Fda Regulations Jobs in Woodstock, ME

This position is Registry status. Casual/Registry status differs from full and parttime statuses Casual/Registry status positions are nonbenefited hours are not guaranteed and your schedule is dependent on the departments staffing needs and your availability.  ThePhlebotomis More...

The Associate Director Immunology Field Training Dermatology is responsible for the team developing the sales franchise curriculum for AbbVie field personnel and field management. This person will create lead and work within crossfunctional teams made of participants from Training Me More...

This position is Registry status. Casual/Registry status differs from full and parttime statuses Casual/Registry status positions are nonbenefited hours are not guaranteed and your schedule is dependent on the departments staffing needs and your availability.  ThePhlebotomis More...

The Senior Manager Regulatory Affairs US Advertising and Promotion ImmunologyDermatology combines knowledge of scientific regulatory and business issues to enable products that are developed manufactured or distributed to meet the required legislation. Additionally the individual deve More...

Responsibilities: Candidate must be able to answer questions in the STAR format (Situation Task Action Result). If they cannot formulate a response this way please coach or whittle down the resume. Note answers should pull from multiple projects and not the same one over and over. C More...

The Senior Director of Regulatory Affairs ensures that all divisions comply with applicable federal state and provincial laws and regulations maintaining continuous operating approvals. This role also leads efforts to develop and influence regulatory policies impacting the delivery of More...

This position is Registry status. Casual/Registry status differs from full and parttime statuses Casual/Registry status positions are nonbenefited hours are not guaranteed and your schedule is dependent on the departments staffing needs and your availability.  ThePhlebotomis More...

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...

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...

This position is Registry status. Casual/Registry status differs from full and parttime statuses Casual/Registry status positions are nonbenefited hours are not guaranteed and your schedule is dependent on the departments staffing needs and your availability.  ThePhlebotomis More...