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Production Operator

Autolus Therapeutics

Stevenage

On-site

GBP 25,000 - 35,000

Full time

Today
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Job summary

Autolus Therapeutics is hiring for multiple positions within its Production Team in Stevenage, UK, including Associate Operator, Operator I, and Operator II. These roles vary in technical responsibilities and experience, suitable for both entry-level candidates and experienced GMP professionals seeking to lead and improve process efficiencies. Join a team transforming patient care through advanced therapies!

Benefits

Opportunities for growth and development
Impactful work in patient care

Qualifications

  • No prior experience required for Associate Operator role.
  • Candidates for Operator I should have ~2 years of GMP manufacturing experience.
  • Operator II role seeks experienced professionals with leadership capabilities.

Responsibilities

  • Routine production tasks like cleanroom maintenance and environmental monitoring.
  • Cell culture activities such as sampling, activation, and harvesting.
  • Leading operational deviations and supporting Continuous Improvement initiatives.

Skills

Attention to Detail
Motivation

Job description

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Building exceptional teams to revolutionize Car T-cell Therapies in Stevenage and beyond

Join Our Production Team at Autolus Therapeutics

Location: Stevenage, UK | Shift-Based Roles

Are you ready to make a difference in the lives of patients? Autolus Therapeutics is at the forefront of cell and gene therapy, delivering cutting-edge autologous treatments to those who need them most. We are currently hiring for multiple roles within our Production Team, based at our state-of-the-art manufacturing site in Stevenage.

Each role contributes uniquely to our shared mission, with responsibilities ranging from hands-on production processes to leadership and improvement initiatives. Here's an outline of the opportunities available:

Associate Operator, Production

No prior experience? No problem! This entry-level role is designed for individuals who are eager to learn and start their career in a cutting-edge manufacturing environment. We'll provide all the training you need to succeed.

Responsibilities include:

  • Performing routine production tasks such as isolator hydrogen peroxide gassing, cleanroom maintenance, and environmental monitoring.
  • Completing raw material transfers, particulate cleaning, and drug product shipment processes.
  • Accurate and timely documentation to ensure compliance with GMP.

Ideal for: Motivated individuals with great attention to detail, who are eager to learn and grow in the pharmaceutical manufacturing industry. No prior GMP or cleanroom experience is required—just bring your enthusiasm and willingness to learn!

Operator I, Production

This role builds on foundational production skills, combining routine activities with advanced technical responsibilities. Key tasks include:

  • Performing cell culture activities, including cell sampling, activation, feeding, and harvesting.
  • Conducting Magnetic Enrichment and Depletion (MACS), drug product visual inspections, and process adjustments.
  • Supporting non-standard or first-time product manufacturing alongside Product Development and MSAT staff.

Ideal for: Candidates with ~2 years of GMP manufacturing experience who are looking to expand their skill set in ATMP and sterile production.

Operator II, Production

This leadership role combines technical expertise with improvement, leadership, and mentoring responsibilities. In addition to core production tasks, you will also play a key role in Continuous

Improvement (CI) initiatives, including:

  • Leading operational deviations, process risk assessments, and change controls.
  • Authoring and updating SOPs, risk assessments, and other documentation to support rapid, controlled improvements.
  • Supporting and mentoring junior team members while taking ownership of personal development.
  • Actively participating in Continuous Improvement (CI) activities, working to identify and implement process enhancements.

Ideal for: Experienced GMP professionals with leadership capabilities, a drive for process improvement, and a passion for mentoring others.

Shift Patterns

This is a shift-based role with the following shift patterns:

  • 4 on, 3 off (Sunday-Wednesday or Wednesday-Saturday)
  • Early shifts: 6:00 AM – 3:45 PM
  • Late shifts: 12:15 PM – 10:00 PM
  • 4 on, 4 off
  • Early shifts: 6:00 AM – 5:00 PM
  • Late shifts: 11:00 AM – 10:00 PM

What Sets Each Role Apart

While all roles focus on delivering high-quality therapies in a GMP-compliant environment, they differ in scope and level of expertise:

  • Associate Operator, Production: Perfect for those new to GMP manufacturing—no experience required!
  • Operator I, Production: Designed for individuals with foundational GMP experience, ready for more advanced technical responsibilities.
  • Operator II, Production: A leadership-focused role for experienced professionals eager to mentor, drive improvements, and support continuous enhancement of production processes.

Why Join Us?

  • Impact: Be part of a team transforming patient care through advanced therapies.
  • Growth: Gain unparalleled experience in a cutting-edge, fast-paced environment with opportunities to learn and develop.
  • Culture: Work with a bright, enthusiastic, and collaborative team that values trust, honesty, and continuous improvement.

If you’re ready to take the next step in your career—whether you’re starting fresh or looking to grow in a leadership role—we want to hear from you. Explore the role that matches your skills and aspirations, and become a part of Autolus Therapeutics’ journey to transform lives.

We will be holding Assessment Centres in the coming months for this role. Apply now and help us shape the future of medicine!

Seniority level
  • Seniority level
    Entry level
Employment type
  • Employment type
    Full-time
Job function
  • Job function
    Manufacturing
  • Industries
    Biotechnology Research and Pharmaceutical Manufacturing

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