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Aseptic Manufacturing Jobs (NOW HIRING)

Careers at RK Pharma Inc.

Aseptic Operator

Pearl River, NY · On-site

$22 - $32/hr

Perform aseptic manufacturing activities in accordance with approved SOPs and GMP requirements * Follow gowning, hygiene, and contamination control procedures required for cleanroom operations * Set ...

Kroger

MFG ASEPTIC PROCESS ENGINEER

Newark, OH · On-site

Provide technical expertise and process guidance in the area of aseptic liquid processing and packaging for all food manufacturing plants. Perform all jobs safely, efficiently and accurately to ...

kindeva

Senior Manufacturing Engineer

Bridgeton, MO · On-site

$86K - $118K/yr

Act as the primary SME for aseptic manufacturing equipment, utilities (WFI, clean steam, compressed gases), and fill-finish systems (vial washers, depyrogenation tunnels, isolators/RABS, filling ...

kindeva

Senior Manufacturing Engineer

Bridgeton, MO

$86K - $118K/yr

Act as the primary SME for aseptic manufacturing equipment, utilities (WFI, clean steam, compressed gases), and fill-finish systems (vial washers, depyrogenation tunnels, isolators/RABS, filling ...

kindeva

Senior Manufacturing Engineer

Bridgeton, MO

$86K - $118K/yr

Act as the primary SME for aseptic manufacturing equipment, utilities (WFI, clean steam, compressed gases), and fill-finish systems (vial washers, depyrogenation tunnels, isolators/RABS, filling ...

kindeva

Senior Manufacturing Engineer

Bridgeton, MO

$86K - $118K/yr

Act as the primary SME for aseptic manufacturing equipment, utilities (WFI, clean steam, compressed gases), and fill-finish systems (vial washers, depyrogenation tunnels, isolators/RABS, filling ...

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Aseptic Manufacturing information

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How much do aseptic manufacturing jobs pay per hour?

As of Jul 6, 2026, the average hourly pay for aseptic manufacturing 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 are some common challenges faced in aseptic manufacturing, and how can new team members prepare for them?

Aseptic manufacturing environments require strict adherence to sterile procedures, and a significant challenge is maintaining contamination-free conditions while meeting production deadlines. New team members need to familiarize themselves with gowning techniques, cleanroom protocols, and documentation practices to avoid procedural errors. Attention to detail, strong communication with colleagues, and a commitment to continuous learning are essential for success in this highly regulated setting. Proactive engagement in training sessions and asking questions about standard operating procedures will help new hires adapt more quickly.

What jobs will no longer exist in 2030?

Aseptic manufacturing jobs are less likely to disappear by 2030 due to the specialized skills required for sterile production, such as cleanroom protocols and equipment handling. However, automation and advanced robotics may reduce roles involving manual tasks, shifting the focus toward technicians and operators skilled in maintaining automated systems. Overall, roles emphasizing manual aseptic techniques may decline, while those involving oversight and technical expertise will remain essential.

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

AspectAseptic ManufacturingPharmaceutical Manufacturing Technician
CredentialsTypically requires GMP training, sterile processing certificationsGMP training, technical certifications often preferred
Work EnvironmentCleanrooms, sterile environments, controlled conditionsManufacturing floors, production areas, some cleanroom work
Industry UsagePrimarily in sterile drug production, vaccinesBroader in pharmaceutical production, including non-sterile products
Job FocusEnsuring sterile conditions, aseptic techniquesOperating equipment, assembling products, quality checks

While both roles are vital in pharmaceutical manufacturing, Aseptic Manufacturing focuses specifically on sterile, contamination-free production environments, requiring specialized skills in aseptic techniques. Pharmaceutical Manufacturing Technicians have a broader scope, working in various production settings within the industry.

What is an aseptic manufacturing technician?

An aseptic manufacturing technician is responsible for preparing, operating, and monitoring equipment used in sterile pharmaceutical production to ensure products are free from contamination. They follow strict aseptic techniques, adhere to Good Manufacturing Practices (GMP), and often require certification or training in sterile processing environments.

What is the highest paying job in manufacturing?

In manufacturing, senior roles such as Manufacturing Director or Plant Manager often have the highest salaries, especially in industries like aerospace or pharmaceuticals. These positions typically require extensive experience, leadership skills, and knowledge of production processes, with salaries varying based on company size and location.

What is aseptic manufacturing?

Aseptic manufacturing is a process used to produce sterile pharmaceutical products by preventing contamination from microorganisms throughout production. This involves sterilizing the product, packaging, and equipment separately, and then bringing them together in a sterile environment. The process is critical in producing injectable medicines, vaccines, and other sterile products where safety and purity are essential. Strict procedures, advanced technology, and rigorous monitoring are used to ensure product sterility and compliance with regulatory standards.

What is aseptic manufacture?

Aseptic manufacturing is a process used in the pharmaceutical industry to produce sterile products by sterilizing both the product and the container separately before filling them in a sterile environment. It requires strict adherence to cleanliness, proper sterilization techniques, and often involves specialized equipment and certifications to ensure product safety and quality.

What are the key skills and qualifications needed to thrive in Aseptic Manufacturing, and why are they important?

To succeed in Aseptic Manufacturing, you need a solid understanding of sterile techniques, GMP (Good Manufacturing Practice) standards, and often a background in life sciences or engineering. Familiarity with cleanroom operations, autoclaves, filtration systems, and quality control documentation are critical, with some roles requiring certifications like GMP or ISO training. Attention to detail, strong problem-solving, and effective teamwork are vital soft skills for maintaining product safety and compliance. These competencies ensure the production of safe, contamination-free products in highly regulated environments.
More about Aseptic Manufacturing jobs
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What states have the most Aseptic Manufacturing jobs? States with the most job openings for Aseptic Manufacturing jobs include:
What job categories do people searching Aseptic Manufacturing jobs look for? The top searched job categories for Aseptic Manufacturing jobs are:
Aseptic Manufacturing jobs near you
Infographic showing various Aseptic Manufacturing job openings in the United States as of June 2026, with employment types broken down into 39% Full Time, 10% Part Time, 29% Contract, and 22% Nights. Highlights an 95% Physical, 2% Hybrid, and 3% 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]

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

Iovance Biotherapeutics

Philadelphia, PA • On-site

Contractor

Posted 3 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.

#LI-onsite
The statements contained in this document are intended to describe the general nature and level of work being performed by a colleague assigned to this description. They are not intended to constitute a comprehensive list of functions, duties, or local variances. Management retains the discretion to add or to change the duties of the position at any time.
Iovance is committed to cultivating and offering a diverse and inclusive work environment. As an equal-opportunity employer, our employees and applicants will be considered without regard to an individual's race, color, religion, sex, pregnancy, national origin, age, physical and mental disability, marital status, sexual orientation, gender identity, gender expression, genetic information, military and veteran status, and any other characteristic protected by applicable law. If you need assistance or accommodation to apply to one of our opportunities, please contact careers@iovance.com.
By voluntarily providing information and clicking "Submit Application", you explicitly consent to the collection and use of your personal information for the purposes described above and in our Candidate Privacy Notice.

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