**Hybrid Position Local to Rochester, NY)**
Job opportunity with a top biopharmaceutical company that is looking for a QA Compliance Manager to join their team on a 6-month contract with a good possibility for conversion or extension!
Requirements and Job Functions:
- Mainly Validation Experience
- Bachelor's degree in a scientific field
- 5-10 years of experience with cGMP, ISO 9001 environment
Job Duties:
- Responsible for maintaining the quality of the products.
- Working knowledge of site processes and procedures as well as current standards and requirements as they relate to the site.
- Receive, investigate, determine root cause, document, and communicate findings for customer complaints valid to the facility
- Initiate process deviations, assist in root cause analysis, investigation, and CAPA related activities for those deviations
- Participate in Quality related investigations for OOS activities
- Review, evaluate and improve processes and procedures as appropriate
- Work with site personnel to provide guidance on current standards and regulations
- Oversite of the release process and individuals performing this process
- Track quality-related issues to identify trends and develop projects and teams to implement corrective actions
- Participate in CAPA program
- Participate in Internal Audits
- Perform other duties as assigned.
Benefits/Perks:
- 401k
- Health Insurance
Please apply here directly if interested but If you are genuinely not interested, is there someone you can recommend?
