Senior Manager, Quality Systems - Devens

This role will encompass laboratory and manufacturing instrument PC support and application administration, local support and liaison for global laboratory and quality systems. · ...

Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. ...

The overall focus of this resource will encompass laboratory and manufacturing instrument PC support and application administration. · ...

WHOOP is looking for a Regulatory Affairs Specialist II to be a core member of the Digital Health team at WHOOP. · This role requires creative problem-solving and adaptability in an innovative and evolving space. · ...

This position plays a key role in supporting daily manufacturing activities by resolving operational issues and driving high-quality investigations. · 6+ years experience in pharma/biotech manufacturing environments. · Proven background in investigations, RCA, QC analytics, and G ...

We are looking for a Regulatory Affairs Specialist II to be a core member of the Digital Health team at WHOOP. As the Regulatory Affairs & Quality Systems Specialist II, you will execute regulatory strategy and support QMS maintenance deliverables for WHOOP SAMDs in a dynamic and ...

EPTAM Precision Molding is looking for a Quality Systems Engineer to join our team in Lancaster, MA. · We are dedicated to supporting the complete product lifecycle in consumer product. healthcare, and defense industries. · ...

We are looking for a Regulatory Affairs Specialist II to execute regulatory strategy and support QMS maintenance deliverables in a dynamic and agile environment. · Support and submit U.S. regulatory documentation including Q-submissions, De Novo requests, 510(k)s, product change ...

We're on a mission to unlock human performance and health span at WHOOP. · Support and submit U.S. regulatory documentation including Q-submissions. · Create detailed regulatory deliverables for global distribution of medical devices. · Prepare regulatory submissions for medical ...

Location: Woburn, MA (on-site 5 days per week) · Vaxess is developing a pipeline of next-generation therapeutics on our novel micro-array patch platform. With only five minutes of wear-time on the skin, the Vaxess' patch combines room temperature stability with simplified applica ...

The Quality System Specialist / Senior Quality System Specialist plays a key role in supporting and enhancing Vaxess Technologies' Quality Management System (QMS) to ensure compliance with applicable GMP/GLP standards. · ...

The evolution and spread of drug-resistant infection is the world's great health care challenge, · Partner with senior stakeholders to design and implement a robust ISO-13485 Quality Management System, · At least 10 years of hands-on experience developing and maintaining ISO-1348 ...

The Quality Manager is responsible for leading quality improvement for an AST processing or lab facility. · ...

The Director, Quality Systems and Compliance provides strategic direction and oversight of the Quality Systems and Quality Compliance functions at ElevateBio to ensure execution and performance meets regulatory requirements and current industry best practices.You will be responsi ...

The Quality Systems Associate will be responsible for assistance with the daily administration of the quality management system document/records management. · Assist with review of documents under revision, issuance of records, tracking of controlled documents, and management of ...

Support the global Quality Systems and their operations in ensuring compliance and fit for intended use in accordance with applicable global SOPs. · ...

We are seeking a dynamic, analytical thinking individual to join our Quality team, · This position is responsible for supporting the overall QMS processes for the organization, · Support CAPA Owners in quality-related technical principles, · Investigate customer complaints, from ...

We are seeking a Director of Quality Systems to oversee all aspects of the Quality Management System (QMS) across the Americas. · Ensures the QMS design maintenance execution and governance supports business objectives through proactive monitoring and application of global regula ...

Lensa does not hire directly for these jobs but promotes them on LinkedIn on behalf of its clients and partners. · Bachelor of Science requiredMinimum of 10 years Regulated Quality Experience.Good analytical toolkit. ...

We are seeking an experienced Senior Quality Systems & Compliance Specialist to support Quality Systems and Compliance activities within a regulated pharmaceutical environment. · ...