- Cipla (Fall River, MA)
- Job TitleMDI Operations Specialist Organization NameInvaGen Pharmaceuticals, Inc. LocationFall River location Employment TypeFull Time ShiftSecond Shift Salary Range ... FDA regulations, and pharmaceutical packaging processes. Experience in SAP system and packaging data analysis tools. Strong problem-solving abilities, attention… more
- Merck & Co. (Durham, NC)
- …Development Life Cycle (SDLC), Systems TroubleshootingPreferred Skills: Automation Systems , Control System , Manufacturing AutomationCurrent Employees ... to ensure the highest quality of raw materials, intermediates and finished products.The Specialist , Manufacturing Automation, is a member of the Focus Factory… more
- Insmed Incorporated (NJ)
- …of science, we're in. Are you?About the Role:We're looking for a Quality Management System (QMS) Specialist on the Analytical Development team to help us expand ... Operations department. You will be responsible for managing the Quality Management System (QMS) for the entire Technical Operations department.What You'll Do: In… more
- Merck & Co. (Rahway, NJ)
- …capital and non-capital improvement projects, and interfacing with the automation system assets spanning production, utility systems and associated ... Job Description Associate Specialist - MACS Operations Specialist (P1)...macrocyclic peptides, bioconjugates) Drug Substance development and GMP clinical manufacturing plant under construction in Rahway, New Jersey. They… more
- Cipla (Fall River, MA)
- …Computer Systems Skills Understanding of machines used in pharmaceutical manufacturing . Must be able to influence decision making and facilitate completion of ... Cipla's US Subsidiaries or Affiliates. Job Title : Quality Assurance Operation Specialist FLSA Classification : Professional, Exempt Work Location : Fall River, MA… more
- Cipla (Fall River, MA)
- …will be given to candidates with experience in generic pharmaceutical manufacturing . Technical Knowledge and Computer Systems Skills Excellent communication ... Job Title : Pkg. Documentation Specialist II FLSA Classification : Professional, Exempt Work...on business needs) Reports To : Department Head - Manufacturing Salary Range: $72,800 - $93,600 Job Overview Invagen… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …experience.Strong knowledge of cell therapy processes strongly preferred.Experience with Manufacturing Execution Systems (MES) design/development and validation ... of an immunotherapy in the treatment of multiple myeloma.Legend Biotech is seeking a Specialist , QA Process Excellence as part of the Quality team based in Raritan,… more
- Merck & Co. (Durham, NC)
- …reliable, consistent manufacturing processes that meet current Good Manufacturing Practices requirements.Knowledgeable of all utility systems regarding ... a sterile, bulk or finished pharmaceutical environmentExperience in automation and manufacturing execution systems (MES), process modeling and process… more
- Merck & Co. (Durham, NC)
- …reliable, consistent manufacturing processes that meet current Good Manufacturing Practices requirements. Knowledgeable of all utility systems regarding ... qualification SAP experience related to plant maintenance and spare parts procurement systems Familiarity with current Good Manufacturing Practices experience in… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …(verbal and written) and strong communication skills. cGMP manufacturing .Maintenance, facilities and utilities.Computerized maintenance management systems ... in the treatment of multiple myeloma.Legend Biotech is seeking a Maintenance Technician Specialist as part of the Technical Operations team based in Raritan, NJ.Role… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …backup for approving printed labels and documents prior to use on the manufacturing floor.Utilize multiple electronic quality systems , batch records and SAP.Work ... multiple myeloma.Legend Biotech is seeking a QA Shop Floor Specialist III as part of the Quality Operations team...oversight of all aspects of the cell therapy clinical manufacturing process.Support manufacturing activities for cGMP compliance… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …assurance, manufacturing compliance, clinical quality, or cell therapy.GxP Quality System knowledge, including relevant regulations and guidances (eg 21 CFR, ICH ... in the treatment of multiple myeloma.Legend Biotech is seeking Document Control Specialist as part of the Quality team based in Raritan, NJ.Role OverviewThe… more
- Merck & Co. (Durham, NC)
- …with validation documentation and executionExperience with SAPExperience with Manufacturing Execution Systems (MES)Experience with Delta VAbility ... Job DescriptionOur Engineers support internal and external manufacturing operations remain operational, continuously improve and innovate. With our extensive range… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …over the validation and qualification activities for equipment, systems , computer systems , and processes within a cell therapy manufacturing plant to support ... protocols, reports).Review and approve periodic review documentation for qualified equipment/ systems (audit trails, user groups, system administration)Provide… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …assurance, manufacturing compliance, clinical quality, or cell therapy.GxP Quality System knowledge, including relevant regulations and guidances (eg 21 CFR, ICH ... Part 11/Annex 11, PIC/S, MHRA).Operational experience with electronic quality systems .Familiarity with core Quality Management System processes.Strong written… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …in the treatment of multiple myeloma.Legend Biotech is seeking QC, Investigations Specialist II/III as part of the Quality team based in Raritan, NJ.Role ... OverviewThe QC Investigations Specialist is an exempt level position with responsibilities for...support of the QC testing laboratories related to the manufacturing of cell therapy products for clinical trials and… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …of an immunotherapy in the treatment of multiple myeloma.Legend Biotech is seeking CQV Specialist II as part of the Technical Operations team based in Raritan, NJ. ... and Validation support to the cGMP Clinical and Commercial Cell Therapy Manufacturing plant. This individual will be responsible in handling day-to-day activities… 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 ... providing operational support to the cGMP Clinical and Commercial Cell Therapy Manufacturing plant. This individual will partner with Technical Operations in support… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …of an immunotherapy in the treatment of multiple myeloma.Legend Biotech is seeking QC Specialist , Lab Services, II/III as part of the Quality team based in Raritan, ... NJ. Role OverviewThe QC Specialist , Lab Services is responsible for sample management. The...sample and retain managementKnowledge and understanding of current Good Manufacturing Practices (cGMP) related to the QC laboratory and… more
- Merck & Co. (Rahway, NJ)
- …a continuous improvement mindsetStrong analytical and presentation skills.Proficient in ERP systems (COMET/SAP in particular), planning software and system ... Research Labs is responsible for developing the drug substance manufacturing processes for our Company's biologics pipeline. We work...product demand is kept current in the site's ERP system in line with the material planning cycleLead facility… more
Related Job Searches:
Manufacturing,
Manufacturing Specialist,
Manufacturing System,
Manufacturing System Specialist Technical,
Specialist,
System,
System Specialist