- Aequor (New Brunswick, NJ)
- …calibrating and performing verification tests on laboratory instruments/equipment in a GMP regulated environment. Associate or Bachelor's degree Familiarity with ... work. Oversee vendors during work execution and need experience in GMP environment. Job Description: 100% onsite Responsibilities: Review and approve vendor-executed… more
- Catalent (San Diego, CA)
- Quality Assurance Associate II - Manufacturing Catalent Pharma Solutions in San Diego is currently hiring a Manufacturing Quality Assurance (MQA) Associate II ... with services that include analytical development, pre-formulation testing, formulation development, GMP manufacturing and stability storage and testing as well as… more
- Merck & Co. (Rahway, NJ)
- …and Experimentation (FLEx) Center to support drug product development and GMP clinical supply of sterile dosage forms.- Positions will support development ... providing feedback on product and process development.These roles require adherence to GMP procedures, strong attention to detail in completing GMP … more
- Catalent (San Diego, CA)
- Quality Assurance Associate I, ManufacturingCatalent Pharma Solutions in San Diego is currently hiring a Quality Assurance Associate I in our QA Manufacturing ... group. A QA Associate I must be familiar with applicable GMPs. This...services that include analytical development, pre-formulation testing, formulation development, GMP manufacturing and stability storage and testing as well… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …in the treatment of multiple myeloma. Legend Biotech is seeking an Associate Director for Operations Compliance and Investigations Managementas part of the Technical ... Operations team based in Raritan, NJ. Role Overview The Associate Director for Operations Compliance and Investigations Management will provide strategic direction… more
- Insmed Incorporated (Bridgewater, NJ)
- …in New York™, and Best Workplaces for Millennials™ lists.OverviewThe Quality Control Associate will serve as a strategic and tactical quality professional in ... ensuring oversight and execution of all aspects of commercial GMP related analytical testing, as well as late stage... related analytical testing, as well as late stage GMP development testing. Responsible for ensuring timely processing of… more
- Catalent (St. Petersburg, FL)
- Associate Scientist II, Analytical Research & Development Position...10 plus years in an analytical lab, 5 in GMP environment, or BS in science with 3 plus ... and St. Petersburg's Quality departmental policies. Once trained, the Associate Scientist II will independently test raw materials to...years in an GMP analytical lab.Expertise in wet chemistry techniques such as… more
- Merck & Co. (Durham, NC)
- Job DescriptionWe are seeking a Growth and Improvement minded Associate Specialist Automation Technician who can help drive our Strategic Operating Priorities.- The ... daily production goals are met safely, efficiently, and in accordance with GMP standards.- They will be responsible for problem resolution, administration and… more
- Merck & Co. (Rahway, NJ)
- …DescriptionAssociate Principal Scientist, Small Molecule Research & DevelopmentIn your role as Associate Principal Scientist, you will be part of a team developing ... shelf-life assessment of clinical supplies under good manufacturing practice ( GMP ) settings.Author investigational new drug (IND), investigational medicinal product… more
- Merck & Co. (Rahway, NJ)
- …job that provides both technical and project management responsibility. The Associate Specialist - Manufacturing Automation position will report to the Director, ... production, utility systems and associated infrastructure.- Responsibilities of the Associate Specialist - Manufacturing Automation include the following: Small… more
- Merck & Co. (Durham, NC)
- …responsibility include but are not limited to activities of: Component Assembly, GMP Autoclaves, Dry Heat Ovens, Parts Washers, and area cleaning. Responsibilities ... may include but are not limited to; Support operations production through start-up and commissioning and qualification through licensure and ramp up. Working in conjunction with all appropriate personnel, performs manual and automated operations, general… more
- Aequor (Devers, TX)
- Job Description: QC Associate Onsite role at the Devens site This position will perform routine testing including testing In support of Manufacturing. Primary ... with minimum of 3-4 years of experience in a GMP QC lab is required (or equivalent experience in...(or equivalent experience in a related biopharmaceutical GLP or GMP lab environment). Strong technical lab skills using pipettes,… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …manufacturing facility to support both clinical and commercial requirements in a sterile GMP environment. This role will serve as the business process owner for the ... (eg 21 CFR parts 210, 211, 1271, 600, 601, 610, ICH Q10, EU GDP/ GMP , Part 11/Annex 11, PIC/S, MHRA). Strong written and verbal communication, analytical problem… more
- Merck & Co. (Millsboro, DE)
- …Delaware seeks to add an Attending Veterinarian in the role of Associate Director.This position will have overall responsibility for oversight and administration of ... DNREC, etc.) of animal facilities and program reviews is required.PurposeThe Associate Director/Attending Veterinarian will report to the Site Quality Head/Director… more
- Aequor (Thousand Oaks, CA)
- …if going well ** Must be within 1hour away or 30/50 miles MCS Mfg Associate MCS Manufacturing Associate -EW Job DescriptionJob Summary The Associate of ... defined manufacturing procedures (MPs) and standard operating procedures (SOPs) Following GMP documents (SOPs, MPs) with strict adherence to safety and compliance… more
- Aequor (Louisville, KY)
- …the team: Strong communication and presentation skills (verbal & written). GMP knowledge and understanding of pharmaceutical regulations with an understanding of ... Actions Manages other projects as assignedBasic Qualifications- Bachelor's degree OR Associate 's degree and 4 years of experience OR High school diploma… more
- Novo Nordisk Inc. (West Lebanon, IN)
- …and EHS projects This position will also support regulatory inspections ( GMP and non- GMP regulatory compliance) including completing assigned corrective ... Exposure to cGMP's, established manufacturing practices and procedures, and compliance with GMP , QS, and ISO regulations and guidelines Ability to read and… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …in the treatment of multiple myeloma. Legend Biotech is seeking an Operations Associate (2nd Shift) as part of the Technical Operations team based in Raritan, ... production. Accurately complete documentation in SOP's, logbooks and other GMP documents. Demonstrate training progression through assigned curriculum. Accountable… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …research areas centered around rare diseases and immune disorders.Summary The Associate Director, RACMC Portfolio Products, will be responsible for regulatory CMC ... presented in a manner that facilitates Health Authority reviews.- Supports company`s GMP Change Management Program. Evaluates CMC changes for portfolio biologics and… more
- Novo Nordisk Inc. (Boulder, CO)
- …external vendors. Ideal candidate would have minimum 5 years of GMP manufacturing experience in the areas of biotechnology/pharmaceuticals. Relationships Senior ... Manager, Material Management. Essential Functions Manage inventory and expiry of raw materials/drug substance/drug product across global network of CDMOs and perform ongoing reconciliations and implement process improvements Support MRP implementation for… more
