- WuXi AppTec (Natick, MA)
- …and training for junior pathologistsResponsible for conducting toxicology and medical device studies in compliance with GLP /CNAS Perform other duties ... Safety, and Biocompatibility. Testing including but not limited to study evaluation for nonclinical studies spanning all...not limited to study evaluation for nonclinical studies spanning all phases of drug development for pharmaceutical… 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 ** Study Monitor** to join our growing team on-site...Generates regulatory documentation based on ISO14155, "Clinical investigation of medical devices for human subjects - Good clinical practice"… 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
- 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 experience and medical device experience preferred For certain roles… 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
- AbbVie (North Chicago, IL)
- …and AbbVie requirements to assure quality, effectiveness and safety of our medical device , clinical materials, and drug suppliers. Responsibilities: + With ... a focus on medical device suppliers, assess compliance to applicable...Must understand a variety of quality/operational systems that support study /product design, device development and understand the… 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
- WuXi AppTec (Boston, 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
- Edwards Lifesciences (Irvine, CA)
- …biology or life Sciences field, with 5 Years experience Class II and III medical device technologies and/or clinical studies background Required **What else ... Full knowledge of US and international medical device regulations, of Good Laboratory Practice ( GLP )...work environment + Knowledge of US/international medical device regulations, of Good Laboratory Practice ( GLP )… 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
- Charles River Laboratories (Memphis, TN)
- …Knowledge of manufacturing processes and safety in GMP regulated facilities Pharmaceutical/ Medical Device /Biotechnology. + Knowledge in operating Kaye Validator ... as contamination and impurity testing, protein characterization, bioassays, viral clearance studies and stability and lot release programs, we support clients… 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
- Tecomet (Riviera Beach, FL)
- …team to solve complex challenges, in partnership with industry-leading clients in medical device technology, aerospace, and defense industries. With the backing ... and knowledge to become a future leader in the medical device technology industry. + Work directly...directly with a mentor in a technical field of study while finding solutions to real world problems. +… more
- Charles River Laboratories (Mattawan, MI)
- …and Engineering experience in a cGxP environments (research, biotech, pharmaceutical, or medical device industries). * Knowledge of the facilities operation ... expert regulatory guidance. From individual specialty toxicology and IND enabling studies to tailored packages and total laboratory support, our deeply experienced… more
- Medtronic (Boston, MA)
- …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
- BioFire Diagnostics, LLC. (San Jose, CA)
- …relevant industry experience. Minimum of 3 years in a managerial role within a medical device diagnostic industry, preferably in the development of AST + Strong ... bioMerieux is a pioneering force in the medical microbiology device industry. Our cutting-edge...research/testing. + Contribute and participate in the execution of studies assigned to the team as needed. + Provide… more
- System One (Oro Valley, AZ)
- …and reports) and Oral presentation skills preferred * Experience from the medical device and/or pharmaceutical industries is preferred * Project management ... Area (RTD) functions, including Tissue procurement & Histology (BAM), Medical Office, Development, Lifecycle, Investigation & Resolution, Manufacturing, Quality,… more
- Edwards Lifesciences (Irvine, CA)
- At Edwards Lifesciences we thrive on discovery and expand the boundaries of medical device technology. We are passionate about providing innovative solutions for ... life around the world. The **Surgical Veterinary Technician** supports in-vivo testing of medical devices to meet R&D and regulatory requirements. They will serve as… 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
