Seeking a Validation Engineer for a high growth pharmaceutical manufacturing client in the Lincoln, RI. The Validation Engineer would be responsible for supporting the installation, operation, performance and environmental qualifications (IQ OQ PQ EQ) to meet required regulatory standards.
Experiene upgrading manufacturing equipment to meet standards is highly desired. The Validation Engineer ideally should have experience with pharmaceuticals and GMP and cGMP guidelines. Apply now!
location: Lincoln, Rhode Island
job type: Contract
salary: $35 - 43 per hour
work hours: 8am to 4pm
education: Bachelors
responsibilities:
- Investigate and troubleshoot validation problems on manufacturing equipment
- Initiate corrective action investigations into non-comformance issues and deviations
- Develop IQ, OQ and PQs with the engineering team
- Ensure all aspects of the facilities validation conform to required internal policies and procedures, including safety and training
- Take ownership of validation related change controls and corrective/preventative actions.
- Assist in the implementation of validation programs.
- Experience with pharmaceuticals and GMP is a must
qualifications:
- Experience level: Experienced
- Minimum 3 years of experience
- Education: Bachelors (required)
skills:
Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.
For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.