Hetero Drugs: Walk-In Drive for Experienced QC, QA & Production Professionals

Hetero Drugs Limited—one of India’s leading generic pharmaceutical companies and the world’s largest producer of anti-retroviral drugs—is hosting an off-campus walk-in recruitment drive for experienced professionals in Quality Control (QC), Quality Assurance (QA), and API Production.

Key Job Details

• Company Name: Hetero Drugs Limited
• Designation: Officer / Executive / Senior Executive
• Target Experience: 2 to 7 Years in API / Formulation Manufacturing
• Educational Qualification: B.Sc / M.Sc (Chemistry / Organic Chemistry) / B.Pharm / M.Pharm
• Job Location: Hyderabad & Visakhapatnam (AP & Telangana Units)
• Employment Type: Full-Time, Permanent

Detailed Department Breakdown

1. Quality Control (QC - API / Formulations)

• Qualifications: M.Sc (Chemistry / Organic Chemistry) / B.Pharm / M.Pharm
• Core Responsibilities:
  • Testing and analysis of Raw Materials, Intermediates, Finished Products, and Stability samples using HPLC, GC, UV-Vis, and Wet Chemistry.
  • Operation of CDS software (Empower 3) in adherence to 21 CFR Part 11 guidelines and data integrity standards.
  • Assisting in handling OOS, OOT, and laboratory investigation reports.

2. Quality Assurance (QA - IPQA & QMS)

• Qualifications: B.Pharm / M.Pharm / M.Sc
• Core Responsibilities:
  • Performing In-Process Quality Assurance (IPQA) checks during manufacturing and packaging.
  • Handling QMS documentation including Deviations, Change Controls, CAPA, and vendor qualification records.
  • Reviewing Executed Batch Production Records (eBPR) and cleaning validation protocols.

3. API Production & Manufacturing

• Qualifications: B.Sc / M.Sc (Chemistry) / Chemical Engineering / B.Pharm
• Core Responsibilities:
  • Handling reactors (GLR/SSR), centrifuges, dryers (FBD, VD, RCVD), and distillation units in compliance with cGMP.
  • Execution of batch manufacturing records (BMR) and shift yield optimization.

📅 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 Certificates & Degree Marksheets
• 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 Hetero talent acquisition desk:

• 📧 Direct HR Email: hdllabs@heterodrugs.com
• 📌 Subject Line Format: Application for [QC/QA/Production] - [Years of Exp] - [Current Location] - [Your Name]
  • Example: Application for QC Executive - 4 Years - Visakhapatnam - K. Srinivas

Aurobindo Pharma: Walk-In Drive for Experienced Regulatory Affairs (RA) Professionals

Aurobindo Pharma Limited—a leading global generic pharmaceutical manufacturer with extensive market presence across US, EU, and Emerging Markets—is conducting a walk-in recruitment drive for experienced Regulatory Affairs (RA) professionals for its corporate R&D centre.

Key Job Details

• Company Name: Aurobindo Pharma Limited
• Designation: Executive / Senior Executive / Assistant Manager – Regulatory Affairs
• Target Experience: 3 to 8 Years in Regulatory Affairs (Formulations / APIs)
• Educational Qualification: B.Pharm / M.Pharm (Drug Regulatory Affairs) / M.Sc
• Job Location: Hyderabad (Telangana)
• Employment Type: Full-Time, Permanent

Detailed Department Breakdown & Scope of Work

1. US & EU Market Submissions (eCTD Dossiers)

• Compilation, formatting, and submission of eCTD / CTD dossiers for ANDAs (USFDA), MAAs (EMA), and UK-MHRA regulatory filings.
• Reviewing Technical Dossiers, Drug Master Files (DMFs), Master Formula Records (MFR), and Process Validation reports to ensure global compliance.
• Preparing responses to Information Requests (IRs), Deficiency Letters, and Complete Response Letters (CRLs) issued by health authorities.

2. Lifecycle Management & Post-Approval Changes

• Handling post-approval regulatory changes including CBE-30, PAS, Special Supplements, and Annual Reports for approved drug products.
• Reviewing plant change controls (QMS) for potential impact on regulatory registrations across global markets.
• Coordinating with R&D, QC, QA, and production units for documentation support for new product submissions.

📅 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 (B.Pharm / M.Pharm / M.Sc)
• 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 updated CV directly to the Aurobindo Pharma HR desk:

• 📧 Direct HR Email: ra.careers@aurobindo.com
• 📌 Subject Line Format: Application for RA - [US/EU] - [Years of Exp] - [Current Location] - [Your Name]
  • Example: Application for RA - US Market - 5 Years - Hyderabad - Venkat Reddy

Lupin Limited: Walk-In Drive for Experienced Production & Manufacturing Professionals

Lupin Limited—a leading global pharmaceutical company—is conducting a walk-in recruitment drive for experienced professionals in Solid Oral Dosage (OSD) & Sterile Production / Packing at its manufacturing facility.

