- Sokol Materials & Services (Skillman, NJ)
- …its equivalent is preferred. QUALIFICATIONS: + Advanced Level of relevant experience in a GMP , GCP, or GXP with at least 8 years focused on product quality. ... Preferred Active member of ASQ or ISPE. + Prior experience of QC equipment Qualification and some project management experience. + Knowledge of biotech, bulk drug substance or finished product manufacturing, medical device analytical testing ishighly… more
- Church & Dwight Co., Inc. (Princeton, NJ)
- …are up-to-date, aligned, understood and followed by all functions involved in GMP activities, including R&D, Supply Chain, Marketing, Legal, Sales, and IT. This ... position is responsible for setting the direction, gaining alignment and implementing globally harmonized processes, including electronic systems, standardized metrics for reporting to the ELT, impacting over all global sites. The role also represents the QMS… more
- Dairy Farmers of America (Burlington, NJ)
- …regarding health and safety issues + Follow all DFA good manufacturing practices ( GMP ) and work in a manner consistent with all corporate regulatory, food safety, ... quality, and sanitation requirements + The requirements herein are intended to describe the general nature and level of work performed by employee, but is not a complete list of responsibilities, duties, and skills required. Other duties may be assigned as… more
- Robert Half Finance & Accounting (Bridgewater, NJ)
- …and performance reports. + Ensure all employees consistently follow FDA, GMP (Good Manufacturing Practices), and internal food safety policies and protocols. ... + Establish and maintain laboratory safety programs; review incident investigations and recommend safety enhancements. + Supervise the HOLD program, including product disposition and recordkeeping, as well as the facility's pest control efforts. + Uphold and… more
- Adecco US, Inc. (New Brunswick, NJ)
- …PLCs, automation systems, and electrical schematics + Familiarity with lean 5S and GMP standards Salary up to $38/hr. Benefits include medical, dental, vision, 401k, ... FSA, etc. **Pay Details:** $28.00 to $38.00 per hour Equal Opportunity Employer/Veterans/Disabled To read our Candidate Privacy Information Statement, which explains how we will use your information, please navigate to… more
- Amneal Pharmaceuticals (Piscataway, NJ)
- …to technical problem solving and troubleshooting as needed. + Contribute towards optimizing laboratory operations to increase efficiency and GMP compliance. ... The preliminary activities include following schedules, direction of compendia standards and in-house standard operating procedures to analyze pharmaceutical drug substance, excipients, drug product testing for release and stability samples. Essential… more
- Astrix Technology (New Brunswick, NJ)
- …NJ **Duties:** + Perform all analytical testing activities within a GMP -compliant environment while collaborating with cross functional teams. + Ensure proper ... chain of custody for samples received in QC. + Develop and manage weekly schedules for QC analysts. + Author, review, and revise technical documents (protocols, specifications, reports, SOPs, test methods, memos, and impact assessments). + Conduct laboratory… more
- Capgemini (Raritan, NJ)
- …documentation, for tracking of NPI/EBR metrics, and for communication between the GMP operations teams and the process development scientific groups. This position ... will be focused on performing PAS-X shopfloor support activities, PAS-X IT support activities, it work closely with MES development team/ MES Operations teams. **KEY RESPONSIBILITIES** **:** Job Scope And Responsibilities Requirements: Manufacturing Electronic… more
- BioLife Plasma Services (Egg Harbor City, NJ)
- …QUALIFICATIONS:** + Associates or Bachelor's Degree + Experience working with SOPs, GDP, GMP , CLIA, and the FDA + Experience working in a highly regulated or ... high-volume retail environment + Excellent interpersonal, organizational, technical, and leadership skills **About BioLife Plasma Services** Every day at BioLife, we feel good knowing that what we do helps improve the lives of patients with rare diseases.… more
- Integra LifeSciences (Plainsboro, NJ)
- …for this position. * High School Diploma. * 1-2 years of relevant GMP /GLP experience specific to incoming, line clearance, in-process, and finished goods inspections ... in pharmaceutical or medical device industry. * QA experience in the medical device industry preferred. * Strong organizational skills, self-directed, strong problem solving and interpersonal skills. * Working knowledge of ISO 13485, 21CFR820 FDA QSR, and cGMP… more