- Curia (Springfield, MO)
- …experience + Minimum 6-8 years' QA experience in pharmaceutical, biotechnology, medical device , and/or cGMP FDA-regulated industry Preferred + Experience ... Position overview The Quality Assurance (QA) Specialist III is responsible for maintaining Quality databases and providing an on-the-floor QA presence and oversight… more
- GRAIL (Durham, NC)
- …metrics) as part of Measurement, Analysis, and Improvement activities, rolling up into medical device QMR and clinical laboratory QMI meetings. + Facilitate ... technical area.8+ years of related experience (Masters 5+ years) working within a medical device , pharmaceutical, or biotech QMS, with expertise in CAPA, NCR,… more
- Crane Payment Innovations (Malvern, PA)
- …to cards and mobile, we keep the world of payments moving with smart validation devices and business management software. Headquartered in Malvern, PA, CPI is ... **Strategic Sourcing Specialist ** Location **PA, Malvern** Department **Supply Chain** Employment...with the aid of one of the 10 million devices designed and manufactured by Crane Payment Innovations (CPI).… more
- Teleflex (Pleasanton, CA)
- …QSR. - Experience developing mechatronic products with IEC 60601 is a plus. - Medical device experience is required. - Experience in robotics, motor control ... in compliance with FDA's Quality System Regulation (QSR), ISO13485, the Canadian Medical Device Regulations, and all other international regulatory requirements… more
- Ascensia Diabetes Care (Portsmouth, NH)
- …improvement. + Preferred experience in glass substrates, screen printing, and medical device manufacturing. + Preferred Knowledge of process historians ... Ascensia Diabetes Care is a global specialist diabetes care company, dedicated to helping people...What you will be doing: + Design and execute Validation and/or Qualification exercises + Lead/Collaborate with internal and… more
- Parexel (Oklahoma City, OK)
- …dynamic Patient Safety team as a **Senior Physician** where you'll leverage your medical expertise to ensure the safety of patients in clinical trials and ... post-marketing settings. In this pivotal role, you'll perform comprehensive medical reviews, provide expert safety monitoring, and deliver pharmacovigilance guidance… more
- Henry Ford Health System (Detroit, MI)
- …Learning Engineer #IND2 Additional Information + Organization: Corporate Services + Department: Ascension MEDICAL DEVICE SECUR + Shift: Day Job + Union Code: Not ... SUMMARY: Reporting to the Emerging Technology Security Manager, the AI Integrity Specialist is a technical role that works collaboratively across all functional… more
- VTI Life Sciences (San Diego, CA)
- … Validation Services to the Pharmaceutical, Biotechnology, Biologics and Medical Device industries. VTI offers professional development, training, competitive ... to accelerate their career in the pharmaceutical, biotechnology and medical device industries. We offer an opportunity...Life Sciences industry. We are looking for a Software Validation Specialist to be responsible for ensuring… more
- Mentor Technical Group (PR)
- …the knowledge and experience to ensure compliance with pharmaceutical, biotechnology, and medical device safety and efficacy guidelines. With offices in Caguas, ... experience + URS, DS, and Equipment Risk Assessments + Device assembly equipment and packaging equipment validation ...+ Device assembly equipment and packaging equipment validation experience Mentor Technical Group es un empleador que… more
- Quality Consulting Group (Villalba, PR)
- QUALITY CONSULTING GROUP, a leader in the pharmaceutical, biotech, medical devices , and manufacturing industry, is looking for a talented, highly motivated and ... instructions and processes. + Prepare and execute computer system validation protocols and generate comprehensive reports. + Develop and... knowledge + Experience in SDLC + Experience in medical devices or other highly regulated industry… more
- Mentor Technical Group (Juncos, PR)
- …the knowledge and experience to ensure compliance with pharmaceutical, biotechnology, and medical device safety and efficacy guidelines. With offices in Caguas, ... experience + URS, DS, and Equipment Risk Assessments + Device assembly equipment and packaging equipment validation ...+ Device assembly equipment and packaging equipment validation experience Mentor Technical Group es un empleador que… more
- Quality Consulting Group (Ponce, PR)
- QUALITY CONSULTING GROUP, a leader in the pharmaceutical, biotech, medical devices , and manufacturing industry, is looking for a talented, highly motivated and ... Puerto Rico & USA. Responsibilities: + Developing, executing, and documenting validation protocols, deviations, and reports to meet company and regulatory… more
- Mentor Technical Group (Caguas, PR)
- …the knowledge and experience to ensure compliance with pharmaceutical, biotechnology, and medical device safety and efficacy guidelines. With offices in Caguas, ... related field. + 2+ years of experience in equipment validation or automation in a regulated industry. + Familiarity...and packaging automation. + Preferred: + Experience in pharmaceutical, medical device , or food manufacturing environments. +… more
- Oracle (Carson City, NV)
- …is standing up a specialized clinical product management team focused on medical device -aligned products. This team bridges clinical practice, product strategy, ... patient safety, usability, and compliance across our next-generation EHR and AI-enabled medical device platforms. As a Clinical Product Manager ( Medical… more
- Oracle (Helena, MT)
- …is standing up a specialized clinical product management team focused on medical device -aligned products. This team bridges clinical practice, product strategy, ... patient safety, usability, and compliance across our next-generation EHR and AI-enabled medical device platforms. As a Clinical Product Manager ( Medical… more
- Lilly (Indianapolis, IN)
- …(SME) Oversight** : + Demonstrate a strong ownership and stewardship for medical device design, manufacturing, labelling, and/or packaging processes you support ... technical change agendas. Understand key regulations and their impact to the medical device design transfer and post-launch surveillance process. + Engage… more
- Pentax Medical (Montvale, NJ)
- …Opening: Senior Regulatory Affairs Specialist Why JOIN Us? We are an established medical device leader that is preparing for high growth. This means that ... regulated employer + Thorough understanding of domestic and international regulatory requirements for medical devices + Experience with reusable medical … more
- Terumo Medical Corporation (Somerset, NJ)
- …(TMC) develops, manufactures, and markets a complete, solutions-based portfolio of high-quality medical devices used in a broad range of applications for ... SAP Extended Warehouse Mgmt Specialist Date: Nov 28, 2025 Req ID: 4412...of Tokyo-based Terumo Corporation; one of the world's leading medical device manufacturers with $6+ billion in… more
- BD (Becton, Dickinson and Company) (Madison, GA)
- …in medical device or GMP regulated environment with process validation of medical devices , pharmaceuticals or biologics. **LANGUAGE** **SKILLS** + ... on government regulations and international regulations regarding the sterilization of medical devices . + Knowledge of hazardous chemical awareness. Proficient… more
- Omaha Children's Hospital (Omaha, NE)
- …for leading the technical activities associated with the delivery of a medical device cybersecurity program. This includes the collection of cybersecurity ... documentation. + Oversees out of the box configuration of medical devices to expected standards. + Leads...Background in Clinical Engineering preferred **Skills and Abilities** + Medical Device knowledge (Medium proficiency) + Software… more
