- TSE INDUSTRIES INC. (Clearwater, FL)
- …processes with the WHK medical device manufacturing department. Work with Quality to ensure all systems are in compliance with ISO 13485. Implement new ... ESSENTIAL DUTIES AND RESPONSIBILITIES include the following. Work with Quality to ensure that all processes are in ...Quality to ensure that all processes are in compliance with ISO 13485 requirements. Write IQ/OQ/PQ validation protocols,… more
- Belmont Village Aventura (Aventura, FL)
- …you will administer medications, support wellness initiatives, help ensure regulatory compliance and assist with quality monitoring. Belmont Village LPN's ... in a positive and constructive manner Update and review resident medical records, clinical documentation, and incident reports MINIMUM QUALIFICATIONS Active LVN… more
- Belmont Village Green Hills (Nashville, TN)
- …of the community while supporting the Director of Nursing in wellness initiatives, regulatory compliance and quality monitoring. You must be a licensed nurse - ... decisions and manage conflict resolution constructively Update and review resident medical records, clinical documentation, and incident reports Assist the Director… more
- Belmont Village Fort Lauderdale (Fort Lauderdale, FL)
- …Village, you will administer medications, support wellness initiatives, help ensure regulatory compliance and assist with quality monitoring in our Assisted ... in a positive and constructive manner Update and review resident medical records, clinical documentation, and incident reports MINIMUM QUALIFICATIONS Active LVN… more
- Unknown (Guilford, CT)
- President About the Company Respected biomedical device company Industry Medical Device Type Privately Held About the Role The Company is in search of a ... of quality , innovation, and customer focus, particularly in the competitive medical device industry. The President will also be tasked with overseeing… more
- JABIL CIRCUIT, INC (Florence, KY)
- …utilize structured, data-driven approaches - while collaborating cross-functionally with Quality , Manufacturing, and Process Engineering teams to identify root ... networking, and storage performance prior to customer shipment. Collaborate with Quality , Process, and Manufacturing Engineering teams to complete in-depth hardware… more
- Unknown (Phoenix, AZ)
- …jurisdiction, and a minimum of 6 years' commercial law experience in the medical device or life sciences industry. Experience in healthcare regulation, including ... Senior Counsel, Commercial About the Company Dynamic manufacturer & marketer of medical devices Industry Medical Devices Type Public Company Founded 1969… more
- Unknown (Chaska, MN)
- …membership, and a minimum of 6 years' commercial law experience, preferably in the medical device or life sciences sector. The Senior Counsel will work closely ... Senior Counsel, Commercial About the Company Dynamic manufacturer & marketer of medical devices Industry Medical Devices Type Public Company Founded 1969… more
- Unknown (Concord, NH)
- …Respected provider of high- quality medical technology & services Industry Medical Device Type Privately Held About the Role The Company is seeking ... role in leading and managing all facets of its medical technology business unit. The successful candidate will be...production, sales, and business development, as well as ensuring quality , compliance , and process improvements across the… more
- Unknown (Kansas City, MO)
- …Fitness Type Non Profit Founded 1969 Employees 201-500 Categories Health & Wellness Health Care Medical Medical Device About the Role The Company is in ... locations. The successful candidate will be tasked with ensuring the integrity, compliance , and growth of all dental programs within the organization. This includes… more
- N1 Discovery, LLC. (Troy, MI)
- …of benefits, including 401k with company match, generous paid time off, full medical /dental/vision starting on day one, and health savings account. N1D values and ... performance metrics such as utilization; rather, we focus on delivering high- quality investigative work and exceeding our clients' expectations. Our leadership… more
- Unknown (Tempe, AZ)
- …a minimum of 10 years' experience in product development, with a focus on aortic medical device development. The role requires a strong track record in leading ... responsibilities include overseeing the entire product development process, ensuring compliance with regulatory standards, and collaborating with cross-functional teams… more
- Oracle (Oklahoma City, OK)
- …Regulatory Affairs, Quality Compliance , Product Development, etc. in medical device industry or equivalent. Experience authoring submissions (510k, EU ... in the healthcare and life sciences sector. As a Medical Device Regulatory Affairs Strategist, you will...design processes, and manufacturing procedures to maintain regulatory and quality compliance . + Maintain compliance … more
- J&J Family of Companies (Santa Clara, CA)
- …related to Design and Development, covering End-to-End Product Quality and Compliance within the Medical Device industry. + Demonstrated experience ... cross-functional teams to reach risk-based decisions in complex capital medical device product reviews. + Uses analytical...investigations of medical devices. + Collaborate with quality and regulatory teams to maintain compliance … more
- Oracle (Augusta, ME)
- …Regulatory Compliance & Quality Alignment + Ensure adherence to medical device software standards including IEC 62304 (software lifecycle) and IEC 82304 ... governance, and scalable design patterns across the organization's medical device portfolio. + Identify opportunities to streamline compliance activities… more
- Actalent (Sacramento, CA)
- …II, you will play a crucial role in ensuring the quality and compliance of new medical device products throughout their development lifecycle. You ... Thorough knowledge of US and International Medical Device Regulations. + Strong knowledge of Quality ...and the ability to work independently. + Experience in compliance risk situations. + Proficiency with computer literacy, including… more
- Actalent (Irvine, CA)
- …II, you will play a pivotal role in ensuring the quality and compliance of new medical device products throughout their development lifecycle. You'll ... conducting reviews. What We're Looking For + Experience with medical device product development lifecycle, including risk...Thorough knowledge of US and international medical device regulations. + Strong understanding of quality … more
- Abbott (Alameda, CA)
- …-related field. + 5+ years of experience in quality assurance or regulatory compliance in the medical device industry. + Strong knowledge of ISO ... medicines. Our 114,000 colleagues serve people in more than 160 countries. **Sr Quality Compliance Specialist** **Working at Abbott** At Abbott, you can do… more
- Takeda Pharmaceuticals (Lexington, MA)
- …true to the best of my knowledge. **Job Description** **About the Role** As Head of Global Quality Device Compliance for the US and Rest of World region, you ... combination devices, and Software as a Medical Device (SaMD). You will ensure that Quality ...**How You Contribute** + Provide strategic quality compliance direction and oversight for GxP medical … more
- Actalent (Lake Forest, CA)
- …Regulatory reporting, Test plan, Regulatory compliance , Compliance , Quality engineering, Medical device , Regulatory affairs, CMC, manufacturing ... both new product development and sustaining activities. - Strong understanding of global medical device regulations (eg, FDA CFR, EU MDR). Skills Regulatory, new… more
