Validation Engineer
Job in
San Jose, Santa Clara County, California, 95199, USA
Listed on 2025-12-13
Listing for:
BEPC Inc. - Business Excellence Professional Consulting
Contract
position Listed on 2025-12-13
Job specializations:
-
Engineering
Biomedical Engineer, Validation Engineer, Pharma Engineer, Quality Engineering
Job Description & How to Apply Below
Validation Engineer I
Benefits: Medical, Dental, Vision, and Life Insurance
Pay Rate: $57-$62 per hour (Paid Weekly)
Term: 6-months contract with possible extensions
Requirements: Bachelor’s degree in engineering, Science, or a related technical field, 1+ year of validation experience within a medical device, pharmaceutical, biotechnology, or other regulated industry.
NO CORP-TO-CORP CANDIDATES WILL BE CONSIDERED
BEPC does not accept C2C, C2H, or W2 referral applications.
Duties & Responsibilities- Develop equipment and fixture matrices with defined qualification requirements in accordance with medical device regulations and client standards.
- Create detailed, compliant Installation Qualification (IQ) and Operational Qualification (OQ) protocols for manufacturing and laboratory equipment.
- Execute IQ/OQ protocols, ensuring accurate data collection, documentation integrity, and adherence to regulatory and client requirements.
- Write and issue validation summary reports following successful protocol execution.
- Provide technical support for the development and implementation of Standard Operating Procedures (SOPs) related to newly qualified equipment and fixtures.
- Perform troubleshooting, root cause analysis, and implement corrective actions to resolve validation and compliance issues.
- Ensure validation activities comply with FDA regulations, ISO 13485, GMP, GAMP, and internal policies.
- Manage multiple validation projects simultaneously, including documentation, scheduling, and communication with internal and client stakeholders.
- Own and execute the full equipment/fixture validation lifecycle, from documentation development through testing and final reporting.
- Bachelor’s degree in engineering, Science, or a related technical field.
- 1+ year of validation experience within a medical device, pharmaceutical, biotechnology, or other regulated industry.
- Working knowledge of:
- ISO 13485
- FDA 21 CFR Part 820
- 21 CFR Part 11
- GMP
- GAMP
- Must be able to speak, read, comprehend, and write English.
Associate
Employment typeContract
Job functionMedical Equipment Manufacturing
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