- Actalent (St. Paul, MN)
- …set up a GLP study ) OR 3 years of medical device microbiology or Sterility assurance experience (bioburden, sterility, endotoxin, cleaning, disinfection, ... <85>, USP <161>, ISO 11737, etc) Skills: Reprocessing, microbiology, glp , medical device Top Skills... Study directing experience AND medical device microbiology experience Experience with reprocessing studies … more
- Actalent (Minneapolis, MN)
- …related scientific field, with the following minimum previous experience working in the pharmaceutical/ medical device industry in GLP /GMP environments: o MS ... of Preclinical (Toxicology and biocompatibility) will support a portfolio of drug, medical device , drug packaging system, and/or combination product development… more
- Avispa Technology (South San Francisco, CA)
- …Biomedical Engineering or the equivalent. * Experience in the Pharmaceutical, Biotech or Medical Device industry is preferred, with previous work on the ... Device Engineer ROCGJP00025353 A leading biotechnology company is...(South San Francisco, CA 94080) * W2 Employment, Group Medical , Dental, Vision, Life, Retirement Savings Program, PSL *… more
- Element Materials Technology (Boulder County, CO)
- … Monitor** will assist the Quality Manager in the review of completed clinical studies , help ensure that study binders include all necessary paperwork and that ... **Overview** Element has a current opening for a **Clinical Study Monitor** to join our growing team on-site in Colorado. Our **Clinical Study… more
- BD (Becton, Dickinson and Company) (Research Triangle Park, NC)
- …evaluation, including microscopic tissue assessment, for GLP and non- GLP studies . This position will serve as Study Pathologist with interpretation and ... functionality support but will also support internal or external GLP and non- GLP studies . The...environment required. + 10+ years of work experiencia and medical device experience preferred For certain roles… more
- BD (Becton, Dickinson and Company) (Warwick, RI)
- …budget, timelines, and milestones 8. Lead study design and execution for preclinical studies ( GLP and non- GLP ) 9. Ensure compliance to all required ... aspects of wound healing. + Demonstrated understanding of analysis/interpretation of medical device histopathology. + Demonstrated understanding of statistical… more
- WuXi AppTec (Plainsboro, NJ)
- **Overview** WuXi AppTec is a leading global pharmaceutical, biopharmaceutical, and medical device open-access capability and technology platform with global ... and development time and lower thecost of drug and medical device R&D through cost-effective and efficient...project development with limited supervision. + Independently devises experimental studies in accordance with GLP , EPA, FDA,… more
- WuXi AppTec (Middletown, DE)
- …training for junior pathologists + Responsible for conducting toxicology and medical device studies in compliance with GLP /CNAS + Perform other duties ... within Toxicology, Safety, and Biocompatibility. Testing including but not limited to study evaluation fornonclinical studies spanning all phases of drug… more
- WuXi AppTec (Natick, MA)
- …training for junior pathologists + Responsible for conducting toxicology and medical device studies in compliance with GLP /CNAS + Perform other duties ... within Toxicology, Safety, and Biocompatibility. Testing including but not limited to study evaluation fornonclinical studies spanning all phases of drug… more
- Kelly Services (Blue Ash, OH)
- …for a Pathology Research Assistant for a long-term engagement at one of our Global medical device clients in Cincinnati, Ohio. The role is eligible for ... is a company that's leading the way in the medical device industry. Day shift Monday through...and/or assisting with the necropsy and histology phases of studies conducted in-house. Additionally, coordinates both internally and externally… more
- Danaher Corporation (Chaska, MN)
- …or related field required with 5+ years' experience in vitro diagnostics (IVD), Medical Device , or Healthcare clinical field, Master's degree in field with ... Affairs Manager, who is responsible for managing the clinical operations for a cardiac study . If you thrive in a an amazing, multifunctional, fast paced role and… more
- BD (Becton, Dickinson and Company) (El Paso, TX)
- …(preferred). + Experience in operating GC and HPLC (preferred). + Conversant with GLP /GCP/cGMP and global Drug and Device Development Processes. + Excellent ... Description** **We are the makers of possible** BD is one of the largest global medical technology companies in the world. Advancing the world of health (TM) is our… more
- GE HealthCare (Marlborough, MA)
- …years of experience in quality leader oversite with Quality Assurance experience in medical device and/or pharmaceutical space; 3 years of experience in ... in a global matrix organization; 3 years of experience with Pharmaceutical and Medical Device QMS requirements and regulatory requirements including but not… more
- Integra LifeSciences (Plainsboro, NJ)
- …appropriate regulations, including FDA and ISO 9001, ISO 13485, CMDR and the Medical Device Directive. + Perform and document in-house microbiological testing on ... testing for in-process and finished good products, water, stability studies , and validation studies as well as...shipment to third party labs when necessary + Maintain GMP/ GLP laboratory notebooks and documentation relevant to the duties… more
- Charles River Laboratories (Memphis, TN)
- …or related field. + Minimum 3-5 years of experience in a biologics, pharmaceutical, medical device , or related industry. + Experience leading and managing people ... as contamination and impurity testing, protein characterization, bioassays, viral clearance studies and stability and lot release programs, we support clients… more
- Medtronic (Lafayette, CO)
- …of managerial experience **Nice to Have** + Proven experience with electromechanical medical device regulatory requirements and submissions, including software + ... thrive. Bring your talents to an industry leader in medical technology and healthcare solutions - we're a market...and Technical Documentation + Knowledge and experience with GCP, GLP and QMS + Expertise in pre-clinical studies… more
- Edwards Lifesciences (Irvine, CA)
- …degree or technical degree/certificate with (2) years of experience in an R&D Lab and/or medical device industry; OR (4) years of overall lab experience within a ... GLP and/or GMP environment providing engineering support with design,...else we look for: (Preferred Qualifications):** + Experience within medical device , pharma, biotech, food, automotive, or… more
- BioFire Diagnostics, LLC. (San Jose, CA)
- …Parental leaves POSITION SUMMARY Specific Diagnostics, a BioMerieux company, is a medical device company that has developed a rapid antimicrobial susceptibility ... research/testing. + Contribute and participate in the execution of studies assigned to the team as needed. + Provide...of 3 years in a managerial role within a medical device diagnostic industry, preferably in the… more
- Kelly Services (Blue Ash, OH)
- …Laboratory Animal Resource (LAR) Technician for a long-term engagement at one of our Global medical device clients in Cincinnati, Ohio. The role is eligible for ... medical benefits, paid time off including vacation (PTO), and...requirements (including but not limited to Animal Welfare Act, GLP , USDA, AAALAC, IACUC, and client policies and procedures).… more