Endo Pharma is a leading pharmaceutical company specializing in sterile manufacturing, ensuring high-quality injectables and pharmaceutical products. With a strong commitment to compliance and innovation, we provide a dynamic work environment for professionals looking to grow in the pharmaceutical industry.
Job Description
As an IPQA (In-Process Quality Assurance) Associate, you will be responsible for ensuring quality compliance during sterile manufacturing and packaging processes. Your key responsibilities include:
- IPQA Activities:
- Monitor and ensure quality at every stage of sterile manufacturing, filling, and packaging.
- Conduct in-process checks to maintain compliance with SOPs and regulatory standards.
- Sampling & Inspection:
- Perform sampling during different stages of product manufacturing.
- Conduct AQL (Acceptable Quality Level) checks post-visual inspection.
- Documentation & Compliance:
- Review and approve audit trails & electronic batch records.
- Handle control samples and stability sample management.
- Visual Inspection Support:
- Assist in the qualification of master kits for visual inspection.
- Review documents related to visual inspector qualifications.
Qualifications & Skills Required
- Education: B.Pharma / M.Pharma / B.Sc / M.Sc in Microbiology or related field.
- Experience: 1-3 years in IPQA within a sterile manufacturing facility (preferred).
- Skills:
- Strong knowledge of GMP, GLP, and regulatory guidelines.
- Attention to detail in documentation and compliance.
- Familiarity with electronic data review and audit trails.
Why Join Us?
✅ Work in a sterile manufacturing environment with cutting-edge technology.
✅ Career growth opportunities in quality assurance.
✅ Competitive salary and benefits.
How to Apply?
Interested candidates can apply before June 18, 2025.
