- Merck & Co. (Rahway, NJ)
- …DescriptionJ ob description This position will be responsible for leading and implementing medical device and combination product design controls for both new ... a culture of operational excellence Ensure processes align with regulatory requirements for medical device and drug combination products (eg, FDA 21 CFR Part… more
- Aptyx (Charlotte, NC)
- …- High School Diploma or equivalent experience 2-5 years inspection experience ( medical device experience preferred) Computer experience and proficiency required ... I position performs component and product inspection in the quality department in support of the department objectives to provide goods and services that meet… more
- Aptyx (Charlotte, NC)
- …accurately fill in LHRs or forms in support of manufacturing Provide job training support to coworkers, as directed Inform lead or supervisor of issues or ... Education Vocational - High School Diploma or equivalent experience Experience Minimum 2 years manufacturing experience, medical device experience preferred more
- Aptyx (Charlotte, NC)
- …position performs the function of design engineer for product development work on medical devices in the Development department in support of the department's ... for following the Quality system, including all applicable SOPs included in the Training Matrix Develop and engineer disposable medical devices from concept to… more
- Eisai, Inc (Dallas, TX)
- …with 3+ years experience in two or more of: infusion, diagnostic, biologic, medical device , buy and bill, rare disease, specialty pharmacy, and/or neurology; ... systems (including buy & bill, specialty pharmacy, distribution models, medical device and/or biologics experience) strongly preferred.Additional commercial… more
- Merck & Co. (Durham, NC)
- …in one or more of the following areas, based on site activities; Medical Device /Combination products, Biologics, Vaccines, API's or Non Sterile or Sterile ... Audits at the site.- - Position Responsibilities: Actively manage, mentor, and support site auditors to ensure performance of auditors contributes to the… more
- Aequor (Aliquippa, PA)
- …inbound/outbound coordination, and ERP transaction execution-preferably within GMP, biotech, medical device , or other regulated environments. They are ... documentation, ensuring accurate execution of GMP processes, records, and data entry. Support and execute the on-site operations strategy in partnership with 3PL… 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, ... services spanning early development to post-market, along with operational strategy and support . With a global team of 400 employees across North America and… more
- Twist BioScience (South San Francisco, CA)
- …Production, Process Development, Product Development, Software Development, R&D, Global Support in addition to building relationships with partners that manufacture ... occur from the improper performance of their specific job; has awareness of device defects that may occur in their area of responsibility, including product design,… more
- ValSource, Inc. (Durham, NC)
- …Commissioning, Qualification and Validation (CQV) experience in Pharmaceutical, Biotech, Medical Device or related GMP manufacturing environment preferred. ... skilled leaders in Commissioning, Qualification and Validation Engineering to support a variety of exciting projects with clients our...ValSource will include: Paid Time Off (PTO) and Holidays Medical / Dental / Vision Insurance - premiums 100%… more
