- Actalent (Watertown, MA)
- …+ Solid understanding of clinical trial operations and industry regulations (eg, ICH-GCP, FDA , EU, APAC, LATAM guidelines). + Proven track record in building and ... maintaining strong relationships with site investigators and stakeholders. + Proficient in speaking and writing English. Additional Skills & Qualifications + Experience in dermatology is preferred. + Onsite Clinical Monitoring or Clinical Research Coordinator… more
- Belcan (Dunn, NC)
- …Diploma or GED * One year experience in Manufacturing, Pharmaceutical or other FDA licensed Industry is desirable. * Experience working with cGMPs and Industry ... Standards desirable * Experience in reading, understanding, and following Standard Operating Procedures desirable * Possess good verbal and written communication skills * Possess basic math skills (addition, subtraction, division, multiplication). * To be able… more
- PCI Pharma Services (Philadelphia, PA)
- …and installation to meet customer requirements. + Assure compliance to GMP's, SOP's, FDA , DEA and OSHA rules and regulations. + Interact with all customers and ... management to achieve objectives. + Able to balance multiple issues simultaneously in a fast pace environment + Coordinate resources with requirements that are driven by the production schedule. + Instruct mechanics on their job assignments and their… more
- Bristol Myers Squibb (Seattle, WA)
- …reports, and regulatory submissions. + Good knowledge of cGMP and ICH/ FDA /EMEA guidance. + Complete regulatory, site, and department training requirements on ... a timely basis. **Qualifications & Experience** + A PhD with 3+ (BS with 10+) years of experience in pharmaceutical research, development, or related industry experience. + Expert in HPLC and LC-MS instrumentation from multiple vendors (eg Vanquish, Waters,… more
- Kelly Services (Clearwater, FL)
- …product meets all acceptable criteria per SOPs + Following all FDA /CGMP regulations regarding traceability and safety procedures + Supporting, encouraging, and ... participating in team-related activities + Assisting in training manufacturing associates + Reporting unusual conditions and problems to supervisor and manufacturing lead + Practicing good housekeeping **This job might be an outstanding fit if you:** + Have a… more
- Charles River Laboratories (Raleigh, NC)
- …proudly supported the development of 86% of the drugs approved by the FDA in 2021. **Equal Employment Opportunity** Charles River Laboratories is an Equal ... Opportunity Employer - all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status. If you are interested in applying to… more
- MD Anderson Cancer Center (Houston, TX)
- …for adverse event and safety reporting to the PI, internal/eternal IRBs and FDA . * Collection of protocol related data and documentation to be entered into ... protocol-specific databases. * Participate in all monitoring and auditing activities to maintain quality assurance. * Training and mentoring research nurses and other clinical research team members and new hires, as it relates to identifying needs, onboarding… more
- ManpowerGroup (Newark, DE)
- …focus on analytical testing and instrumentation. + Knowledge of quality management systems, FDA , QSR, ISO, and IVDD standards. + Proficiency with MS Office, SAP, ... LIMS, and Siemens Clinical testing software. + Strong laboratory skills, including operation, maintenance, and troubleshooting of analytical instruments. + Excellent communication skills and the ability to work independently or as part of a team. **What's in… more
- ZOLL Medical Corporation (Pittsburgh, PA)
- …Super Saturated Oxygen (SSO2) Therapy is the first FDA -approved therapy since the stent 20+ years ago to ... reduce infarct size in patients with the most severe heart attacks. Heart disease is the leading cause of death for both men and women in the US At ZOLL, your work will help to ensure cardiac patients get the life-saving therapy they need.ZOLL has been… more
- Penn Medicine (Philadelphia, PA)
- …standards and requirements, including TJC, Department of Health, funding agencies, FDA , HIPPA, HCFA, DPW, LCGME, SCGME, department specific guidelines and other. ... + Ensures patients have been properly registered and referred to Financial Counseling. + Makes sure new patients arrive for new patient appointment with referral and copays, as appropriate. + Maintains an excellent understanding of managed care plans and… more
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