QA Compliance Specialist
Are you an accomplished Quality Assurance professional looking for their next venture?
INCOG Biopharma Services is searching for someone to join them in contributing towards a better path to market for life-saving drugs. Having recently been voted as one of the Best Places To Work in Indiana for the second year in a row, INCOG is the perfect place to continue building your career.
The QA Compliance Specialist will work closely with the Sr Quality Engineering Validation Manager, and will play a key role in helping implement the highest quality procedures and standards throughout all manufacturing, packaging, and release stages.
Main aspects of the role include:
- Generate and review supplier/ contractor documentation including: supplier evaluations, questionnaires, and audit reports
- Generate and review quality agreements between suppliers and INCOG
- Review and approve material specifications
- Provide oversight for shipping and receiving activities
- Internal audit planning and tracking of mitigations
The ideal candidate will have a Bachelor’s degree in a related scientific field (or appropriate industry experience), as well as a minimum of 5 years of supply chain experience within the biopharma industry. Audit experience and/or certification is preferred but not required, so don’t let this stop you from applying!
Interested? Send us your resume at firstname.lastname@example.org or you can find the full job specification here: INCOG – QA Compliance Specialist
Don’t meet all the requirements? Don’t sweat! We’re always looking for an excuse to discuss your next opportunity. You might just surprise yourself…
Lead Candidate wholeheartedly supports Equality and Diversity in employment and opposes all forms of unlawful or unfair discrimination on the grounds of age, disability, sex, gender reassignment, sexual orientation, pregnancy and maternity, race, religion or belief and marriage and civil partnerships.