1.0 Core Jobs
1.1 To ensure timely testing and release of Raw Materials, Packaging Materials and Finished Products as per cGMP.
1.2 To ensure effective implementation of systems and procedures as per GMP, GLP and other regulatory requirements.
1.3 To ensure timely withdrawal and analysis of stability samples as per the plan.
1.4 To ensure that Work Plan targets and KPIs for self and team are met.
1.5 To manage all aspects of Laboratory services to the Manufacturing sites.
1.6 Preparation of SOPs, Standard Test procedures and General Test Procedures etc..
1.7 To ensure calibration & maintenance of laboratory equipments.
1.8 To develop cost-effective ways of working to ensure quality, compliance, service and safety.
1.9 To promote high standards of service for internal and external customers.
1.10 To ensure that effective failure investigation is done with identification of CAPA within stipulated period.
1.11 On job training as necessary to develop skills and improve productivity.
1.12 Allocation of work as per the skills of persons & supervision.
1.13 To optimize resources, utilize and develop skills across the Quality team to increase flexibility and to meet specific site business requirements.
1.14 To create an environment within QC where each member can understand their role and contribution and produce their best work.
2.0 Other Jobs
2.1 Develop and build team to meet business objective for future.
2.2 Develop and build culture which encourages Quality improvement programs.
2.3 To ensure development, training and motivation of team members.
Special Responsibilities (if any)
1 To participate as an auditor for vendor approval.
(Mention only direct reportees) Senior Executives Quality Control
Executives Quality Control
Officer Quality Control
Designee in case of absence of Job Holder Manager Quality Control
10-14 Years in QC lab (Solid oral dosage)