Actalent • Allendale, NJ 07401
Job #2696194562
Support tracking of supplier manufacturing information
manage the testing conducted by external laboratories according to procedures and standards regarding reprocessing activities (cleaning and sterilization) and biocompatibility.
Complete documentational gap assessments as needed for reprocessing activities (cleaning and sterilization) and biocompatibility for EU MDR compliance.
Reviewing and approving microbiological testing data ensuring compliance to the applicable methods and regulatory standard requirements
Ability to work cross-functionally with R&D, Operations and Regulatory.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
Diversity, Equity & Inclusion
At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through:
Hiring diverse talent
Maintaining an inclusive environment through persistent self-reflection
Building a culture of care, engagement, and recognition with clear outcomes
Ensuring growth opportunities for our people
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email ~~~ (~~~) for other accommodation options.
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