- 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
- 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
- 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
- Sodexo (Hyannis, MA)
- …role is responsible for the technical execution of cybersecurity initiatives across medical device inventories in hospital and clinical environments. You will ... will collaborate with HTM teams, hospital IT departments, and medical device manufacturers to ensure medical...the gathering of manufacturer documentation and security guidelines for medical devices . + Conduct technical risk assessments… more
- Abbott (Plymouth, MN)
- …the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices , nutritionals and branded generic medicines. Our 114,000 ... help of international regulatory affiliates. + Compile, prepare, review and submit medical device submissions to regulatory agencies + Interfaces directly with… 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 FICO Specialist Date: Oct 30, 2025 Req ID: 3552...of Tokyo-based Terumo Corporation; one of the world's leading medical device manufacturers with $6+ billion in… more
