Executive Documentation
2 days ago
From 2 to 5 year(s) of experience
- 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
- capadocumentation
Education
- UG:_B.Sc in Any Specialization
- PG:_MS/M.Sc(Science) in Any Specialization
**Company Profile**:
BROOKS STERISCIENCE LIMITED
BROOKS STERISCIENCE LIMITED
- Company Info
- X- Contact Company:_BROOKS STERISCIENCE LIMITED
- Address:_UNIT - II,,VILLAGE MANGLEJ,NARESHWAR ROAD, OFF NH-, VADODARA, Gujarat, India
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