Medical and Clinical Affairs Specialist - Raynham, United States - Med Device, Biotech and Pharma Consulting

Principal Regulatory Affairs Specialist

2 days ago

**Job Title**: Principal Regulatory Affairs Specialist · **Principal Regulatory Affairs Specialist · - Software & Artificial Intelligence (U.S. Hub Based)** · The Principal Regulatory Affairs Specialist · - SW & AI will shape, lead and execute innovative regulatory strategies to ...

Regulatory Affairs Specialist I

3 weeks ago

DePuy Synthes, part of Johnson & Johnson MedTech, is recruiting for a Regulatory Affairs Specialist I to support our Spine business. This role is located on-site in Raynham, MA and will work a Flex/Hybrid schedule with three days of on-site and two days of off-site work . · Ab ...

Regulatory Affairs Specialist II

3 weeks ago

DePuy Synthes, Inc. is currently recruiting for a Regulatory Affairs Specialist II to support Life Cycle Management and New Product Development. This role will work a Hybrid/Flex schedule with 3 days in office each week, located in Raynham, MA or West Chester, PA . · About Joh ...

Regulatory Affairs Specialist

4 days ago

The Regulatory Affairs (RA) Specialist within the BD Interventional Surgical Devices Business unit will work on global regulatory strategy and submissions for implantable and absorbable devices. Under the mentorship of the Senior Regulatory Affairs M Regulatory Affairs, Specialis ...

Regulatory Affairs Specialist

1 week ago

As a core member of multiple new product development teams, the Regulatory Affairs Specialist will provide timely and valued regulatory guidance (written and / or verbal) by owning the following tasks: 1. Advise internal stakeholders (marketing, manu Regulatory Affairs, Specialis ...

Regulatory affairs specialist

6 days ago

job summary: · Your Responsibilities: · As a core member of multiple new product development teams, the Regulatory Affairs Specialist will provide timely and valued regulatory guidance (written and / or verbal) by owning the following tasks: · 1. Advise internal stakeholders (m ...

Regulatory Affairs Specialist

4 days ago

**Job Description Summary** · The Regulatory Affairs (RA) Specialist within the BD Interventional Surgical Devices Business unit will work on global regulatory strategy and submissions for implantable and absorbable devices. Under the mentorship of the Senior Regulatory Affairs ...

Regulatory Affairs Specialist III_US

1 week ago

OVERVIEW · We are currently searching for a skilled professional to join a well-known client's team as a Remote Regulatory Affairs Specialist. The Regulatory Affairs Specialist role will independently provide EU regulatory requirements and guidance to EU MDR project teams. Lead ...

Regulatory Affairs Specialist III

3 days ago

We're looking for a Regulatory Affairs Specialist III , working in Pharmaceuticals and Medical Products industry in Bridgewater, New Jersey, United States .Contributes to the development and oversees the successfulimplementation of regulatory strategies for assigned products, inc ...

Regulatory Affairs Specialist III #:

1 week ago

Job Title - Regulatory Affairs Specialist III · Location - Bridgewater, NJ · Duration - 9 Months · Job Description · Manager will consider candidates to be based in either Bridgewater, New Jersey or Cambridge, Massachusetts. Please specify on resume which location candidate i ...

Regulatory Affairs Specialist

1 week ago

Job Title · Regulatory Affairs SpecialistJob Description · Looking at the challenges the world is facing today Philips' purpose has never been more relevant. So, whatever your role, if you share our passion for helping others, you'll be working towards creating a better and faire ...

CMC Regulatory Affairs Specialist

1 week ago

Job title: CMC Regulatory Technical Writer II · Location: Bridgewater, NJ, Hybrid · Duration: 1 year · SHIFT SCHEDULE 1st shift, 9-5 EST Mon-Fri · Pay Rate starts: $47/ HOUR · HM Notes: · Hybrid - onsite Tuesday & Thursday - This can change at any time. · 5 years experie ...

Regulatory Affairs Specialist III

1 week ago

Remote · Description: · 1) Independently provide EU regulatory requirements and guidance to EU MDR project teams. · 2) Lead the preparation of the EU MDR technical documentation for Class III, IIa, IIb, or Class I sterile or reusable medical devices to support timelines for C ...

Principal Regulatory Affairs Specialist

4 days ago

Job Title Principal Regulatory Affairs Specialist Job Description This requisition is expected to stay active for 45 days but may close earlier if a successful candidate is selected or business necessity dictates. Interested candidates are encouraged to apply as soon as possible ...

Principal Regulatory Affairs Specialist

5 days ago

Job Title Principal Regulatory Affairs Specialist Job Description · This requisition is expected to stay active for 45 days but may close earlier if a successful candidate is selected or business necessity dictates. Interested candidates are encouraged to apply as soon as possib ...

Principal Regulatory Affairs Specialist

1 week ago

Job TitlePrincipal Regulatory Affairs Specialist · Job Description Principal Regulatory Affairs Specialist (U.S. Hub based) · Clinical Integration and Insight (CII) is changing the way healthcare is delivered at the point of care. Our Capsule Surveillance product is a clinical ...

Principal Regulatory Affairs Specialist

1 week ago

Job Title · Principal Regulatory Affairs Specialist Job Description · Principal Regulatory Affairs Specialist (U.S. Hub based) · Clinical Integration and Insight (CII) is changing the way healthcare is delivered at the point of care. Our Capsule Surveillance product is a clini ...

Principal Regulatory Affairs Specialist

1 week ago

Job Title · Principal Regulatory Affairs SpecialistJob Description · Principal Regulatory Affairs Specialist (U.S. Hub based) · Clinical Integration and Insight (CII) is changing the way healthcare is delivered at the point of care. Our Capsule Surveillance product is a clinical ...

Senior Regulatory Affairs Specialist

1 week ago

The Senior Regulatory Affairs Specialist will support and carry out the regulatory strategy and other regulatory aspects of product development and processes for the Biofourmis pharma partnerships and DTx algorithms. · Reporting to the SVP of Q&R, the Senior Regulatory Affairs S ...

Senior Regulatory Affairs Specialist

1 week ago

Contract Role: · Schedule: It will be on average 20 hours per week, preferably 4 hours a day M-F, but we can be flexible depending on the candidate. · -REMOTE- Regulatory Affairs Specialist DS Process Expert with NDA filing experience. · May – September (20 hours week) · Cont ...