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Manager, QA and Regulatory Affairs
Laerdal Medical
-
New York, NY
This position will provide Regulatory Affairs oversight to Laerdal to assure FDA and Health Canada medical device and establishment requirements are met and both Laerdal Medical Corporation (LMC) and Laerdal Medical Canada (LMCA) remain compliant to medical device regulations. This position will provide Quality Assurance oversight to both the Laerdal Medical Canada (LMCA)
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Posted Today
Associate Director, Regulatory Affairs - Therapeutic Area Strategy
Ferring Pharmaceuticals Inc.
-
Parsippany, NJ
US Regulatory TA Strategy Lead the development and execution of US regulatory strategy in conjunction with Global Regulatory Lead (GRL), Global Regulatory Team and Global project teams. Partner with the GRL to understand the competitive landscape, e.g., views of US HAs, regulatory precedents, labeling differences and TA specific issues. Utilize US regulatory expertise and
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Posted Today
Manager, Reg Affairs NAM
International Flavors and Fragrances
-
Ridgefield, NJ
We are searching for a candidate to provide North America (including US and Canada) regulatory support for IFF Health and Biosciences business unit with focus on dietary supplement ingredients. The successful candidate will work as part of a global regulatory team within IFF Health and collaborate with internal business partners including R&D, Quality, Commercial and Mark
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Posted Today
Management and Program Assistant (Office Automation) (6 Month Register)
Internal Revenue Service
-
Hartford, CT / New Haven, CT / Norwalk, CT / 57 more...
Duties WHAT IS THE LARGE BUSINESS AND INTERNATIONAL (LBI) DIVISION? A description of the business units can be found at Vacancies will be filled in the following specialty areas Large Business and International Director Northeastern Compliance Practice Area (NECPA) The following are the duties of this position at the full working level. If this vacancy includes more than
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Posted Today
US Head of Regulatory Affairs Wellness
Haleon
-
Warren, NJ
Active Haleon Representative on Industry association, CHPA, and relevant Wellness associations in region and globally as appropriate Lead Wellness regulatory intelligence evaluation and communication process to guide strategic portfolio choices. Regulatory lead on governance and management of current/emerging wellness ingredient issues and risk management. Set Wellness Re
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Posted 3 days ago
Director, Regulatory Affairs - Advertising, Promotion and Regulatory Compliance
Ferring Pharmaceuticals Inc.
-
Parsippany, NJ
Manage Regulatory Affairs, Advertising & Promotion and Compliance Group Manage the US RA Ad Promo, submission operations, labeling and compliance group staff, including objective setting and career development activities and motivate line reports to achieve shared and individual goals. Regulatory Leadership of Advertising and Promotional Materials Serve as subject matter
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Posted 4 days ago
Associate Director, Regulatory Affairs - Athens, OH, San Diego, CA, or Remote
QuidelOrtho
-
Raritan, NJ / Athens, OH / San Diego, CA
Prepares /oversees the preparation of various regulatory submissions including Pre Submissions, 510(k) submissions, CLIA Waiver Applications, Dual 510(k)/Waiver by Applications, technical files, and license applications. Monitors new and changing regulations and guidance and disseminates information to stakeholders. Identifies regulatory trends and conducts key regulatory
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Posted 4 days ago
Senior Manager, Regulatory Affairs Operations and Intelligence
QuidelOrtho
-
Raritan, NJ
Develop solutions to improve processes for global regulatory submissions. Identify, implement, support validation and manage software tools for organizing regulatory files, registration tracking and documentation for submissions Manage Regulatory tools/database and new enhancements. Interact with global regulatory leaders and peers to share and manage department metrics a
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Posted 5 days ago
Regulatory Affairs Sr. Manager- Raritan, NJ, Rochester, NY, San Diego, CA or Rem
QuidelOrtho
-
Raritan, NJ / Rochester, NY / San Diego, CA
Reviews and interprets regulations/guidance documents to develop regulatory strategy to support Transfusion Medicine project teams in terms of regulatory submission pathway, IND & CMC strategies, submission requirements, timing and risks. Interact with US FDA and acts as a liason with Corporate International RA and/or country RA to define submission content, expedite pend
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Posted 5 days ago
State and Local Government Account Executive - MA, RI, VT, NH, ME
SAS Institute
-
Cary, NC / Arlington, VA / Pittsburgh, PA / 1 more...
State and Local Government Account Executive MA, RI, VT, NH, ME Job Locations US NC Cary HQ | US MA Requisition ID 20060332 Category Sales/Pre Sales Visa Sponsorship No Travel Requirements 50% Location Strong preference for New England or North Carolina based candidate. Nice to meet you! We're the leader in analytics. Through our software and services, we inspire customer
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Posted 6 days ago
Senior Associate, Regulatory Affairs
Alvogen
-
Pine Brook, NJ
OF POSITION Independently authors, compiles, reviews, and schedules high quality regulatory submissions in adherence with standards that are fully compliant with FDA and ICH requirements within company timelines. Plans, coordinates and writes, clear, concise and accurate, responses to inquiries from FDA resulting from their review of the submissions. Submissions will inclu
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Posted 7 days ago
Contracts Associate
Macmillan Learning
-
New York, NY
The Contracts Associate will handle Subsidiary Rights licensing agreements for the various publishers in the Macmillan Trade group of publishers, including Celadon Books, Farrar, Straus & Giroux, Picador, Flatiron Books, Henry Holt & Co., Metropolitan Books, St. Martin's Publishing Group, Tor, and the Macmillan Children's Publishing Group. The Associate will be responsibl
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Posted 10 days ago
MLTC-Dir of Contracts/Compliance
RiverSpring Living
-
Bronx, NY
MLTC Dir of Contracts/Compliance Job Locations US NY Bronx ID 2024 4997 Category Regulatory Compliance Position Type Regular Full Time Overview RiverSpring Health Plans serves over 16,000 frail individuals and help them live in their homes and independently for as long as possible. Join our compassionate and dedicated team and make a difference in the lives of our members
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Posted 10 days ago
Director, Interoperability Regulatory Lead
Quest Diagnostics Incorporated
-
Secaucus, NJ
The Interoperability Regulations and Standards, Director will work with key external stakeholders to summarize lab related industry standards and regulations and translate any business impact to internal stakeholders. When impactful, this role will be responsible to coordinate internal stakeholders to further assess any impact and help establish solutions. The role will c
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Posted 11 days ago
Manager, Regulatory Affairs Operations (Submission publishing)- Remote
PTC Therapeutics, Inc
-
South Plainfield, NJ
The Manager, Regulatory Affairs Operations is responsible for supporting the development of documents created for, and as a result of, worldwide regulatory submissions. The incumbent utilizes and supports systems and processes by which regulatory documentation (internally generated or received) is created, approved, submitted, and maintained for use and made readily searc
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Posted 11 days ago
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