At a Glance
- Tasks: Support quality assurance for innovative cancer therapies in a dynamic team environment.
- Company: Join Autolus, a pioneering biopharmaceutical company focused on life-changing treatments.
- Benefits: Enjoy competitive salary, bonuses, private medical insurance, and flexible working options.
- Other info: Be part of a diverse team committed to excellence and innovation.
- Why this job: Make a real impact in the fight against cancer while developing your career.
- Qualifications: Ideal for those with a background in pharmaceuticals or related fields.
The predicted salary is between 30000 - 42000 £ per year.
Our team are passionate in the pursuit of excellence and in pushing the boundaries of cancer therapy and Autoimmune disease to deliver life-changing treatments to patients. Whilst working at Autolus you will enjoy a flexible, diverse and dynamic working environment which actively promotes creativity, leadership and teamwork – together we are ONE Autolus.
Job Description:
Reports to: QA Manager / Senior QA Specialist
Department: Quality Assurance – QA Operations
Hours: Full Time, Sunday – Wednesday 08:00 – 17:45
Location: Stevenage
About Autolus
Autolus is a biopharmaceutical company, advancing innovative therapies at both clinical and commercial stages of development, focused on next-generation, programmed T cell therapies for the treatment of cancer.
Role Summary
Based in Stevenage, the post-holder will work within the Quality Assurance team, supporting the delivery of autologous CAR T-cell products for commercial purposes and clinical trials operating in sites across the UK, EU and US from a central Good Manufacturing (GMP) site in Stevenage (UK). You will be expected to work with a team of quality professionals to provide a high-quality service to external service users.
Key Responsibilities
- Maintaining the requirements of Good Manufacturing Practice in a multi-product facility delivering cell and gene therapies for clinical trial and commercial purposes.
- Interact with various functions to ensure cGMP compliance in batch release related activities. Report or escalate to Line Manager any issues.
- Control of record forms for use in production and QC, applying batch or test article identity traceability features and maintaining an audit trail of issue, use and reconciliation.
- Review of Batch Manufacturing Records and Quality Control records and escalation of quality issues.
- Preparation and checking of in-process and Drug Product labels, ensuring compliance with the authorised template and the batch-specific/patient-specific data thus maintaining product traceability and regulatory compliance.
- Identify potential compliance risks/gaps and recommend improvements.
- Under supervision, review of premises and equipment documentation including; logbooks, protocols, reports and equipment maintenance forms.
- To liaise with internal departments regarding quality issues when required.
- Under supervision, supports in the generation of departmental metrics.
- Conduct the archiving of documentation and records within the QA team.
- Support inspection readiness activities.
- Work in adherence to local Health and Safety policies and SOPs.
- To perform other duties which are directed by the line manager/QA Team Lead.
- Any other duties as required following consultation with the post holder.
- Contribute to the continuous improvement of the Pharmaceutical Quality System (PQS).
- Contribute and facilitate in quality event investigations and in the determination of root cause.
Demonstrated skills and competencies
- E – Essential
- P – Preferred
Experience
- Experience working with GMP systems and controlled documentation (P).
- Meet requirements to work in cleanroom environment (P).
Qualifications
- Higher education (P)
- BSc in pharmaceutical services, immunology, biology, chemistry or relevant discipline (P)
Skills/Specialist knowledge
The post holder will bring expertise related to:
- Good communications skills
- Good eye for detail
- Accurate data entry skills
- Good workload prioritisation skills, decision-making and scheduling skills
- Reliability, flexibility, motivation and a responsible team-orientated attitude
- Ability to manage multiple activities to tight deadlines
Autolus Core Competencies
- Focus on Results: Works to meet business goals set by management and leaders
- Builds Trust and Relationships: Ensures trust with internal and external partners by delivering on commitments
- Resilience: Has the capacity to recover quickly from difficulties; toughness
- Communicates and Collaborates: Builds partnerships and works collaboratively with others to meet objectives
Autolus’ success is driven by equality and inclusion; we believe all voices are of equal value and must be heard. Whilst operating with focus and integrity, we are committed to improving diversity and inclusion within our business and our industry.
Associate, QA Operations in Stevenage employer: Autolus Limited
Contact Detail:
Autolus Limited Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Associate, QA Operations in Stevenage
✨Tip Number 1
Network like a pro! Reach out to people in the industry, attend events, and connect on LinkedIn. You never know who might have the inside scoop on job openings or can put in a good word for you.
✨Tip Number 2
Prepare for interviews by researching Autolus and understanding their mission. Be ready to discuss how your skills align with their goals in cancer therapy and quality assurance.
✨Tip Number 3
Practice common interview questions and answers with a friend or in front of a mirror. This will help you feel more confident and articulate during the real deal!
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets seen by the right people. Plus, it shows you’re genuinely interested in joining the Autolus team.
We think you need these skills to ace Associate, QA Operations in Stevenage
Some tips for your application 🫡
Tailor Your CV: Make sure your CV reflects the skills and experiences that match the Associate, QA Operations role. Highlight any experience with GMP systems and controlled documentation, as these are key for us.
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you're passionate about quality assurance and how you can contribute to our mission at Autolus. Be genuine and let your personality come through.
Showcase Your Attention to Detail: In QA operations, attention to detail is crucial. Make sure your application is free from typos and errors. This shows us that you take pride in your work and understand the importance of accuracy.
Apply Through Our Website: We encourage you to apply directly through our website. It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, it’s super easy!
How to prepare for a job interview at Autolus Limited
✨Know Your GMP Basics
Make sure you brush up on Good Manufacturing Practice (GMP) principles before your interview. Autolus is all about delivering high-quality therapies, so being able to discuss GMP systems and controlled documentation will show that you're serious about the role.
✨Showcase Your Attention to Detail
In a QA role, attention to detail is key. Prepare examples from your past experiences where your keen eye for detail made a difference. Whether it was catching an error in documentation or ensuring compliance with regulations, these stories will highlight your suitability for the position.
✨Demonstrate Team Spirit
Autolus values teamwork, so be ready to talk about how you've collaborated with others in previous roles. Share specific instances where you worked with cross-functional teams to solve problems or improve processes, as this will resonate well with their focus on collaboration.
✨Prepare for Compliance Questions
Expect questions around compliance risks and quality issues. Think about potential gaps you've identified in past roles and how you recommended improvements. This will not only show your proactive approach but also align with Autolus' commitment to continuous improvement.