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  Assist with routine validation activities, including periodic reviews and requalification efforts, as required.
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  Support cleaning validation activities for assigned process train.
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  Execute cleaning validation activities in accordance with approved protocols and regulatory requirements.
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  Draft and support the review of cleaning validation protocols and final reports.
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  Participate in project‑related meetings and provide validation updates as needed.
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  Support documentation activities to ensure compliance with site procedures and GMP expectations.

Requirements

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  Bachelor’s degree in engineering, life sciences, or a related technical discipline.
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  3-5 years experience supporting cleaning validation activities in a GMP‑regulated pharmaceutical or biotechnology environment.
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  Working knowledge of validation lifecycle principles, including execution, documentation, and requalification activities.
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  Experience drafting or supporting validation protocols and reports.
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  Ability to work under direction while managing assigned validation tasks and timelines.
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  Strong written and verbal communication skills.
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  Ability to work flexible hours with some overtime and weekend shifts required.
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  Must be authorized to work in the U.S.
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  No C2C at this time.

Benefits