Torrent Pharmaceuticals: Walk-In Drive for Experienced Bioanalytical R&D & Quality Control (QC) Scientists

Torrent Pharmaceuticals Limited—a leading multinational pharmaceutical major with state-of-the-art USFDA, MHRA, and WHO-GMP approved manufacturing and R&D facilities—is hosting a walk-in recruitment drive for experienced Bioanalytical R&D Scientists and Quality Control (QC) professionals.

Key Job Details

• Company Name: Torrent Pharmaceuticals Ltd.
• Designation: Executive / Technical Assistant – Bioanalytical R&D & Quality Control
• Target Experience: 2 to 8 Years in Bioanalytical Method Development / QC Operations
• Educational Qualification: M.Sc / M.Pharm / B.Pharm / B.Sc
• Job Location: R&D Centre (Gandhinagar, Gujarat) / Baddi Plant (Himachal Pradesh)
• Employment Type: Full-Time, Permanent

Detailed Department Breakdown

1. Bioanalytical R&D (Gandhinagar R&D Centre)

• Qualifications: M.Pharm / M.Sc (Analytical / Bio-analytical Chemistry)
• Core Responsibilities:
  • Method development, validation, and sample analysis using LC-MS/MS, SPE, and LLE extraction techniques for drug substance and bio-equivalence studies.
  • Routine maintenance, calibration, and operation of high-sensitivity mass spectrometers in compliance with GLP and Good Documentation Practices (GDP).
  • Assisting in bioanalytical study report generation for USFDA, EMA, and ANVISA regulatory filings.

2. Quality Control (QC - Formulation & Finished Products)

• Qualifications: B.Sc / M.Sc / B.Pharm / M.Pharm
• Core Responsibilities:
  • Testing finished products, stability samples, and raw materials using HPLC, GC, UV-Vis, FTIR, and KF titrators.
  • Data processing and audit trail management using Empower CDS software strictly following 21 CFR Part 11 guidelines and ALCOA+ data integrity norms.
  • Laboratory investigation management for OOS, OOT, and Unconfirmed Test Results.

📅 Walk-In Schedule & Venue Details

📋 Checklist of Documents Required

• Updated Resume / CV (2 Copies)
• Academic Certificates & Marksheets (Graduation / Post-Graduation)
• Current Employer Appointment Letter & Recent Salary Revision / Increment Letter
• Last 3 Months' Pay Slips & Bank Statements
• Government Photo ID Proof (Aadhaar Card and PAN Card)

📩 Direct E-mail Application Channel

Candidates unable to attend the walk-in interview in person can submit their CV directly to Torrent Pharma's Talent Acquisition Desk:

• 📧 Direct HR Email: meghamaheshwari@torrentpharma.com / vilshashah@torrentpharma.com
• 📌 Subject Line Format: Application for [Bioanalytical/QC] - [Years of Exp] - [Current Location] - [Your Name]
  • Example: Application for Bioanalytical Executive - 4 Years - Ahmedabad - Viral Patel

Fortrea India: Hiring Experienced Clinical Data Managers & Clinical Data Scientists (CDM / CDISC)

Fortrea India—a global Contract Research Organization (CRO) leading clinical development solutions—is actively hiring experienced Clinical Data Managers (CDM) and Clinical Data Scientists to drive end-to-end data validation, database design, and risk-based data monitoring for global Phase I–IV clinical trials.

Key Job Details

• Company Name: Fortrea India
• Designation: Senior Clinical Data Manager / Lead Clinical Data Scientist
• Target Experience: 3 to 8 Years in Clinical Data Management (CDM) & CDISC Standards
• Educational Qualification: B.Pharm / M.Pharm / B.Tech (Biotechnology/Bioinformatics) / M.Sc (Bio-Statistics / Life Sciences) / MCA
• Job Location: Bengaluru / Hyderabad / Mumbai / Remote (Hybrid)
• Employment Type: Full-Time, Permanent

Detailed Scope of Work & Responsibilities

1. Data Management Plan (DMP) & Electronic Data Capture (EDC)

• Designing and reviewing Data Management Plans (DMP), Data Transfer Agreements (DTA), and Case Report Form (eCRF) completion guidelines.
• Overseeing EDC platform database setup, testing User Acceptance Testing (UAT) scripts, and defining edit check specifications on Medidata Rave, Oracle InForm, or Veeva EDC.
• Managing external data reconciliation (Central Lab, eCOA/ePRO, PK/PD, and Biomarker data) against study databases.

