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This is a highly autonomous Quality Engineer role where you'll lead US regulatory and quality oversight for FDA‑cleared implantable medical devices manufactured overseas. You'll act as the primary FDA liaison while building and maintaining a compliant, inspection‑ready quality system across international partners.
The Spinal Implant Instruments Development Engineer will play a key role in designing and developing innovative spinal implant instruments within the medical industry. This position requires expertise in engineering and manufacturing, with a focus on delivering high-quality solutions.
This role serves as the U.S. quality and regulatory owner for FDA‑cleared implantable medical devices manufactured overseas. You'll lead QMS execution, design controls, supplier quality, and regulatory compliance while working closely with global partners.
Our client, a well-known producer and distributor of branded food products, is seeking a Regulatory Specialist to oversee and drive regulatory initiatives across North America. Amid rapid growth, they are looking for a candidate who can help develop, enhance, and scale their regulatory function.
This Quality Engineer will play a critical role in maintaining regulatory compliance while supporting production, investigations, and facility transfer activities. The position blends hands‑on manufacturing support with system‑level quality engineering in a fast‑paced medical device environment.
This role offers the opportunity to shape next‑generation spinal implant and instrument systems by translating surgeon feedback into meaningful design improvements. You will work closely with clinicians, engineers, and manufacturing partners to refine products throughout their lifecycle.
This is a Quality/Regulatory Specialist role with a growing manufacturer of various baked goods and pantry items you see everyday. This role will have exposure to big name brands and help lead the regulatory arm of quality.
My client is seeking a Senior Regulatory Affairs Specialist to support regulatory strategy and execution across a growing portfolio of healthcare products. This individual will play a critical role in ensuring compliance with U.S. and international regulatory requirements while partnering cross‑functionally to enable timely product development, approval, and lifecycle management.
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