(Fixed Term) Analyst, Quality Control, Microbiology

ModernaTX; Oxford; On-site; GBP 40,000 - 60,000; Full time

Job summary

A pioneering biotechnology company in the UK is looking for a Microbiology Quality Control Analyst to support its GMP manufacturing operations. This full-time role involves conducting environmental monitoring, executing microbiological analyses, and collaborating with cross-functional teams to ensure compliance with quality standards. Candidates should have a BSc and at least 5 years of Quality Control experience in a cGMP environment. The position offers significant opportunities for professional growth while contributing to the advancement of mRNA technology.

Benefits

Quality healthcare and insurance benefits

Lifestyle Spending Accounts

Free premium access to fitness classes

Generous paid time off

Qualifications

• 5 years of Quality Control experience in a cGMP organization with a focus on Microbiology.
• Hands-on experience with methods like Bioburden and Sterility.
• Working knowledge of FDA, EU, and ICH guidelines preferred.

Responsibilities

• Conduct routine environmental monitoring in a GMP facility.
• Perform microbiological analyses including TOC and Endotoxin tests.
• Support GMP testing for product release and stability.

Skills

Microbiology testing techniques

Collaboration in cross-functional teams

Ability to prioritize tasks

Investigation skills

Education

BSc in a relevant scientific discipline

Tools

Vitek Isolator Technology

Job description

The Role :

Joining Moderna offers the unique opportunity to be part of a pioneering team thats revolutionizing medicine through mRNA technology with a diverse pipeline of development programs across various diseases.

As an employee youll be part of a continually growing organization working alongside exceptional colleagues and strategic partners worldwide contributing to global health initiatives.

Modernas commitment to advancing the technological frontier of mRNA medicines ensures a challenging and rewarding career experience with the potential to make a significant impact on patients lives worldwide.

Modernas mission is to establish a leading-edge research development and manufacturing facility at Harwell as part of a long-term commitment to onshore mRNA vaccine production for respiratory diseases. This initiative will create a multitude of highly skilled jobs and foster collaboration with academic NHS and government partners across the UK. Were looking for global experts eager to join us in this endeavour contributing to a future where access to life-saving vaccines is a reality for all.

In this essential role you will serve as the Microbiology Quality Control Analyst at our Harwell facility directly supporting GMP manufacturing operations. Reporting to the Associate Director of Quality Control you will carry out routine environmental and critical utility monitoring while performing key microbiological testing across raw materials excipients and drug substances for mRNA products. Youll collaborate cross-functionally on method transfers validations and contribute to laboratory systems aligned with current Good Manufacturing Practices (cGMP). With the opportunity to operate at the interface of digital systems and biotechnological innovation this position offers access to tools and data environments closely tied to Generative AI platforms supporting Quality Operations across Moderna globally.

Heres What Youll Do :

• Conducting routine environmental monitoring (EM) and sampling of critical utilities such as water systems in a GMP manufacturing facility.
• Executing microbiological analyses including TOC Conductivity Bioburden Endotoxin Sterility and other GMP QC methods.
• Supporting GMP testing for product release stability and validation samples.
• Preparing shipping and receiving contract laboratory samples including those for microbiological identification.
• Participating in new microbiological method transfers in collaboration with Analytical Sciences & Technology (AS & T) teams.
• Supporting development implementation and maintenance of laboratory systems in line with cGMP expectations.
• Performing general laboratory support activities including reagent preparation equipment maintenance and housekeeping.
• Participating in audit readiness activities including support to internal and external audit teams.
• Assisting in equipment and method qualifications and potentially troubleshooting assay methods and instrumentation.
• Drafting and revising SOPs protocols reports and contributing to quality system documentation (e.g. deviations CAPAs EM excursions and change controls).
• Applying Good Documentation Practices and ensuring full compliance with GxP and Data Integrity requirements.
• Completing all assigned training per schedule and requalification timelines.
• Supporting junior team members as required with data review troubleshooting and training.