Key Job Details

• Company Name: Lupin Limited
• Designation: Associate / Officer / Executive – Production & Packing
• Target Experience: 2 to 8 Years in Formulations (OSD / Injectable)
• Educational Qualification: Diploma (Pharmacy/Mechanical) / B.Sc / B.Pharm / M.Pharm
• Job Location: Nagpur / Goa / Pithampur (Madhya Pradesh)
• Employment Type: Full-Time, Permanent

Detailed Department Breakdown

1. Solid Oral Dosage (OSD Production & Packing)

• Qualifications: B.Pharm / M.Pharm / B.Sc
• Core Responsibilities:
  • Operations involving Granulation, Compression (Fette, Korsch), Coating (Glatt, ACG), and Capsule Filling machines.
  • Supervising primary and secondary packaging activities including Blister Packing (BVM, Uhlmann), Strip Packing, and Bottle Lines.
  • Managing electronic batch manufacturing records (eBMR), line clearance, and shift yield calculations in compliance with cGMP.

2. Sterile Injectable Manufacturing

• Qualifications: Diploma / B.Pharm / M.Pharm
• Core Responsibilities:
  • Handling aseptic filling lines, compounding vessels, isolators, autoclaves, and lyophilizers.
  • Performing CIP/SIP procedures, filter integrity testing, and cleanroom environmental monitoring coordination.

📅 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
• Academic Certificates & Marksheets (Graduation / Diploma)
• 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 send their CV directly to the Lupin recruitment team:

• 📧 Direct HR Email: production.careers@lupin.com
• 📌 Subject Line Format: Application for Production - [OSD/Sterile] - [Years of Exp] - [Current Location] - [Your Name]
  • Example: Application for Production - OSD - 5 Years - Nagpur - Anil Deshmukh

Zydus Lifesciences: Walk-In Drive for Experienced Quality Control (QC) Professionals

Zydus Lifesciences Limited—a leading innovative global healthcare provider—is conducting a walk-in recruitment drive for experienced Quality Control (QC) professionals to support its formulation manufacturing plants.

Key Job Details

• Company Name: Zydus Lifesciences Limited
• Designation: Officer / Executive / Senior Executive – Quality Control
• Target Experience: 2 to 7 Years in Oral Solid Dosage (OSD) / Injectable Quality Control
• Educational Qualification: B.Sc / M.Sc (Analytical Chemistry / Organic Chemistry) / B.Pharm / M.Pharm
• Job Location: Ahmedabad (Moraiya / Pharmez) & Vadodara (Gujarat)
• Employment Type: Full-Time, Permanent

Detailed Scope of Work & Responsibilities

1. Analytical Testing & Instrument Handling

• Analysis of Raw Materials, In-Process, Finished Products, and Stability samples using advanced analytical tools (HPLC, GC, UV-Vis Spectrophotometer, KF Titrator, and Dissolution Apparatus).
• Operations using CDS software (Empower 3) in strict compliance with 21 CFR Part 11 guidelines and ALCOA+ data integrity standards.
• Calibration, routine maintenance, and volumetric solution standardization for QC laboratory instruments.

2. Lab Compliance & Investigations

• Handling laboratory investigation workflows for Out of Specification (OOS), Out of Trend (OOT), and Unconfirmed Test Results.
• Preparation and review of Analytical Test Reports (ATR), Specifications, and Standard Operating Procedures (SOPs).
• Adherence to cGMP norms and readiness for global regulatory inspections (USFDA, MHRA, ANVISA).

📅 Walk-In Schedule & Venue Details

📋 Checklist of Documents Required

• Updated Resume / CV (2 Copies)
• Academic Marksheets and Degree Certificates (Graduation / PG)
• 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 Zydus recruitment desk:

• 📧 Direct HR Email: qc.careers@zyduslife.com
• 📌 Subject Line Format: Application for QC - [Years of Exp] - [Current Location] - [Your Name]
  • Example: Application for QC Executive - 4 Years - Vadodara - Parth Patel

Ajanta Pharma: Walk-In Drive for Experienced Quality Assurance (QA) Professionals

Ajanta Pharma Limited—a specialty pharmaceutical company with USFDA and international regulatory approvals—is hosting a walk-in recruitment drive for experienced Quality Assurance (QA) professionals for its advanced formulation facilities.

