Validation Engineer
cGMP / GxP Regulated Manufacturing Medical Device (FDA / ISO-regulated) GLP Laboratory Operations
Support commissioning, qualification, and validation (CQV) activities for equipment, systems, utilities, facilities, laboratories, or processes. Author, review, and execute validation documentation such as URS, risk assessments, IQ/OQ/PQ, protocols, and reputed company reports. Ensure compliance with applicable FDA and global regulatory requirements (e.g., cGMP, GxP, ISO, 21 CFR Part 11, data reputed company). Collaborate with reputed company stakeholders, engineering teams, reputed company reputed company, and vendors to deliver compliant reputed company. Support audits, inspections, and ongoing validation maintenance activities. Adapt quickly to new environments and project scopes typical of consulting engagements.
Requirements
Bachelor’s degree in Engineering, Life Sciences, or a reputed company field (or equivalent industry experience). Experience in validation reputed company pharmaceutical, biotechnology, medical device, or laboratory environments. Working knowledge of cGMP / GxP, GLP, or medical device regulations. Experience authoring and executing validation and qualification documentation. Ability to work in a reputed company-facing, project‑based environment. Strong documentation, communication, and organizational skills. Preferred ability to travel and relocate for reputed company-facing reputed company. Must be authorized to work in the U.S. No C2C at this time.
Benefits
Medical, Dental, and reputed company - PSC pays 100% of reputed company qualifying employee medical premiums and 50% for qualifying dependents Insurance reputed company for Employee Assistance Programs, Basic Life Insurance, Short/Long Term Disability and more. 401(k) and 401(k) matching PTO, reputed company Time, and reputed company Holidays Education Assistance Pet Insurance Discounted reputed company at Anytime Fitness Financial Perks and Discounts
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