Responsibilities:
- Leading and managing change controls, CAPAs and investigations
- Reviewing and maintaining procedures, polices and other instructional documents with a focus on continuous improvement
- Generating, monitoring and tracking performance metrics
- Reviewing documentation and records to assess for compliance with established quality standards, policies and procedures
- Assisting in maintenance of product integrity and company reputation by assisting in the monitoring of cGMP compliance
This might appeal to you if you are:
- Someone who demonstrates strong communication, interpersonal and coordination skills
- Someone who has the ability to interact with others with tact and diplomacy
- Resilient and flexible and thrive in a dynamic environment
- Passionate about GMP compliance
To be considered for this role you should have a BS/BA in scientific discipline and 2 years of related experience in cGMP manufacturing operations (clinical and/or commercial External Manufacturing) or equivalent combination of education and experience.
