Validation Engineer (Contractor)

Title: Validation Engineer (Contractor)
Description:

Working Model: 5 days onsite at Oceanside location, CA
Working Days: Monday through Friday
Working Hours: 9 AM to 5:30 PM PT
Interview Format: Two Rounds (1. Hiring Manager [virtual - 30 minutes]; 2. Panel interview [Onsite 1hr)

Focus Areas: Equipment Validation & Cleaning Validation

Position Summary
We are seeking an experienced Validation Engineer (Contractor) to support the Validation Engineering team at the Genentech Oceanside manufacturing facility. In this role, you will be responsible for authoring, executing, and summarizing equipment qualification and cleaning validation activities supporting both commercial stainless steel and single-use manufacturing facilities. The ideal candidate brings hands-on experience with GMP manufacturing equipment, Clean-in-Place (CIP)/Steam-in-Place (SIP) systems, and strong verbal and written communication skills.

Key Responsibilities

Protocol Authoring & Execution

Author, review, and execute qualification protocols (IQ, OQ, PQ) for systems and equipment.

Develop and execute Cleaning Validation (CV) and cleaning verification protocols, including sampling plans, visual inspections, and analytical test data coordination (e.g., TOC, conductivity, bioburden, and endotoxin).

Evaluate validation test results against defined acceptance criteria, resolve execution discrepancies via structured troubleshooting, and author protocol exceptions with cross-functional stakeholders.

Support continuous improvement in validation processes.

Document validation activities and maintain records.

Regulatory Compliance & GMP Standards

Ensure all qualification deliverables are in compliance with industry and regulatory standards, and Roche/Genentech quality standards.

Qualifications

Education: B.S. or M.S. in Chemical Engineering, Biomedical Engineering, Mechanical Engineering, Biochemistry, or a related technical discipline.

Experience:

8-10+ years of direct validation engineering experience within a cGMP biopharmaceutical or biotechnology manufacturing facility.

Direct hands-on experience authoring and executing both Equipment Validation (bioreactors, chromatography skids, TFF systems, autoclaves) and Cleaning Validation (CIP/SIP, residue limits, recovery studies).

Soft Skills:

Excellent technical writing, cross-functional collaboration, and communication skills.

Proven ability to independently manage timelines.



Skills: