- ValSource, Inc. (Durham, NC)
- …Qualification and Validation (CQV) experience in Pharmaceutical, Biotech, Medical Device or related GMP manufacturing environment preferred. Recent ... Validation Specialist / Validation ... Validation Specialist / Validation Engineer / CQV...ValSource will include: Paid Time Off (PTO) and Holidays Medical / Dental / Vision Insurance - premiums 100%… 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
- Bluepeak (Denver, CO)
- …Communities." **Overvie** **w** **of the Position Responsibilities:** The CRM Program Specialist serves as the organizational expert and primary administrator for ... integrity across all customer-facing and back-office. The CRM Program Specialist provides ongoing feedback for system enhancements, partners with cross-functional… more
- Integra LifeSciences (Braintree, MA)
- …I Regulatory Compliance environment with a working knowledge preferably in the medical device , diagnostics or pharmaceutical industries. Familiarity with FDA ... but not limited to, ECRs, DCRs, ECOs, DCOs, and MCOs. deviations, validation records, batch records, and notebooks. + Responsible for processing change orders… 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
- Cognizant (Highland Heights, KY)
- **About the role** As an ** Validation Specialist - Medical Devices & Instruments** , you will make an impact by ensuring software installed on laboratory ... validation test cases and protocols for instruments and medical devices . . Create infrastructure and data.... 8+ years of extensive experience in instrument or medical device validation within a… more
- Cognizant (Highland Heights, KY)
- **About the role** As an ** Validation Specialist - Medical Devices & Instruments** you will make an impact by ensuring software installed on laboratory ... need to have to be considered** + 6-10+ years of experience in Instrument/ Medical Device validation within a regulated (GxP) environment. + Strong technical… more
- Cognizant (Highland Heights, KY)
- **About the role** As an **Instrument/ Medical Device Validation Specialist ** , you will make an impact by ensuring software installed on laboratory ... need to have to be considered** + 6-10+ years of experience in Instrument/ Medical Device validation within a regulated (GxP) environment. + Strong technical… more
- Novo Nordisk (Petersburg, VA)
- …and a minimum of five (5) years of related validation experience in pharmaceutical or medical device industry + In lieu of BS degree + five (5) years of ... of seven (7) years of relevant validation experience in pharmaceutical or medical device industry + In lieu of BS degree + five (5) years of experience,… 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
- 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
- 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 (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
- 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
- VTI Life Sciences (San Diego, CA)
- … Validation Services to the Pharmaceutical, Biotechnology, Biologics, and Medical Device industries. VTI offers professional development, training, ... to accelerate their careers in the pharmaceutical, biotechnology, and medical device industries. We offer an opportunity...industries. We are looking to staff a highly motivated Validation Specialist / Engineer 1 responsible for delivering… 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: Oct 30, 2025 Req ID: 4412...of Tokyo-based Terumo Corporation; one of the world's leading medical device manufacturers with $6+ billion in… 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...Sciences industry. We are looking for a Computer System Validation (CSV) Specialist to be responsible for… more