2. Clinical Data Validation, Discrepancy Management & CDISC Standards

• Executing query management, issuing manual queries, reviewing auto-queries, and resolving data discrepancies following Good Clinical Data Management Practices (GCDMP).
• Standardizing raw clinical data into CDISC SDTM (Study Data Tabulation Model) and ADaM (Analysis Data Model) specifications.
• Conducting database lock procedures, blinded data reviews (BDR), and final audit reconciliation prior to statistical analysis.

Selection & Interview Process

1. Profile Shortlisting: Technical assessment of EDC system proficiency, SDTM domain knowledge, and experience handling global trial databases.
2. Technical Discussion: Technical interview with CDM Leads focusing on complex edit check logic, UAT validation, lab data reconciliation scenarios, and ICH-GCP E6(R2) risk-based monitoring.
3. HR & Delivery Management Review: Evaluation of remote/hybrid alignment, client communication skills, notice period, and compensation package.

📋 Checklist of Documents Required

• Updated Resume / CV (2 Copies)
• CDISC / EDC Platform Certifications (if applicable)
• Academic Marksheets & Degree Certificates (Graduation / Post-Graduation)
• Current Employer Appointment Letter & Recent Salary Revision Letter
• Last 3 Months' Pay Slips & Bank Statements
• Government Photo ID Proof (Aadhaar Card and PAN Card)

📩 Direct E-mail Application Channel

Qualified Clinical Data Management professionals can submit their CV directly to Fortrea India's Clinical Data Science Recruitment Team:

• 📧 Direct HR Email: cdm.careers@fortrea.com
• 📌 Subject Line Format: Application for CDM - [EDC Platform/SDTM] - [Years of Exp] - [Current Location] - [Your Name]
  • Example: Application for Senior CDM - Medidata Rave - 5 Years - Bengaluru - Rajesh Kumar

Syngene International: Walk-In Drive for Experienced Analytical R&D (AR&D) & Formulation R&D (F&D) Professionals

Syngene International Limited—a world-class Contract Research, Development, and Manufacturing Organization (CRDMO) under the Biocon Group—is hosting a walk-in recruitment drive for experienced Analytical R&D (AR&D) and Formulation R&D (F&D) scientists for its integrated R&D centre.

Key Job Details

• Company Name: Syngene International Limited
• Designation: Research Associate / Senior Research Associate / Scientist
• Target Experience: 2 to 8 Years in Pharma R&D / CRDMO Operations
• Educational Qualification: M.Sc (Analytical / Organic Chemistry) / M.Pharm (Pharmaceutics) / Ph.D.
• Job Location: Bengaluru (Biocon Park, Karnataka) / Hyderabad (SEZ, Telangana)
• Employment Type: Full-Time, Permanent

Detailed Department Breakdown

1. Analytical R&D (AR&D - Small Molecules & Biologics)

• Qualifications: M.Sc (Analytical Chemistry) / M.Pharm / Ph.D.
• Core Responsibilities:
  • Analytical method development, validation, and forced degradation studies using HPLC, UPLC, LC-MS/MS, GC-MS, and ICP-MS.
  • Structural characterization of impurities, degradation products, and extractables & leachables (E&L).
  • Adherence to ICH Q2(R1) guidelines, electronic lab notebooks (ELN), and 21 CFR Part 11 data integrity compliance under CDS platforms (Empower 3).

2. Formulation R&D (F&D - Oral Solids & Injectables)

• Qualifications: M.Pharm (Pharmaceutics) / Ph.D.
• Core Responsibilities:
  • Formulation design, execution, and lab-scale process development for Oral Solid Dosage (OSD) forms, Sterile Injectables, and Complex Drug Delivery Systems.
  • Applying Quality by Design (QbD) principles, Design of Experiments (DoE), and scale-up studies from lab to pilot plant.
  • Stability testing evaluation and technology transfer documentation to commercial manufacturing units.

📅 Walk-In Schedule & Venue Details

📋 Checklist of Documents Required

• Updated Resume / CV (2 Copies)
• Current Employer Appointment Letter & Latest Salary Increment Letter
• Last 3 Months' Pay Slips & Bank Statements
• Post-Graduation / Ph.D. Degree Certificates & Transcripts
• Government Photo ID Proof (Aadhaar Card and PAN Card)

📩 Direct E-mail Application Channel

Candidates unable to attend the walk-in drive in person can submit their CV directly to the Syngene Talent Acquisition team:

• 📧 Direct HR Email: ard.careers@syngeneintl.com / fnd.careers@syngeneintl.com
• 📌 Subject Line Format: Application for [AR&D/F&D] - [Years of Exp] - [Current Location] - [Your Name]
  • Example: Application for AR&D Scientist - 5 Years - Bengaluru - Priya Nair

Micro Labs: Walk-In Drive for Experienced Quality Control (QC), QA & Production Professionals

Micro Labs Limited—a leading research-driven healthcare organization with USFDA, WHO-GMP, and MHRA accreditations—is hosting a walk-in recruitment drive for experienced professionals in Quality Control (QC), Quality Assurance (QA), and Production for its formulation plants.

