- Lilly (Durham, NC)
- …engineering or related technical field. + Minimum 5-15 plus years in cGMP manufacturing or manufacturing support experience + Extensive knowledge of **parenteral ... processing equipment** and operations including formulation, filling, freeze drying, and isolation equipment. Deliverables include input and support of facility design, equipment layout, technical specifications, and equipment optimization, testing and… more
- J&J Family of Companies (Wilson, NC)
- …utilities, and media or buffer preparation. + Working knowledge of cGMP 's in a biopharmaceutical manufacturing or pharmaceutical distribution environment is ... preferred. + The ability to apply basic project management skills to complete assigned projects effectively and consistently to meet challenging schedules is required. + Influencing skills, partnering and collaboration skills, analytical skills and good oral… more
- Lilly (Concord, NC)
- …continuous improvement in deviation writing practices. + Good knowledge of cGMP , regulatory standards, and quality system requirements. Preferred Attributes: + 7+ ... years in QA roles within the pharmaceutical or medical device industry. + Experience with GMP systems, including Deviation Management and Document Control systems. + Advanced technical proficiency in deviation management, CAPA, change control, and product… more
- Pfizer (Sanford, NC)
- …will: + Perform tasks associated with maintaining Good Manufacturing Practices ( cGMP ) compliant Quality Control and Stability laboratories. + Support environmental ... monitoring/water testing in the QC Raw materials laboratory. + Test incoming raw materials per compendial methods. + Follow Environment Health and Safety requirements for site and QC laboratories. + Support product transfers, new product development,… more
- Pfizer (Rocky Mount, NC)
- …Relevant pharmaceutical experience + The ideal candidate should have background in cGMP regulations and the practical application of those methodologies to control ... systems. + Understanding of programming, and proficiency in at least one language + Understanding of network infrastructure, windows servers, and virtualization + Technical Troubleshooting experience within tight timelines. + Knowledge of site systems such as… more
- Herbalife (Winston Salem, NC)
- …in Food/Dietary/Nutritional/Pharmaceutical kindred product industries with working knowledge of cGMP other regulatory environments \#LI-TK1 At Herbalife, we value ... doing what's right. We are proud to be an equal opportunity employer, making decisions without regard to race, color, religion, sex, sexual orientation, gender identity, marital status, national origin, age, veteran status, disability, or any other protected… more
- Kedplasma (Greenville, NC)
- …Operates within the scope of EU Guidance on Good Manufacturing Practice and FDA cGMP 21CFR. **ESSENTIAL JOB FUNCTIONS** Every effort has been made to make your job ... description as complete as possible. However, that in no way states or implies that these duties/responsibilities are the only duties you will be required to perform. The omission of specific duties/responsibilities does not exclude them from the position if… more
- Actalent (Holly Springs, NC)
- …of Good Documentation Practices (GDP) and current Good Manufacturing Practices ( cGMP ). Additional Skills & Qualifications + Experience with DeltaV batch processes ... is preferred. + Familiarity with DeltaV Live is an advantage. + Experience in the pharmaceutical industry is beneficial. Work Environment This is an onsite position with working hours from 8 AM to 5 PM. The engineer will report directly to the Project Manager… more
- Merck (Wilson, NC)
- …experience encompassing a working knowledge of FDA regulatory requirements * cGMP experience in a pharmaceutical manufacturing, packaging, or device assembly ... environment * SAP working knowledge * Green or Black Belt Certification in Lean Six Sigma * Knowledge and/or experience with formal problem solving techniques as it relates to a hands-on approach to problem solving, such as root cause analysis * Proficiency in… more
- ThermoFisher Scientific (Greenville, NC)
- …years of experience in Quality and/or Validation. + 7+ years of cGMP experience in the pharmaceutical industry, Steriles manufacturing experience strongly preferred. ... + Proven ability to lead and mentor multi-functional teams. + Strong leadership skills and ability to work within a matrix organization. + Ability to support and lead multi-functional and multi-site initiatives involving integration. + Excellent written and… more