- Omnicell (Warrendale, PA)
- …The individual will maintain positive customer relations, and support OSHA, FDA , Green Initiatives, and ISO requirements. The individual will develop facility ... maintenance programs and drive continuous process improvement and best practices across the facilities organization. **Responsibilities** + Responsible for all aspects of facility operations at our Warrendale and Cranberry Township, Pennsylvania locations… more
- Bristol Myers Squibb (Princeton, NJ)
- …PowerPoint, etc.) as well as job-related programs such as SpotFire. + Knowledge of FDA , EMA and ICH regulations and guidelines a must. + Ability to effectively ... collaborate cross-functionally, across all levels of the organization. \#Rayzebio If you come across a role that intrigues you but doesn't perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will… more
- BioLife Plasma Services (Worcester, MA)
- …highly desirable. Demonstrated understanding of quality assurance in an FDA -regulated environment. Demonstrated understanding of plasma center operations. Effective ... organizational, technical and problem-solving skills. Leadership Integrity Fairness Honesty Perseverance Putting the patient at the center Building trust with society Reinforcing our reputation Developing the business Decision-making and Autonomy Responsible… more
- Amgen (Washington, DC)
- …+ Biotech, pharma, or healthcare domain exposure. + Familiarity withGxP, HIPAA, or FDA guidance. + Experience leading AI Centers of Excellence. + Patents or ... open-source RL contributions. + Prior collaborations with academia or top AI labs **What you can expect of us** As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our… more
- 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