Key Job Details

• Company Name: Micro Labs Limited
• Designation: Officer / Executive / Senior Executive
• Target Experience: 2 to 7 Years in Oral Solid Dosage (OSD) / Injectable Manufacturing
• Educational Qualification: B.Pharm / M.Pharm / B.Sc / M.Sc (Analytical / Organic Chemistry)
• Job Location: Bengaluru (Bommasandra / Veerasandra, Karnataka) & Goa
• Employment Type: Full-Time, Permanent

Detailed Department Breakdown

1. Quality Control (QC - Formulations & Injectables)

• Qualifications: M.Sc (Chemistry) / B.Pharm / M.Pharm
• Core Responsibilities:
  • Routine, stability, and raw material testing using HPLC, GC, UV-Vis Spectrophotometer, and Dissolution test apparatus.
  • Operation and data management via Empower 3 CDS following 21 CFR Part 11 guidelines and ALCOA+ principles.
  • Handling laboratory investigations for Out of Specification (OOS), Out of Trend (OOT), and laboratory incidents.

2. Quality Assurance (QA - IPQA & QMS)

• Qualifications: B.Pharm / M.Pharm
• Core Responsibilities:
  • Execution of In-Process Quality Assurance (IPQA), line clearance, and environmental monitoring checks in OSD/Sterile areas.
  • Managing QMS elements: Deviations, Change Control, CAPA, and vendor qualification records using TrackWise.
  • Reviewing Executed Batch Manufacturing Records (eBMR) and cleaning validation protocols.

3. Production & Packaging (OSD / Sterile)

• Qualifications: B.Pharm / M.Pharm / B.Sc
• Core Responsibilities:
  • Operation and supervision of high-speed Granulation, Compression (Fette/Korsch), Coating, and Aseptic Filling machinery.
  • Managing primary and secondary packaging compliance, line clearance, and shift throughput metrics under cGMP standards.

📅 Walk-In Schedule & Venue Details

📋 Checklist of Documents Required

• Updated Resume / CV (2 Copies)
• Current Employer Appointment Letter & Recent Increment Letter
• Last 3 Months' Pay Slips & Bank Statements
• Academic Marksheets & Degree Certificates (Graduation / Post-Graduation)
• Government Photo ID Proof (Aadhaar Card and PAN Card)

📩 Direct E-mail Application Channel

Candidates unable to attend the walk-in drive in person can submit their CV directly to the Micro Labs recruitment desk:

• 📧 Direct HR Email: ta.blr@microlabs.in / exihr@microlabs.in
• 📌 Subject Line Format: Application for [QC/QA/Production] - [Years of Exp] - [Current Location] - [Your Name]
  • Example: Application for QC Executive - 4 Years - Bengaluru - Suresh Kumar

Caplin Point Laboratories: Walk-In Drive for Experienced Sterile Injectables & Analytical R&D Professionals

Caplin Point Laboratories Limited—a fast-growing, research-driven pharmaceutical major with USFDA, EU-GMP, and INVIMA approvals—is conducting a walk-in recruitment drive for experienced professionals in Sterile Injectables (Production & QA) and Analytical R&D (AR&D) for its state-of-the-art facilities.

Key Job Details

• Company Name: Caplin Point Laboratories Ltd.
• Designation: Executive / Senior Executive / Assistant Manager
• Target Experience: 2 to 7 Years in Injectables / Ophthalmic / API & Formulation AR&D
• Educational Qualification: B.Pharm / M.Pharm / M.Sc (Chemistry / Analytical Chemistry)
• Job Location: Chennai (Gummidipoondi / Perungudi, Tamil Nadu)
• Employment Type: Full-Time, Permanent

Detailed Department Breakdown

1. Analytical Research & Development (AR&D - Formulations / API)

• Qualifications: M.Sc (Analytical Chemistry / Organic Chemistry) / M.Pharm
• Core Responsibilities:
  • Method development, validation, and transfer for Sterile Injectables, Ophthalmic, and Complex Formulations using HPLC, UPLC, GC, and LC-MS.
  • Structural elucidation, degradation product analysis, and impurity profiling in compliance with ICH Q2(R1) guidelines.
  • Operation and maintenance of CDS platforms (Empower 3) following strict 21 CFR Part 11 data integrity standards.

