Onsite Validation Engineer – GMP/CIP-SIP Specialist

BEPC Inc. - Business Excellence Professional Consulting; Oceanside (CA); On-site; USD 103,000 - 117,000; Full time

Job summary

BEPC Inc. is actively seeking a Validation Engineer for our client site in Oceanside, CA. The role focuses on authoring, executing, and summarizing equipment qualification and cleaning validation activities in GMP manufacturing environments.

5‑day onsite schedule, 9:00 AM–5:30 PM PT, with a 24‑month W2 contract. The ideal candidate will have 8–10+ years of direct validation experience in cGMP biopharma, strong technical writing, and hands‑on expertise with CIP/SIP, IQ/OQ/PQ, and regulatory

Qualifications

• Bachelor of Science (B.S.) or Master of Science (M.S.) in Chemical Engineering or related technical discipline.
• 8–10+ years of direct validation engineering experience in a cGMP biopharmaceutical or biotechnology facility.
• Hands‑on experience with equipment validation, CIP/SIP systems, and strong technical writing.

Responsibilities

• Author, review, and execute IQ, OQ, and PQ protocols for manufacturing systems and equipment.
• Support validation activities across commercial stainless steel and single‑use facilities.
• Develop and execute cleaning validation protocols and sampling plans.
• Document validation activities and maintain accurate records.

Skills

Technical writing

Communication

Project management

Troubleshooting

Education

B.S./Bachelors in Chemical Engineering

M.S. in Chemical Engineering

Job description

BEPC Inc. is actively seeking a Validation Engineer for our client site in Oceanside, CA. The role focuses on authoring, executing, and summarizing equipment qualification and cleaning validation activities in GMP manufacturing environments.

5‑day onsite schedule, 9:00 AM–5:30 PM PT, with a 24‑month W2 contract. The ideal candidate will have 8–10+ years of direct validation experience in cGMP biopharma, strong technical writing, and hands‑on expertise with CIP/SIP, IQ/OQ/PQ, and regulatory