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Aseptic Manufacturing Technician Jobs (NOW HIRING)

Iovance Biotherapeutics

The Aseptic Manufacturing Technician II, role is crucial for the autologous cell therapy manufacturing program. This position requires a broad understanding of theories, techniques, and principles to ...

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Iovance Biotherapeutics

The Aseptic Manufacturing Technician I, role is crucial for the autologous cell therapy manufacturing program. This position requires a broad understanding of theories, techniques, and principles to ...

New

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How much do aseptic manufacturing technician jobs pay per hour?

As of Sep 3, 2026, the average hourly pay for aseptic manufacturing technician in the United States is $24.95, according to ZipRecruiter salary data. Most workers in this role earn between $20.19 and $28.85 per hour, depending on experience, location, and employer.

What is an aseptic manufacturing technician?

An Aseptic Manufacturing Technician is a professional responsible for preparing, operating, and monitoring processes that produce sterile pharmaceutical products, such as injectable drugs or biologics. They work in specialized cleanroom environments to maintain strict contamination control, following Good Manufacturing Practices (GMP). Their duties include equipment setup, material handling, documentation, and ensuring that all procedures are performed under aseptic conditions to guarantee product safety and efficacy.

What are the key skills and qualifications needed to thrive as an aseptic manufacturing technician?

To thrive as an Aseptic Manufacturing Technician, you need knowledge of sterile manufacturing processes, strong attention to detail, and often a background in life sciences or related technical training. Familiarity with cleanroom environments, Good Manufacturing Practices (GMP), and use of aseptic processing equipment is typically required. Excellent teamwork, communication, and strict adherence to protocols distinguish high-performing technicians. These skills are vital to ensure product safety, regulatory compliance, and consistent quality in pharmaceutical or biotechnology manufacturing.

What are some common challenges faced by aseptic manufacturing technicians, and how can they be addressed?

Aseptic Manufacturing Technicians often face challenges such as maintaining strict sterility standards, accurately following complex protocols, and working for extended periods in cleanroom environments. Adapting to the physical demands of wearing protective gear and maintaining concentration during repetitive tasks are also common hurdles. These challenges can be addressed through thorough training, practicing good communication with team members, and adhering to established SOPs. Regular feedback and teamwork help ensure high-quality results and a safe, compliant manufacturing process.

What is the difference between Aseptic Manufacturing Technician vs Pharmaceutical Manufacturing Technician?

AspectAseptic Manufacturing TechnicianPharmaceutical Manufacturing Technician
CredentialsTypically requires a high school diploma or equivalent; certifications in aseptic techniques are a plusSimilar credentials; may include certifications in GMP and safety procedures
Work EnvironmentCleanroom settings focused on sterile product preparationGeneral manufacturing areas, sometimes including cleanrooms
Industry UsagePrimarily in sterile drug production, vaccines, and biotech productsBroader in pharmaceutical production, including non-sterile drugs

While both roles involve working in pharmaceutical manufacturing, the Aseptic Manufacturing Technician specializes in sterile, contamination-free environments, whereas the Pharmaceutical Manufacturing Technician may work in both sterile and non-sterile settings. The roles often overlap in credentials and industry usage, but the focus on aseptic techniques distinguishes the Aseptic Manufacturing Technician.

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Aseptic Manufacturing Technician jobs near you
Infographic showing various Aseptic Manufacturing Technician job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 82% Full Time, 13% Part Time, 3% Contract, and 1% Nights. Highlights an 99% Physical, and 1% Remote job distribution, with an average salary of $51,890 per year, or $24.9 per hour.

Aseptic Manufacturing Technician I - Day Shift B [Contract to Hire]

Iovance Biotherapeutics

Philadelphia, PA • On-site

Contractor

Re-posted 2 days ago

Job description

Rotation Schedule:

Week 1: Shift B: Thursday to Saturday from 0700 to 1930

Week 2 Shift B: Wednesday to Saturday from 0700 to 1830

Overview

Iovance Biotherapeutics is an immuno-oncology company focused on the development and commercialization of novel cancer immunotherapies based on tumor infiltrating lymphocytes (TIL). 

The Aseptic Manufacturing Technician I, role is crucial for the autologous cell therapy manufacturing program. This position requires a broad understanding of theories, techniques, and principles to support manufacturing processes.

As an Aseptic Manufacturing Technician I, you will primarily be responsible for the following tasks: suite preparation for cell processing, material transfer, environmental monitoring, BSC runner duties, final product inspection, and final product cryopreservation in controlled rate freezers, for commercial and clinical use.

This position works across different shifts. Depending on your assigned shift, you may be required to work overtime, weekends, and holidays to ensure the manufacturing process is completed.

As this person will be a key member of the autologous cell therapy manufacturing program, a background in cell culture, aseptic gowning and qualifications, as well as ISO class 5 (Grade A) cleanroom operations is strongly desired.