2. Sterile Injectable Production & Aseptic QA

• Qualifications: B.Pharm / M.Pharm
• Core Responsibilities:
  • Operations involving Vial Filling, Lyophilizers, Isolators, Autoclaves, and CIP/SIP systems.
  • Executing In-Process Quality Assurance (IPQA), line clearance, environmental monitoring supervision, and media fill trial validations.
  • Investigation of deviations, CAPA execution, and eBMR review for USFDA / EU-GMP compliance.

📅 Walk-In Schedule & Venue Details

📋 Checklist of Documents Required

• Updated Resume / CV (2 Copies)
• Academic Marksheets & Degree Certificates (Graduation / Post-Graduation)
• Current Employer Appointment Letter & Recent Increment Letter
• Last 3 Months' Pay Slips & Bank Statements
• Government Photo ID Proof (Aadhaar Card and PAN Card)

📩 Direct E-mail Application Channel

Candidates unable to attend the walk-in drive in person can submit their CV directly to the Caplin Point recruitment desk:

• 📧 Direct HR Email: careers@caplinpoint.net / hr@caplinpoint.net
• 📌 Subject Line Format: Application for [AR&D/Injectable QA/Production] - [Years of Exp] - [Current Location] - [Your Name]
  • Example: Application for AR&D Executive - 4 Years - Chennai - K. Ramesh

Dr. Reddy’s Laboratories: Hiring Experienced Pharmacovigilance (PV) & Drug Safety Professionals

Dr. Reddy’s Laboratories Ltd.—a leading multinational pharmaceutical enterprise with global footprints across US, Europe, and Emerging Markets—is actively hiring experienced Pharmacovigilance (PV) & Drug Safety professionals for its Global Safety & Regulatory Operations unit.

Key Job Details

• Company Name: Dr. Reddy’s Laboratories Ltd.
• Designation: Safety Analyst / Drug Safety Associate / Senior Specialist – Pharmacovigilance
• Target Experience: 2 to 6 Years in Individual Case Safety Report (ICSR) Processing / Aggregate Safety Reporting
• Educational Qualification: B.Pharm / M.Pharm / Pharm.D / MBBS / BDS / M.Sc (Life Sciences)
• Job Location: Hyderabad (Telangana) / Remote (Hybrid)
• Employment Type: Full-Time, Permanent

Detailed Department Breakdown & Scope of Work

1. ICSR Case Processing & Medical Assessment

• End-to-end processing of Individual Case Safety Reports (ICSRs) from clinical trials (spontaneous, solicited) and post-marketing sources using industry-standard safety databases (Argus Safety / ARISg).
• Performing MedDRA coding of adverse event terms, medical history, and suspect drugs; drafting comprehensive narrative writing for serious and non-serious cases.
• Evaluation of causality, unexpectedness, and expectedness against Reference Safety Information (RSI), USPI, SmPC, and Investigator's Brochure (IB).

2. Aggregate Safety Reporting & Signal Management

• Assisting in authoring and medical review of aggregate safety documents including DSUR (Development Safety Update Reports), PSUR/PBRER (Periodic Safety Update Reports), and PADER.
• Performing signal detection, risk management plan (RMP) reviews, and adverse event surveillance across global health authority platforms (USFDA, EMA, MHRA, CDSCO).
• Handling safety query responses and supporting regulatory inspections and internal PV audits.

Selection & Interview Process

1. Profile Shortlisting: Technical screening based on hands-on Argus Safety usage, MedDRA coding proficiency, and ICSR workflow understanding.
2. Technical Interview: In-depth evaluation covering ICH-E2D guidelines, GVP modules, narrative framing, causality assessment models, and SAE handling timelines.
3. HR & Line Management Review: Notice period review, hybrid work arrangement discussions, and compensation alignment.

📋 Checklist of Documents Required

• Updated Resume / CV (2 Copies)
• Academic Marksheets & Degree Certificates (B.Pharm / M.Pharm / Pharm.D / Life Sciences)
• Current Employer Appointment Letter & Recent Increment Letter
• Last 3 Months' Pay Slips & Bank Statements
• Government Photo ID Proof (Aadhaar Card and PAN Card)

📩 Direct E-mail Application Channel

Qualified Pharmacovigilance professionals can submit their updated CV directly to the Dr. Reddy’s Global Safety Talent Acquisition Desk:

• 📧 Direct HR Email: pv.careers@drreddys.com
• 📌 Subject Line Format: Application for PV - [ICSR/Aggregate Reporting] - [Years of Exp] - [Current Location] - [Your Name]
  • Example: Application for PV Specialist - ICSR Argus - 4 Years - Hyderabad - Sumanth Rao