QA

Review and approve development protocols, reports, and technical documents for formulation, analytical, and process development.

Responsible for quality oversight of personnel, process and practice to meet the cGMP and compliance requirement.

Monitoring production processes, ensuring adherence to Good Manufacturing Practices, and conducting real-time quality checks and inspections on the manufacturing floor. 

M.Pharm, B.Pharm, M.Sc, B.Sc Openings at Stallion Laboratories Pvt. Ltd. For following Positions at OSD Formulation facility - Unit-ll

Person should know IPQA related activities of OSD Manufacturing activity. B.Pharm, MSc in Production, QA, QC

EHS Monitoring PTW Compliance. Safety Audit Inspection lmpart training. Safety engagement, GMP. Experience of Store activities. SAP knowledge must.

Require young and skilled employees with experience in Parenteral/ Injectable formulations for our manufacturing facility. Equipment Qualification & Validation/ IPQA

Walk In Drive for B.Pharmacy/ M. Pharmacy / Diploma / ITI in OSD Manufacturing - Softgel , OSD IPQA, OSD Manufacturing- Granulation, Compression

Having IPQA experience in manufacturing & Packing of OSD. Proven experience in IPQA or a related field, with a strong understanding of pharmaceutical regulations and standards.