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Sr. Medical Device, Pharmaceutical & Engineering Recruiter
Job Title: Sr. Validation Engineer
Contract Type: Short-term Contract
Job Description:
We are seeking an experienced Validation Engineer to support equipment qualification activities for a medical device manufacturing facility in San Francisco, CA. The role involves authoring, executing, and documenting IQ/OQ/PQ protocols to ensure compliance with FDA, ISO 13485, and cGMP standards.
Key Responsibilities:
Develop, review, and execute equipment qualification protocols (IQ/OQ/PQ).
Conduct risk assessments, deviation investigations, and support change control activities.
Collaborate with quality, engineering, and manufacturing teams to meet project timelines.
Ensure compliance with FDA, ISO 13485, and company SOPs.
Qualifications:
Bachelor’s degree in Engineering, Life Sciences, or related field.
4+ years of experience in equipment validation within the medical device industry.
Knowledge of FDA 21 CFR Part 820, ISO 13485, and validation best practices.
Seniority level
Seniority level
Mid-Senior level
Employment type
Employment type
Contract
Job function
Industries
Medical Equipment Manufacturing
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