- BD (Becton, Dickinson and Company) (Tempe, AZ)
- …In-depth knowledge of medical communications, claims management, regulatory requirements ( FDA and international), and compliance with company policies regarding ... promotional and educational materials. Capable of understanding complex legal and technical standards while effectively communicating their intent. + Strong background in clinical study design, technical writing, and critical literature appraisal. Proven… more
- Eurofins US Network (Columbia, MO)
- …and procedures in accordance with all applicable regulatory (eg DEA, EPA, FDA , FIFRA, OECD, etc.) requirements as defined by protocol, method, and standard ... operating procedures (SOPs). + Perform method establishment and validations on a diverse set of methods including multiplex ELISAs using ECL platforms. + Analyze data with software including Molecular Devices Softmax Pro and effectively communicate results. +… more
- Cardinal Health (Deland, FL)
- …and perform repairs on associated departmental equipment in conformance to FDA , GMP's, ISO 13485 standards and finished product specifications. Minimize scrap ... generation from processes and promote workplace safety. Provide process information to management so production equipment may be optimized and/or process corrected. Assist with training of personnel to perform various functions within each assigned area.… more
- GE HealthCare (Waukesha, WI)
- …in highly regulated environments. + Expertise in healthcare regulations ( FDA , Medicare/Medicaid, anti-kickback statutes) and compliance frameworks. + Strong ability ... to prioritize competing demands and make rapid, informed risk assessments. + Exceptional communication skills; Ability to navigate diverse legal systems and cultural contexts. **Desired:** + Experience in medical device industry, particularly Imaging. +… more
- Abbott (Altavista, VA)
- …reports You'll be accountable for meeting our compliance standards including FDA , OSHA and Abbott policies and procedures. **Required Qualifications** + Bachelor's ... degree in accounting, business, science, food technology, engineering or equivalent combination of education and experience + Demonstrated leadership skills + Knowledge of project planning tools and experience using them + Proven plant financial understanding… more
- Agiliti Health (Branch, AR)
- …of assembly by maintaining equipment and inventory levels; adhering to ISO and FDA regulations; completing work order forms for parts needed to keep production ... running by reading, listening, interpreting, and implementing both oral and written directions from a variety of sources. **QUALIFICATIONS** + Must use critical thinking to make independent decisions. + Must be able to work independently with little… more
- Aerotek (Irvine, CA)
- …**Why Work Here?** The company offers growth opportunities with the product aiming for FDA approval in the US this year. For the 3rd shift, employees receive full ... 8 hours' pay even if they work less than 8 hours, provided it's not due to a call-out. Additionally, a $500 bonus is provided upon conversion and $1,000 retention bonuses at 6 months and 12 months. **Work Environment** The work environment is a cleanroom… more
- Kelly Services (Coralville, IA)
- …operations. + Ensure all animal care practices meet or exceed USDA, OLAW, FDA , and AAALAC requirements and accreditation standards. + Participate as a key member ... of the IACUC, reviewing and advising on animal use protocols. **Preclinical Research & Client Support** + Serve as a scientific and technical expert for preclinical studies utilizing minipig disease models. + Participate in client-facing discussions to… more
- Vitality Works Inc (Albuquerque, NM)
- …vitamin and nutraceutical supplements to help people get and stay well. While the FDA defines minimum quality, we strive for the highest level of quality. Vitality ... Works also operates in an environmentally sustainable way, recycling, composting, reducing energy and water consumption in a conscientious way. Our dedicated and passionate employees strive to produce amazing products in an uncompromising yet affordable way so… more
- Actalent (Irvine, CA)
- …software. + Medical device industry experience with a deep understanding of FDA regulations, ISO standards, and global quality systems. Additional Skills & ... Qualifications + 10+ years of Project/Program Management experience in the medical device industry preferred. + Demonstrated success managing QA activities in M&A environments, preferred. + Experience coordinating with Regulatory Affairs and Clinical Affairs… more
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