Fda Regulations Jobs in Brewster, MA

The Manager Regulatory Affairs US Advertising & Promotion combines knowledge of scientific regulatory and business issues to enable products that are developed manufactured or distributed to meet required legislation. The Manager has the responsibility for 12 of the following: the More...

As a leading pharmaceutical company AbbVie is constantly striving to discover and deliver innovative medicines and solutions that address complex health issues and enhance peoples lives. Bringing a new drug to patients is a complex process that involves not only scientific research an More...

The Associate Director Market Access Field Training has primary responsibility to partner with Leaders across AbbVies portfolio of businesses to help diagnose needs and develop solutions that support skill development across market access competencies to create a world class Market Ac More...

Why We Work at Dun & BradstreetDun & Bradstreet unlocks the power of data through analytics creating a better tomorrow. Each day we are finding new ways to strengthen our awardwinning culture and accelerate creativity innovation and growth. Our 6000 global team members are pas More...

Why We Work at Dun & BradstreetDun & Bradstreet unlocks the power of data through analytics creating a better tomorrow. Each day we are finding new ways to strengthen our awardwinning culture and accelerate creativity innovation and growth. Our 6000 global team members are pas More...

Why We Work at Dun & BradstreetDun & Bradstreet unlocks the power of data through analytics creating a better tomorrow. Each day we are finding new ways to strengthen our awardwinning culture and accelerate creativity innovation and growth. Our 6000 global team members are pas More...

Responsibilities: Lead the validation team in a strategic riskbased approach that optimizes legacy Computer System documentation CSA strategies and strong SAP ECC>S/4 HANAconversion knowledge to successfully deliver a validated system meeting all project requirements. Review approva More...

*Employee can work remotely anywhere in the U.S.  The Principal Medical Writer is responsible for providing writing support and advanced scientific writing expertise to the teams ensuring successful preparation of high quality documents and effective implementation of the wr More...

*Employee can work remotely anywhere in the U.S. The Senior Medical Writer is responsible for providing medical writing ensuring successful preparation of high quality documents and effective implementation of the writing process. Provides medical writing expertise for multiple c More...

*Employee can work remotely anywhere in the U.S. The Senior Medical Writer is responsible for providing medical writing ensuring successful preparation of high quality documents and effective implementation of the writing process. Provides medical writing expertise for multiple c More...

*Employee can work remotely anywhere in the U.S.  The Principal Medical Writer is responsible for providing writing support and advanced scientific writing expertise to the teams ensuring successful preparation of high quality documents and effective implementation of the wr More...

Roles & Responsibilities: Full lifecycle validation for all applicable computerized systems ensuring they are designed validated operated and retired in compliance with GxP regulation and computer system validation (CSV) guidance. Compiling and maintaining accurate CSV documentation More...

About This Role The Associate Director Quality Assurance & Governance R&D Quality & Compliance (RDQC) will provide strategic guidance oversight and support for the quality activities within the Quality Management System (QMS) including regulatory health inspections and th More...

As a leading pharmaceutical company AbbVie is constantly striving to discover and deliver innovative medicines and solutions that address complex health issues and enhance peoples lives. Bringing a new drug to patients is a complex process that involves not only scientific research an More...

Responsibilities: Lead validation planning risk assessment and for R Studio GitLab and Medidata Rave EDC. Develop and execute validation documentation including: Validation Plans (VP.. User Requirements Specifications (URS.. Risk Assessments (RA.. Functional and Design Specification More...

Prysmian is the world leader in the energy and telecom cable systems industry. Each year the company manufactures thousands of miles of underground and submarine cables and systems for power transmission and distribution as well as medium low voltage cables for the construction and in More...

General SummaryUnder limited supervision is responsible for the collection of the account balances from all third party payors and patients for services rendered at UMMC Kernan and Specialty Hospital. Manages the Cash Posting area and Followup. Develops and maintains the policies and More...

Reporting to the Manager of Technical Services this position is responsible for conducting the mixing and testing of experimental polymeric compound formulation. This work is conducted under the direction of Polymer Engineers and industry/customer specifications and internal procedure More...

Working with UsChallenging. Meaningful. Lifechanging. Those arent words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here uniquely interesting work happens every day in every department. From optimizing a production line to the lat More...

The Policy and Regulatory Affairs team at Zoox is a crossfunctional organization responsible for advancing Zooxs public policy and regulatory goals including working with federal agencies such as the US Department of Transportation (USDOT) National Highway Traffic Safety Administratio More...