Validation Engineer Jobs

About The Position

Requirements

• Bachelor’s degree in a Technical or Life Sciences discipline with two years of experience in the pharmaceutical industry; or Associate degree in a Technical or Life Sciences discipline with four years of experience in the pharmaceutical industry.
• One year of validation experience.
• Some exposure to hazardous chemicals and other active chemical ingredients.
• Capacity to handle and manipulate objects using hands and arms.

Nice To Haves

• Oral solid dosage (OSD) experience.
• Process validation experience.
• Experience in a Catalent production role with a demonstrated solid understanding of internal manufacturing processes may be considered in lieu of direct validation experience.

Responsibilities

• Collaborate with the Cleaning Verification and Validation Analytical Group to develop draft cleaning verification and validation protocols.
• Review cleaning validation protocols, residue limits, reports, and cleaning verification/validation summary packages.
• Evaluate the impact of planned and unplanned changes to formulations, processes, or equipment on cleaning validation status.
• Author and review equipment and utilities qualification protocols and summary reports.
• Review executed qualification protocols and summary reports for completeness, accuracy, and compliance.
• Assist with the execution of equipment and utilities qualification activities as required.
• Ensure validation documentation is archived in accordance with GMP documentation retention requirements.
• Other duties assigned.

Benefits

• Competitive medical benefits
• 401K
• 152 hours PTO
• 8 Paid Holidays
• Opportunity to work on Continuous Improvement Processes