4-5

Should have good exposure in injectable manufacturing in-process. Manpower handling, Good documentation Practices, should have basic knowledge of machine , Breakdown, operation and troubleshooting during machine operation, QMS, elogbook, Audit exposure.

Ph.D. or MS in Organic chemistry or related field with 2 plus years post-Ph.D. experience and 7 plus years of post-MS experience relevant to job requirements.

GCP Subject Matter Expert, Provide independent and objective quality advice in support of clinical trial activities and in line with current standard methodology. Experience in Quality Management, Quality Assurance. pharmaceuticals

Laboratory Quality Assurance Reviewer. Quality Assurance - Documentation Cell. Injectable / Parenteral / Sterile - Aseptic, Clean area, Manufacturing.

B.Pharm / M.Pharm career in Pharma packing, Production, Quality Assurance, Quality Control. freshers or Having experience in analysis of raw materials / stability / finished product with hands on experience on HPLC and other instruments.

Automatic Visual Inspection / Manual Visual Inspection / Labelling Machine and Packing Machine with Track N Trace

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