- Catalent Pharma Solutions (Morrisville, NC)
- …or pharmaceutical science is required. + 5+ years of experience in cGMP laboratory environment required. + Experience with scheduling, planning, or coordination of ... laboratory activities. + Familiarity with laboratory information management systems (LIMS) and electronic record-keeping systems as well as laboratory workflows. + Strong organizational and ability to manage multiple priorities. + Excellent communication and… more
- 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
- Catalent Pharma Solutions (Morrisville, NC)
- …required + Preferred industry experience in research or Good Manufacturing Practice ( cGMP ) laboratory setting + Problem solving, critical thinking skills and ability ... to follow a variety of instructions furnished in written or oral form + Mathematical and scientific reasoning ability and ability to learn and retain technical information + Experience with Microsoft Office and Excel is required + Individual may be required to… more
- Merck (Wilson, NC)
- …Skills** + Knowledge of continuous improvement principles. + Knowledge of regulatory and cGMP principles. **Preferred Skills** + 2 years of experience working in a ... text verification role. + Experience utilizing SAP. + Experience using Global Artwork Management System (GLAMS) + Experience utilizing Text Verification Systems and barcode scanners. + Execution of root cause analysis. + Background in technical writing… more
- ThermoFisher Scientific (Greenville, NC)
- …pharmaceutical products are manufactured in accordance to area SOPs and current cGMP . Verify and document production activities in batch records, logbooks and ... controlled forms. Complete assembly, disassembly and operation of area manufacturing equipment outside of the aseptic core: Trayloader Vial Washer SMEJA stopper processor Equipment and component sterilizers Filter integrity testers Piping changeover's on the… more
- Fujifilm (Holly Springs, NC)
- …and protocols to ensure compliance with safety and Good Manufacturing Practices ( cGMP ) quality standards * Performs loop checks for new instrumentation to ensure ... proper functionality * Assists and performs lock out tag out (LOTO) as required to complete I&C/Metrology activities * Adheres to all safety requirements and follows safe work practices * Notifies management or Environmental Health & Safety (EHS) when unsafe… more
- Medtronic (Charlotte, NC)
- …understand schematics and engineering drawings + Familiar with the FDA 21 CFR, CGMP for Medical devices + Demonstrable skills in Microsoft Office products as well ... as ERP and CRM software packages (such as SAP, ServiceMax and SalesForce.com) + Excellent analytical and communication skills with the ability to communicate complex technical issues in an easy to understand manner, are necessary to accomplish this task +… more
- ThermoFisher Scientific (Greenville, NC)
- …(cGMPs), safety precautions and housekeeping practices in performing duties. Align with cGMP , Occupational Safety Health Agency (OSHA) and company rulings. Keep area ... neat and clean. + Assist supervisor in training in Standard Operating Procedures (SOPs), cGMPs, safety procedures. + Perform other duties as assigned. **How will you get here?** **Education** + High school diploma or equivalent is minimally required.… 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