Senior Regulatory Manager Job Description 1. Job purpose 1) Acts as business contact for product regulatory advice, substance registration and/or emerging regulations management. 2) Ensure product ...

The Manager of Clinical and Regulatory Services is a dedicated individual (RN) who supports the Clinic Managers and Regional Vice Presidents of Operations in the opening of new facilities, assistin...

Ashley Addiction Treatment is seeking a Regulatory/Accreditation Coordinator, FT. This professional works in coordination and cohesively with the Director of Corporate Compliance, Quality and Risk ...

Founded in 1979, Technical Resources International, Inc. (TRI) is a full-service contract research organization plus (CRO+) providing product development support services to the global drug, biolog...

Here's What You'll Do: Develop effective CMC regulatory strategies for submissions (e.g. IND/CTA/BLA/MAA) and identify regulatory risks Provide guidance for regulatory CMC aspects of product develo...

• Under the direction of the Senior Vice President of Regulatory Affairs is an essential point of contact/liaison with FDA and related health authorities where applicable. Responsible for establish...

Title: Regulatory & Medical Affairs Project Manager Location: Lawrenceville, NJ Start date: ASAP Responsibilities: This position will plan and manage projects of moderate-to-high complexity in ...

Jazz Pharmaceuticals is an international biopharmaceutical company focused on improving patients’ lives by identifying, developing and commercializing meaningful products that address unmet medical...

The Director Regulatory Affairs is responsible for planning, coordinating and implementing regulatory strategies for products that require government approval. Accountabilities Deliver innovativ...

The Regulatory Affairs Manager is responsible for providing regulatory expertise to the site and, as directed, to other FDB sites. Performs regulatory surveillance, interpreting regulatory document...

You will be responsible for the oversight of all aspects of submitting protocols to the Healthcare NCAL (KPNCAL) Regional Institutional Review Board (IRB) and central IRBs for review regulatory act...

Bayside Solutions is seeking a Regulatory Affairs Manager to be part of our client's team in the North Bay. This is an opportunity to work with the largest privately held pharmaceutical corporation...

QA and Regulatory Affairs Manager have primary responsibility for our ISO13485/cGMP compliant quality system for Foamtec’s regulated businesses, including Medical Device, Pharmaceutical, and Life S...

We're an established, yet growing medical device manufacturer comprised of dedicated, passionate industry veterans. Our company provides a unique to the industry medical device aimed at helping peo...

The Project Manager will be responsible for specific deliverables within the global/regional/line of business focused on program initiatives. Profile Candidate Profile Requirements Proactive delive...

With supervision by the Head, Global Regulatory Affairs Labeling Strategy, PDT BU, the Regulatory Labeling Strategy Lead, is responsible for providing regulatory expertise, strategic insight, and g...

Under general supervision by the Lead, CMC Regulatory Affairs, Plasma-Derived Therapies Business Unit (GRA PDT BU) the Strategist is responsible for developing, coordinating and implementing global...

Lead the promotional material review committee (PMRC) for assigned products/therapeutic areas for the company. Under the direction of the US lead Promotional Regulatory Affairs, provides input on d...

This position will report to the Vice President, Regulatory Affairs and will be responsible for developing and implementing global regulatory strategies, establishing and maintaining effective rela...

The Director US Regulatory Affairs supports the contract development and manufacturing of client cell therapy products for the US market. This individual collaborates cross-functionally to support ...

Determine global regulatory strategies for market introduction of new and modified device (technology) platforms. Ensure proper communication of regulatory strategies to responsible functions, incl...

Our client, a top multinational pharmaceutical and biopharmaceutical company, is currently seeking a Global Regulatory Affairs Compliance Manager for a 6 month assignment, with potential to convert...

This position is designed to develop, implement, and oversee the Quality Assurance and Regulatory Compliance strategies of the company. This position is responsible for providing leadership and tec...

Prepares, reviews and submits high quality regulatory submissions to Regulatory Agencies (primarily FDA) within company timelines and in accordance with regulatory guidelines and applicable federal...

Activities will include the intake and execution of applying data standards and date remediation efforts on the centralized administrative functions leveraged as keystone activities across RIMS ( E...