Manager, Quality Salary at 908 Devices Inc BETA

Company Overview: Dyne Therapeutics is discovering and advancing innovative life-transforming therapeutics for people living with genetically driven neuromuscular diseases. Leveraging the modularity of its FORCE™ platform, Dyne is developing targeted therapeutics that deliver to muscle and the central nervous system (CNS). Dyne has a broad pipeline for neuromuscular diseases, including clinical programs for myotonic dystrophy type 1 (DM1) and Duchenne muscular dystrophy (DMD) and preclinical programs for facioscapulohumeral muscular dystrophy (FSHD) and Pompe disease. For more information, please visit https://www.dyne-tx.com/, and follow us on X, LinkedIn and Facebook. Role Summary: The Manager, Quality Control will support and oversee stability programs as well as QC testing and release of antibody drug conjugates and intermediates. This role will also contribute to the management of analytical development and QC activities in Phase 1 through BLA and commercial production. These acti

Why Sarepta? Why Now? The promise of genetic medicine has arrived, and Sarepta is at the forefront. We hold leadership positions in Duchenne muscular dystrophy (DMD) and limb-girdle muscular dystrophies (LGMDs), and we currently have more than 40 programs in various stages of development in gene therapy, RNA and gene editing. In 2023, we launched our fourth therapy and the first ever gene therapy to treat Duchenne. We're looking for people who see unlimited potential in themselves and who are motivated by an unwavering commitment to patients. What Sarepta Offers At Sarepta, we care deeply about all the people in our community and believe in the importance of supporting them in all aspects of their lives. We aspire to maintain a culture that acknowledges people bring their whole selves to work, and we will strive to help everyone in our community integrate their work and personal lives while maintaining productivity. We are committed to offering a range of benefits and work-life resourc

The Quality Manager position, based in Bedford, MA, will be responsible for: Supporting quality engineering requirements for new product development activities ISO certification and ongoing maintenance of the Quality Management System Driving a cultu Manager, Quality Engineer, Product Development, Management, Quality, Manufacturing, Technology

Quality Manager Cytonome, LLC. – Lexington, MA Job Overview Cytonome is a subsidiary of the global STgenetics group, an international leader of livestock reproductive services. Cytonome is based in the heart of the Massachusetts technology corridor and has additional research and development (R&D) teams in Texas and New Zealand. In 2021, we expanded our software capability via acquisition of Verity Software House, the cytometry software experts. Our facilities include an ISO 8 cleanroom for GMP consumable manufacturing, biological laboratory facilities (BSL2), and extensive engineering and R&D facilities. Cytonome operates under a quality management system compliant to ISO 9001:2015 and ISO 13485:2016 We are seeking an experienced Quality Manager to add to our team. As the Quality Manager, you will be responsible for delivering safe, reliable, compliant, and quality products that meet customer expectations. Reporting to the General Manager of Operations, you will be responsible for lea

Technology & Industry Leaders (Electronics - Automotive) Career Advancements About Our Client My client stands out as a pioneering force in the power electronics industry, known for its cutting-edge and innovative solutions. The company's commitment to high power density and efficiency has positioned it as a leader in the market. They have a global presence, providing reliable power components, modules, and systems to a diverse range of industries, including data centers and telecommunications. Its emphasis on quality management systems ensures products adhere to the highest standards, fostering trust among clients and partners. With a focus on continuous improvement and a reputation for technological excellence, my client remains at the forefront of advancing power electronics worldwide. Job Description Quality Manager key responsibilities: Oversee the RMA (Return Merchandise Authorization) process, including customer requests, return evaluations, and authorization issuance. Serve as

Job Description Job Description At Vericel Corporation, we are pioneers in advanced cell therapies for sports medicine and severe burn care, transforming patient lives through cutting-edge regenerative medicine. Our commitment to innovation, patient-centered focus, and scientific excellence drives us to develop groundbreaking treatments including MACI (knee cartilage repair), Epicel and Nexobrid (burn care).  Position Summary: The Quality Operations (QAOps) Manager is responsible for the oversight of the quality compliance activities associated with the day-to-day Quality Operations which includes CMO relationships. The individual will work cross functionally to support site projects as well as clinical and commercial products. This role will be focused on Vericel’s Medical Device products. Schedule: As a company that thrives on teamwork and collaboration, this role will be required to work five days per week on-site. Position Scope: Quality Ops Responsibilities: Provide guidance and e

Job Description Job Description At Vericel Corporation, we are pioneers in advanced cell therapies for sports medicine and severe burn care, transforming patient lives through cutting-edge regenerative medicine. Our commitment to innovation, patient-centered focus, and scientific excellence drives us to develop groundbreaking treatments including MACI (knee cartilage repair), Epicel and Nexobrid (burn care).  Position Summary: The Quality Operations (QAOps) Manager is responsible for the oversight of the quality compliance activities associated with the day-to-day Quality Operations which includes CMO relationships. The individual will work cross functionally to support site projects as well as clinical and commercial products. This role will be focused on Vericel’s Medical Device products. Schedule: As a company that thrives on teamwork and collaboration, this role will be required to work five days per week on-site. Position Scope: Quality Ops Responsibilities: Provide guidance and e

Why Sarepta? Why Now? The promise of genetic medicine has arrived, and Sarepta is at the forefront. We hold leadership positions in Duchenne muscular dystrophy (DMD) and limb-girdle muscular dystrophies (LGMDs), and we currently have more than 40 programs in various stages of development in gene therapy, RNA and gene editing. In 2023, we launched our fourth therapy and the first ever gene therapy to treat Duchenne. We're looking for people who see unlimited potential in themselves and who are motivated by an unwavering commitment to patients. What Sarepta Offers At Sarepta, we care deeply about all the people in our community and believe in the importance of supporting them in all aspects of their lives. We aspire to maintain a culture that acknowledges people bring their whole selves to work, and we will strive to help everyone in our community integrate their work and personal lives while maintaining productivity. We are committed to offering a range of benefits and work-life resourc