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Aseptic Processing Jobs (NOW HIRING)

Aseptic Process Expert

Morris Plains, NJ · On-site

$88K - $132K/yr

Supporting investigation and leading continuous improvement to improve aseptic processing and training within the manufacturing area. 365 days a year, we aspire to be the best manufacturer of Cell ...

... aseptic processing Additional Information Please attach a WORD resume to your submission All of your information will be kept confidential according to EEO guidelines. ON-SITE only This is a FT role ...

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Aseptic Processing information

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How much do aseptic processing jobs pay per hour?

As of Jul 6, 2026, the average hourly pay for aseptic processing in the United States is $24.67, according to ZipRecruiter salary data. Most workers in this role earn between $19.71 and $28.12 per hour, depending on experience, location, and employer.

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

To thrive in Aseptic Processing, you need knowledge of sterile manufacturing practices, attention to detail, and often a background in microbiology, biotechnology, or a related field. Familiarity with cleanroom operations, automated filling equipment, and compliance with Good Manufacturing Practices (GMP), as well as certifications like HACCP or aseptic processing training, are valuable. Strong teamwork, communication skills, and a commitment to safety set top performers apart. These skills are crucial to maintaining product purity, preventing contamination, and meeting strict regulatory standards in industries such as pharmaceuticals or food production.

What are the typical daily responsibilities of someone working in an Aseptic Processing role?

Aseptic Processing professionals are responsible for preparing, operating, and monitoring equipment within sterile environments, ensuring all procedures are performed according to strict quality and safety guidelines. Tasks may include gowning and entering cleanrooms, performing aseptic transfers, documenting activities for regulatory compliance, and troubleshooting equipment or process deviations. Teamwork is essential, as you will collaborate closely with quality assurance, maintenance, and production teams to maintain consistent standards. The role requires a high level of concentration, adherence to protocols, and readiness to promptly address any contamination risks or procedural issues.

What is an Aseptic Processing job?

An Aseptic Processing job involves maintaining sterile conditions while handling pharmaceutical or food products to prevent contamination. Responsibilities typically include sterilizing equipment, monitoring environmental conditions, and following strict regulatory guidelines. Workers must adhere to Good Manufacturing Practices (GMP) and use specialized techniques to ensure product integrity and safety.

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What are the most commonly searched types of Aseptic Processing jobs? The most popular types of Aseptic Processing jobs are:
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Advanced Research Associate - Aseptic Processing

Advanced Research Associate - Aseptic Processing

Bio-Techne

Saint Paul, MN • On-site

$49K - $81K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 9 days ago


Bio-Techne rating

8.5

Company rating: 8.5 out of 10

Based on 14 frontline employees who took The Breakroom Quiz


Job description

By joining Bio-Techne, you'll join a company with a powerful and positive purpose of enabling cutting-edge research in Life Sciences and Clinical Diagnostics. Bio-Techne, and all of its brands, provides tools for researchers to further treat and prevent disease worldwide.
Pay Range:
$49,700.00 - $81,650.00
Position Summary:
The Advanced Research Associate supports the development and sustained manufacture of Bio-Techne's diverse product portfolio. This role involves executing and revising standard operating procedures, facilitating controlled experiments, and collaborating cross-functionally to advance new and existing products. The position implements process improvements, ensures compliance with quality standards, and supports operational excellence within a fast-paced environment.
Key Responsibilities:
  • Author, revise, and execute Standard Operating Procedures (SOPs) for manufacturing reagents and consumables.
  • Facilitate moderately complex controlled experiments to support new product development.
  • Perform validation activities for equipment used in GMP manufacturing processes.
  • Follow Good Documentation Practices (GDP) to capture results, analyze generated data, and prepare comprehensive reports.
  • Perform timely reviews of in-process manufacturing documentation.
  • Identify and resolve observed manufacturing process issues.
  • Investigate and author non-conformance reports; lead troubleshooting activities.
  • Propose process improvement initiatives and lead implementation efforts.
  • Conduct periodic workspace walkthroughs, close out actions, and perform device calibrations to maintain compliance.
  • Collaborate with cross-functional teams to achieve project objectives.
  • Perform training for new employees and contribute to team development.
  • Follow company guidelines and comply with all safety, quality, and regulatory requirements.
  • Perform additional duties as assigned.

QUALIFICATIONS
Education and Experience:
  • Bachelor's degree with 3-5 years of relevant experience, or
  • Master's degree in a related field with up to 2 years of relevant experience.
  • GMP laboratory experience required.

Knowledge, Skills, and Abilities:
  • Knowledge of GMP and Good Documentation Practices (GDP) required.
  • Strong technical knowledge of aseptic filling.
  • Exposure to media fills and aseptic process qualification.
  • Ability to work in laminar flow hoods and RABS.
  • Proficiency in Microsoft Word, Excel, and PowerPoint.
  • Ability to perform moderately complex data analysis.
  • Strong organizational skills and attention to detail.
  • Ability to work independently and collaboratively in a fast-paced environment.
  • Ability to perform moderate complex calculations.
  • Effective verbal and written communication skills.
  • Ability to conduct training effectively.
  • Ability to multitask and prioritize effectively.

Working Conditions:
  • Onsite work required during standard business hours.
  • Occasional extended hours may be necessary to meet project deadlines.

Physical Requirements:
  • Ability to stand or sit for extended periods.
  • Ability to wear PPE and clean room attire.
  • Manual dexterity for handling laboratory equipment.
  • Ability to lift up to 25 lbs as needed.

Why Join Bio-Techne:
  • We offer competitive insurance benefits starting on day one: medical, dental, vision, life, short-term disability, long-term disability, pet, and legal and ID shield.
  • We invest in our employees' financial futures through 401k plans, an employee stock purchase plan (ESPP), Health Saving Account (HSA), Flexible Spending Account (FSA), and Dependent Care FSA.
  • We empower our employees develop their careers through mentorship, promotional opportunities, training and development, tuition reimbursement, internship programs, and more.
  • We offer employee resource groups, volunteer paid time off, employee events, and charity drives to build a culture of caring and belonging.
  • We offer an accrued leave policy with paid holidays, paid time off, and paid parental leave.
  • We foster a culture of empowerment and innovation, where employees feel valued and encouraged to bring their new ideas to the table.

Bio-Techne is an E-Verify Employer in the United States.
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.
To protect the interests of all, Bio-Techne will not accept unsolicited resumes from any source other than a candidate application. Any unsolicited resumes sent to Bio-Techne will be considered Bio-Techne property.
If you require a reasonable accommodation to complete an application, participate in an interview, or take part in any other stage of the recruitment process, please contact hr@bio-techne.com for assistance.

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