Operator I, Production

Operator I, Production

Stevenage Full-Time 30000 - 42000 £ / year (est.) No home office possible
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At a Glance

  • Tasks: Join our GMP manufacturing team to produce life-changing cell therapies.
  • Company: Autolus Therapeutics is an inclusive biotech company focused on innovative cell therapies.
  • Benefits: Gain hands-on experience in a cleanroom environment with opportunities for career growth.
  • Why this job: Be part of a dynamic team making a real impact in patient care and cell therapy.
  • Qualifications: GMP manufacturing or cleanroom experience is essential; shift work experience required.
  • Other info: This role requires weekend shifts within operational hours of 6 AM – 10 PM.

The predicted salary is between 30000 - 42000 £ per year.

Job Description

This job is with Autolus Therapeutics, an inclusive employer and a member of myGwork – the largest global platform for the LGBTQ+ business community. Please do not contact the recruiter directly.

Autolus is looking for a motivated and detail-oriented Operator I to join our GMP manufacturing team in Stevenage. This shift-based role requires weekend working within the operational hours of 6 AM – 10 PM. As part of the Production team, you will contribute to the manufacture and delivery of Autologous cell therapies for patients. This is an excellent opportunity to develop your skills in a cleanroom environment while working within a dynamic and evolving team.

Key Responsibilities

  • Execute GMP manufacturing processes under strict regulatory guidelines to produce high-quality cell-based products.
  • Follow Standard Operating Procedures (SOPs) and Standard Work Instructions (SWIs) in compliance with Good Manufacturing Practices (GMP).
  • Perform cleanroom activities, including cell culture sampling, counting, washing, activation, feeding, and harvesting.
  • Support aseptic processing activities such as Magnetic Enrichment & Depletion (MACS), drug product visual inspection, and process adjustments.
  • Assist with raw material transfers, environmental monitoring, labelling, reconciliation, and documentation management.
  • Maintain a strong focus on safety, quality, and compliance, raising any issues proactively.
  • Participate in continuous improvement (CI), root cause analysis (RCA), and corrective & preventive action (CAPA) initiatives.
  • Support training and development of junior staff, contributing to a collaborative team environment.

Skills & Experience

  • GMP manufacturing or cleanroom experience (essential) or relevant transferable skills.
  • Prior experience in shift-based work (essential).
  • Ability to work effectively in high-performance environments.
  • Strong understanding of GxP production (essential) and knowledge of ATMP manufacturing (preferred).
  • Basic awareness of environmental, health & safety requirements.
  • Excellent time management, decision-making, and risk assessment skills.

Working Pattern

  • This is a shift-based role requiring weekend working.
  • Shifts will fall within 6 AM – 10 PM.
  • The role is based at our Stevenage manufacturing site, with occasional travel to other locations.

This role offers a fantastic opportunity to grow within a cutting-edge biotech company. If you’re looking to develop your career in GMP manufacturing and be part of an innovative team shaping the future of cell therapy, we’d love to hear from you!

#LI-DNI

Operator I, Production employer: Autolus Therapeutics

Autolus Therapeutics is an exceptional employer that fosters an inclusive and dynamic work environment in Stevenage, where you can thrive as an Operator I in our GMP manufacturing team. We prioritize employee growth through continuous training and development opportunities, while our commitment to safety and quality ensures a rewarding experience in the cutting-edge field of cell therapy. Join us to be part of a collaborative team dedicated to making a meaningful impact on patients' lives.
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Contact Detail:

Autolus Therapeutics Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land Operator I, Production

✨Tip Number 1

Familiarize yourself with Good Manufacturing Practices (GMP) and the specific processes involved in cell therapy production. Understanding these concepts will help you demonstrate your knowledge during the interview.

✨Tip Number 2

Highlight any previous experience you have in cleanroom environments or shift-based work. Be prepared to discuss how you managed time and tasks effectively in those settings.

✨Tip Number 3

Show your enthusiasm for continuous improvement and teamwork. Think of examples where you've contributed to process enhancements or supported colleagues, as this aligns with the collaborative culture at Autolus.

✨Tip Number 4

Research Autolus Therapeutics and their mission in the biotech field. Being knowledgeable about the company’s goals and values will help you connect your personal aspirations with their vision during the interview.

We think you need these skills to ace Operator I, Production

GMP Manufacturing Experience
Cleanroom Procedures
Attention to Detail
Standard Operating Procedures (SOPs)
Cell Culture Techniques
Aseptic Processing
Environmental Monitoring
Documentation Management
Safety Compliance
Continuous Improvement (CI)
Root Cause Analysis (RCA)
Corrective and Preventive Actions (CAPA)
Time Management
Decision-Making Skills
Risk Assessment

Some tips for your application 🫡

Understand the Role: Take the time to thoroughly read the job description for the Operator I position at Autolus Therapeutics. Make sure you understand the key responsibilities and required skills, especially regarding GMP manufacturing and cleanroom experience.

Tailor Your CV: Customize your CV to highlight relevant experience in GMP manufacturing or cleanroom environments. Emphasize any shift-based work you've done and showcase your understanding of GxP production.

Craft a Strong Cover Letter: Write a cover letter that reflects your motivation for applying to Autolus. Mention specific experiences that align with the job requirements, such as your ability to follow SOPs and your commitment to safety and quality.

Proofread Your Application: Before submitting your application, carefully proofread all documents for spelling and grammatical errors. Ensure that your application is clear, concise, and professional, as attention to detail is crucial in this role.

How to prepare for a job interview at Autolus Therapeutics

✨Understand GMP and Cleanroom Protocols

Make sure you have a solid grasp of Good Manufacturing Practices (GMP) and cleanroom protocols. Be prepared to discuss your previous experiences in these areas, as they are crucial for the role.

✨Showcase Your Attention to Detail

As an Operator I, attention to detail is key. Prepare examples from your past work where your meticulousness led to successful outcomes, especially in a manufacturing or laboratory setting.

✨Demonstrate Team Collaboration Skills

This role requires working within a dynamic team. Think of instances where you contributed to team success, particularly in high-pressure environments, and be ready to share those stories.

✨Prepare for Shift Work Discussion

Since this position involves shift-based work, be ready to discuss your flexibility and experience with such schedules. Highlight your ability to adapt to different working hours and maintain productivity.

Operator I, Production
Autolus Therapeutics
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  • Operator I, Production

    Stevenage
    Full-Time
    30000 - 42000 £ / year (est.)

    Application deadline: 2027-04-22

  • A

    Autolus Therapeutics

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