- Merck & Co. (Boston, MA)
- Job DescriptionOur company is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products. The difference ... and an inspiring mission to achieve new milestones in global healthcare.At our company, we are inspired by the...is seeking a dynamic, strategic thinking and collaborative Associate Principal Scientist to contribute to our small molecule and… more
- Olympus Corporation of the Americas (Westborough, MA)
- …The position will provide guidance, training, and coaching to team on quality compliance matters including on communication on responses. The individual ... compliance response communications working cross functionally with Market Quality , Marketing, Operations/Ops Quality , Regulatory, Risk and R&D in… more
- Takeda Pharmaceuticals (Boston, MA)
- …is true to the best of my knowledge. **Job Description** **Job Title** : Principal Manager, Cell Therapy Quality Compliance **Location** : Cambridge, MA ... + Establish and maintain productive relationships with Takeda Global Quality and R&D Quality Compliance & Systems personnel to represent CT/CTQ in … more
- Sanofi Group (Framingham, MA)
- …infectious diseases and bring hope to patients and their families. Your job, as Principal Compliance Specialist on our Quality Assurance (QA) Operations team ... of operations at Sanofi's Framingham Biologics facilities. The Principal Compliance Specialist is responsible for providing quality support and guidance… more
- Takeda Pharmaceuticals (Boston, MA)
- …function to ensure compliance to company quality standards and global regulatory requirements. The Principal Archivist contributes to company success by ... across the global enterprise with key stakeholders (eg, in Research, Global Quality , Pharmaceutical Sciences, Plasma-Derived Therapies) to implement, as well… more
- Merck (Boston, MA)
- **Job Description** **Position Title** -Director/ Principal Scientist, Regulatory Compliance **Department** - Device Quality & Regulatory **Brief Description ... Position-** This position will be part of the Device Quality & Regulatory Team within Global Regulatory...data for management review. **Reports to** - Director Regulatory Compliance , Device Quality and Regulatory **Location** -… more
- Takeda Pharmaceuticals (Boston, MA)
- …is true to the best of my knowledge. **Job Description** **Job Title** : Principal Quality Manager **Location** : Cambridge, MA **About the role:** The ... Principal QA Manager, Cell Therapy Quality (CTQ),...and partners with team members and stakeholders in advancing quality and compliance . + Lead across the… more
- RTX Corporation (Andover, MA)
- …solves tough, meaningful problems that create a safer, more secure world. The Patriot Principal Program Quality Lead (PQL) in Land and Air Defense Systems ... engage with the product line and work in partnership with Program Leadership, Engineering, Global Supply Chain, Operations and the Quality team. These roles will… more
- RTX Corporation (Tewksbury, MA)
- …world. We have an immediate need for onsite Principal Software Systems Quality Engineers ( Quality Assurance/ Compliance ) to support Land & Air Defense ... Technology, Engineering or Mathematics (STEM) Education and eight (8) years of Quality Experience (Assurance, or Compliance , or Engineering) or Engineering… more
- J&J Family of Companies (Lexington, MA)
- …all necessary procedures are followed to secure new equipment and technology and compliance with local and country safety and quality guidelines and regulations. ... Principal Engineer - 2406210334W **Description** Johnson and Johnson...position is Lexington, MA. It is part of the global PC&D Team. The position reports to the Director,… more
- Catalent Pharma Solutions (Chelsea, MA)
- …Development. **Catalent is committed to a Patient First culture through excellence in quality and compliance , and to the safety of every patient, consumer, ... ** Principal Scientist, DMPK Advisory Services** **Position Summary:** Catalent is a global , high-growth, public company and a leading partner for the… more
- Sanofi Group (Framingham, MA)
- **About the Job** We are an innovative global healthcare company with one purpose: to chase the miracles of science to improve people's lives. We're also a company ... get started? Purification Process Development (part of Sanofi R&D and Global CMC Development) is responsible for development, scale-up, transfer, and… more
- Takeda Pharmaceuticals (Lexington, MA)
- …with company policies and procedures. + Maintain continuous awareness around cGMP and quality ; follow compliance requirements. + Travel: You may travel for ... is true to the best of my knowledge. **Job Description** **Job Title** : Principal Automation Hardware Engineer **Location** : Lexington, MA **About the role:** As a… more
- Editas Medicine (Cambridge, MA)
- … assurance and validation deliverables are met. + Have knowledge and ensure compliance with all relevant quality guidelines, including FDA, EMA, ICH, and ... global regulatory requirements. + Ability to support other Quality Assurance tasks as needed. Requirements The Ideal Transcript:... activities. This role is critical for maintaining our compliance and quality standards in a fast-paced… more
- Medtronic (Boston, MA)
- …posted on our career site for at least 3-7 days. This aligns with our Global Job Posting Standards and ensures compliance with the new legislation. No ... world. **A Day in the Life** Medtronic is a global leader in medical technology, alleviating pain, restoring health,...providers. Medtronic is seeking a highly skilled and experienced Principal Associate for Strategy to join our Medical Surgical… more
- AbbVie (Cambridge, MA)
- …Description AbbVie Analytical Research & Development (Analytical R&D) is a global analytical scientific organization responsible for all CMC analytical activities ... Careers in AbbVie Analytical R&D provide unique opportunities to work with global and cross-functional teams to drive exceptional science and innovative product… more
- Philips (Cambridge, MA)
- …regulatory entities on regulatory filings at the reviewer level. Provide guidance on global compliance such as CE Marking and product registrations, clinical ... The Principal Regulatory Affairs Specialist will play a critical...regulatory professionals; drive improvement in regulatory aspects of the Quality Management System, in developing/documenting processes and procedures to… more
- Medtronic (Boston, MA)
- …be joining our Product Development Organization as a Senior Principal Development Engineer responsible for the Verification Strategy, Requirement Decomposition, ... responsible for partnering with Systems Engineering, Marketing, the design teams, Quality and Project Management to drive meaningful product requirements, a robust… more
- Bristol Myers Squibb (Devens, MA)
- …for transfer and validation of methods in the commercial environment in compliance with global regulatory requirements. + Implement method lifecycle and ... Read more: careers.bms.com/working-with-us . **Position Summary:** BMS is seeking a Principal Scientist for the Cellular Therapies Development and Operations (CTDO)… more
