REGULATORY PARTNER MEDICAL DEVICES jobs in ENGLAND EUROPE, United Kingdom

prioritisation and resourcing. This grouping is not fixed, so can flex over time. Regulatory Partner (Medical Devices): The... advice to the commercial teams on business-related activities Regulatory Partner (Medical Devices) People: With a good...

CK Group are recruiting for a Regulatory Partner (Medical Devices) to join a company in the Pharmaceutical industry... working from home/remotely. Regulatory Partner Medical Devices Role: Support the team in ensuring that regulatory...

CK Group are recruiting for a Regulatory Partner Medical Devices to join a company in the Pharmaceutical industry... is based at our clients site in Welwyn Garden City. Regulatory Partner Medical Devices Role: Support the team in ensuring...

Zest Scientific is actively recruiting for a Senior Regulatory Specialist in the field of medical devices for a leading... medical devices industry (coupled with some work in the pharmaceutical sector), you will leverage your regulatory knowledge...

medical devices - from proof-of-concept through to market launch. You’ll oversee a diverse and fascinating range of front-end... on your experience of developing and launching medical devices, you’ll also be able to advise colleagues and clients on the appropriate...

we are looking for Do you have...? Pharmacy/Chemistry or Life Sciences degree Regulatory Affairs experience ideally with medicines, medical devices, OTCs... for the role of Regulatory Affairs Associate at our Harlow office to support European Generic new submissions via...

. As required, participate in medical device reporting, product recall and withdrawals events, liaising with internal management, regulatory... authorities, and partner organisations. Support the regulatory requirements of the product development process, contributing...

. As required, participate in medical device reporting, product recall and withdrawals events, liaising with internal management, regulatory... authorities, and partner organisations. Support the regulatory requirements of the product development process, contributing...

within the Global Regulatory Affairs, CMC Biologics, Devices department as a Director, Regulatory Affairs CMC Combination... Products to provide global regulatory CMC strategy and guidance for combination products, platform devices and assigned...

Experience in Medical Devices and their clinical evaluation International Regulatory experience – specifically USA Knowledge... in development of any future clinical development plans working closely with medical office and regulatory new products...

medical data software. This includes conceptualizing, designing, and prototyping wearable devices that are not only functional... you to push boundaries. Key Responsibilities: Design and develop hardware for wearable medical devices, including watches...

medical data software. This includes conceptualizing, designing, and prototyping wearable devices that are not only functional... you to push boundaries. Key Responsibilities: Design and develop hardware for wearable medical devices, including watches...

/leadership experience with IVD medical devices. Extensive knowledge of international IVD medical device quality systems... would be a plus if you also possess previous experience in: Supplier Auditing and/or Quality Assurance. IVD medical device regulatory affairs...

/ clinical or engineering with 5 or more years of marketing/commercial work experience in medical devices is preferred... healthcare market and medical device regulatory requirements. It would be a plus if you also possess previous experience in...

, automotive, pharmaceuticals and medical devices, technology, chemical, tobacco, industrial engineering, food and drink, safety... international businesses on product safety compliance, consumer protection legislation, the management of regulatory notifications...

Qualifications: Knowledge in medical devices and/or regulated OTC packaging. Excellent team player, eager to contribute to the... (internal and regulatory framework) are met during the development to reach a smooth handover to Supply Chain at validation...

: HEOR experience in diagnostics/medical devices Experience with infectious diseases and oncology Experience... opportunity to: Collaborate with cross-functional leadership across Government Affairs, Market Access, Medical Affairs...