- Daiichi Sankyo, Inc. (Bernards, NJ)
- …or basic research in a pharmaceutical company, a Medical device /Diagnostic company, Academic Research Organization (ARO), hospital/medical setting or Contract ... Research Organization (CRO). Clinical Project Management experience required. required- CRA experience is preferred preferred- Familiarity with a Japan-based organization is beneficial preferred TravelAbility to travel up to 10% Daiichi Sankyo, Inc. is an… more
- Syner-G BioPharma Group (Boston, MA)
- …Experience: 4-7 years of experience within the biotech, pharmaceutical, or medical device industry.Knowledge and experience working with FDA cGMP, FMEA, and Risk ... Analysis required.Validation expertise in Equipment, CSV, Method, and Process.Protocol generation experience of automated production systems, with a concentration on computerized equipment and systems validation.Report writing experience for IQ, OQ, PQ, and… more
- Tris Pharma (St. Louis, MO)
- …pharmaceutical, biotechnology, business to business (B2B), capital equipment, medical device and/or related industry REQUIRED.(SR)/Healthcare Sales Rep - Bachelors ... degree and minimum 2 years sales experience in a pharmaceutical or biotechnology industry with documented sales success REQUIRED. Job title, level and salary determination will be commensurate with experience. Proven track record of exceeding sales targets and… more
- ValSource, Inc. (Durham, NC)
- …Qualification and Validation (CQV) experience in Pharmaceutical, Biotech, Medical Device or related GMP manufacturing environment preferred. Recent college graduates ... with an Engineering or STEM related degree also considered for entry level career opportunities. Prior practical experience at a GMP facility in a Process Engineering, Facilities or Operations role with skills that transfer to CQV duties also considered.… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …higherA minimum of two (2) years related experience in medical device , biopharmaceutical, or pharmaceutical industryA degree in Biology, Biochemistry, Microbiology, ... Chemistry or related fieldSolid understanding of regulatory requirements, policies and guidelinesExperience with Quality Control document reviews and regulatory inspection processesWorking knowledge of Quality systemsExperience in management of retain samples… more
- Merck & Co. (Rahway, NJ)
- …technologies for pharmaceutical products including parenteral and/or medical device and combination products.Demonstrated experience in a leadership role, ... managing technical team in support of packaging or distribution operations, or related functions.Strong problem-solving and decision-making skills with an ability to interrogate the science, identify true requirements, and detect critical flaws including… more
- Merck & Co. (Rahway, NJ)
- …transportation technologies for pharmaceutical products including parenteral and/or medical device and combination products. Demonstrated experience in a leadership ... role, managing technical team in support of packaging or distribution operations, or related functions. Strong problem-solving and decision-making skills with an ability to interrogate the science, identify true requirements, and detect critical flaws… more
- Hackensack Meridian Health (Holmdel, NJ)
- …Demonstrates appropriate judgment in ordering and measuring the resident for a prosthetic/orthotic device . Assesses the fit and function of the device and the ... use. Educates the resident/family about the proper fit and function of the device and signs of malfunction which would indicate the need for intervention. Resident… more
- Frito-Lay North America (Cleveland, OH)
- …degree Company discounts and perks Our application takes 20-25 minutes to finish on any device . Our mission is to get you in for an interview instead of jumping ... through hoops. Just keep an eye on your e-mail, and we will take care of the rest. All qualified applicants will receive consideration for employment without regard to age, race, color, religion, sex, sexual orientation, gender identity, national origin,… more
- Eckert & Ziegler Isotope Products, Inc. (Valencia, CA)
- …Security (BIS), DOT 49 CFR / IAEA, DAkkS / ISO 17025 , and Medical Device Directive (93/42/EEC) and Medical Device Regulation (EU 2017/745) CE Mark compliant ... Burbank and in Valencia. Experience with compliance to MDSAP, European Medical Device Directives (MDD), EU MDR/IVD, FDA, QSR/QMSR, ISO standards, and other… more
