Associate, Manufacturing, Cell Therapy
Job in
West Jordan, Salt Lake County, Utah, 84088, USA
Listed on 2026-07-04
Listing for:
Dormont Manufacturing Co
Full Time
position Listed on 2026-07-04
Job specializations:
-
Manufacturing / Production
Manufacturing & Industrial Operations, Pharmaceutical Manufacturing
Job Description & How to Apply Below
Position Summary
Our Associates perform a crucial role in driving our novel cell therapy programs by supporting routine manufacturing operations. We are searching for innovative, intellectually curious individuals with a general understanding of Good Manufacturing Practices (GMPs) to support routine manufacturing operations for Cell Therapy. Successful candidates must be goal-oriented and flexible, with the ability to work effectively and efficiently on a team while demonstrating safety, quality, and GMP compliance at all times.
Duties & Responsibilities- Learn and execute Cell Therapy Manufacturing operations compliantly
- Execute operations as outlined in Source Governing Documents (including but not limited to: Standard Operating Procedures, Work Instructions, Batch Records, Forms)
- Execute transactions and processes in all electronic systems and adheres to business continuity processes
- Prioritize safety of self and others
- Reports safety events within 24 hours
- Immediately escalates any/all issues that may impact compliance or safety of self and/or others
- Complete documentation required by Source Governing Documents contemporaneously
- Perform all tasks in a manner consistent with the safety policies, SOPs, quality systems, and GMP requirements including ALCOA+
- Complete training assignments prior to assigned due date to ensure necessary technical skills and knowledge
- Train for proficiency in process systems and some supporting business systems
- Execute the daily unit operations schedule, that includes people, product, and material flow across multiple shifts
- Work within a control cleanroom environment and execute aseptic processing procedures (as assigned)
- Maintain manufacturing environmental conditions (Non‑Viable Particulate(s) and Viable microbial levels per controlled area classification specifications) by performing area disinfection regiment as required to meet global Health Authority requirements
- Continues to refine and improve manufacturing process technique to improve individual operational times
- Verifies training completion prior to performing any GxP tasks
- Author Manufacturing operating procedures that are technically sound, promote effective and efficient operations and comply with cGMP requirements
Manager/Supervisor
QualificationsEducation:
- Associate or bachelor’s degree in related field is preferred
- A minimum high school diploma and/or equivalent combination of education and experience is required
Experience:
- 0–1 years of cGMP cell therapy manufacturing, bioprocessing manufacturing, or relevant experience and education
- Proven experience working on teams where collaboration and results were expected
- Proficiency in common computer tools such as word processing, spreadsheet, and web‑based applications
- Meticulous attention to detail and personal accountability is critical to success
- Possess excellent interpersonal skills, is attentive and approachable
- Maintain a professional and productive relationship with area management and co‑workers
- Basic understanding of cGMP regulations and FDA guidance applicable to biologics and cell therapy manufacturing is preferred
Working Conditions:
- Must be able to stand/walk for extended periods of time
- Must be able to work in a cleanroom environment and perform aseptic processing in ISO 5 biosafety cabinets (as assigned), which require gowning and personal protective equipment (PPE), including but not limited to: safety shoes, safety glasses, aprons, face shields, powered air purifying respirators (PAPR), lab coats, full body gowns, hairnets, gloves, and hearing protection
- Required to carry and/or lift up to 30 pounds / 15 kg, several times a day, while handling production equipment and/or materials
- Required to push and/or pull up to 50 pounds / 25 kg, several times a day, while handling production equipment and/or materials
- Work in areas that may have strong magnets
- Must be able to work in a BSL2 / ML1 work environment handling human blood components
- Work in areas with exposure to vapor phase liquid nitrogen
- Must be able to work assigned shift (Day, Evening, Night, Weekends and/or Holidays)
Summit West - NJ - US: $27.83 - $33.72 per hour
The…
Position Requirements
10+ Years
work experience
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