Website Lenox Executive Search
Fully Onsite: Swiftwater PA
12 Month Contractual Role
- Validation and Quality background necessary – need to have both.
- Sterilization validation would be a plus.
- Equipment validation is important.
- Lab equipment qualifications.
- Must work independently.
- Might be final approver for documents.
- Excel knowledge
- Reviewing and approving documents a major plus.
- Must be able to work with others.
- Bachelor’s Degree/Undergraduate Degree in engineering or technical discipline.
- Master Degree preferred.
- Experience in pharmaceutical/biopharmaceutical industry or related industry/manufacturing environment
- Ability to work on strict deadlines.
- Background in life science.
- Ability to interface with cross-functional teams.
- Detail oriented.
- Strong working knowledge of Quality System Regulations.
- Experience leading CAPA (Corrective and Preventive Action) activities.
- Ability to handle multiple projects concurrently.
- Well-developed communication skills, both verbal and written..
- Years of Experience: 5+