Key Job Details

• Company Name: Ajanta Pharma Limited
• Designation: Senior Officer / Officer / Executive – Quality Assurance
• Target Experience: 3 to 8 Years in Oral Solid Dosage (OSD) / Formulations
• Educational Qualification: B.Pharm / M.Pharm / M.Sc
• Job Location: Dahej (Gujarat) / Paithan (Chhatrapati Sambhajinagar, Maharashtra)
• Employment Type: Full-Time, Permanent

Detailed Department Breakdown & Scope of Work

1. Quality Management Systems (QMS & Compliance)

• Key Responsibilities: Managing QMS processes including Deviations, Change Control, Out of Specification (OOS), Out of Trend (OOT), and CAPA investigations.
• Conducting risk assessments, impact analyses, and root cause analysis (RCA) using 5-Why and Fishbone tools.
• Assisting during internal cGMP audits and USFDA / MHRA regulatory site inspections.

2. Process & Cleaning Validation / Qualification

• Key Responsibilities: Reviewing equipment qualification protocols (URS, DQ, IQ, OQ, PQ) and HVAC validation reports.
• Overseeing cleaning validation, process validation protocols, and analytical quality assurance (AQA) support.

📅 Walk-In Schedule & Venue Details

📋 Checklist of Documents Required

• Updated Resume / CV (2 Copies)
• Academic Certificates & Degree Marksheets
• Current Employer Appointment Letter & Recent Increment Letter
• Last 3 Months' Salary Slips & CTC Break-up Document
• Recent Passport-Size Photographs & Government Photo ID Proof

📩 Direct E-mail Application Channel

Candidates unable to attend the walk-in drive in person can submit their updated CV directly to the recruitment team:

• 📧 Direct HR Email: referral.dhi@ajantapharma.com / cv.ptn@ajantapharma.com
• 📌 Subject Line Format: Application for QA - [Years of Exp] - [Current Location] - [Your Name]
  • Example: Application for QA Executive - 5 Years - Goa - Rajesh Kulkarni

Dr. Reddy’s Laboratories: Career Expo Walk-In Drive for Injectables (Manufacturing, Engineering & QC)

Dr. Reddy’s Laboratories Ltd.—a global pharmaceutical giant—is hosting a major Injectables Career Expo walk-in recruitment drive for experienced professionals in Injectables Manufacturing, Process Engineering, Equipment Qualifications, and Quality Control.

Key Job Details

• Company Name: Dr. Reddy’s Laboratories Ltd.
• Designation: Team Member / Specialist / Executive
• Target Experience: 3 to 8 Years in Injectable / Parenteral Operations
• Educational Qualification: Diploma / B.Tech / B.Pharm / B.Sc / M.Sc (Min. 60% Marks Mandatory)
• Job Location: Visakhapatnam (Duvvada / Pydibhimavaram Plants, Andhra Pradesh)
• Employment Type: Full-Time, Permanent

Detailed Department Breakdown

1. Production Filling & Compounding (Injectables)

• Qualifications: B.Pharm / M.Pharm / B.Sc / M.Sc / Diploma
• Key Responsibilities:
  • Hands-on aseptic operations including Vial Filling, Cartridge Filling, Lyophilizer management, Isolators, and Autoclaves.
  • Complex injectable compounding using CIP, SIP, SKIDS, solution preparation, filtration, and equipment cleaning.
  • Handling QMS events including Investigations, Deviations, and Change Controls.

2. Process Engineering & Utilities

• Qualifications: Diploma / B.Tech (Mechanical, Electrical, Instrumentation)
• Key Responsibilities:
  • Maintenance of parenteral equipment (BFS, Vial filling, Autoclaves, Tunnels, and Isolators) and PLC/SCADA automation.
  • Managing sterile utilities: Purified Water, Water for Injection (WFI), Clean Steam, Compressed Air, Nitrogen, and Chillers.

3. Equipment Qualification & Quality Control (Chemical)

• Qualifications: B.Sc / M.Sc / B.Pharm
• Key Responsibilities:
  • Qualifications: Execution of SAT, IQ, OQ, PQ protocols for sterile equipment (filling lines, capping machines, washing systems).
  • Quality Control: Chemical analysis of raw materials and finished injectables using HPLC, GC, KF, IR, and UV in USFDA-regulated environments.

📅 Walk-In Schedule & Venue Details

📋 Checklist of Documents Required

• Updated Resume / CV (2 Copies)
• Academic Certificates & Marksheets (Minimum 60% aggregate overall)
• Current Employer Appointment Letter & Latest Increment Letter
• Last 3 Months' Pay Slips & Bank Statements
• Government Photo ID Proof (Aadhaar Card and PAN Card)

📩 Direct Contact & Registration Channel

Candidates planning to attend can pre-register or submit their profile directly to Dr. Reddy's Talent Acquisition team:

• 📧 Direct HR Email: talent@drreddys.com
• 📌 Subject Line Format: Application for Injectables [Dept] - [Years of Exp] - [Current Location] - [Your Name]
  • Example: Application for Injectables Production - 5 Years - Hyderabad - Karthik V