Aseptic Manufacturing Technicians are required to work their assigned schedule. The first few months of onboarding training for this position will occur during regular work week hours (1st shift M-F); however, once the technician is trained, they will be assigned to a shift that include weekends, evenings, and holidays, as needed (i.e. Shifts may be Sunday to Wednesday, Wednesday to Saturday days or nights). May be required to work overtime. 

Essential Functions and Responsibilities:

  • Develop a comprehensive understanding of and be able to proficiently execute Iovance's GMP cell therapy manufacturing process(es).
  • Complete training sessions and ensure training documentation is maintained.
  • Understand and comply with quality standards and requirements as documented.
  • Adhere to Good Manufacturing Practices (GMP) and Standard Operating Procedures (SOPs), including Good Documentation Practices (GDP).
  • Preps:
    • Provide operational support functions including:
      • Materials stocking and transfer.
      • Kit preparation.
      • Room readiness.
      • Equipment cleaning activities.
      • And inventory transactions using electronic inventory systems.
    • Hallway:
      • Material transfer.
      • Tumor receipt.
      • Chain of Information/Chain of Custody transactions.
      • Material incubation.
      • Feeder cell retrieval from liquid nitrogen (LN2) tanks.
      • Able to perform final product visual inspection.
      • Final product cryopreservation in controlled rate freezers.
    • BSCR:
      • Perform biosafety cabinet (BSC) runner duties as assigned.
      • Balance weight checks and operation.
      • Operation of liquid repeater pump.
      • Operation of tube sealers and welders.
      • Incubator-use for cell culture.
    • EM:
      • Perform in-suite environmental monitoring during the day of process
      • Perform document Environmental Monitoring duties using sample management electronic system.
    • Miscellaneous:
      • Able to train, pass and maintain gowning qualification.
      • Perform logbook review.
      • Attend the daily Tier 1 meeting and escalate issues/concerns at that forum to Area Management for further investigation.
      • Ability to work in a team environment and independently as required.
      • Must adhere to Iovance Biotherapeutics' core values, policies, procedures, and business ethics.
      • Must comply with Safety SOPs, SDS sheets, and laboratory procedures per company policy and OSHA regulations.
      • Adherence to production schedule while maintaining internal production priorities.
      • Perform other duties as assigned.

Required Education, Skills, and Knowledge

  • Bachelor's degree or equivalent experience.
  • Minimum 0-1 year of experience in biopharmaceutical-based GMP manufacturing operations, including, aseptic technique, aseptic liquid transfers, use of welders and sealers, BSC aseptic operations and associated downstream processing is a plus.
  • Must be able to read, write and understand English especially for Good Documentation Practices.
  • Proficiency in Microsoft (Excel, Word, Outlook and Teams).
  • Ability to accurately and reproducibly perform arithmetic calculations including fractions, decimals and percentages and basic algebraic and geometric calculations.
  • May work on moderately complex assignments, requiring judgment to resolve operational issues without negatively impacting manufacturing efforts.
  • Quality mindset, familiar with 21 CFR Part 11 and standard GxP best practices and FDA regulations.
  • Ability to build relationships quickly and credibly.
  • Ability to work successfully in a fast-paced team-oriented environment and manage constant change.

The physical demands described here represent those that an employee must meet to perform the essential functions of this job successfully. Reasonable accommodation may be made upon request to enable individuals to perform essential functions. Please contact Human Resources to request accommodation.

For the Visual Inspection Program, the technician must be able to pass a Vision Exam that includes the following: 

  • Must not be color blind.
  • Must have 20/20 near vision in both eyes (can be corrected)
  • Clarity of vision at near and mid-range, depth perception, and ability to identify and distinguish colors may be given a visual exam for visual acuity and color perception.

Physical Demands and Activities Required:

  • You must be able to wear appropriate cleanroom attire and all Personal Protective Equipment (PPE), i.e., scrubs, gowning coveralls, masks, gloves, etc.
  • Must meet requirements for and be able to wear a half-faced respirator for use of hazardous chemicals.
  • Able to stand and/or walk 90% (and sit 10%) within your scheduled workday, which may include climbing ladders or steps.
  • Able to crouch, bend, twist, reach, and perform activities with repetitive motions.
  • Must be able to lift and carry objects weighing 50 pounds. 

Mental:

  • Clear and conceptual thinking ability; excellent judgment, troubleshooting, problem-solving, analysis, and discretion; ability to handle work-related stress; ability to handle multiple priorities simultaneously; and ability to meet deadlines. 

Work Environment: 

  • This position will work in both an office and a manufacturing setting.
  • When in the cleanroom setting, must be able to work with various chemical/biochemical exposures with appropriate PPE.
  • Potential exposure to noise and equipment hazards and strong odors. 

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