Roles & Responsibilities:
- Strong working knowledge of Quality System Regulations.
- Experience leading CAPA (Corrective and Preventive Action) activities.
- Quality review for documents associate with protocols functional spec detail design specs site acceptance test data packs.
- Also investigate deviations and will be final approver on such documents.
- Ability to work on strict deadlines.
- Ability to interface with crossfunctional teams.
- Detail oriented.
- Ability to handle multiple projects concurrently.
- Welldeveloped communication skills both verbal and written.
- Bachelors Degree/Undergraduate Degree in engineering or technical discipline. Masters degree preferred.
- 10 Years Experience in pharmaceutical/biopharmaceutical industry or related industry/manufacturing environment.
- Experience in Bulk Formulation and Aseptic Filling.
Additional Information :
All your information will be kept confidential according to EEO guidelines.
Remote Work :
No
Employment Type :
Contract