. Demonstrated supplier quality experience within the medical device industry.... skills to lead and influence others to drive change. Desired Characteristics: * ASQ Certified Quality Engineer or CQA...
and regulatory compliance in the medical device industry? Do you thrive in a leadership role, guiding teams to achieve excellence... within the medical device industry; 3-5 years in quality auditing. Education: Bachelor’s degree in a relevant field...
within the medical device industry. Interested and Qualified candidates, please send your most recently updated word document...Our client, a leading medical devices company, is looking for a Supplier Quality Engineer. This is for an initial...
to patients through risk-reward-sharing partnerships with leading medical device companies. Orchestra BioMed’s vision... is to accelerate medical innovation to patients through risk-reward-sharing partnerships with leading medical device companies...
with company policies specifications procedures and medical device regulations. The Director of Supplier Quality will partner... in Engineering required. Minimum 10 years of experience in Supplier Quality or Quality Engineering in the Medical Device Industry...
of experience in a medical device R&D / manufacturing environment preferred Familiarity with ISO 13485:2016 and FDA 21 CFR Part 820... and lead continuous improvement initiatives with engineering team. Drive closure of quality improvement plans and activities...
with company policies specifications procedures and medical device regulations. The Director of Supplier Quality will partner... in Engineering required. Minimum 10 years of experience in Supplier Quality or Quality Engineering in the Medical Device Industry...
or Life science related manufacturing, R&D, Quality or Operational environment with Medical Device or Research Use or Lab... medical device experience (preferred). Ability to provide support to internal / external audits. Proficiency MS Excel...
throughout all phases of the life cycle of BD's dispensing medical devices and solutions. They will lead cross-functional teams... and ISO 13485. IEC 60601 and IEC 62304 experience a plus. Experience in medical device and/or regulated industry...
Overview: About QTS QTS offers critical end-of-line services for medical device OEMs including finished device... assembly, packaging and sterilization management. QTS is part of the Cretex Medical family of companies. Learn more at www...
The audit focus will be primarily medical device software, product security, and risk management. We look for leaders who... in medical device software. Provide detailed functional knowledge and maintain insight to current industry best practices...
, and compliance of the cybersecurity program for the medical device software products manufactured at Sysmex America, Inc. The role... compliance and standardization. As part of this responsibility, this role will lead efforts to maintain the independent 3rd party...
/defense, automotive, or medical device fields Experience working in a ISO 9001 and/or AS9100 regulated environment Working... Experience as a lead auditor for AS9100 or other ISO 9001-based QMS standard (e.g., ISO 13485, IATF 16949). Experience with high...
in a biologics, pharmaceutical, medical device, or related industry. 15 years' experience is preferred Minimum 5 years experience... modalities, cell-based gene therapies. ISO Lead Auditor training, desirable. Certified Quality Engineer (ASQ), desirable...
. At least 5 years of engineering experience; preferably in the medical device industry. CQE/CQA certification helpful... use of engineering tools and methodologies in order to support production, design, and development of medical devices. ESSENTIAL...
throughout all phases of the life cycle of BD's dispensing medical devices and solutions. They will lead cross-functional teams... and ISO 13485. IEC 60601 and IEC 62304 experience a plus. Experience in medical device and/or regulated industry...
’s leading medical device manufacturers with $6+ billion in sales, 30,000+ employees worldwide and operations in more than 160..., or similar. Requires six to ten years increasing responsibility and experience in a medical device quality assurance environment...
to apply light in ways that improve life. Our mission is to develop innovative medical device laser solutions that make the world...: Working experience in a medical device or life sciences industry. Strong written/verbal communication skills and demonstrated...
, operations, and quality experience in the US medical device, pharmaceutical, or combination products industries (this includes... 820.30). Working knowledge of device risk management (ISO 14971) and drug risk management (ICH Q9). Working knowledge of EU medical...
’s leading medical device manufacturers with $6+ billion in sales, 30,000+ employees worldwide and operations in more than 160... including Quality System Regulations, 21 CFR 820, 21CFR 803 and 804 (MDR regulations), Canadian Medical Device Regulations, ISO...