| Resume alert | Resumes 21 - 30 of 300 |
Quality Management System
Cherry Hill, NJ
... Built and maintained capability within the assigned sub-system for compliance with QMS, ISO, and FDA GMP's. Ensured activities and items were in compliance with both company quality assurance standards and applicable government regulations, such as ... - 2023 Dec 11
... Built and maintained capability within the assigned sub-system for compliance with QMS, ISO, and FDA GMP's. Ensured activities and items were in compliance with both company quality assurance standards and applicable government regulations, such as ... - 2023 Dec 11
Quality Control Specialist
Somerset, NJ, 08873
... Knowledge of GMP, ISO, and FDA regulations and audit Experience with environmental monitoring, air and water sampling with GMP regulations. Performed Cross Functional Lab audits for FDA Inspection. Worked according to the approved validation ... - 2023 Dec 07
... Knowledge of GMP, ISO, and FDA regulations and audit Experience with environmental monitoring, air and water sampling with GMP regulations. Performed Cross Functional Lab audits for FDA Inspection. Worked according to the approved validation ... - 2023 Dec 07
Human Resources Production Line
Skillman, NJ
... Knowledge of health and safety procedures including OSHA, SOP, GMP regulations. Extensive knowledge of the inner workings of production line companies from human resources down to production line workers. EDUCATION 2009 - Paraprofessional ... - 2023 Dec 04
... Knowledge of health and safety procedures including OSHA, SOP, GMP regulations. Extensive knowledge of the inner workings of production line companies from human resources down to production line workers. EDUCATION 2009 - Paraprofessional ... - 2023 Dec 04
Regulatory Affairs United States
Mount Laurel, NJ, 08054
... Job Title Manager CMC Regulatory CATALENT Dates Position Held March 2018 June 2018 Responsibilities As Regulatory Affairs Manager it was my primary duty to support: ●Product development ●Manufacturing activities ●Compliance with GMP regulations. ... - 2023 Nov 29
... Job Title Manager CMC Regulatory CATALENT Dates Position Held March 2018 June 2018 Responsibilities As Regulatory Affairs Manager it was my primary duty to support: ●Product development ●Manufacturing activities ●Compliance with GMP regulations. ... - 2023 Nov 29
CSV Specialist, Compliance Specialist, Quality Control and AR&D Lab
Hillsborough, NJ
... Summary of Qualifications • 12 years of analytical experience in Quality Control and R&D Laboratory • 11 years of Computerized System validation/qualification experience in the Validation Department • 2 years of GMP quality compliance/quality ... - 2023 Nov 17
... Summary of Qualifications • 12 years of analytical experience in Quality Control and R&D Laboratory • 11 years of Computerized System validation/qualification experience in the Validation Department • 2 years of GMP quality compliance/quality ... - 2023 Nov 17
Quality Assurance Business Development
Somerset, NJ
... Highly effective at contributing to drug development and technology transfer, facilitating GMP audits, CAPA, and root cause analysis, and clearly and concisely liaising with agencies and clients. Encouraging mentor, excellent team leader and ... - 2023 Nov 16
... Highly effective at contributing to drug development and technology transfer, facilitating GMP audits, CAPA, and root cause analysis, and clearly and concisely liaising with agencies and clients. Encouraging mentor, excellent team leader and ... - 2023 Nov 16
Quality Assurance Operations
Monmouth Junction, NJ
... Specialist Operations – Americas (Aug 2021 - Present) • Conducting thorough Quality Assurance review and release of Small Molecules for contract manufacturing, packaging, labeling, and analytical records, ensuring strict adherence to GMP regulations ... - 2023 Nov 10
... Specialist Operations – Americas (Aug 2021 - Present) • Conducting thorough Quality Assurance review and release of Small Molecules for contract manufacturing, packaging, labeling, and analytical records, ensuring strict adherence to GMP regulations ... - 2023 Nov 10
Quality Control Associate
Robbinsville Center, NJ
... Worked on raw material, packaging materials, in-process, finished product and stability Education testing as per GMP, GLP standards using instruments such as HPLC, UV/Vis, FTIR, Dissolution apparatus USP (I & II), Particle size analysis. Prepared ... - 2023 Oct 24
... Worked on raw material, packaging materials, in-process, finished product and stability Education testing as per GMP, GLP standards using instruments such as HPLC, UV/Vis, FTIR, Dissolution apparatus USP (I & II), Particle size analysis. Prepared ... - 2023 Oct 24
Strategic Business Quality Control
Franklin Park, NJ
... Performed packaging room clearance, count material available, and reconcile items as per GMP and SOP. Handled in-process checks, visual inspections, routinely inspected transdermal products for quality i.e. proper placement of cutting, printing, and ... - 2023 Oct 23
... Performed packaging room clearance, count material available, and reconcile items as per GMP and SOP. Handled in-process checks, visual inspections, routinely inspected transdermal products for quality i.e. proper placement of cutting, printing, and ... - 2023 Oct 23
Manufacturing Operations Compliance Officer
Moorestown, NJ
... ●Follow GMP, PPE, GLP, Safety Health & Environmental and FDA procedures MetLife, Convent Station, NJ - Compliance Officer/Metadata Collector September 2013 - November 2015 ●Responsible for the management of MetLife’s Investments IT Department’s ... - 2023 Oct 08
... ●Follow GMP, PPE, GLP, Safety Health & Environmental and FDA procedures MetLife, Convent Station, NJ - Compliance Officer/Metadata Collector September 2013 - November 2015 ●Responsible for the management of MetLife’s Investments IT Department’s ... - 2023 Oct 08