- Merck & Co. (Rahway, NJ)
- …for independent approval of documentation to support GMP clinical supply drug product manufacture, testing, release, and maintenance in support of our company's ... or more functional areas such as quality control, quality assurance , analytical laboratories, manufacturing, production support area, clinical development.-Strong… more
- Merck & Co. (Durham, NC)
- Job DescriptionWe're looking for a Director of Quality Assurance to lead quality across the full value chain for a late-stage ophthalmic program. In this role, ... thrive.Bring energy, knowledge, innovation to carry out the following:Own the product 's quality strategy, aligned to supply strategy, and ensure clear documentation… more
- Formation Bio (New York, NY)
- …the PositionWe are seeking a highly accomplished, strategic Vice President of Quality Assurance . In this pivotal role, you will have the opportunity to establish the ... strategic development and operational management of Formation Bio's quality assurance program to support the growing drug development capabilities. This position… more
- Insmed Incorporated (NJ)
- …of science, we're in. Are you?About the Role:The Sr. Director CMC QA will lead QA CMC oversight for drug products, biologics, and combination product programs ... 3, ensuring compliance with GMPs and internal standards.Serve as the Quality lead for GMP activities supporting clinical trial materials, including DS/DP used in… more
- Cipla (Fall River, MA)
- …To : QA Manager Purpose: The purpose of the Quality Assurance Production Lead (QMS) is to monitor and ensure product quality is maintained throughout all ... Job Title : Quality Assurance (QMS) Production Lead FLSA Classification : Professional, Exempt Work Location : Fall River, MA Work Hours: General: 8:30AM -… more
- Novo Nordisk Inc. (Boulder, CO)
- …well as perform formulation studies in a laboratory setting as needed. This position will lead a team of Drug Product Managers and manage their own projects. ... Functions Lead , manage, and advise all aspects of drug product manufacturing operations at CMOs to manufacture clinical parenteral medicines according to… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …an immunotherapy in the treatment of multiple myeloma.Legend Biotech is seeking QA Investigations Lead I as part of the Quality team based in Raritan, NJ. Role ... OverviewThe QA Investigation Lead is an exempt level position reporting to the...occur in the production of a personalized cell therapy product in a sterile GMP environment. The ideal candidate… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …an immunotherapy in the treatment of multiple myeloma.Legend Biotech is seeking QA Investigations Lead III as part of the Quality team based in Raritan, NJ. Role ... OverviewThe QA Investigations Lead is responsible for providing quality oversight over the...of quality metrics while ensuring high quality and complaint product supply.Key Responsibilities Support compliance activities for site Quality… more
- Cipla (Fall River, MA)
- Job Title: Analytical Quality Assurance Supervisor FLSA Classification: Professional, Exempt Work Location: Fall River, MA Work Hours: General: 8:30AM - 5:00PM (may ... vary based on business needs) Reports To: Quality Assurance Manager Salary Range: $78,000 - $99,840 Purpose This position requires a strong analytical chemistry/lab… more
- Cipla (Fall River, MA)
- Job Title : Quality Assurance Operation Specialist FLSA Classification : Professional, Exempt Work Location : Fall River, MA Work Hours: General: 8:30AM - 5:00PM ... (may vary based on business needs) Reports To : Quality Assurance Manager Salary Range: $72,800 - $93,600 Purpose: The QA operation specialist (MDI) position is an… more
- Cipla (Hauppauge, NY)
- …- 5:00PM (may vary based on business needs) Reports To : Quality Assurance Manager Purpose: This position requires a strong analytical chemistry/lab background and ... include but are not limited to the following: Scope : The Analytical Quality Assurance (AQA) associate I position is an team contributor role and reports to the… more
- Cipla (Central Islip, NY)
- …include but are not limited to the following: Scope : The Analytical Quality Assurance (AQA) associate III position is an team or individual contributor role and ... reports to the Supervisor Analytical Quality Assurance for InvaGen Pharmaceuticals, Inc., a Cipla subsidiary located at Hauppauge, NY . The job duties for this… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …FDA to providing medical education and collecting data to support efficacy and new product development, CMR is involved. The one thing that keeps us all marching to ... Programs, and other CMR Functional areas. This job will lead a team of Patient Safety training and vendor...Bachelor's degree in a relevant field (Life Sciences, Quality Assurance , Regulatory Affairs, etc.); advanced degree preferred 7+ years… more
- Cipla (Fall River, MA)
- …Shift: 07:00AM - 03:30PM (May vary based on business needs) Reports To : Quality Assurance Manager Salary Range : $21 - $26 PURPOSE The purpose of the QA ... Manufacturing Inspector position is to monitor and ensure product quality is maintained throughout all phases of the manufacturing process in compliance with… more
- Cipla (Fall River, MA)
- …readiness. Responsible for collaborating with Cipla global stakeholders particularly Integrated Product Development (IPD) and Quality Assurance (QA) to ... R&D technical staff, supply chain management, medical affairs, regulatory affairs, quality assurance , procurement etc. Act as the custodian of the project governance… more
- Insmed Incorporated (NJ)
- …Role:The Associate Director, Patient Services Quality & Process leads quality assurance and process improvement initiatives to ensure compliance, consistency, and ... and operational excellence across all patient services functions. You will lead a team focused on monitoring program execution, identifying improvement… more
- Merck & Co. (Rahway, NJ)
- …regulatory standards (eg, FDA, cGMP), maintain optimal environmental conditions for product quality, and support continuous operations. The ideal candidate will have ... strategies that ensure compliance with GxP (as applicable) and other regulatory requirements. Lead the operation of the site BAS and HVAC control systems. Manage… more
- Cipla (Fall River, MA)
- …procedure as per Current Good Manufacturing Practices (cGMP) guidelines by Quality Assurance (QA). Check and monitor for cleanliness, maintenance, upkeep of the ... and troubleshoot facility electrical systems. Coordinate in Technology Transfer / Product Transfer with other departments. Coordinate with other departments for… more
- Cipla (Hauppauge, NY)
- …benefits. Overview The QA Inspector is responsible for monitoring and ensuring product quality is maintained through all phases of manufacturing and packaging in ... & batch packaging record instructions. Collection of in-process blend, finished product , validation samples for analysis, sample collection as per protocols.… more
- Insmed Incorporated (NJ)
- …and timely completion and hand-off to routine commercial manufacture.What You'll Do: Lead project teams for Technical Operations activities, both within Insmed and ... with external contractors. Lead the transition of projects from Research into Technical...aligned with project goals including Manufacturing, Analytical Development, Quality Assurance , and Regulatory, with input from Commercial, Research, and… more
