What are the responsibilities and job description for the Quality Engineer - Medical Device - Contract position at VTI Life Sciences?
Quality Engineer – Medical Device -Contract
VTI Life Sciences (VTI) is seeking a forward-thinking and ambitious Medical Device Quality Engineer looking to accelerate their careers in the pharmaceutical, biotechnology, and medical device industries. We offer an opportunity to support our teams of industry subject matter experts and thought leaders while consulting with leading companies in the Life Sciences industry.
The successful candidate will lead and coordinate validation execution activities with operations and engineering teams for special processes.
PROJECT OVERVIEW
Education
As one of the leading global Commissioning, Qualification and Validation Services organizations, VTI is always looking for innovative, talented and experienced validation professionals for our multinational and global offices. We offer some of the best salary and benefit packages in the industry for our full-time/permanent employees. www.validation.org
VTI Life Sciences (VTI) is seeking a forward-thinking and ambitious Medical Device Quality Engineer looking to accelerate their careers in the pharmaceutical, biotechnology, and medical device industries. We offer an opportunity to support our teams of industry subject matter experts and thought leaders while consulting with leading companies in the Life Sciences industry.
The successful candidate will lead and coordinate validation execution activities with operations and engineering teams for special processes.
PROJECT OVERVIEW
- Location: Pendleton, SC
- Start date: Monday, November 2nd
- Length of Project: Approximately 4 months
- Employment Classification: Contract
- Inspecting, Review Protocols, Support, SOP Development, Feedback, Execution
- Equipment: Grinders, Laser Welders
- Lead and coordinate validation execution activities with operations and engineering teams for special process related areas (Laser marking, Laser welding).
- Review equipment validation protocols (IQ, OQ, PQ) and reports for equipment used for manufacturing medical devices such as metal instruments/ implants, ABS/Peek instruments/implants.
- Execute validation protocols for manufacturing equipment such as Laser marking, Laser welding, grinders
- Compile executed validation packages.
- Support SOP development
- Perform and assist in any validation activities but not limited to: SOP, Work instruction, forms, templates.
- Lead and write deviation investigations related to validations or assist in non-conformances/CAPA investigations.
Education
- Minimum Bachelor’s degree in Life Sciences, Computer Science, Engineering, or a related discipline.
- Minimum 2 years of experience in GMP-regulated Medical Device industry
- Hands-on experience writing and executing validation protocols
- Strong technical writing and documentation skills
- Excellent organizational and project coordination abilities
- Ability to communicate effectively with multi-disciplinary IT teams
- Detail-oriented with strong compliance mindset
- Ability to manage multiple priorities in a fast-paced environment
As one of the leading global Commissioning, Qualification and Validation Services organizations, VTI is always looking for innovative, talented and experienced validation professionals for our multinational and global offices. We offer some of the best salary and benefit packages in the industry for our full-time/permanent employees. www.validation.org