Director of Quality and Compliance
EPS Connects LLC
Director of Quality & Compliance Beverly, Massachusetts Help Build the Next Generation of Global Quality. EPS Connects is conducting a confidential search on behalf of a global medical device manufacturer seeking a Director of Quality & Compliance to help shape the future of its enterprise Quality Management System. This is not a traditional Quality Director role focused on maintaining compliance. The organization has experienced significant growth, and they’re looking for a leader who can help evolve their Quality Management System to support the next stage of that growth. Working closely with the Vice President of Quality, you’ll evaluate existing quality systems, identify opportunities for improvement, harmonize processes across global manufacturing sites, and help build a scalable quality organization capable of supporting continued expansion. If you’re energized by improving systems rather than simply maintaining them, this opportunity offers the chance to make a lasting impact. What You’ll Be Doing Evaluate and improve an enterprise Quality Management System supporting multiple global manufacturing sites. Drive practical, measurable improvements to quality processes, systems, and performance metrics. Partner with Operations, Engineering, Regulatory Affairs, and executive leadership to strengthen quality throughout the organization. Lead Quality initiatives involving FDA, ISO 13485, MDSAP, and other global regulatory requirements. Support quality harmonization across manufacturing locations. Build dashboards and meaningful quality metrics that drive better business decisions. Mentor and influence quality leaders throughout the organization. Help develop the long-term quality strategy for a growing global medical device company. We’re Interested In Leaders Who Have Progressive leadership experience in medical device manufacturing quality. Experience improving or transforming Quality Management Systems—not simply maintaining them. Strong understanding of ISO 13485, FDA Quality System Regulation, MDSAP, and global regulatory expectations. Experience working across multiple manufacturing sites or global operations. Strong collaboration skills with Engineering, Operations, Regulatory Affairs, and executive leadership. A practical continuous improvement mindset focused on sustainable progress rather than perfection. Excellent communication skills with the ability to influence without relying solely on organizational authority. Why This Opportunity Stands Out This position offers the opportunity to work directly with executive leadership while helping shape the future direction of Quality across a growing global organization. The successful candidate will have meaningful influence on systems, strategy, and organizational development—not simply day-to-day compliance. #J-18808-Ljbffr
$168.28k - $252.43k
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...of biological discovery. We are seeking a highly motivated Quality Control Manager to lead Quality Control activities supporting... ...partner closely with cross-functional teams to ensure sustained compliance and uninterrupted product supply.Your Tasks- Lead and develop...SuggestedFull timeLocal area- ...and recognize their merit. Job Function: Quality Job Sub Function: Customer/Commercial... ...are searching for the best talent for a Director, Commercial Quality - Americas to be based... ...Commercial Quality function focused on compliance for Americas commercial operations, field...Suggested
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...applicants must be eligible to work in the US. Your Role:The Head of Quality Operations will develop and lead the Quality Organization at... ...will be responsible for:Taking overall ownership of ensuring compliance of the Danvers Quality System to ISO 9001-2015, ISO 14001-2015...Work experience placementShift work- The Senior Director, Quality — Post-Market Surveillance and Innovation Excellence at Johnson & Johnson leads enterprise quality strategy supporting... ...Post-Market Surveillance, ensuring governance, regulatory compliance, and risk-based decision making across the product portfolio...
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...QIAGEN seeks a Quality Control Manager to lead QC operations for molecular biology reagents in a regulated manufacturing environment... ...oversight of laboratory testing, batch release activities, and compliance management while supervising a QC team. Responsibilities...$163.1k - $260.9k
We are the global test and automation specialists, powering next-generation technologies through sophisticated solutions. Behind every electronic device you use, Teradyne's test technology ensures your device works right the first time, every time! Our portfolio of automation...Local areaRelocationFlexible hours$155.5k - $248.7k
...Experience with either AMD or Altera FPGAs and development tools (Vivado/Quartus), preferably both. Experience using digital design quality tools e.g. LINT, CDC. Experience with bug tracking tools (Jira etc.) Experience with source control systems (Clearcase, Git, CVS)...Full timeContract workRemote workFlexible hours- Teradyne in North Reading, MA, seeks an ASIC and Logic Design Engineering Manager to lead a 4–6 person FPGA/ASIC team for Compute Test products. You will oversee 2–3 FPGA/digital IP projects, collaborate across disciplines, and ensure timely deliverables in budget. ...
- ...lead lab technicians, establish preventive maintenance, and collaborate with facilities and engineering to enable new product introductions while maintaining safety and compliance. This role requires strong leadership and hands-on technical expertise. #J-18808-Ljbffr
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