- Jabil (West Chester, PA)
- …diverse communities around the globe. How will you make an impact? As a Quality Engineer, you will support key quality systems, ensure compliance with internal ... and procedures. + Support key business metrics by providing Quality Engineering expertise for manufacturing processes. + Conduct root...for manufacturing processes. + Conduct root cause analyses for quality issues using tools such as 8D, A3, and… more
- Philips (New Kensington, PA)
- …+ You have a minimum of 5+ years' experience within FDA regulated medical device Quality environments, with a focus on CAPA reviews, investigations, root cause ... The Senior Quality Engineer-CAPA will play a critical role within...for improvement. + You have detailed knowledge of medical device regulations, requirements, and standards, such as 21 CFR… more
- Olympus Corporation of the Americas (Center Valley, PA)
- …to meet regulatory/ procedural deadlines. + Demonstrated working knowledge of Medical Device Quality Systems regulations including ISO 13485, 21CFR820, and ... . **Job Description** Responsible for the review of medical device global complaints and coordinate the resolution of complex complaints… more
- Merck (West Point, PA)
- **Job Description** **Job Summary:** The Associate Director of Device Technology is a key leadership role within the Device Development and Technology ... The associate director will be a technical subject matter expert on the device components and combination products and lead a cross functional team members to… more
- Geisinger (Scranton, PA)
- …Assists with the day-to-day function of the outpatient Electrophysiology (EP) Heart Rhythm Device Clinic (HRDC). This specialist will collaborate with the Device ... RN in order to provide continuity of care. Follows device protocols set by the Electrophysiologist based on industry...Evaluates, manages and provides support in the delivery of quality clinical care of patients with implanted cardiac pacemakers,… more
- Teva Pharmaceuticals (West Chester, PA)
- …or medical device industry. . Exposure to regulated environments or quality systems (eg, ISO 13485, GMP). . Familiarity with Microsoft Excel, basic statistical ... Device Engineer I Date: Aug 8, 2025 Location:...testing, and documentation to support regulatory filings and product quality . **How you'll spend your day** . Perform physical… more
- Jabil (West Chester, PA)
- …preferably QA exempt personnel + Knowledge of the US and international medical device quality system regulations, standards and best practices (21 CFR 820, ... audit. The qualified person will have the objective of maintaining high quality standards for the product manufacturing process and compliance with all applicable… more
- WellSpan Health (York, PA)
- …Coordinates inpatient and outpatient care for patients with a ventricular assist device (VAD), including, but not limited to, patient education, staff education, ... for VAD intervention: Coordinates transplant evaluation for patients who would receive a device as a bridge to heart transplant; Collaborates with medical team about… more
- West Pharmaceutical Services (Exton, PA)
- Senior Specialist, Regulatory Affairs - Medical Device Requisition ID: 69746 Date: Aug 8, 2025 Location: Exton, Pennsylvania, US Department: Regulatory Affairs ... Documentation for CE Marking. The Senior Specialist ensures timely and high- quality execution of all regulatory deliverables. In addition, the Sr. Specialist… more
- dsm-firmenich (Exton, PA)
- **Technician Manufacturing, (Mechanical Device ) 2nd** shift **Exton, PA (USA)** **Onsite (Monday - Friday 2:00 PM - 10:30 PM)** As a **Manufacturing Technician in ... Mechanical Device ,** you will assure that dsm-firmenich products are of...assure that dsm-firmenich products are of consistent and high quality by producing products in compliance with established DSM/GMP… more