Cgmp Jobs in Urbandale

Description: 3rd shift role - 10pm - 8am Could be any of the following shift but will be set once they start working 3rd shift. MUST train on 1st for the first couple weeks. Sun-Wed, Mon-Thurs, Tues-Fri, or Wed - Sat - flexible to work OT on weekends 1. Can it extend - Yes 2. Is th More...

Fremont, CA Contract Duration: 5-36 months Rate: Negotiable Responsibilities: Excellent employment opportunity for a Manufacturing Technician in the Fremont, CA area. Executes fundamental unit operations in Upstream or Downstream manufacturing related to the manufacturing of bulk More...

Responsibilities: Responsible as Quality focal point for MQSA by providing quality leadership for site. Lead monthly quality review meetings for MQSA to ensure health of quality at site. Ensure compliance towards GLP regulations for site. Mitigate any compliance gaps if identified. P More...

Job Summary Performs a variety of chemical analysis and GMP review of raw materials, packaging components, ancillary solutions, in-process samples, finished product and stability samples in accordance with cGMP, GLP, DEA and company policies and procedures. Assists in writing and perf More...

Job Title: Validation Engineer Job Location: Framingham, MA.(Onsite Role) Job Duration: Long-Term Job Description: Leads and performs Commissioning, Qualification, and Validation (CQV) activities in support of early phase cGMP clinical manufacturing, fill finish, and QC labora More...

Job Title: QA Specialist II Location: Buffalo Grove, IL - On-site Contract Duration: Contract until 06/11/2023 Work Hours: Monday to Friday, 9AM - 6PM MAIN PURPOSE OF ROLE This position is responsible for developing and maintaining quality engineering methodologies and providing More...

Santa Monica, CA Contract Duration: 4-18 months Rate: Negotiable Responsibilities: Excellent employment opportunity for an Packaging Engineering in the Santa Monica, CA area. (onsite) The position will report to the Associate Director of Packaging Engineering. The ability to work More...

Frederick, MD Contract Duration: 5-18 months Rate: Negotiable Responsibilities: Excellent employment opportunity for a Cell Therapy Specialist I in the Frederick, MD area. 100% on site roles - No flex or WFH available Must meet the company Covid Vaccination requirements PRIOR to star More...

Frederick MD Contract Duration: 5-18 months Rate: Negotiable Responsibilities: Excellent employment opportunity for a Manufacturing Associates in the Frederick MD area. 100% on site roles - No flex Successful candidate must meet the Company Covid Vaccination requirements PRIOR to s More...

Frederick MD Contract Duration: 5-18 months Rate: Negotiable Responsibilities: Excellent employment opportunity for a Manufacturing Technician in the Frederick MD area. 100% on site roles - No flex Successful candidate must meet the Company Covid Vaccination requirements PRIOR to s More...

Production Technician Contract Duration: 5-18 months Rate: Negotiable Responsibilities: Excellent employment opportunity for a Production Technician in the Frederick MD area. 100% on site roles - No flex Successful candidate must meet the Company Covid Vaccination requirements PRIO More...

Description: The successful candidate must have knowledge &/or experience in the development of chemical/biochemical processes. In addition to understanding process design considerations the candidate must be assist in the validation of associated equipment and process steps including More...

Description: This role will require the ability to develop the understanding of the critical quality aspects of the biologic products the design of which is to be transferred into manufacturing as well as the details of the manufacturing system used. This will entail working closely More...

Description: Job Description: This role is for a person to engage as part of a team with Healthineers staff to participate in the development and commissioning of production processes for the manufacture of biochemical reagents, calibrator and control products and other fluidic chemi More...

Senior Validation Engineer Contract Woburn, Massachusetts The Senior Validation Engineer will support a diverse variety of Quality Control and Manufacturing instrumentation, including analytical and microbiological instruments, maintaining the validated state of the instruments fro More...

Description: Job Description: This role is for a person to engage as part of a team with Siemens-Healthineers staff to participate in the development and commissioning of production processes for the manufacture of biochemical reagents, calibrator and control products and other fluid More...

Provide expertise and guidance to the Business and other laboratory system groups in the planning, use, and adoption of the LabWare LIMS system (EM, Sample, Lot Manager, Stability). Review and Assessment of risk as well as work with QA to ensure accuracy and timeliness for change More...

Responsibilities: Executes the commissioning, qualification, requalification, validation and any associated maintenance activities within the plant Manages multiple and complex CQV projects, provides status reports and coordinates with other departments or outside contractors/vendo More...

Job Responsibilities: Person must be able to know how to operate pharmaceutical production machinery independently. Execute procedures for manufacturing processes in accordance with batch manufacturing record (BMR) and Standard Operating Procedures (SOP) requirements. Perform More...

Job Summary Performs a variety of chemical analysis and GMP review of raw materials, packaging components, ancillary solutions, in-process samples finished product and stability samples in accordance with (GMP, GLP, DEA and company policies and procedures. Assists in writing and perfo More...