The key Moderna Mindsets youll need to succeed in the role :

We obsess over learning. We dont have to be the smartest we have to learn the fastest.

In this technically rigorous environment your growth mindset and rapid adaptability will be critical as you integrate advanced microbiology testing techniques evolving quality standards and support ongoing method transfers in a dynamic manufacturing setting.

We digitize everywhere possible using the power of code to maximize our impact on patients.

While hands-on microbiological testing is central you will be immersed in Modernas digital-first culture leveraging automation electronic lab records and systems designed to integrate data into scalable AI-driven quality frameworks.

Heres What Youll Bring to the Table :

• BSc in a relevant scientific discipline with 5 years Quality Control experience in a cGMP organization with a focus on Microbiology.
• Hands-on experience of various Microbiology testing techniques and analyses (e.g. Vitek Isolator Technology Bioburden BET Sterility others)
• Working knowledge of relevant and current FDA EU ICH guidelines and regulations preferred.
• Working experience in a GMP environment.
• Ability to collaborate effectively in a dynamic cross-functional matrix environment.
• Ability to efficiently prioritise and complete multiple projects and tasks in a fast-paced environment.
• Proven ability to conduct investigations.

This position is site-based requiring you to be at Modernas site full-time. This position is not eligible for remote work.

Benefits

• Quality healthcare and insurance benefits
• Lifestyle Spending Accounts to create your own pathway to well-being
• Free premium access to fitness nutrition and mindfulness classes
• Family planning and adoption benefits
• Generous paid time off including vacation bank holidays volunteer days sabbatical global recharge days and a discretionary year-end shutdown
• Savingsandinvestments
• Location-specific perks and extras!

The benefits offered may vary depending on the nature of your employment with Moderna and the country where you work.

About Moderna

Since our founding in 2010 we have aspired to build the leading mRNA technology platform theinfrastructure to reimagine how medicines are created and delivered and a world-class team. We believe in giving our people a platform to change medicine and an opportunity to change the world.

By living our mission values and mindsets every day our peopleare the driving force behind our scientific progress and our we are creating a culture of belonging and building an organization that cares deeply for our patients our employees the environment and our communities.

We are proud to have been recognized as a Science Magazine Top Biopharma Employer a Fast Company Best Workplace for Innovators and a Great Place to Work in the U.S.

As we build our company we have always believed an in-person culture is critical to our success. Moderna champions the significant benefits of in-office collaboration by embracing a 70 / 30 work model. This 70% in-office structure helps to foster a culture rich in innovation teamwork and direct mentorship. Join us in shaping a world where every interaction is an opportunity to learn contribute and make a meaningful impact.

If you want to make a difference and join a team that is changing the future of medicine we invite you to visit to learn more about our current opportunities.

Moderna is a smoke-free alcohol-free and drug-free work environment.

Moderna is a place where everyone can grow. If you meet the Basic Qualifications for the role and you would be excited to contribute to our mission every day please apply!

Moderna is committed to equal opportunity in employment and non-discrimination for all employees and qualified applicants without regard to a persons race color sex gender identity or expression age religion national origin ancestry or citizenship ethnicity disability military or protected veteran status genetic information sexual orientation marital or familial status or any other personal characteristic protected under applicable law. We consider qualified applicants regardless of criminal histories consistent with legal requirements.

We're focused on attracting retaining developing and advancing our employees. By cultivating a workplace that values diverse experiences backgrounds and ideas we create an environment where every employee can contribute their best.

Moderna is committed to offering reasonable accommodation or adjustments to qualified job applicants with disabilities. Any applicant requiring an accommodation or adjustment in connection with the hiring process and / or to perform the essential functions of the position for which the applicant has applied should contact the Accommodations and Adjustments team at .

Required Experience :

IC

Key Skills

Computer,IT Audit,CAD CAM,ABAP,Exterior Designing,HR Operations

Employment Type : Full-Time

Experience : years

Vacancy : 1