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Biomanufacturing Associate

Job in Frederick, Frederick County, Maryland, 21701, USA
Listing for: Net2Source (N2S)
Full Time position
Listed on 2025-12-09
Job specializations:
  • Manufacturing / Production
    Pharmaceutical Manufacturing, Manufacturing Engineer, Operations Engineer, Manufacturing Operations / Plant Manager
Job Description & How to Apply Below

Cell Therapy Technician –

Location:

Frederick, Maryland

2 days ago – Be among the first 25 applicants

Direct message the job poster from Net2

Source (N2S).

Key Details:

  • Contractor work schedule: 6 weeks of Monday–Friday (07:30‑16:00) for orientation and training, followed by shift deployment as needed.
  • Shift times:
    Day Shift (07:00‑16:30) Sun–Wed, Wed–Sat;
    Swing Shift (15:00‑01:30) Sun–Wed, Wed–Sat.
  • Role type:
    Full-time 4/10, with shift flexibility directed by manager or department leads.
Position Summary

Everyone at this facility is grounded by one common goal – curing cancer. Every single day, we seek to establish a direct line between that purpose and our day-to-day work. We are seeking a highly motivated, Cell Therapy Technician to join our newly formed Cell Therapy Manufacturing team in a brand‑new, state‑of‑the‑art commercial Cell Therapy facility in Frederick, Maryland.

The Cell Therapy Technician will perform and/or verify all tasks associated with the manufacture of commercial product following batch records and standard operating procedures (SOPs) to ensure safe and compliant operations, and will work as part of a team to execute GMP runs in close collaboration with Materials Management, Quality Control, and Quality Assurance.

Are you passionate about making an impact on people’s lives? Would you be excited to work for a company leading the way in developing and producing unique, innovative immunotherapies? Do you have a background in cGMP manufacturing? If the answer is yes, we’d like to consider you!

Responsibilities
  • Successfully troubleshoot processing and equipment issues while communicating said issues to management.
  • Complete required training assignments to maintain necessary technical skills and knowledge and to ensure compliance with cGMP requirements.
  • Routinely monitor, clean, prepare and operate sophisticated automated cell processing, cell expansion and filling equipment in Grade B/C clean rooms. All required PPE and gowning for classified GMP manufacturing areas are provided by the company.
  • Find opportunities for improvement in manufacturing efficiencies and compliance while assisting with investigations/deviations and change controls.
  • Ability to wear a respirator during use of certain cleaning chemicals.
Qualifications
  • 1+ years related experience with High School Diploma.
  • 0+ years related experience with Associate’s Degree.
Seniority Level

Entry level

Employment Type

Contract

Job Function

Other – Industries:
Pharmaceutical Manufacturing

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Position Requirements
10+ Years work experience
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