This job is closed
We regret to inform you that the job you were interested in has been closed. Although this specific position is no longer available, we encourage you to continue exploring other opportunities on our job board.
About the position
The primary purpose of the role is to support the Operations team with documentation and processes to meet production needs.
Responsibilities
- Assist engineers in developing, building, or testing prototypes/new products, processes, validations or procedures.
- Adhere to all applicable regulations, policies, and procedures for health, safety and environmental compliance.
- Monitor and adjust production processes or equipment for quality and productivity gains.
- Provide training to operators as needed.
- Assist in providing information to Transfer Tech and Validation Crew on investigations.
- Assist/Support OPS Management and QA: Open, Follow up, and close deviations, CAPAs, QA Investigations and TA’s.
- Assist work team in the achievement of goals/commitments and achieves own goals/commitments regardless of obstacles.
- Update Operation’s SOP’s, as needed, and perform periodic review of procedures.
- Assist in driving continuous improvement activities.
Requirements
- At least 2 years working within a manufacturing environment, cGMP/pharmaceutical manufacturing preferred.
- Operational capacity working with batch records.
- Experience with technical writing.
