the walk-in interview should carry:

• Updated Resume
• Educational Documents
• Experience Documents
• Salary Documents

Candidates should carry the required original and photocopies of their final-year mark sheets / degree certificate / CTC breakup / salary slip, as mentioned in the recruitment notification.

How to Apply

Interested candidates can attend the Intas Pharmaceuticals Walk-In Drive for SEZ between 30th September 2026 and 3rd October 2026, from 09:00 AM to 04:00 PM.

Walk-In Venue

Intas Pharmaceutical Ltd. (Pharmez)
Plot No. 5 to 14, Pharmez, Near Village: Matoda,
Sarkhej – Bavla National Highway No. 8-A,
Taluka: Sanand, Dist: Ahmedabad – 382213

Candidates should attend the walk-in interview with their updated resume and required educational, experience and salary documents.

Company Website

www.intaspharma.com

Important Note

Intas Pharmaceuticals Ltd. does not directly or indirectly charge any fee for job application, processing, training or testing. Candidates should not participate in any such invitation or payment request claiming to represent the company.

Job Summary

**Omega Healthcare Hiring Medical Coding Freshers 🔥**
**Medical Coding Trainee – Specialty Coding | Chennai**
**Paramedical | Life Sciences | Certified & Non-Certified**
**Freshers | 400+ Openings | Anatomy | Training + Placement**
**₹19,000/Month |

Apply Here ❤️** https://pharmastuff.org/job/omega-healthcare-fresher-medical-coders

MSN Laboratories Walk-In Interview 2026 – R&D Center

MSN Laboratories is conducting a Walk-In Drive at its R&D Center in Hyderabad for experienced professionals across Regulatory Affairs and Kilo Lab (Production, Pilot Plant) departments.
The recruitment drive includes opportunities for candidates with 1–15 years of experience and qualifications ranging from B.Sc. and M.Sc. to M.Pharm.
Open positions are available in Regulatory Affairs – API, Kilo Lab (Production, Pilot Plant), and Regulatory Affairs – Formulation.
Eligible candidates can attend the walk-in interview on 9 October 2026, with free transportation and a subsidised canteen listed among the available perks.

MSN Laboratories R&D Walk-In Drive

Regulatory Affairs – API

Experience: 3–15 Years
Qualification: M.Sc.

Candidates with an M.Sc. qualification and relevant experience can attend the walk-in drive for opportunities in the Regulatory Affairs – API department.

Kilo Lab – Production, Pilot Plant

Experience: 1–5 Years
Qualification: B.Sc., M.Sc.

The Kilo Lab opportunity covers Production and Pilot Plant activities at the MSN Laboratories R&D Center.

Regulatory Affairs – Formulation

Experience: 1–10 Years
Qualification: M.Pharm

Candidates with M.Pharm qualification and relevant experience can attend the walk-in interview for the Regulatory Affairs – Formulation department.

Eligibility & Qualifications

The recruitment drive lists the following qualifications according to the respective departments:

• M.Sc. – Regulatory Affairs – API
• B.Sc. / M.Sc. – Kilo Lab (Production, Pilot Plant)
• M.Pharm – Regulatory Affairs – Formulation

Eligible Qualification Courses

B.Sc. | M.Sc. | M.Pharm

Job Location & Work Details

Company: MSN Laboratories Pvt. Ltd.

Location: R&D Center, Hyderabad, Telangana

Job Type: Full Time

Work Location: MSN Laboratories R&D Center

Perks

• Free Transportation
• Subsidised Canteen

Walk-In Interview Details

Date & Time

Date: 9 October 2026, Friday
Time: 9:30 AM to 4:00 PM

Interview Venue

MSN Laboratories Pvt. Ltd., R&D Center
Pashamylaram,
Patancheru Mandal,
Sangareddy District,
Hyderabad, Telangana – 502307

Documents to Carry

Candidates are requested to bring the following documents:

• Resume
• Photocopies of educational certificates
• Passport-size photographs
• Aadhaar Card copy
• PAN Card copy

Candidates should carry the required documents to the interview venue.

Contact Details

For recruitment-related queries:

Dinesh Baratam
Phone: 9154811048
Email: dinesh.baratam@msnlabs.com

Teja Mani Varma
Phone: 9247908031
Email: tejaman i.vemanamanda@msnlabs.com

Vijay G
Phone: 9247949257
Email: vijay.gajjina@msnlabs.com

How to Apply

Interested and eligible candidates can attend the MSN Laboratories Walk-In Drive on 9 October 2026 between 9:30 AM and 4:00 PM at the R&D Center in Pashamylaram, Patancheru Mandal, Sangareddy District, Hyderabad.

Candidates should bring their resume, educational certificates, passport-size photographs, Aadhaar Card copy, and PAN Card copy.

Job Summary

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

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

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