Monitoring and guiding for day to day activities to ensure the GLP compliance in the lab. Reviewing the Quality, production & analytical documents for compliance.
Keeping the plant & lab all the time ready for customer audits and regulatory inspections.
Handling regulatory and customer inspections and audits. Preparing internal audit calendar & conducting internal audit.
Ensure standardized Quality Control (QC) practices and systems across all QC functional areas and drive the implementation of Operational Excellence best practices and tools in support of an efficient QC operation.
Develop and manage the operating budget and capital expenditure proposals for the laboratory to ensure achievement of operational targets.
Act as primary QC representative during Regulatory Inspections and audits (e.g. client and corporate)
Ensure that own, and teams work aligns with GLP, Data Integrity & Good Documentation Practice (GDP) and is undertaken in accordance with GMP
Knowledge of testing and associated equipment protocols and requirements and analytical instrumentation.
QC Department Sr Executive / Assistant Manager Experience 5-8 yrs. Education : B. pharm , M. Pharm , B.Sc, M.Sc Industry : Pharmaceutical Formulation Manufacturing Unit Skills : Quality Control, Audit Exposures, FDA Approval Salary : Assistant Manager - 5-7 LPA Job Type: Full-time Salary: 500,000.00 - 700,000.00 per year Benefits:
Provident Fund
Schedule:
Day shift
Supplemental pay types:
Overtime pay
Shift allowance
Experience:
total work: 5 years (Preferred)
Ability to Commute:
Solan, Himachal Pradesh (Preferred)
Ability to Relocate:
Solan, Himachal Pradesh: Relocate before starting work (Preferred)