SRG is seeking a Validation Engineer Level II to join our client's pharmaceutical manufacturing team in Vacaville, CA! This person will be responsible for support and execution of QC laboratory equipment qualification activities while in full compliance with current cGMP regulations.

M-F 8am - 4pm onsite

Responsibilities:

• Perform qualification of laboratory equipment in accordance with EQ policies, plans and procedures.
• Coordinate with laboratory personnel to define qualification requirements.
• Author, review and execute equipment qualification protocols.
• Coordinate equipment qualification activities with vendors and other support groups.
• Identify business, quality, and compliance gaps.

Requirements:

• BS/BA degree (preferably in relevant scientific discipline)
• Experience in the pharmaceutical, biopharmaceutical industry or an equivalent combination of education and experience.
• Knowledge of cGMP or equivalent regulations.
• Minimum of two years experience in Validation or equipment qualification is desired.
• Ability to make sound decisions about scheduling and managing of priorities.

Impellam Group and its brands are equal-opportunity employers committed to diversity and inclusion. All qualified applicants will receive consideration without regard to race, color, religion, gender, sexual orientation, pregnancy or maternity, national origin, age, disability, veteran status, or any other factor determined to be unlawful under applicable law. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application, interview process, pre-employment activity, and the performance of crucial job functions.

If you require additional disability considerations, modifications, or adjustments please let us know by contacting HR-InfoImpellamNA@impellam.com or fill out this form to request accommodations.