Validation Engineer (CQV)

Piper Health & Sciences is seeking a Validation Engineer to support a highly successful biotech organization in Silver Spring, MD. The ideal candidate will have direct experience with Steam-in-Place (SIP), Clean-in-Place (CIP), autoclaves, and dry heat sterilization, as well as a strong working knowledge of IQ/OQ/PQ protocols.

Responsibilities for the Validation Engineer include:

·       Perform hands-on validation activities for equipment and systems in a GMP-regulated environment.

·       Execute IQ/OQ/PQ protocols for sterilization systems and other critical equipment.

·       Support sterilization processes including SIP, CIP, autoclaves, and dry heat systems.

·       Collaborate with cross-functional teams including Engineering, Quality, and Manufacturing to ensure validation tasks are completed on time and in compliance.

·       Maintain accurate documentation of validation activities and ensure alignment with regulatory standards.

·       Assist in preparing for audits and inspections by providing validation records and technical support.

Qualifications for the Validation Engineer include:

·       Bachelor’s degree in Engineering, Life Sciences, or a related field is required.

·       3–7+ years of validation experience in the pharmaceutical or biopharmaceutical industry.

·       Strong hands-on experience with sterilization systems: SIP, CIP, autoclaves, and dry heat is required.

·       Knowledge of IQ/OQ/PQ protocols and their execution in a GMP environment.

·       Ability to work independently and efficiently with minimal supervision.

·       Excellent attention to detail and documentation skills.

Compensation for the Validation Engineer includes:

·       Salary: approximately $38.00 - $52.00 hourly, commensurate with experience

·       Comprehensive Benefits: Cigna Medical/Dental/Vision, ADP 401k, PTO, Paid Holidays, STD, LTD, Sick leave (as required by law)

This job is open for applications on 8/12/2025. Applications will be accepted at least 30 days from the posting date.

Validation engineer, equipment engineer, equipment validation, iqoqpq, installation, qualification, optimization, sterilization, sip, cip, clean in place, steam in place, autoclave, dry heat, manufacturing, quality control, biotechnology, biopharmaceutical, life sciences, biopharma, gmp, cgmp, good manufacturing practices

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