- BioFire Diagnostics, LLC. (Durham, NC)
- …guidelines of bioMerieux's Quality System. Adhere to Regulatory requirements, including FDA , ISO, Legal, Ethical, and bioMerieux-specific procedures. + Source a ... 10 years of Purchasing experience + Procurement experience preferred + Manufacturing experience preferred Knowledge, Skills, and Abilities + Negotiation (Contracts,… more
- ThermoFisher Scientific (Raleigh, NC)
- …Schedule** Standard (Mon-Fri) **Environmental Conditions** Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Office **Job Description** **Job ... Title: Senior Manager , Platform Engineering** Role Summary Lead development of our...platform compliance with healthcare regulations including HIPAA, CLIA, IVDR, FDA , and GLP. + Work cross-functionally with product management,… more
- Pilgrim's (Sanford, NC)
- …performing regular housekeeping audits. + Develops sanitation procedures according to Good Manufacturing Practice (GMP), USDA and FDA regulations for all ... **Description** Sanitation Manager SUMMARY: This position will be responsible for directing the cleaning and sanitizing of the plant to maintain conformance to USDA… more
- Gilead Sciences, Inc. (Raleigh, NC)
- …with EDI/OTC/FSS/3PL's and trading partners + Working experience with pharama manufacturing processes + Hands-on DevOps & Agile delivery experience + Track ... record working in a fast paced, FDA regulated IT environment + Experience managing consultants and providing technical recommendations + Ability to work… more
- Grifols Shared Services North America, Inc (Clayton, NC)
- …and department safety practices. + Provides guidance as well as consults with manufacturing and internal regulatory departments on GXP matters. + Uses expertise and ... of 10 years relevant experience - Experience in dealing with the FDA regarding license submissions, inspections and audit follow-up required - Aeseptic/sterile… more
- Reckitt (Wilson, NC)
- …a talented team of Process Engineers and Process Technologists, the Technical Manager ensures the efficient, safe, and high-quality manufacturing of liquid ... liquid and oral solid dosage (OSD) forms. + Strong understanding of GMP, FDA regulations, and pharmaceutical manufacturing standards. + Hands-on experience with… more
- ManpowerGroup (Raleigh, NC)
- …Tech II, Tech III, Tech SR) reports directly to the Team Leader, Manager , or Director depending on the organizational structure. These positions are non-exempt. ... train on new instrumentation areas and build an understanding of pharmaceutical and FDA requirements. Increased client interaction will occur and the Tech II will… more
- Grifols Shared Services North America, Inc (Goldsboro, NC)
- …of operational priorities, and provides direct support to the Center Manager in driving performance, donor satisfaction, and continuous improvement. **Primary ... Responsibilities** + Serves as acting leader in the absence of the Center Manager as assigned. Maintains the ability to perform any/all tasks within the plasma… more
- US Tech Solutions (Wilson, NC)
- …NC (later referred to as BioNC) as required by current Good Manufacturing Practices (cGMP). These activities include the administration of the electronic document ... new users to the system and assign privileges as directed by the QA Systems Manager + Set up review and approval routings for SOPs and other GMP regulated documents… more
- Reckitt (Wilson, NC)
- …writing skills + Must be familiar with Good Documentation Practices (GDP) and Good Manufacturing Practices (GMP), as well as FDA and ICH guidelines + Proficient ... in the compliance programme under your remit, working closely with the technical project manager to ensure tasks are completed by you and your team on time to… more