About us Based in Parma, Italy, Chiesi is an international research-focused pharmaceuticals and healthcare group with over 85 years’ experience, operating in 30 countries with more than 6,000 employees (Chiesi Group). To achieve its mission of
About the Department Our Boston Research & Development hub, anchored in the greater Boston area, brings together the best minds in life science innovation. The teams located in facilities in Lexington, Watertown and Cambridge reflect the
Intertek Scientific and Regulatory Consultancy Group is looking for a motivated and client focused senior regulatory affairs professional who is seeking an opportunity to be a Program Manager to promote our food, nutrition and regulatory consulting services. The Principal Scientist/Associate
Johnson and Johnson Medical Device Companies is recruiting for an Associate Director, Regulatory Affairs - Special Projects. The preferred location for this role is Raynham, MA however remote options within United States will be considered on a case
DePuy Synthes, Inc., part of the Johnson & Johnson MedTech companies, is currently recruiting for a Senior Regulatory Affairs Specialist to support Life Cycle Management and New Product Development. This role will work a Hybrid/Flex schedule with 3
Job Description Job Description About Us Leap’s mission is to combat climate change by enabling a reliable electric grid that runs on clean energy. The electric grid is transforming from dirty (but predictable) fossil fuels to
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,
Job Description Job Description Exciting opportunity for a Full Time Senior Vice President, Regulatory Affairs and Quality to lead regulatory strategy and quality systems for cutting-edge biotech projects at Beacon Therapeutics. As a pivotal member of our team, you
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The Associate Director RA serves as the regulatory lead on Review Committees (RCs). As the RC RA representative, work with brands on competitively positioning assigned products appropriately while maintaining compliance with applicable FDA regulations, company policies, and
About the Role The Associate Director, US Regulatory Affairs (RA) serves as the regulatory lead on relative Review Committees (RCs), for products in the Rare Disease, Rare Blood Disorder and Neurology portfolio. As the RC RA representative, work with
Job Description Job Description Company Description Corbus Culture: Our passion. Our purpose. At Corbus, it starts at our core. We look for unique talent. Our people are brilliant, they break barriers and are not defined by
Company Overview: Dyne Therapeutics is a clinical-stage muscle disease company focused on advancing innovative life-transforming therapeutics for people living with genetically driven diseases. With its proprietary FORCE platform, Dyne is developing modern oligonucleotide therapeutics that are
This position can be fully remote PURPOSE AND SCOPE: Ensures company products meet regulatory requirements by supporting all assigned regulatory aspects of product approval and post-marketing compliance. Develops, coordinates, reviews and prepares documentation packages for pharmaceutical regulatory submissions (Primarily
DePuy Synthes, part of the Johnson & Johnson family of companies, is current recruiting for a Regulatory Affairs Specialist II role to support our Sports Medicine business. The preferred location is within a commutable distance of Raynham, MA
Abiomed, part of Johnson & Johnsons MedTech, is recruiting for a Senior Regulatory Affairs Specialist . Remote work options may be considered on a case-by-case basis and if approved by the Company Abiomed, part of Johnson & Johnson
Title: Regulatory CMC Specialist Location: Worcester, MA (Open to Hybrid or Remote) Pay: $65-69/hr Contract: 12+ months Responsibilities: Leads and influences peers and colleagues within the scope of their work. Responsible for various aspects of quality assurance
Shorla Oncology develops innovative solutions into effective oncology treatments to improve patients’ lives. The patients’ needs are at the heart of our innovation, ensuring we deliver affordable, accessible medicines and provide a significant clinical impact. Shorla
Job Description: • The Manager/Sr. Manager of Regulatory Affairs will work closely with the Regulatory Leads and cross-functional development teams to assist in the development, communication, and execution of regulatory strategy and submission timelines. • Manage document and submission preparation
Regulatory Affairs Manager Reporting Reports to VP, Quality Assurance and Regulatory Affairs Company Akston Biosciences is inventing, developing, and manufacturing breakthrough protein therapeutics for Companion Animal Health. Our integrated capabilities, from discovery to commercial manufacturing, give us unique advantages. Our