- US Tech Solutions (San Bruno, CA)
- …Quality System Regulations, ISO 13485, and integration of best practices from the medical device industry. **Documentation and Support:** 1. Support the creation ... and support CAPA, complaints, audits, and overall QMS functions. **Experience:** ** Medical Device Software Experience:** 1. Proven experience in software… more
- Bausch + Lomb (Greenville, SC)
- …with manufacturing or manufacturing quality in a sterile dosage pharmaceutical or medical device facility. (ie, 21CFR211, 21CFR820, ISO 9001, ISO 13485). ... directly to the Site Quality Leader, the Manager of Quality Systems & Compliance is responsible for the maintenance and execution of the Greenville Quality System… more
- Lilly (Indianapolis, IN)
- …execution and reporting of design and human factors activities across all medical device , combination product and packaging programs, according to current ... regulations and appropriate guidelines within the medical device and biopharmaceutical industries. **Position responsibilities** : **Design and Human Factors:**… more
- Globus Medical, Inc. (Eagleville, PA)
- …of directly related experience, having experience in a class II or III medical device environment quality inspection is preferred, complaints lab inspection or ... an organized and retrievable state (manual or electronic) for compliance to procedures, regulations and standards + Safekeeping all...using a microscope is preferred + Experience in the medical device industry and with knowledge performing… more
- Abbott (Princeton, NJ)
- …for diversity, working mothers, female executives, and scientists. For years, Abbott's medical device businesses have offered technologies that are faster, more ... help people with chronic pain or movement disorders, our medical device technologies are designed to help...providing subject matter expertise and leadership as directed. + ** Compliance & Collaboration** : Ensure adherence to FDA regulations,… more
- J&J Family of Companies (White Plains, NY)
- …Medical portfolio aims to establish a new standard of care for medical device treatment of atherosclerotic cardiovascular disease through its differentiated ... of clinical research, Good Clinical Practice (GCP) and regulatory compliance guidelines for clinical trials. + A history of...market releases. + Product knowledge including product vigilance and medical device reporting. + High attention to… more
- Terumo Medical Corporation (Elkton, MD)
- …TMC is part of Tokyo-based Terumo Corporation; one of the world's leading medical device manufacturers with $6+ billion in sales, 30,000+ employees worldwide ... replacement of various types of facilities infrastructure in support of a medical device cleanroom manufacturing facility. The primary responsibility is to… more
- Terumo Medical Corporation (Elkton, MD)
- …TMC is part of Tokyo-based Terumo Corporation; one of the world's leading medical device manufacturers with $6+ billion in sales, 30,000+ employees worldwide ... replacement of various types of facilities infrastructure in support of a medical device cleanroom manufacturing facility. The primary responsibility is to… more
- Glenmark Pharmaceuticals Inc., USA (Monroe, NC)
- …Minimum 3 years in Quality Assurance in the pharmaceutical, biopharmaceutical, or medical device industry, or a combination of education and experience. ... Quality Compliance Specialist Department: Data Management Location: Monroe, NC...SUMMARY: Under the direction of the Senior Manager, Quality Compliance , the Quality Compliance Specialist is responsible… more
- Regeneron Pharmaceuticals (East Greenbush, NY)
- …experience: + Associate Director: 10+ years of experience in the pharmaceutical or medical device industry or equivalent combination of education and experience. ... + Director: 12+ years of experience in the pharmaceutical or medical device industry or equivalent combination of education and experience. Does this sound like… more