Lee Pharma Limited has announced multiple vacancies at its Unit-I API manufacturing facility in Hyderabad. The recruitment drive provides opportunities for professionals across manufacturing, quality, analytical research, engineering, regulatory and support functions.
Lee Pharma is a research-driven pharmaceutical company established in 1997, with operations focused on APIs, intermediates, semi-finished dosage forms and finished formulations. Its manufacturing facilities have approvals/certifications including USFDA, EU GMP and WHO GMP.
The company’s API and R&D activities cover areas including process development, analytical research, technology transfer and quality assurance.
Departments With Vacancies
Lee Pharma Unit-I, Hyderabad has openings in the following departments:
- Quality Control (QC)
- IPQA
- Quality Assurance (QA)
- Production
- Production Documentation
- Microbiology
- Water Plant Operator
- Maintenance
- Warehouse
- Engineering Store – SAP
- Research & Development (R&D)
- Regulatory Affairs
- Development Quality Assurance (DQA)
- Project Management
- TSD
- Analytical Research & Development (AR&D)
Eligibility & Experience
Candidates with 1 to 7 years of relevant pharmaceutical industry experience are invited to apply.
The exact educational qualification may vary according to the department and position. Candidates with relevant qualifications and experience in API manufacturing, QC, QA, IPQA, analytical R&D, production, engineering, warehouse, regulatory affairs, microbiology and pharmaceutical operations can submit their resumes for consideration.
Key Responsibilities
Responsibilities will depend on the department and position. Typical responsibilities may include:
Quality Control / Analytical R&D
- Performing analysis of pharmaceutical/API samples.
- Handling laboratory instruments and analytical procedures.
- Maintaining laboratory documentation and records.
- Supporting testing, investigation and compliance activities.
- Following applicable GMP and laboratory procedures.
QA / IPQA / Development QA
- Monitoring manufacturing and quality activities.
- Reviewing batch and quality documentation.
- Supporting deviation, CAPA and investigation processes.
- Ensuring compliance with established SOPs and GMP requirements.
- Participating in audits and inspection-readiness activities.
Production
- Supporting API manufacturing operations.
- Monitoring production activities and process parameters.
- Ensuring adherence to SOPs, safety requirements and GMP practices.
- Maintaining production documentation and records.
Production Documentation
- Preparing and reviewing manufacturing documentation.
- Maintaining batch records and production-related documents.
- Coordinating with Production and Quality teams.
R&D / AR&D
- Supporting process development and analytical research activities.
- Conducting laboratory experiments and analysis.
- Maintaining scientific and technical documentation.
- Supporting development and scale-up activities.
Regulatory Affairs
- Supporting regulatory documentation and submissions.
- Coordinating technical information required for regulatory activities.
- Maintaining regulatory records and documentation.
Engineering / Maintenance / Utilities
- Supporting plant equipment maintenance.
- Troubleshooting equipment and utility-related issues.
- Ensuring safe and reliable plant operations.
Warehouse / Engineering Store – SAP
- Handling material receipt, storage and inventory activities.
- Maintaining warehouse documentation.
- Supporting SAP-based inventory and store operations.
- Following material handling and safety procedures.
Why Consider This Opportunity?
Lee Pharma operates across APIs, intermediates and pharmaceutical formulations, with a research and manufacturing focus. The company states that its facilities have international regulatory approvals including USFDA, EU GMP and WHO GMP, providing professionals exposure to regulated pharmaceutical manufacturing environments.
Professionals joining the Hyderabad API facility may gain experience in areas such as:
- API manufacturing operations
- GMP and quality systems
- Pharmaceutical analytical activities
- R&D and process development
- Regulatory compliance
- Cross-functional pharmaceutical operations
How to Apply for Lee Pharma Jobs
Interested candidates should send their updated resume to:
Email: talentacquisition@leepharma.com