Join Hetero Labs Ltd – Empowering Pharmaceutical Excellence!
Hetero Labs Ltd, a leading pharmaceutical company committed to global health, is actively seeking dedicated and experienced professionals to expand our teams. We offer dynamic opportunities for individuals ready to contribute to cutting-edge pharmaceutical manufacturing and quality assurance.
1. Senior Chemist, Quality Control (QC) – Nakkapally
We are seeking a skilled Senior Chemist to join our Quality Control department in Nakkapally, Andhra Pradesh.
- Experience: 3-6 Years in a relevant QC role.
- Qualification: M.Sc. Chemistry or B. Pharmacy.
- Key Responsibilities:
- Perform analysis of Active Pharmaceutical Ingredients (API), in-process, and finished product samples.
- Operate and troubleshoot analytical instruments including HPLC and GC.
- Ensure all testing strictly adheres to approved Standard Operating Procedures (SOPs), specifications, and Standard Testing Procedures (STPs).
- Review analytical results and maintain meticulous documentation.
- Support Out-of-Specification (OOS) and Out-of-Trend (OOT) investigations and laboratory activities.
- Ensure compliance with Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), and data integrity.
- Collaborate effectively with Quality Assurance (QA), Production, and other cross-functional teams.
- Special Note: Immediate joiners for this position are eligible for a joining bonus.
2. Tech Transfer – Injectables (Multiple Roles) – Jadcherla
Hetero is also searching for talented professionals to join our Tech Transfer – Injectables team at Unit – VI, Jadcherla. We have openings for Junior Research Associate, Research Associate, and Senior Research Associate positions.
- Experience: 2-8 Years in pharmaceutical tech transfer.
- Qualification: B.Pharma, M.Pharma, or M.Sc.
- Key Responsibilities:
- Execute technology transfer of injectable products from development or other manufacturing sites to the target facility.
- Prepare and execute Tech Transfer protocols, plans, and reports.
- Coordinate with Research & Development (R&D), Quality Assurance (QA), Quality Control (QC), Production, Engineering, and Regulatory teams.
- Manage the transfer of manufacturing processes, analytical methods, equipment, and documentation.
- Support process validation/Process Performance Qualification (PPQ), risk assessment, gap analysis, and troubleshooting.
- Ensure stringent compliance with current Good Manufacturing Practices (cGMP) and regulatory requirements.
- Maintain complete and accurate technology transfer documentation.
- Preferred Profile: Candidates with hands-on experience in Injectable Tech Transfer, particularly involving Liquid or Lyophilized products, are highly encouraged to apply.
How to Apply:
If you meet the qualifications and are eager to join a growing pharmaceutical leader, we invite you to submit your updated resume for consideration through our official career channels.
