At a Glance
- Tasks: Lead microbiological investigations and ensure compliance with sterility assurance standards.
- Company: Join Autolus, a pioneering biopharma company focused on innovative therapies.
- Benefits: Enjoy competitive pay, career growth opportunities, and a collaborative work environment.
- Why this job: Make a real impact in a fast-paced setting while enhancing your technical expertise.
- Qualifications: MSc or PhD in Microbiology with 10+ years of relevant experience required.
- Other info: This is a leadership role with direct management responsibilities.
The predicted salary is between 48000 - 72000 £ per year.
Associate Director, Sterility Assurance page is loaded## Associate Director, Sterility Assurancelocations: UK – Stevenagetime type: Full timeposted on: Posted 21 Days Agojob requisition id: JR100025**Work with us** 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:**Job Title – Associate Director, Sterility AssuranceReports to Director, MicrobiologyDepartment – Quality ControlHours- Monday – Friday, Core Office HoursLocation – Stevenage**About Autolus**Autolus is a clinical-stage biopharmaceutical company developing next-generation, programmed T cell therapies for the treatment of cancer. Using a broad suite of proprietary and modular T cell programming technologies. The company is engineering precisely targeted, controlled and highly active T cell therapies that are designed to better recognise cancer cells, break down their defence mechanisms and eliminate these cells. Autolus has a pipeline of product candidates in development for the treatment of haematological malignancies and solid tumours.**Why Autolus**Our team is passionate in the pursuit of excellence and in pushing the boundaries of cancer therapy 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. In addition to this Autolus is proud to offer a competitive salary, performance related bonus as well as private medical insurance, life assurance, pension and access to an employee share scheme. Autolus promotes flexible working.**Our Promise**Autolus is developing complex, breakthrough therapies for a globally diverse market and equally recognises that diversity amongst our people is critical to our mission. As we draw on our differences, what we’ve experienced, and how we work, we celebrate diversity and are committed to creating an inclusive environment for all employees**Role Summary**Autolus is seeking an experienced sterility assurance professional to take on a senior technical role within the Microbiology function as Associate Director, Sterility Assurance. This role is accountable for leading microbiological investigations related to sterility failures, environmental monitoring (EM) excursions, and contamination events across our GMP operations.As Associate Director, Sterility Assurance, you will act as the subject matter expert (SME) for microbiological deviations, ensuring rigorous root cause analysis, strong scientific rationale, and effective CAPAs. You will work closely with cross-functional teams including QA, QC Microbiology, Manufacturing, Validation, and Engineering to resolve complex issues and strengthen the site\’s contamination control strategy.This is a role for an experienced microbiologist with deep technical expertise, strong investigational skills, and the ability to influence across functions. It is a leadership position with direct line management.**Key Responsibilities*** Lead site investigations involving sterility failures, contamination events, and EM excursions, ensuring scientific integrity and timely resolution* Serve as the SME for sterility assurance within the QC Microbiology team, representing the function during audits and inspections* Identify true root causes and drive implementation of sustainable, risk-based CAPAs* Support and enhance the site’s contamination control strategy, including microbial risk assessments and trending* Collaborate with QA, QC, Manufacturing, Validation, and Engineering to ensure alignment on microbiological issues and preventive actions* Promote consistent use of structured root cause analysis tools and data-driven decision-making in microbiology investigations* Ensure all sterility assurance activities comply with EU GMP Annex 1, FDA aseptic guidance, and other relevant regulatory expectations* Provide technical leadership within the QC Microbiology function to embed best practices and support continuous improvement.