ABOUT COMPANY:
Stark Pharma Solutions Inc is a life sciences staffing and consulting firm supporting pharmaceutical, biotechnology and medical device organizations across the United States. We place quality, validation, manufacturing and regulatory professionals with companies building and scaling FDA-regulated operations. Our clients range from established manufacturers to early-stage sites standing up their first quality systems.
Quality Engineer Medical Device (CAPA, ISO 13485, Risk Management)
JOB SUMMARY:
Our client, a medical device manufacturer, is seeking a Quality Engineer to support quality systems and product quality activities in an FDA-regulated environment. The role covers CAPA and non-conformance investigations, risk management, design control support and process validation, working cross-functionally with Manufacturing, Engineering and Regulatory teams.
RESPONSIBILITIES:
QUALIFICATIONS:
HOW TO APPLY:
Please send your resume to deepika.b@starkpharma.com . In your email, please include your current location, your hourly rate expectation on W2, and your availability to start.
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