- Novo Nordisk (Clayton, NC)
- …(5) years of managing other managers experience required, preferably in a pharmaceutical manufacturing environment + Experience with method validation and/or ... for millions of people around the world. In NC, we operate three pharmaceutical manufacturing facilities that are responsible for fulfilling different steps in our… more
- ThermoFisher Scientific (Greenville, NC)
- …+ Knowledge of aseptic process simulations (media fills). + Experience with pharmaceutical industry technology, especially from a validation , technical or ... Laboratory or Environmental Monitoring experience, and ideally within a sterile pharmaceutical manufacturing facility). + 5 years of leadership experience required.… more
- Fujifilm (Holly Springs, NC)
- …Biological Science, or related fields, with 3 years of direct Computer System Validation experience in a cGMP pharmaceutical facility working with FDA ... Expert (SME) and leads tasks associated with Computer System Validation (CSV). This role provides input and determine action...5 years of direct CSV experience in a cGMP pharmaceutical facility working with FDA regulations + Experience in… more
- ThermoFisher Scientific (Greenville, NC)
- …meticulous QA Engineer III to join our Quality Assurance team as a Quality Validation Specialist. The ideal candidate will have a strong background in quality ... validation processes, excellent analytical skills, and a dedication to...5-7 years of experience in quality assurance in a pharmaceutical or similar GMP environment, with at least 3… more
- ThermoFisher Scientific (Greenville, NC)
- …Description** The Staff QA Engineer will lead the quality oversight of validation activities with a strategic focus on continuous improvement and regulatory ... senior-level position involves leadership, mentorship, and high-level coordination of validation processes across multiple sites. **Typical work hours are Monday… more
- Lilly (Durham, NC)
- …shifts, weekends for facility startup. + Experience maintaining Computer Systems Validation in line with pharmaceutical computer system quality regulations ... (eg cGMP's, FDA 21 CFR Part 11) and other applicable regulations (eg privacy, OSHA, etc.). + Demonstrated ability to lead and influence cross-functional teams with a strong customer service focus. + Strong analytical and problem-solving skills. + Highly… more
- Merck (Wilson, NC)
- …+ Bachelor of Science (BS) in packaging/ mechanical/ chemical/ biochemical engineering, pharmaceutical science or chemistry or related fields with fifteen (15) years ... relevant experience pharmaceutical packaging, combination product assembly and packaging, or related...components, process, and equipment, as well as qualification and validation . + Demonstrated experience in a leadership role; managing… more
- Merck (Wilson, NC)
- …continuous improvement. + Deliver the development, design, construction, qualification/ validation and/or initial operation of complex tertiary packaging components ... for new and commercial human health products including active pharmaceutical ingredients, drug substance, drug product, finished goods including combination… more
- Cognizant (Raleigh, NC)
- …or equivalent experience. . 12+ years of automation experience in the pharmaceutical industry, with a strong preference for API/bulk manufacturing environments. . ... Proven experience leading cross-functional automation teams on large-scale pharmaceutical projects or programs. . Demonstrated ownership of full project lifecycle… more
- Merck (Wilson, NC)
- …high liability to projects of varying scopes. Expertise in qualification and process validation practices for complex systems is essential to success in this role. ... equipment qualification, process demonstration, process performance qualification, and process validation . + Responsible for managing capital and expense projects… more