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Material Control Coordinator II

Employer
FUJIFILM Diosynth Biotechnologies
Location
Research Triangle Park, NC
Start date
Aug 16, 2022

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Job Details

Fujifilm Diosynth Biotechnologies U.S.A., Inc. is seeking a Material Control Coordinator to work in our Biotechnology Manufacturing Plant in RTP, NC.  The successful candidate will be responsible for performing tasks at pre-defined levels within projects or operations. 

The candidate is a competent operation professional responsible for performing tasks at predefined levels within projects or operations. Tasks may be routine in nature, expertise is generally limited to areas of responsibility. The candidate understands the “why” part of the job and demonstrates knowledge of internal customers and support area requirements.

External US

Fujifilm Diosynth Biotechnologies U.S.A., Inc. is seeking a Material Control Coordinator II to work in our Biotechnology Manufacturing Plant in RTP, NC.  The successful candidate will be responsible for performing tasks at pre-defined levels within projects or operations. 

The candidate is a competent operation professional responsible for performing tasks at predefined levels within projects or operations. Tasks may be routine in nature, expertise is generally limited to areas of responsibility. The candidate understands the “why” part of the job and demonstrates knowledge of internal customers and support area requirements.

Major areas of Responsibility include:

  • Raw Material and Gas sampling
  • Executing shipping and receiving procedures for all GMP and Non-GMP materials and/or finished products
  • Dispensing Raw Materials, Acids, Caustic and Consumables to Manufacturing Formulation or Batch Records
  • Receiving verification and staging of Raw Materials, Acids, Caustic and Consumables
  • Labeling and staging dispensed materials for manufacturing
  • Performing Formulation or Batch record materials issuance calculations
  • Performing inventory cycle counts/transactions within a specified time period
  • Equipment cleaning
  • Transportation of raw materials and consumables
  • Other duties as assigned

Background requirements

  • High school Diploma/GED and 2-4+ years in a GMP environment or equivalent

 

FDBU works with technical data, technology and materials that are subject to U.S. export laws and regulations. This position will require access to technical data, technology and source code that is controlled under U.S. export laws and regulations, including but not limited to the International Traffic in Arms Regulations at 22 C.F.R. Parts 120 – 130 and Export Administration Regulations in 15 C.F.R. Part 730 – 774, as may be amended. To conform to these laws and regulations, applicants must be U.S. citizens, lawful permanent residents of the U.S., protected individuals as defined by 8 USC 1324(b)(a)(3) (i.e., asylees and refugees) or otherwise eligible for an export authorization from the U.S. Department of State or U.S. Department of Commerce. Offers of employment will be contingent on the Company's ability to secure an export authorization.

 

FDBU is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability, protected veteran status, sexual orientation, gender identify or any other protected class. If an accommodation to the application process is needed, please e-mail FDBUHR@fujifilm.com.

 

To all agencies: Please, no phone calls or emails to any employee of FUJIFILM about this requisition. All resumes submitted by search firms/employment agencies to any employee at FUJIFILM via-email, the internet or in any form and/or method will be deemed the sole property of FUJIFILM, unless such search firms/employment agencies were engaged by FUJIFILM for this requisition and a valid agreement with FUJIFILM is in place. In the event a candidate who was submitted outside of the FUJIFILM agency engagement process is hired, no fee or payment of any kind will be paid.

Company

FUJIFILM Diosynth Biotechnologies is an industry leading cGMP Contract Development and Manufacturing Organization (CDMO) supporting our partners in the biopharmaceutical industry with the development and production of their biologic, vaccines and gene therapies.

With over 30 years of experience in process development and cGMP manufacturing, a dedicated staff of over 2,000 and a reputation for excellent customer service, flexibility and responsiveness, we’ve become a trusted partner to some of the most prominent biotech developers and pharmaceutical companies in the industry.

Our Process Development experience includes the development of processes for molecules expressed via fermentation (e.g., E. coli, P. pastoris), cell culture systems including CHO, HEK, Vero, MDCK, EB66 and insect cells, and from transgenic sources.

Our network expands within five development and manufacturing facilities located in Teesside, United Kingdom; Research Triangle Park, North Carolina, USA; College Station, Texas, Thousand Oaks CA USA and Hillerød, Denmark.

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Website
Phone
919-337-4400
Location
Thousand Oaks, CA
Research Triangle Park, NC
College Station, TX
Holly Springs, NC
Watertown, MA
United States
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