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Quality Validation Specialist - Fishers, United States - INCOG BioPharma Services
Description
Quality Validation Specialist
WHO?
INCOG BioPharma is looking for a Quality Validation Specialist to join their QA team This individual will be working closely with the Manager of QA, and will be instrumental in ensuring site compliance and reviewing and approving various organizational documentation.
INCOG is offering the opportunity to contribute 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.
WHAT?
YOU
The ideal candidate will have a Bachelors Degree (Chemistry, Biology, Biochemistry, Microbiology etc.). They will also have at least 2 years of biopharma industry experience with increasing responsibilities in Commissioning, Qualification, and Validation. Experience with CQV activities for aseptic manufacturing facilities or clean utilities (e.g. Water for Injection, Clean Steam, etc.) is preferred but not required.
Dont meet all the requirements? Dont sweat Were 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.
