- Cipla (Fall River, MA)
- Job Title : QA Document Control Associate FLSA Classification : Full-Time, Professional Work Location : Fall River, MA Work Hours: General Shift: 08:30 AM - 5:00 ... PM (May vary based on business needs) Reports To : QA QMS Lead Salary...Range : $64,272 - $77,662 PURPOSE The QA Document Control Associate in a pharmaceutical environment is… more
- Merck & Co. (Millsboro, DE)
- Job DescriptionA Senior Laboratory Technician, Quality Control /Senior QC Lab Tech is responsible for performing advanced laboratory procedures independently for the ... types of cell culture, substrates, and viruses, per Quality Control Procedures.Write laboratory investigations as neededPerform troubleshooting of test methods,… more
- Repligen (Hopkinton, IA)
- OverviewThe Distribution and Inventory Control Supervisor oversees all warehouse operations, including shipping, receiving, storing, and distributing products, ... regular blind cycle counts, physical inventory checks, and other control methods to ensure efficient product flow and accountability.ResponsibilitiesOversee all… more
- Aequor (Thousand Oaks, CA)
- …determined by the Variation Lead for reportable changes for Global Distribution control . May also translate product launch/variation strategy as determined by the ... to an executable implementation plan for launch/variation changes for Customer Facing SKU control . This role will own the execution of the implementation plan in… more
- Insmed Incorporated (NJ)
- …includes supporting GxP-regulated applications, while also functioning as strategic IT business partner for Compliance. The position requires a blend of technical ... expertise and business acumen to ensure regulatory compliance, system integrity, and...external audits to ensure regulatory complianceManage technical ownership, change control , and documentation while ensuring system integrity and regulatory… more
- Merck & Co. (North Wales, PA)
- Job DescriptionThe Associate Director, Regulatory Affairs, supports products in the Oncology therapeutic area as part of a regulatory team.- The individual will have ... in Regulatory Operations, Clinical Safety, Labeling, Regulatory Chemistry, Manufacturing and Control (CMC) as well as other functional areas (eg, clinical research,… more
- Merck & Co. (Rahway, NJ)
- …DescriptionAssociate Principal Scientist - Device Technical and Engineering Lead ( Associate Director Equivalent) Our company's Device Product & Process Development ... development; manufacturing process development, qualification, and validation; and design control and risk management techniques to positively support and influence… more
- Aequor (Thousand Oaks, CA)
- …banks for cell-based potency assay methods in Process Development (PD) and Quality Control (QC), with a primary focus on adherent mammalian cell lines. Support ... can scale effectively. Clear, influential communication: Present technical findings and business cases to technical colleagues and senior leaders; write clear SOPs… more
- Cipla (Hauppauge, NY)
- …working outside of Cipla's US Subsidiaries or Affiliates. Job Title : QA Associate I AQA FLSA Classification : Professional, Exempt Work Location : Happauge, NY ... Hours: General: 8:30AM - 5:00PM (may vary based on business needs) Reports To : Quality Assurance Manager Purpose:...the following: Scope : The Analytical Quality Assurance (AQA) associate I position is an team contributor role and… more
- Merck & Co. (Rahway, NJ)
- …areas and routes of administration, including inhalation, implantation, and injection.The Associate Principal Scientist will lead the definition and execution of ... product development, such as manufacturing process development and validation, design control , risk management, material and molding, design validation to create and… more
- Merck & Co. (Baton Rouge, LA)
- …Operation, Maintenance Processes, Manual Dexterity, Manufacturing Quality Control , Manufacturing Techniques, Packaging Operations, Production Efficiencies, ... by site or organization, with Friday designated as a remote-working day, unless business critical tasks require an on-site presence.This Hybrid work model does not… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionWe are seeking an Associate Principal Scientist to join our Data-Rich Experimentation (DRE) organization, within Process Research & Developing ... develop are as diverse as the team developing them, and in this Associate Principal Scientist role, the chosen candidate will leverage their laboratory robotics and… more
- Cipla (Central Islip, NY)
- …working outside of Cipla's US Subsidiaries or Affiliates. Job Title: QA Associate II AQA FLSA Classification: Professional, Exempt Work Location: Central Islip, NY ... Hours: General: 8:30AM - 5:00PM (may vary based on business needs) Reports To: Quality Assurance Manager Purpose: This...to the following: Scope: The Analytical Quality Assurance (AQA) associate II O III position is an team or… more
- Merck & Co. (Rahway, NJ)
- …DescriptionReporting into the Director, Logistics and Distribution Technology the Associate Director, Logistics and Distribution Technology will be responsible and ... to shape the technical capabilities lead a global, cross-modality technical team.The Associate Director will lead a team of technical experts responsible providing… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …insights and intelligence to inform decision making & drives digitalization and business solutions to attain NNI goals. Finance & Operations works closely across ... maintaining our facilities and assuring the integrity and completeness of all business transactions. At Novo Nordisk, you will have the opportunity to build… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …of an immunotherapy in the treatment of multiple myeloma.Legend Biotech is seeking Associate Director, Engineering as part of the Technical Operations team based in ... Raritan, NJ. Role OverviewThe Associate Director of Engineering is a strategic and operational leader responsible for the management, development, and performance of… more
- Novo Nordisk Inc. (Boulder, CO)
- …of both worlds to develop new medicines for patients. The Position The Associate Director of Drug Product Manufacturing is accountable for all clinical drug product ... continuous improvement initiatives that are essential to meeting patient and business needs Rapidly and accurately communicate issues to Senior Leadership. Resolve… more
- Lupin Pharmaceuticals (Coral Springs, FL)
- …commercial divisions. Together these entities make up the generic and branded US business . Lupin has a significant generic pipeline, and a branded focus on women’s ... of success but rather the people we help along the way. The Associate Director, Finance will be responsible for accounting and management reporting for Lupin’s… more
- NatWest Markets (Stamford, CT)
- Product Control Associate Closing date for applications: 07/12/2025...the business ._ **Join us as a Product Control Associate ** + Join a team that is ... career in this challenging role. **What** **you'll** **do** As a Product Control Associate ,you'llbe responsible foroverseeing the daily P&L and monthly balance… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …This individual will be responsible for performing training activities for Quality Control Microbiology team members who support cGMP Clinical and Commercial Cell ... as needed.Key ResponsibilitiesLead, coach, and deliver trainings for the Quality Control Microbiology team and Operations team (as needed).Be responsible for… more
