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Manufacturing Associate I

External
csusystem logoCsusystem · Fort Collins, CO
$50K–$65K/yrContractOn-site2w ago
Clinical TrialsDocumentationSAFe
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Requirements

  • Bachelor's degree in the Sciences or a field related to the responsibilities of the assignment with 0-1 years of experience; OR
  • Bachelor's degree in an unrelated field plus at least 1 years of professional experience related to the specific assignment.
  • Experience working within a cGMP quality system.
  • Experience working in a contract manufacturing or similar regulated environment.
  • Experience working in BSL-2 or BSL-3 clean room spaces.
  • Application Instructions
  • Please note, applicants may redact information from their application materials that identifies their age, date of birth, or dates of attendance at or graduation from an educational institution.
  • Employee Benefits
  • Review our detailed benefits information here.
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  • For the total value of CSU benefits in addition to wages, use our compensation calculator.
  • Lastly, click here for more information about why Fort Collins is consistently ranked in the top cities to live in!
  • Background Check Policy Statement
  • EEO

Benefits

Vision insurance

Additional Information

Job Description Position Summary The MF Associate I primary role is to assist in the planning, preparation and execution of laboratory-based activities related to the production of cGMP biological material for use in early Phase Clinical trials. Additional roles include the maintenance of laboratory spaces and equipment in a ready state for cGMP manufacturing. A detailed description of the Infectious Disease Research Center is available on the department website: https://www.research.colostate.edu/idrc/ Salary Range $50,000 - $65,000 Essential Job Duties Executes approved documentation for the preparation of media & solutions used in GMP production. Assist in the execution of approved batch records and SOPs for the production of GMP material in one or more of the following: upstream processing (e.g., cell culture), downstream processing (e.g., UF/DF, chromatography), and fill/finish activities. Assist in the execution of non-GMP production activities in support of process development, pilot production, and engineering runs. Perform assigned activities in cleanroom environments up to and including ISO 5 spaces. Also requires work within BSL-1, BSL-2, and BSL-3 spaces with biological agents. Conditions of Employment Standard background check expected. Expected to work under BSL-3 conditions and may require work with CDC Select Agents. Supervision None expected.


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