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Responsible for manufacturing process development, implementation, and continuous improvement to enhance yield, reduce cost and improve productivity. Represent Process Engineering in assigned R&D and Project Team meetings for technology transfers and provide technical expertise and support in analytical method development, validation and process scale, and current production capabilities in manufacturing. Performs or manages process validations (IQ/OQ, OQ, PQ). Troubleshoot production line issues related to yield, quality, and throughput. Leads scaling up processes from development to full scale manufacturing. Supports evaluation of NCMR, CAPA, SCAR, Failure investigation and Deviation requests arising from Contract Manufacturers/Suppliers. Creates/Updates manufacturing instructions, routings, bills of materials and SOPs.
Skills:
process validation, class iii medical devices, product transfer, implant
Top Skills Details:
process validation,class iii medical devices,product transfer
Additional Skills & Qualifications:
BA/BS in life sciences or engineering (Biomedical, Manufacturing, Mechanical). 4+ years of experience of medical device manufacturing - class 3 preferred (live implants) Experience managing contract manufacturers Experience Process Validations at external suppliers (CMO). Experience transferring product from R&D to production
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.
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Full Time