- Cipla (Fall River, MA)
- Job Title : Pkg. Documentation Specialist II FLSA Classification : Professional, Exempt Work Location : Fall River, MA Work Hours: General Shift: 8:30AM - 5:00PM ... Pharmaceuticals is searching for experienced candidates for the position of Documentation Specialist . The Documentation Specialist is responsible for… more
- Merck & Co. (Rahway, NJ)
- Job Description Associate Specialist - MACS Operations Specialist (P1) - - Description- - The Enabling Facilities (EF) group within the Chemical Engineering ... and a strong understanding of engineering fundamentals. The MACS Operations Specialist position will report to the Associate Director, Engineering and will… more
- Cipla (Fall River, MA)
- …Cipla's US Subsidiaries or Affiliates. Job Title : Quality Assurance Operation Specialist FLSA Classification : Professional, Exempt Work Location : Fall River, MA ... : Quality Assurance Manager Salary Range: $74,984 - $96,408 Purpose: The QA operation specialist (MDI) position is an individual contributor role and a member of the… more
- Bayer (Ankeny, IA)
- …minds to make a real difference, there’s only one choice. Research and Development Specialist II - 3rd Shift (Monday through Friday 1am to 10am.) YOUR TASKS AND ... RESPONSIBILITIES This production genotyping role (Research and Development Specialist II) is accountable for working collaboratively with lab team members to ensure… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …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 ... status in at least one.Reads and interprets blueprints, P&IDs, and drawings.Utilize good documentation practices (GDP) for all work performed on the CMMS system work… more
- Merck & Co. (Durham, NC)
- …last several years; currently Durham employs 1,000+ people.Durham's Technology Transfer Specialist will be an energetic, technical leader with strong interpersonal, ... related to the vaccine processLead technical studies and author documentation associated with site commercialization effortsParticipate in the equipment… more
- Aequor (Framingham, MA)
- Mon-Fri 800-430 EST The Third Party Management Specialist will oversee Third Party Quality operations for the MA BioCampus, ensuring excellence in quality standards ... investigations, supporting quality agreement programs including periodic reviews and documentation , and collaborating cross-functionally with QC, Facilities, and Manufacturing… more
- Aequor (Golden Valley, MN)
- Job Title: Packaging Development Specialist Location: Golden Valley, MN 55427 (Hybrid) (temp-to-hire)Duration: 12 Months Shift: M-F Job Title: Packaging Development ... Specialist - Integrated Project Solutions About the Role: This...manufacturing feasibility and regulatory compliance. Manage project data and documentation using GMI systems (RDSS, Optiva, TOPS, ConnectedITQer, and… more
- Shimadzu Scientific Instruments (Dallas, TX)
- QX Service Specialist Location: Dallas, TX Salary: $97,000 - $99,000 per year Who are we? Established in 1975, Shimadzu Scientific Instruments is one of the largest ... Adjustment (COLA). Position Summary: Shimadzu Scientific Instruments is seeking an QX Service Specialist to join our team! As the regional expert in our LCMS QX… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …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, ... NJ.Role OverviewThe QA Process Excellence Specialist III role is an exempt level position with responsibilities for providing quality oversight for the manufacturing… more
- Insmed Incorporated (NJ)
- …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 what's possible for ... be essential to maintaining the integrity, accuracy, and compliance of all documentation within the Technical Operations department. You will be responsible for… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …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 ... QA Document Control Specialist role is an exempt level position with responsibilities...the periodic review process for procedures.Issuance of batch related documentation in support of GMP manufacturing.Reconcile GMP documentation… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …in the treatment of multiple myeloma.Legend Biotech is seeking a QA Shop Floor Specialist III as part of the Quality Operations team based in Raritan, New Jersey. ... Role OverviewThe QA Shop Floor Specialist is an exempt level position responsible for the...immediate path forward for manufacturing quality issues.Review of all documentation , in accordance with Good Documentation Practices… more
- Merck & Co. (Rahway, NJ)
- …both GMP and developmental use.- Author, review, and update GMP procedures and documentation , with an emphasis on Qualification / Validation plans and annual reports ... and execute qualifications, commissioning, and decommissioning activities.- Maintain GMP documentation where applicable, such as GMP engineering drawings and… more
- Merck & Co. (Durham, NC)
- …of design & engineering records and related Good Manufacturing Practices documentation , identifying and resolving discrepancies in a timely manner, and implementing ... corrective actions to improve the execution/review process for equipment.Develop training material. Working as a subject matter expert (SME), provide necessary training for system maintenance.Work alongside operations and lean six sigma team members to develop… more
- Merck & Co. (Durham, NC)
- …of design & engineering records and related Good Manufacturing Practices documentation , identifying and resolving discrepancies in a timely manner, and implementing ... corrective actions to improve the execution/review process for equipment. Develop training material. Working as a subject matter expert (SME), provide necessary training for system maintenance. Work alongside operations and lean six sigma team members to… more
- Aequor (Framingham, MA)
- …methodology transfer from Research to Quality Control. Interpret complex, explicit documentation to ensure quality standards and compliance. May provide training to ... new employees. Work under only very general supervision. Work is reviewed for soundness of judgment and overall adequacy and accuracy. Contribute to the completion of organizational projects and goals. Errors in judgment or failure to achieve results would… more
- Cipla (Fall River, MA)
- Job TitleMDI Operations Specialist Organization NameInvaGen Pharmaceuticals, Inc. LocationFall River location Employment TypeFull Time ShiftSecond Shift Salary Range ... operational inefficiencies, escalating complex issues when necessary. Ensure proper documentation of batch records, logs, and deviations. Monitor production… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …in the treatment of multiple myeloma.Legend Biotech is seeking a QA Validation Specialist III as part of the Quality team based in Raritan, NJ.Role OverviewThe ... QA Validation Specialist role is an exempt level position with responsibilities...protocols, reports, risk assessments, technical studies, and any associated documentation in support of computer systems validation, equipment, utilities,… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …in the treatment of multiple myeloma.Legend Biotech is seeking a QA Change Control Specialist II as part of the Quality team based in Raritan, NJ.Role OverviewThe QA ... Change Control Specialist II role is an exempt level position with...systems and cGMP requirements.Review change controls, SOPs, and other documentation .Require minimal direction to complete tasks, knows how to… more
