Job Description

Adecco is working with a pharmaceutical manufacturing company that is looking for a Deviation Investigator for their Manufacturing Department. This role is located in Lakewood, NJ. The Deviation Investigator will be the primary investigator and ensure that investigations are completed timely and accurately. They will also implement changes from corrective actions as a result of the investigations.

The Deviation Investigator will be responsible for:

• Own the investigations and ensure that root cause evaluations are performed according to cGMPs and SOPs.
• Observe activities on the manufacturing floor and collaborate with colleagues to gain process knowledge for investigations
• Utilize investigational tools like 6M, Fishbone and 5 Why's
• Identify probable root causes and determine preventative and corrective actions

Requirements for the Deviation Investigator are:

• Bachelor's degree in Science/Engineering
• 3 years of relevant experience in the pharmaceutical industry or additional education in project or documented investigational coursework may be substituted
• Experience with cGMP software (ex: Trackwise) preferred

Equal Opportunity Employer/Veterans/Disabled. To read our Candidate Privacy Information Statement, which explains how we will use your information, please visit http://www.adeccousa.com/candidate-privacy/. The Company will consider qualified applicants with arrest and conviction records.