Vacancy for M.Pharm, B.Pharm in Quality assurance at Mankind Pharma

Mankind Pharma, the 7^th largest Pharmaceutical Company of India, was incepted in 1995 with a meagre capital of 50 lakhs and 20 employees. Today, we are amongst the top 5 fastest growing Pharmaceutical companies of India with an employee base of more than 10000 and heading towards a turnover of INR 3000 crores.

Executive / Sr. Executive (QMS)
Qualification : B. Pharma / M. Pharma
Experience : 6 to 8 Years
Expertise Area :
Sterile Injectable exposure is mandatory for the position.
• Preparation, Review and approval of Standard Operating Procedures.
• Handling of Deviations, Investigations, CAPA, Change Control, Product recall, NCR, and Market Complaint
• Protocols Validation Reports, Review Calibration / Validation/Qualification activities
• Issuance & Retrieval of BMR/BPR, SOP's, Specifications etc.
• Review & Updating of Site Master File

Officer (Doc Cell)
Qualification : B. Pharma / M. Pharma
Experience : 1 to 4 Years
Expertise Area :
• To issue controlled copies of BMR / BPR, log books and monthly formats of all departments.
• Issuance of distribution copies of SOP's, MSDS, Specification / STP to respective departments.
• To maintain and storage of master copies of all controlled documents.
• Issuance and archival of controlled copies of documents related to change control.
• Management of Doc cell.

Officer / Sr. Officer (IPQA)
Qualification : B. Pharma / M. Pharma
Experience : 1 to 6 Years
Expertise Area :
Sterile Injectable exposure is mandatory for the position.
• Line clearance different stage of manufacturing and packing
• Sampling of Process validation and Cleaning Validation and control sample.
• In process checks during product manufacturing and packing
• Handling of Visual inspector qualification program
• AQL inspection of finish product and control sample inspection.
• Review of batch manufacturing records, batch packaging records.
• Participating in media fill activity and visual inspection of the media fill units.
• Issuance and archival of documents
• Assist to carryout investigations and implementation of action plan
• Review of validation /Qualification documents.