Job Description

Are you ready to lead the charge in ensuring excellence in pharmaceutical production? Our client is looking for a dynamic Validation Supervisor to oversee critical validation activities, drive innovation, and build strong client relationships—all while working at the forefront of the pharmaceutical industry in New Jersey.

If you are interested in learning more, apply to this ad or reach out to Jessica Goodman for more information!

Key Responsibilities:

• Manage validation activities for manufacturing and packaging equipment, critical utilities (e.g., WFI, clean steam, compressed gases), and facilities.
• Develop, review, and approve qualification protocols, deviations, and reports.
• Serve as the Subject Matter Expert (SME) for Process Performance Qualifications (PPQs) and related activities.
• Plan and execute validation schedules, manage resources, and oversee protocol execution.
• Collaborate with clients to discuss timelines, project deliverables, and technical updates.
• Lead investigations into process and product issues and ensure batch records align with the validated state.
• Ensure compliance with FDA, ISO, EMA, and other international regulations.
• Supervise and mentor the validation team, including hiring, training, and performance management.

Qualifications:

• Bachelor of Science degree (advanced education preferred).
• Minimum of 5 years’ relevant experience in validation within an aseptic pharmaceutical environment.
• Familiarity with FDA, ISO, EU, and ICH guidelines.
• Certifications such as ASQ, PMP, ISPE, or PDA are a plus.

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