- ThermoFisher Scientific (Lawrenceville, NJ)
- …including PPD and client SOPs, ICH guidelines, USP requirements, and FDA regulations + Demonstrated experience with laboratory documentation, including data ... recording, protocol execution, deviations, investigations, and report writing in compliance with GLP standards + Proficient in Microsoft Excel and Word for data analysis, documentation, and reporting + Comfortable working with technical operating systems and… more
- CBRE (Durham, NC)
- …be considered. Prior shift management or supervisory experience preferred. + GMP/ FDA regulated experience highly desired. + Meet the physical requirements of this ... role including stooping, standing, walking, climbing stairs/ladders, and the ability to lift/carry heavy loads of 50 lbs. or more. + The innovative mentality to develop methods that go beyond existing solutions. + Ability to solve unique problems using… more
- Charles River Laboratories (Ashland, OH)
- …worked on 80% of the drugs approved by the US Food and Drug Administration ( FDA ) in the past five years. We're committed to providing benefits that elevate your ... quality of life. Based on your position these may include: bonus/incentives based on performance, 401K, paid time off, stock purchase program, Health and wellness coverage, employee and family wellbeing support programs, and work life balance flexibility.… more
- Stryker (Fremont, CA)
- …will gain hands-on exposure to clinical trial operations, compliance activities, and FDA readiness efforts, providing a valuable opportunity to learn how medical ... devices progress through the final stages prior to approval. **Majors Targeted:** Biomedical Engineering, Mechanical Engineering, Electrical Engineering, Software Engineering / Computer Engineering, Manufacturing Engineering, Industrial Engineering, Quality… more
- Aerotek (Rockville, MD)
- …devices required. **Additional Skills & Qualifications** + Experience working in a regulated ISO/ FDA (GMP) environment preferred. **Why Work Here?** Join a team in a ... well-equipped facility with supportive management and ample opportunities for growth. Employees speak highly of the work environment and potential for advancement. **Work Environment** Work in a production environment with bench work, testing units, and… more
- Danaher Corporation (Hialeah, FL)
- …in: + Previous laboratory work experience preferred, especially in an FDA /ISO regulated manufacturing environment + Experience with highly regulated work ... environments with stringent PPE requirements + Experience with MS Office products, Microsoft Excel, email Beckman Coulter Diagnostics, a Danaher operating company, offers a broad array of comprehensive, competitive benefit programs that add value to our lives.… more
- Jabil (Hunt Valley, MD)
- …a regulated life-science (Pharmaceutical, aseptic preferred). + Strong understanding of FDA 's Six-System Audit Schema + Ability to effectively present information ... and respond to questions from managers, clients, customers, and other entities. + Ability to define problems, collect data, establish facts, and draw valid conclusions. + Advanced skill to operate a personal computer including using a Windows based operating… more
- Actalent (Waltham, MA)
- …of compliance, audits, and quality systems management. + Familiarity with cGMP, FDA regulations (21 CFR Parts 211, 212), and ICH guidelines. Additional Skills ... & Qualifications + Bachelor's degree with 3-5 years of experience. + Experience supervising or managing direct reports. + Capability to support GMP requirements and compliance. Work Environment The role involves working with a team of 3-4 individuals. It is a… more
- Roper St. Francis (Moncks Corner, SC)
- …satisfactory diagnostic images for interpretation preferred. Knowledge of OSHA, DHEC, FDA and TJC standards and regulations. Ability to operate standard office ... equipment. **Other:** Requires a mature individual who projects a professional and business-like appearance. Must maintain strict confidentiality of work-related information. **Contacts** **:** Frequent personal contact with patients, staff, physicians and… more
- Actalent (Ocala, FL)
- …enrollment, and retention. Responsibilities + Conduct clinical studies in compliance with FDA /GCP and ICH regulations and guidelines. + Provide medical care to ... patients, prioritizing their safety at all times. + Schedule subject visits within protocol windows to maximize scheduling capacity. + Perform defined study activities such as informed consent, screening, and protocol procedures including vital signs,… more