Associate Specialist, Cell Therapy

The primary purpose of this role is to support routine manufacturing execution, cleanroom readiness, material preparation, equipment setup, documentation accuracy, and real-time issue escalation under the guidance of Specialists, Leads, or Manufacturing management. The role is expected to recognize when an activity, condition, or observation may differ from accepted practice and escalate appropriately.

Typical Accountabilities

• Execute assigned manufacturing steps according to batch records, SOPs, electronic work instructions, and cGMP requirements.

• Support GMP readiness activities including equipment setup, cleanroom preparation, material staging, basic qualification support, and facility readiness.

• Prepare, stage, verify, and transfer materials and consumables requiredfor manufacturing activities.

• Routinely monitor, clean, prepare, and operateautomated or manual cell therapy processing equipment under guidance.

• Follow proper gowning, cleaning, sanitization, aseptic technique, and contamination control procedures.

• Maintain cleanroom standards and support routine area readiness, 5S, and housekeeping activities.

• Maintain accurate, complete, and timelydocumentation in batch records, logbooks, electronic systems, and other production records.

• Support batch record reconciliation and timelydocumentation closure as assigned.

• Support material and componentinventory control within manufacturing areas, including bill of material awareness and inventory transactions as assigned.

• Escalate issues, errors, abnormal conditions, visible defects, or potential deviations in real time.

• Participate in deviation, non-conformance, OOS, or quality record support by providing factual input as requested.

• Participate in shift handover communication and ensure relevant production information is shared clearly.

• Collaborate with Manufacturing, Quality, Process Development, MSAT, Supply Chain, EHS, and Facilities and Engineering as needed.

• Support SOP drafting, document revisions, visual management, and continuous improvement activities under guidance.

• Participate in required training and work toward qualification onassigned unit operations.

• Perform or support Final Drug Product Visual Inspection activities, when assigned, in accordance withsite procedures, including annual visual acuity qualification.

• Perform other responsibilities as assigned to support daily manufacturing operations and project goals.

You Are Accountable For

• Safe and compliant execution of assigned manufacturing tasks.

• Following approved procedures and batch records without unapproved variation.

• Accurate, complete, and timelydocumentation.

• Timely escalation of issues that may impactproduct quality, schedule, safety, compliance, or patient supply.

• Maintainingcleanroom discipline and contamination control expectations.

• Achieving qualificationon assigned processes within expected timelines.

• Supporting team performance through reliable execution and communication.

• Demonstrating increasing technical proficiencyand progress toward independent execution of core manufacturing processes.

Minimum Qualifications:

• • High School Diploma with at least 2 years of GMP, laboratory, manufacturing, or relevant technical experience, or an equivalent combination of education and experience. Associate degree or Bachelordegree in science, engineering, or a relateddiscipline with 0-2 years experience is preferred

  • Basic understanding of cGMP requirements, aseptic technique, cleanroom procedures, and documentation practices.

  • Familiarity with cleanroom operations, equipment setup, regulated manufacturing, or laboratory environments.

  • Ability to follow detailed instructions and established procedures with strong attention to detail.

  • Ability to work effectively in a team-based manufacturing environment and learn on the fly.

  • Sound judgment to identifyand escalate issues to senior team members.

  • Ability to prioritize assigned tasks and manage time effectively to support production schedules.

  Preferred Qualifications

  • Cell therapy, biologics, pharmaceutical, biotech, or vector manufacturing experience.

  • Experience working in a cleanroom or aseptic processing environment.

  • Experience with paper or electronic batch records, MES, inventory systems, or quality systems.

  • Familiarity with primary human cell culture, single-use technologies, or automated cell processing equipment.

  • Proficiencyin Microsoft Word, Excel, and basic data entry or data review.

  The annual base pay (or hourly rate of compensation) for this position ranges from $81,992.80 - 122,989.20. Our positions offer eligibility for various incentives-an opportunity to receive short-term incentive bonuses, equity-based awards for salaried roles and commissions for sales roles. Benefits offered include qualified retirement programs, paid time off (i.e., vacation, holiday, and leaves), as well as health, dental, and vision coverage in accordance with the terms of the applicable plans.

Date Posted

Closing Date

Our mission is to build an inclusive environment where equal employment opportunities are available to all applicants and employees. In furtherance of that mission, we welcome and consider applications from all qualified candidates, regardless of their protected characteristics. If you have a disability or special need that requires accommodation, please complete the corresponding section in the application form.