* Support sterility assurance assessments for new systems including process, equipment and facility* Contribute to the existing collaborative attitude in a fast paced, high impacting environment**Demonstrated skills and competencies**Essential (E)Preferred (P)* MSc or PhD in Microbiology, Biochemistry, or a related life science discipline (P)* Minimum 10 years of microbiology experience in a GMP-regulated biopharma, ATMP, or sterile manufacturing environment (E)* Strong track record in leading microbiological investigations, including sterility failures and contamination events (E)* Deep expertise in aseptic manufacturing, cleanroom microbiology, EM programs, and contamination control (E)* In-depth knowledge of EU GMP Annex 1, FDA aseptic guidance, and other relevant global regulations (E)* Experience acting as SME during MHRA, FDA, or other regulatory inspections (E)* Excellent written and verbal communication skills, with the ability to clearly present complex technical information (E)* Demonstrated ability to work cross-functionally and influence without direct authority (E)* Experience with ATMPs, CAR-T manufacturing, or small-scale aseptic operations (P)* Skilled in microbial data trending, EM analytics, and risk-based investigation approaches (P)* Formal training in structured RCA tools (e.g. 5 Whys, Fishbone, Fault Tree Analysis) (P)* Understanding of contamination risks associated with facility and equipment design (P)* Experience contributing to or maintaining a Contamination Control Strategy in a GMP environment (P)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.### Get In TouchIntroduce yourself to our recruiters and we\’ll get in touch if there\’s a role that seems like a good match. #J-18808-Ljbffr
Associate Director, Sterility Assurance employer: Autolus Limited
Contact Detail:
Autolus Limited Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Associate Director, Sterility Assurance
✨Tip Number 1
Network with professionals in the microbiology and sterility assurance fields. Attend industry conferences or webinars where you can meet potential colleagues and learn about the latest trends and challenges in the sector.
✨Tip Number 2
Familiarise yourself with the latest EU GMP Annex 1 and FDA aseptic guidance. Being well-versed in these regulations will not only boost your confidence but also demonstrate your commitment to compliance during interviews.
✨Tip Number 3
Prepare to discuss specific examples of your experience with microbiological investigations and CAPAs. Highlighting your problem-solving skills and how you've successfully led teams through complex issues will set you apart.
✨Tip Number 4
Showcase your leadership abilities by discussing how you've influenced cross-functional teams in previous roles. Emphasising your collaborative approach will resonate well with hiring managers looking for a strong Associate Director.
We think you need these skills to ace Associate Director, Sterility Assurance
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights relevant experience in microbiology, particularly in GMP-regulated environments. Emphasise your leadership roles and any specific achievements related to sterility assurance and contamination control.
Craft a Compelling Cover Letter: In your cover letter, express your passion for sterility assurance and detail how your background aligns with the responsibilities of the Associate Director role. Mention specific experiences that demonstrate your ability to lead investigations and implement CAPAs.
Highlight Technical Expertise: Clearly outline your technical skills and knowledge in aseptic manufacturing, cleanroom microbiology, and regulatory compliance. Use examples from your past work to illustrate your expertise and problem-solving abilities.
Showcase Communication Skills: Since excellent communication is crucial for this role, provide examples of how you've effectively communicated complex technical information to diverse teams. This could include presentations, reports, or leading cross-functional meetings.
How to prepare for a job interview at Autolus Limited
✨Showcase Your Technical Expertise
As an Associate Director in Sterility Assurance, it's crucial to demonstrate your deep understanding of microbiology and contamination control. Be prepared to discuss specific examples from your past experiences where you successfully led investigations or implemented CAPAs.
✨Prepare for Regulatory Questions
Given the importance of compliance in this role, expect questions related to EU GMP Annex 1 and FDA aseptic guidance. Brush up on these regulations and be ready to explain how you've ensured compliance in previous roles.
✨Highlight Cross-Functional Collaboration
This position requires working closely with various teams. Share examples of how you've effectively collaborated with QA, QC, and Engineering teams to resolve microbiological issues and enhance contamination control strategies.
✨Demonstrate Leadership Skills
As a leadership role, it's essential to convey your ability to influence and lead teams. Prepare to discuss your management style and provide examples of how you've motivated teams to achieve common goals in a high-pressure environment.