Validation Engineer - Experienced

Responsibilities

• Work with teams to support capital projects and implement solutions for clients.
• Develop and execute validation and FDA compliance documents and protocols for pharmaceutical equipment.
• Create and execute FAT, SAT, IQ, and OQ documentation for automated systems in the pharmaceutical industry.
• Assist in developing and executing QMS procedures, ICH Q1 Stability Protocols/Reports, CFR 21 Part 211, CFR 21 Part 820, ICH Q8, Q9, and Q10.
• Perform investigations and troubleshoot issues related to validation.
• Prepare written validation reports.
• Travel to client sites across the country to assist with design, project management, and facility development, demonstrating integrity and professionalism.

• Good communication and interpersonal skills, flexibility with tasks, and ability to interact at all management levels, with clients, and vendors.
• Minimum 3 years of project experience validating automation, packaging, utilities, or facilities.
• Preferred 3 years of project experience in pharmaceutical or medical device environments.
• Strong technical writing and oral communication abilities.
• Proficient in Microsoft Office, Microsoft Project, and AutoCAD.
• Willingness and ability to travel as required for project installation, start‑up, client meetings, training, industry seminars, and conventions.
• B.S. in Bioengineering, Biomedical Engineering, Chemical Engineering, or related technical degree.

• Supportive environment offering first‑year experience program, individual development plans, and career path resources.

Barry‑Wehmiller is an equal‑opportunity employer. M/F/D/V.

This organization uses E‑Verify. Applicants may be subject to pre‑employment screening which may include drug screening, reference checks, employment verifications, background screening and/or skills assessments.