To identify and address areas of non conformance and take appropriate corrective and preventive actions, further control non conformance till adequate actions are taken up.
Conduct and review Internal Quality Audits.
Line clearance at various manufacturing stages.
Issuance and verify of batch records.
Checking of master formula records and entered in software.
Logbooks and records of different department shall be checked.
To investigate out of specification results or failure investigation related to testing or manufacturing etc.
SOP preparation, verification and control monitoring, issuance as well as retrieval.
Monitoring of process validation activity and raw data compilation. To prepare or verify the final report of Process Validation.
Handling and control monitoring over all controlled documents issuance and retrieval.
To handling and investigate deviations.
Part of Market complaints investigation.
Change control handling and record maintain.
Sampling of products at various stages.
Handling of software.
Responsible for product release.
Desired Candidate Profile
UG:B.Sc - Any Specialization, B.Pharma - Pharmacy
PG:Post Graduation Not Required, MS/M.Sc(Science) - Any Specialization, M.Pharma - Pharmacy
Baroque Pharmaceuticals Pvt Ltd
Recruiter Name:Kalpit Darji
Contact Company:Baroque Pharmaceuticals Pvt Ltd