Executive Documentation

2 weeks ago

Vadodara, India Brooks Laboratories Full time

Responsible for management of Drug product manufacturing and QMS compliance.
- Documents preparation and changes in existing documents as per cGMP requirements.
- Responsible for investigation of non-conformities, identification of root cause, suggestion of CAPA, preparation review and compliance of investigation reports.
- Responsible for raising and execution of change control and CAPA and its implementation.
- Responsible for preparation and review of Risk assessment related to process and product attributes.
- To review and compliance of Audit points and to implement audit CAPAs.
- Responsible to prepare and execute /support for the process protocols and its reports preparation.
- Responsible to prepare and revise batch production, MPR, SOPs, etc.
- To provide the cGMP training to production personnel and maintain the training document.
- Role:
Production & Manufacturing - Other
- Salary:
Not Disclosed by Recruiter
- Industry:
Pharmaceutical & Life Sciences
- Functional Area:
Production, Manufacturing & Engineering
- Role Category:
Production & Manufacturing - Other
- Employment Type:
Full Time, Permanent
- Key Skills

capa

documentation
- Education
- UG:
B.Sc in Any Specialization
- PG:
MS/M.Sc(Science) in Any Specialization

Company Profile
- BROOKS STERISCIENCE LIMITED
- BROOKS STERISCIENCE LIMITED

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