- Catalent Pharma Solutions (Chelsea, MA)
- ** Quality Control Analyst IV** **Position...SD1, SD4 and SD7, the latter being the largest CGMP unit of its kind for DPI in North America. ... Catalent Pharma Solutions is hiring a Quality Control Analyst IV who...IV who is a key analytical leader in a cGMP laboratory capable of both clinical development and commercial… more
- Catalent Pharma Solutions (Chelsea, MA)
- ** Quality Control Analyst III**...knowledge of cGMP 's and their application to Quality Control required; + Ability to effectively ... 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 III 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
- Catalent Pharma Solutions (Chelsea, MA)
- ** Quality Control Analyst II** **Position...SD1, SD4 and SD7, the latter being the largest CGMP unit of its kind for DPI in North America. ... Catalent Pharma Solutions is hiring a Quality Control Analyst who is...determine root causes of OOTs and/or OOSs according to cGMP standards required; + Ability to troubleshoot and repair… 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
- Nitto Denko Corp. (Milford, MA)
- …raw materials, in-process materials and finished products in accordance with cGMP guidelines. The appropriately trained individual may provide training and guidance ... manner in support of project plans in accordance to cGMP guidelines + Review analytical data for compliance with...related discipline + 4-7 years' experience as a QC analyst /chemist in a GMP environment + Experience and familiarity… 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) Type: ... Hire / Permanent 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
- Nitto Denko Corp. (Milford, MA)
- …and QC reports, documents analytical procedures, and authors QA documents. The Sr. QC Analyst may review the work of other analysts, schedule work within the lab, ... manner in support of project plans in accordance to cGMP guidelines + Review analytical data for compliance with...related discipline + 8+ years' experience as a QC chemist/ analyst . + Interpersonal skills to lead and train less… 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
- Curia (Albany, NY)
- QUALITY CONTROL ANALYST II in Camarillo, CA Build your future at Curia, where our work has the power to save lives Curia is a global contract development and ... to cure and ultimately to improve patients' lives. The Quality Control Analyst II is...of education and experience Preferred + Experience working in cGMP or GLP pharmaceutical industry environment Knowledge, skills and… 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
- Novo Nordisk (Clayton, NC)
- …our employees to embark on life-changing careers, and the opportunity to help improve the quality of life for millions of people around the world. In NC, we operate ... release & stability samples of API &/or filled product in accordance with cGMP , site & corporate procedures & policies. Transfer of technology & processes in… more
- Teva Pharmaceuticals (Davie, FL)
- Quality Analyst Date: Jun 7, 2025...+ Work closely with Project Managers, R&D, Regulatory Affairs, Quality Control , Quality , Operations and ... Equipment Qualifications, Process Validations. Also, review and approve Change Control System, LIMS/MES/SAP changes, Electronic Document Management System for the… more
- BeOne Medicines (Pennington, NJ)
- …potency assay, capillary electrophoresis, 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
- Eurofins (Indianapolis, IN)
- …physical sciences field, or at least 3-5 years of laboratory experience in a cGMP pharmaceutical Quality Control laboratory. + Fundamental knowledge of and ... 20 years. The Container Closure Integrity testing laboratory analysts in the Analytical Quality Control Operations (AQCO) organization will serve as a technical… 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
- Takeda Pharmaceuticals (Round Lake Beach, IL)
- …& Risk Management: Revise procedures, forms, and specifications; identify and assess quality risks in production operations, reporting findings in quality ... Review: Release pre-printed manufacturing materials, maintain the label cage per cGMP , and follow EHS/5S guidelines. + Manufacturing Support Activities: Oversee… more
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