- Cordis (Irvine, CA)
- …practices. + Audit Support: Support internal and external audits, including FDA inspections, by providing documentation, data, and expertise related to manufacturing ... quality. + Product Testing: Support and coordinate product testing, equipment qualifications, validation and verification processes to ensure required specifications are met. + Mentor and provide technical guidance to junior engineers, fostering their… more
- Abbott (Plymouth, MN)
- …chain solutions. + Complies with US Food and Drug Administration ( FDA ) regulations, other regulatory requirements, Company policies, operating procedures, processes, ... and task assignments. + Able to build collaborative relationships with and influence a matrixed organization of R&D, NPI, Finance, PMO, Site SC, Manufacturing teams + Maintains positive and cooperative communications and collaboration with all levels of… more
- Steris Corporation (Atlanta, GA)
- …but not limited to, radioactive materials, licensing compliance, safety, EPA, OSHA, NFPA, FDA rules and regulations are adhered to. Maintains a working knowledge of ... regulations. The Experience, Skills, and Abilities Needed Required: + Bachelor's Degree in a technical discipline with minimum of 10 years' experience or minimum of 20 years' experience in lieu of degree + Minimum of 5 years of related experience in complex… more
- Imperative Care (Campbell, CA)
- …combination of education and work experience. + Working knowledge of quality system requirements ( FDA 21 CFR Part 820, ISO 13485 or ISO 9001), and good manufacturing ... practices. + Excellent communications skills (both written and verbal). + Ability to provide thorough and meticulous review of documents. + Ability to perform multiple tasks concurrently timely with accuracy and organized. + Proficient in Microsoft Office… more
- Danaher Corporation (New York, NY)
- …working in a Healthcare regulated Product Development and Sales environment, eg, FDA , IVD Beckman Coulter Diagnostics, a Danaher operating company, offers a broad ... array of comprehensive, competitive benefit programs that add value to our lives. Whether it's a health care program or paid time off, our programs contribute to life beyond the job. Check out our benefits at Danaher Benefits Info… more
- TestPros (MD)
- …and OSC Project Manager (PM). Document that the documents fully passes the HHS and FDA checklists. Notify the PM when a document requires the insertion of Alt text. ... Perform final document remediation within ten (10) business days after the PM has reviewed and returned the work product to the contractor for final remediation. The process for remediation shall include: 1) The first remediation work product. 2) Review and… more
- Emmi Roth (Stoughton, WI)
- …safety policies and all government food safety and sanitation regulations (ex. FDA , HACCP, GMP, OSHA, FSSC 22000) Qualifications * Associates Degree or combination ... of High School Diploma and two years of quality inspection experience* HACCP certification within first year* Preventative Controls for Qualified Individual Certification, or within first year* Microbiology and food safety training, preferred* Knowledge of… more
- Abbott (Casa Grande, AZ)
- …tasks. **You'll be accountable for meeting our compliance standards including FDA , OSHA and Abbott policies and procedures.** **Required Qualifications** + High ... school diploma or GED + One year production experience + Must be able to work effectively within a team environment, possess excellent attention to detail and problem-solving skills **Preferred Qualifications** + One year production experience within food… more
- Houston Methodist (Houston, TX)
- …bench research, to prototyping and development, to clinical trials and FDA approval. The Research Institute supports clinical research protocols and extramurally ... Under minimal supervision, this position is responsible for ensuring accurate data collection, documentation, organization and safety of research participants, gathering patient data for clinical research activities via methods specified in the study protocol… more
- Actalent (Lexington, MA)
- …+ Familiarity with pharmaceutical and medical device sectors + Understanding of FDA regulations Additional Skills & Qualifications + Training in health economics, ... outcomes research, epidemiology, and/or health services research. + Direct analytics experience with HEOR, Data Management vendors, Pharma, or Medical device companies. + 5+ years of related experience with a Master's degree. + 1+ years of related experience… more
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