- Legend Biotech USA, Inc. (Raritan, NJ)
- …immunotherapy in the treatment of multiple myeloma.Legend Biotech is seeking a CQV Specialist (Contract) as part of the Technical Operations team based in Raritan, ... OverviewThis position will be responsible for providing Commissioning, Qualification and Validation support to the cGMP Clinical and Commercial Cell Therapy… more
- Merck & Co. (Durham, NC)
- …the bulk active ingredient, finished product, and laboratory testing for vaccines.The Specialist , Quality Control participates in a team of analysts in the ... development, validation , and routine testing for product. Initially the position..., and GMP laboratory readiness.- The Quality Operations Laboratory Specialist performs laboratory testing on a variety of product… more
- Merck & Co. (Rahway, NJ)
- …vaccines, antibody drug conjugates (ADCs), in addition to others.- --The Senior Specialist , Engineering will serve as a business representative in the FLEx Sterile ... drug product GMP facility startup.Experience with Commissioning, Qualification and Validation .Knowledge of Investigational drug regulatory requirements.Understanding of Clinical Supply… more
- Aequor (Davie, FL)
- …be considered for the role: 1. At least 1 year experience as a MS&T Specialist 2. PhD in chemistry Screening Requirements: 1. Medical Screenings: a) Vision Screen - ... to critical aspects of products and processes, including process development, pre- validation and optimization of solid oral dosage forms after Abbreviated New… more
- Merck & Co. (Durham, NC)
- …while developing and expanding your careerThe main function of the Associate Specialist , Quality Control is to receive and transport starting materials and ... value to the achievement of team goals Functional Expertise The Associate Specialist , Quality Control - will be responsible for performing Sample Transfers, sampling… more
- Merck & Co. (Rahway, NJ)
- …and patients on time, every time, across the globe. This QA Senior Specialist in Digital and Data Quality will be responsible for the quality/compliance, ... Supporting the preparation, review, and approval of documentation related to validation and quality operation of above requirements including core requirements,… more
- Aequor (Thousand Oaks, CA)
- 100% ONSITE ROLE SUPPORTING ATO FACILITY. Manufacturing Specialist Job Description: Part of the Drug Product New Product Introduction Team at Thousand Oaks, Building ... both within and outside of the immediate team. The Manufacturing Specialist will successfully inform, influence, and assign accountability to members of… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …in the treatment of multiple myeloma.Legend Biotech is seeking an Operations Specialist as part of the Technical Operations team based in Raritan, NJ.Role ... GMP investigations, change controls, document control, process improvement, process validation and data managementPartners with Operational Excellence to implement… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …of multiple myeloma.Legend Biotech is seeking a QA Warehouse Incoming Raw Material Specialist as part of the Quality team based in Raritan, NJ. Role OverviewThe ... QA Warehouse Incoming/Raw Material Specialist is an exempt level position with responsibility to be part of the team responsible for Warehouse activities that will… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …an immunotherapy in the treatment of multiple myeloma.Legend Biotech is seeking QC Specialist , Equipment Management as part of the Quality team based in Raritan, NJ. ... Role OverviewThe QC Specialist , Equipment Management is responsible for equipment lifecycle management...(cGMP) related to the QC laboratory.Experience developing content for Validation Life Cycle documents (eg, Master Validation … more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …in the treatment of multiple myeloma.Legend Biotech is seeking QA Lab Oversight Specialist as part of the Quality team based in Raritan. Role OverviewThe QA ... Lab Oversight Specialist role is an exempt level position with responsibilities...for reviewing and approving, of standard operating procedures (SOPs), validation / qualification/ method.Key Responsibilities Be responsible for providing quality… more
- Merck & Co. (Durham, NC)
- …and reviewDirect support of regulatory inspections and auditsDirect support of validation activities and all other associated quality functionsOther duties as ... requested by management.PROBLEM SOLVING:Identifies and solves a range of problems in straightforward situations; analyzes possible solutions and assesses each using standard procedures.INTERNAL CLIENT/EXTERNAL CUSTOMER FOCUS:Responds to standard requests from… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …in the treatment of multiple myeloma.Legend Biotech is seeking QA Document Control Specialist as part of the Quality team based in Raritan, NJ. Role OverviewThe ... Quality Assurance Document Control Specialist role is an exempt position responsible for supporting the document management process within a cell therapy… more
- Novo Nordisk Inc. (West Lebanon, IN)
- …Possess signature authority for deviation closure Reviews and approves Validation Documentation Reviews and assesses Corrective and Preventive Action Reports ... Participates in Regulatory Inspections Other duties as assigned Performs all job duties and responsibilities in a compliant and ethical manner and in accordance with all applicable healthcare laws, regulations and industry codes Incorporates the Novo Nordisk… more
- Axelon Services Corporation (Bothell, WA)
- …PURPOSE AND SCOPE OF POSITION (Position Summary): The MES Recipe Engineer and Validation Specialist role will deliver electronic batch record (EBR) configuration ... and validation in the Emerson Syncade Manufacturing Execution System (MES)....will be considered. - Experience with writing and executing validation protocols. - Strong technical writing competency and GMP… more
- Creative Financial Staffing (Stamford, CT)
- …Finance, for someone looking for upward mobility. What you'll do as the AP Specialist :* Responsible for data input, validation , and processing of invoices in ... in Stamford, is looking for a bright, driven AP Specialist to join their team ASAP!Why should you join...and effectiveness.What we are looking for in an AP Specialist :* Associates degree in Accounting or other business-related field… more
- The Bartech Group Inc (Pontiac, MI)
- …are powered by Impellam Group, a connected group providing global workforce and specialist recruitment solutions. Our client has engaged us to assist them in hiring ... a contract Validation Test Engineer. If you are interested in an...hour: Salary:We are seeking a hard-working, innovative, and curious Validation Test Engineer and Lead System Test Engineer to… more
- The Bartech Group Inc (Pontiac, MI)
- …are powered by Impellam Group, a connected group providing global workforce and specialist recruitment solutions. Our client has engaged us to assist them in hiring ... a contract Validation Engineer. If you are interested in an opportunity...Salary: 35-40 HRWe are looking for high-performing development and validation engineers with engine, transmission, and drive unit experience.… more
- Kaukahi (Fort Meade, MD)
- …the regular and consistent use of discretion and judgmentMay require field validation of the Installation Real Property Inventory by conducting in-depth base-wide ... will report directly to Project Manager and Sr. Real Property Specialist . Requirements Associate or Bachelor's degree in related fieldStrong organizational… more
- PrideStaff (Hattiesburg, MS)
- PrideStaff Hattiesburg is seeking an experienced Data Entry Specialist on behalf of our client in Hattiesburg, MS. In this role, the Data Entry Specialist will ... information, relationships, and involvements for returned mail, call center updates, data validation queries and other projects as needed Processes gifts for all… more
