A small-scale medical device organization based in Chelmsford, MA that focus on plastic injection molding has focused their efforts on brining in a Manager of QARA on a full-time basis. This individual is expected to come in
Position Summary BostonGene is seeking a Regulatory Manager to join our team and play a crucial role in supporting our ISO certification efforts and regulatory compliance. The primary focus of this position will be on ensuring Good Laboratory Practice
Work Your Magic with us! Start your next chapter and join EMD Serono. Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe
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
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
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 and
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.
Job Description Job Description The Company Verve Therapeutics is a biotechnology company created with a singular focus: to protect the world from heart disease. Founded by world-leading experts in cardiovascular medicine, human genetics and gene-editing, the
Job Description Job Description Salary: About Us: Pramand, LLC, is a medical device company based in Bedford, MA. We develop implantable medical devices from novel, proprietary hydrogel materials that improve patient outcomes while lowering the cost
Job Description Job Description Vericel Corporation, a leader in advanced therapies for the sports medicine and severe burn care markets, has an exciting opportunity for a top performing Regulatory professional looking to join and contribute to a
Job Description Job Description Lantheus is headquartered in Bedford, Massachusetts with offices in New Jersey, Canada, and Sweden. For more than 60 years, Lantheus has been instrumental in pioneering the field of medical imaging and has
Job Description Job Description Position Summary: The main responsibilities of this role are to participate in regulatory projects to achieve program deliverables and provide regulatory support to global clinical trial teams or other cross-functional teams. This individual will
Job Description Job Description Company Description Deciphera is a biopharmaceutical company focused on discovering, developing and commercializing important new medicines to improve the lives of people with cancer. We are leveraging our proprietary switch-control kinase inhibitor
Regulatory Affairs Senior Manager-Director Company Summary: My client is a growing leader in developing breakthrough protein therapeutics for Companion Animal Health. They are looking to add a Senior Manager-Director of Regulatory Affairs to support their growing pipeline of animal health
Job Description Job Description The Company Verve Therapeutics is a biotechnology company created with a singular focus: to protect the world from heart disease. Founded by world-leading experts in cardiovascular medicine, human genetics and gene-editing, the
Senior Manager level Recommended experience: minimum 4 years of pharma industry experience with a minimum of 2 years within a strategy role. Description: Accountabilities Assists in the creation and execution of global regulatory strategies for assigned programs and
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 and timelines
Looking to work at a firm that encourages a work life balance? Withum is a forward-thinking, technology-driven advisory and accounting firm, helping clients to Be in a Position of StrengthSMin today’s modern business landscape. Withum empowers
Looking to work at a firm that encourages a work life balance? Withum is a forward-thinking, technology-driven advisory and accounting firm, helping clients to Be in a Position of StrengthSMin today’s modern business landscape. Withum empowers