- ThermoFisher Scientific (Pittsburgh, PA)
- …Minimum of 3+ years of experience in quality assurance or regulatory affairs , preferably in the pharmaceutical, biotechnology, or medical device ... and suppliers. This role ensures that all quality standards and regulatory requirements are met, fostering strong relationships and maintaining compliance across… more
- Takeda Pharmaceuticals (Cambridge, MA)
- …Pharmacometrics, Statistics, Drug Safety, Clinical Sciences, Outcomes, Digital Health, Pharmaceutical Sciences/ Device , and Global Regulatory Affairs . + ... approaches (eg, QSP, MBMA) to inform internal decisions and external regulatory interactions. + Represents Clinical Pharmacology in meetings with global or… more
- System One (Park Ridge, NJ)
- …directly impact product safety, regulatory success, and speed-to-market for critical medical devices and healthcare products. As a recognized authority, you ... + Partner with product development, packaging, operations, quality, and regulatory affairs to integrate microbiological and sterilization requirements… more
- Patterson Companies, Inc. (St. Paul, MN)
- …and service performance. + Collaborate with internal teams (marketing, quality assurance, regulatory affairs , supply chain and finance) to ensure product ... of experience in sourcing, procurement, or supply chain management, ideally in healthcare, medical device , or pharmaceutical industries. + At least 3 years of… more
- Imperative Care (Campbell, CA)
- …directly with customer representatives, marketing, physicians, pre-clinical engineering, and regulatory affairs to understand user interactions, identify product ... discipline and a minimum of 8 years of related experience developing flexible medical device instruments; or equivalent combination of education and work… more
- Danaher Corporation (Vista, CA)
- …procedures and transfer schedules + Work closely with Research and Development and Regulatory Affairs on deliverables for global regulatory submissions, ... + Minimum of five years of experience in quality field in a medical device , IVD, or similarly regulated industry with emphasis on software development +… more
- ManpowerGroup (Mendota Heights, MN)
- …and service performance. + Collaborate with internal teams (marketing, quality assurance, regulatory affairs , supply chain and finance) to ensure product ... of experience in sourcing, procurement, or supply chain management, ideally in healthcare, medical device , or pharmaceutical industries. + At least 5 years of… more
- Takeda Pharmaceuticals (Boston, MA)
- …among functions represented at the Labeling cross functional teams including clinical, safety, medical affairs , and commercial, to ensure the highest level of ... and assures that Takeda labeling content and processes conform to regulatory requirements. Management of Local Exceptions and LOC Interactions + Manages… more
- Mentor Technical Group (Gurabo, PR)
- …the knowledge and experience to ensure compliance with pharmaceutical, biotechnology, and medical device safety and efficacy guidelines. With offices in Caguas, ... and company SOPs. + Collaborate with cross-functional teams including R&D, QA/QC, Regulatory Affairs , and Manufacturing. Qualification: + Bachelor's degree in… more
- ThermoFisher Scientific (Waltham, MA)
- …across IVD assays, instruments, and software. You'll partner closely with R&D, Clinical Affairs , Regulatory Affairs , and Operations to design and analyze ... studies that directly support regulatory submissions and improve patient outcomes. **A Day in...1+ years of experience as a statistician in IVD, medical devices , pharmaceutical, or life sciences settings… more