- Actalent (Louisville, CO)
- Job Title: Quality Control Microbiology Senior Analyst Job Description We are seeking a Quality Control Microbiology Senior Analyst to perform ... cGMP regulated QC environment. + Experience with microbiology, quality control , environmental monitoring, laboratory practices, aseptic technique, chemistry,… more
- Catalent Pharma Solutions (Chelsea, MA)
- ** Quality Control Analyst II -...knowledge of cGMP 's and their application to Quality Control required; + Ability to effectively manage ... SD1, SD4 and SD7, the latter being the largest CGMP unit of its kind for DPI in North...in North America. Catalent Pharma Solutions is hiring a Quality Control Analyst II who… more
- Glenmark Pharmaceuticals Inc., USA (Monroe, NC)
- Senior Quality Control Analyst Department: Chemistry Location: Monroe, NC START YOUR APPLICATION ... position is for a highly motivated member of the Quality Control (QC) Lab at the Monroe...position will be: perform QC analysis in compliance to cGMP in line with standards prescribed by USFDA. Maintain… more
- Glenmark Pharmaceuticals Inc., USA (Monroe, NC)
- Quality Control Analyst Department:...position will be: perform QC analysis in compliance to cGMP in line with standards prescribed by USFDA. Maintain ... position is for a highly motivated member of the Quality Control (QC) Lab at the Monroe...compliance to data integrity and cGMP in QC lab in line with standards prescribed… more
- Procter & Gamble (Inwood, WV)
- …and quality for the consumers P&G serves. We have several types of Quality Control roles available at our Tabler Station Plant. As a QC Laboratory ... goods, packaging materials and other samples. Tracking, trend analysis, and other Quality Control (QC) related responsibilities will be performed as directed… more
- System One (Piscataway, NJ)
- Job Title: QC Analyst II Location: Piscataway, NJ Hours/Schedule: M-F, 8:30 am - 5:00 pm (May require extended hours or weekends during manufacturing runs) Overview ... We are seeking a QC Analyst II with a strong background in small molecule...chemistry to support our client's QC laboratory in a cGMP -compliant environment. The role involves analytical testing and data… more
- Nitto Denko Corp. (Milford, MA)
- About this opportunity : The QC Analyst II is responsible for conducting routine and non-routine analyses of raw materials, in-process materials and finished ... products in accordance with cGMP guidelines. The appropriately trained individual may provide training...related discipline + 2-5 years' experience as a QC analyst /chemist in a GMP environment + Experience and familiarity… more
- Curia (Springfield, MO)
- Quality Control Analyst I in Springfield, MO Night Shift Build your future at Curia, where our work has the power to save lives Curia is a global contract ... contributions + Learning platform + And more! Summary The Quality Control Analyst I is...of education and experience Preferred + Experience in a cGMP or GLP pharmaceutical industry environment Education, experience, location… more
- J&J Family of Companies (Raritan, NJ)
- …more at https://www.jnj.com/innovative-medicine **We are searching for the best talent for Associate Analyst Quality Control to be in Raritan, NJ.** ... profoundly impact health for humanity. Learn more at https://www.jnj.com **Job Function:** Quality **Job Sub** **Function:** Quality Control **Job… more
- Takeda Pharmaceuticals (Social Circle, GA)
- …the highest standards of quality and consistency throughout the production process. Quality Control Lead is also responsible for leading a team of analysts, ... continuous improvement, consistent with plant objectives. Additionally, the Lead Analyst is responsible for leading a team of QC...Own and manage special projects as defined by the Quality Control Leadership Team (QCLT). + Support… more
- Mentor Technical Group (Marion, NC)
- …to lift up to 50 pounds. Preferred Experience and Skills: + Quality Control , Quality Assurance and/or cGMP experience Mentor Technical Group es un ... + Attention to detail, flexibility and an awareness of production and attendant quality control problems. + Strong understanding of GMPs and of regulatory… more
- BeiGene (Hopewell, NJ)
- …International Regulations, BeiGene processes and procedures. As a Senior level analyst , demonstrate proficiency and expertise in environmental monitoring program for ... indicators, environmental monitoring, etc. + Familiar with the USP/EP and the cGMP /EU GMP. + Familiar with instrument and equipment validation. + Demonstrated… more
- BeiGene (Hopewell, NJ)
- …(cIEF), cell-based potency assay, etc. + Working knowledge with USP/EP and cGMP /EU GMP regulations. + Familiar with instrument and equipment validation. + ... Impressive, demonstrable track record and skills/experience gained within a similar position(s), at a similar level. + Strong leadership/team management skills and experience. + Credible and confident communicator (written and verbal) at all levels. + Strong… more
- BeiGene (Hopewell, NJ)
- …wet chemistry compendial methods, etc. + Working knowledge with USP/EP and cGMP /EU GMP. + Familiar with instrument and equipment validation. + Impressive, ... demonstrable track record and skills/experience gained within a similar position(s), at a similar level. + Strong leadership/team management skills and experience. + Credible and confident communicator (written and verbal) at all levels. + Strong analytical… more
- Sanofi Group (Framingham, MA)
- …method transfers, product release, stability, process validations, and investigation, in compliance with cGMP . The Quality Control Data Reviewer is also ... **Job Title:** QC Analyst **Location:** Framingham, MA **About the Job** We...diseases and bring hope to patients and their families. Quality Control is responsible for testing intermediate… more
- Mallinckrodt Pharmaceuticals (Raleigh, NC)
- Job Title Quality Analyst II Requisition JR000014866 Quality Analyst II (Open) Location Raleigh, NC Additional Locations Job Description Summary Job ... Description SUMMARY OF POSITION: The Quality Analyst II has responsibility for Product...Review, Management Review, Audits, Product Complaints, CAPA, and Change Control . ADDITIONAL FUNCTIONS: + Function as a secondary back-up… more
- Astellas Pharma (Westborough, MA)
- …to join us as a QC Analyst II, Raw Materials. This position provides Quality Control compliance and release testing of raw materials used in the manufacture ... **QC Analyst II, Raw Materials** Do you want to...and testing. + Ensure data integrity of all generated quality control data from QCRM laboratory function.… more
- Takeda Pharmaceuticals (Thousand Oaks, CA)
- …management, change control , document control , product release, supplier quality . + General knowledge of cGMP manufacturing and processes. + Proficient ... my knowledge. **Job Description** **About the Role:** As the Quality Systems Analyst II, you will participate... System department activities for Thousand Oaks including Change Control , Deviations, CAPA, and Quality Documentation. This… more
- Unilever (Chicago, IL)
- …and instead we will equip you with the tools you need to shape your own future. The Quality analyst , Night Shift (10 PM - 6 AM) reports to the Quality Lead ... safety through monitor ing and perform ing the daily Quality Control & Assurance activities in the...for you! WHAT WILL YOUR MAIN RESPONSIBILITIES BE The Quality Analyst , Night Shift will: + Perform… more
- University of Pennsylvania (Philadelphia, PA)
- …+ Assign, and maintain the Eternal Report, and CVPF Correspondences. + Review other control quality documents such as SOPs, WIs, and guidance as needed. ... programs and resources, and much more. Posted Job Title Quality Assurance Analyst (Regulatory) CVPF (Center for...of custody, and all applicable records adhere to GDP, cGMP and applicable internal SOPs. + Communicate errors and… more
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