Quality Engineer at Edison

Job Description

Quality Engineer (Pharma )

About our client
Global publically traded pharmaceutical organization
Job description
Quality Engineer- in a GMP Regulated EnvironmentOur client is planning to add several Quality Engineers to their staff in the coming weeks/months.RESPONSIBILITIES: Multiple concurrent project oriented deliverables. Create SOPs and work instruction sheets. Perform quality audits internally. Lead CAPA investigations. Summarize root cause analyses, IQ/OQ, and PQ reports and quality performance metrics.
Whats on offer
Competitive Salary + Benefits Package + Bonus

Job Requirements

Who we are looking for
SKILLS: Ideally experience in a GMP regulated environment. Ideally a thorough understanding of FDA regulations, ideally 21 CFR Parts 210, 211, and 820. Experience in pharmaceutical or medical device Quality Assurance. ASQ Certification, Certified Quality Engineer, preferred. Microsoft Office Suite and Microsoft Project. Experience with statistical software packages. Effective oral and written communication skills.

For further information please forward a detailed resume along with current salary, in strict confidence by applying on Michael Page website
Country: USA, State: New Jersey, City: Edison, Company: Michael Page.