Are you a Validation professional looking for an exciting opportunity with an organization where you can have an impact on global health and wellness? Do you naturally create new ways to deliver exceptional results? We want to meet you!
INCOG Biopharma Services is seeking a highly motivated Principal Validation Engineer to help execute and develop the validation qualification programs at their state-of-art CDMO during an exciting time of growth. 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.
- Develop, perform, and review Validation and Qualification activities on software, utilities, equipment and laboratory systems.
- Interact with clients to provide validation support, provide validation oversight for CAPEX projects, and develop & maintain the CQV program.
- Assess risks involved processes related to equipment, developing and/or reviewing validation requirements and design deliverables.
The ideal candidate will have a Bachelor’s degree in a STEM discipline, at least 10 years experience within Validation, including 8 years of GMP experience in a regulated industry. Experience of working with Vapor Hydrogen Peroxide decontamination processes for isolators, steam sterilization processes, and performing cleaning validations is preferred but not essential.
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.