After having met several important milestones including exciting clinical data, we are poised for new strategic objectives which will require significant new resources. Those new resources include a well-qualified Cellular Manufacturing Associate.

Responsible for production of clinical and commercial products, including operating production equipment, manual operations, maintaining records and a clean room environment.


  • Manufacturing Operations – Execute approved or draft procedures to manufacture product. Ensure that production batch records are completed at the highest standards according to company policies and procedures. Execute startup and specific process operations related to Argos product manufacturing. Perform daily manufacturing activities (process, equipment/component preparation and cleaning/sanitization of equipment and rooms) while ensuring adherence to company and governmental GMP regulations, policies and procedures. Assist Supervisor with technical review and implementation of new procedures. Ensure training is current for processes and procedures relevant to all manufacturing activities. In cooperation with others, assist in ordering supplies and maintaining an inventory adequate for production needs.
  • Environmental Monitoring – Execute and document environmental monitoring in classified areas as required.
  • Documentation – Ensure that all processes and procedures that are performed are documented in a timely manner in accordance with company and regulatory regulations. As necessary, provide assistance with the review and revision of Batch Records, SOPs, Item Specifications and PFDs necessary for the manufacture of product.
  • Personnel Training – Assist with the training of new employees in accordance with company and governmental GMP regulations, policies and procedures. Assist with the oversight of temporary, part-time and/or contract personnel to ensure adherence to company procedures at all times. Ensure that all training documentation is current and complete. Ensure all qualifications required for GMP manufacturing are current.
  • Validation – Assist with executing validation protocols associated with manufacturing equipment and procedures including revalidation as scheduled or required to maintain systems in a validated state.
  • Confidentiality – Ensure that information and documentation pertaining to Argos Therapeutics, Inc. is treated as confidential information and handled appropriately as confidential information.
  • Safety – Perform all job functions and responsibilities in a safe and responsible manner. Ensure compliance of co-workers with all safety policies and procedures at all times.
  • Other duties as required.


  • Requires Associate Degree with 0-2 years’ experience. May have a Bachelors degree; however, not required.
  • Basic aseptic technique required. Experience with PCR and other molecular biology techniques and/or cell culture required. Experience cGMP preferred.
  • Good interpersonal and communication skills are required.
  • Flexibility on work schedules and duties.
  • Ability and willingness to be regularly, predictably and reliably at work.

We offer a competitive compensation package along with outstanding benefits. For confidential consideration, please submit a resume with a cover letter and salary history.

No phone calls please.

Argos Therapeutics is an Equal Opportunity Employer.