We are looking for a Validation Engineer II, working in the Biotechnology/Medical Devices industry in Oceanside, California, United States.
Prepares and authors qualification and commissioning protocols.
Performs testing, collects samples, analyzes test results and prepares commissioning and qualification summary reports.
Plans, performs and coordinates installation qualification (IQ), inclusive of test generation and execution.
Provides technical assessment and validation review/ approval for engineering, process and standard operating procedure changes.
We are offering Competitive Compensation and Benefits. This position may present an opportunity to go permanent.
Our client is an award-winning clinical development company. Improving lives globally with 20+ years experience in clinical research and strategic resourcing. Elevating results with proven strategies, comprehensive solutions, and customized delivery models.
Serving pharmaceutical, biopharmaceutical, biotechnology, and medical device organizations.
Strong relationships provide you connections and access to great opportunities. Industry expertise sets you up for success with helpful insights, career coaching, and professional training. Grow and learn while you put your skills to work.
Experience Required for Your Success
BS degree in Life Science, Engineering, Biology, Biochemistry or equivalent.
3 to 6 years of direct GMP/ validation experience with increasing levels of responsibility for protocol generation, execution and planning of wide range of validation equipment and software.
Experience with Emerson DeltaV, Emerson Syncade and Pi software preferred.
Thorough knowledge of validation of principles, manufacturing processes, quality systems, engineering design fundamentals, regulatory agency expectation and industry trends.
Strong technical writing, verbal communication, interpersonal and problem solving skills.
Strong computer skills and familiarity with Microsoft office suite programs.
Excellent collaboration and ability to communicate information to a varied audience.
Compliance to cGMP requirements.
Demonstrated good record keeping practices and attention to detail.
What Do You Think?
Does your experience reflect what it takes to be successful in this role? Do the work and challenges get you excited about what's possible? Apply here.