At a Glance
- Tasks: Conduct microbiological testing and environmental monitoring in a cutting-edge GMP facility.
- Company: Join Moderna, a leader in mRNA technology and innovation.
- Benefits: Enjoy competitive healthcare, generous paid time off, and wellness resources.
- Other info: Collaborative culture with opportunities for mentorship and career growth.
- Why this job: Make a real impact in the future of medicine while growing your skills.
- Qualifications: BSc in a scientific discipline with 2 years of Quality Control experience.
The predicted salary is between 40500 - 49500 £ per year.
The Role
Reporting to the Manager, Microbiology, the Individual will perform routine environmental monitoring (EM) and water sampling of the GMP manufacturing facility. The analyst will also support microbiological testing for GMP QC raw materials, excipients, drug substances, and drug product intermediates for mRNA products produced at Moderna’s manufacturing facility and affiliated contract organizations. This position will contribute to related method transfers and qualification activities. The QC Analyst may perform projects as assigned.
Here’s What You’ll Do
- Perform routine environmental monitoring and critical utility sampling activities.
- Conduct analysis of water samples to include TOC, Conductivity, Bioburden and Endotoxin.
- Execute GMP QC Microbiology methods, focusing on Sterility testing, Bioburden analysis, Endotoxin, and other methodologies as needed.
- Support testing for release, stability, and method and verification/validation samples.
- Collaborate with AS&T groups on new methods transfers.
- Participate in method transfer projects for internal and external testing labs.
- Assist in development, implementation, and maintenance of general laboratory operational systems in accordance with cGMP requirements.
- Provide support to audit teams for internal and vendor audits.
- Prepare and ship/receive contract laboratory testing samples including those intended for microbiological identification.
- Perform general laboratory support activities including reagent preparation, equipment maintenance and housekeeping.
- May participate in equipment and method qualifications, validations, and method transfers.
- Perform data entry utilizing good documentation practices.
- May assist with troubleshooting assay methods and equipment.
- Supports more junior staff with data review, training, and troubleshooting.
- Participate in authoring quality systems records such as EM excursions, investigation, deviations, change controls, CAPAs; Write/revise SOPs, protocols, and reports.
- Foster a positive and inclusive work culture that promotes collaboration, innovation and continuous improvement.
- Follow all relevant GxP regulations, guidelines, and company policies to ensure compliance with regulatory and internal requirements.
- Execute tasks precisely as defined in internal guiding documents including but not limited to standard operating procedures (SOPs) and work instructions.
- Follow Good Documentation Practices and Data Integrity requirements to ensure data, documentation, and records are completed and maintained for use by the business and available to support audits or inspections.
- Complete training in assigned required learning plan according to the defined timing and the prescribed requalification cadence.
The Key Moderna Mindsets You’ll Need to Succeed in the Role:
- We obsess over learning. We don’t have to be the smartest—we have to learn the fastest.
- In a technically evolving Quality Control environment, your success will depend on your ability to rapidly absorb new testing technologies, regulatory standards, and evolving data workflows. Your mindset must be tuned to constant growth and curiosity.
- We digitize everywhere possible using the power of code to maximize our impact on patients.
- This role engages heavily with digital platforms like LIMS for sample tracking, inventory control, and data analysis. Embracing digital workflows and analytical tools is key to ensuring speed, precision, and scalability in QC operations.
Here’s What You’ll Need (Basic Qualifications)
- BSc in a relevant scientific discipline with a minimum of 2 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 prioritize and complete multiple projects and tasks in a fast-paced environment.
- Proven ability to conduct investigations.
As part of Moderna’s commitment to workplace safety, this role may require an enhanced pre-employment check. This position is site-based, requiring you to be at Moderna’s site full-time. This position is not eligible for remote work.
Pay & Benefits
At Moderna, we believe that when you feel your best, you can do your best work. That’s why our benefits and well-being resources are designed to support you—at work, at home, and everywhere in between.
- Competitive healthcare, plus voluntary benefit programs to support your unique needs.
- A holistic approach to well-being with access to fitness, mindfulness, and mental health support.
- Family building benefits, including fertility, adoption, and surrogacy support.
- Generous paid time off, including vacation, bank holidays, volunteer days, sabbatical, global recharge days, and a discretionary year-end shutdown.
- Savings and investments to help you plan for the future.
- 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, the infrastructure 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 people are the driving force behind our scientific progress and our culture. Together, 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 modernatx.com/careers 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 person's 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 leavesandaccommodations@modernatx.com.
Homebased Disability Analyst in Oxford employer: Moderna Therapeutics
Moderna Therapeutics is an exceptional employer located in Oxford, offering a dynamic work culture that fosters innovation and collaboration. With a strong emphasis on employee well-being and career development, the company provides a comprehensive benefits package and ample opportunities for professional growth, making it an ideal place for those passionate about advancing the future of medicine.
StudySmarter Expert Advice🤫
We think this is how you could land Homebased Disability Analyst in Oxford
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We think you need these skills to ace Homebased Disability Analyst in Oxford
Some tips for your application 🫡
Show Off Your Lab Skills:In the biotechnology field, it's super important to highlight your lab experience in your CV. Be sure to mention specific techniques or instruments you've mastered (think PCR, gel electrophoresis, etc.) and any relevant projects you've worked on. This will show Moderna Therapeutics that you have the hands-on skills they need.
Tailor Your Technical Skills:Make sure to emphasise your technical skills, especially those relevant to the biotechnology sector. Include any software tools or programming languages you've used, like R or Python for data analysis, which could be key for this role at Moderna Therapeutics.
Craft a Compelling Cover Letter:Since this is a full-time role, your cover letter should reflect not only your passion for biotechnology but also your long-term career ambitions. Share why you're excited about the work that Moderna Therapeutics does and how you envision contributing to their goals. This shows that you’re not just looking for any job, but you're genuinely invested in this opportunity.
Include Your Papers and Projects:If you've published any papers or contributed to significant projects, mention them! These documents can boost your application and provide tangible evidence of your expertise in the biotechnology field. Don’t forget to link to any relevant publications or project summaries—this can set you apart from other candidates.
How to prepare for a job interview at Moderna Therapeutics
✨Brush Up on Lab Techniques
Since you're eyeing a full-time gig in biotechnology, make sure you're well-versed in the lab techniques relevant to the role. Be ready to talk about PCR, CRISPR, or any specific methods mentioned in the job description at Moderna Therapeutics. You might even be asked to demonstrate your understanding of these processes.
✨Know Your Bioinformatics Tools
Get comfortable with bioinformatics tools that are commonly used in the industry, like BLAST or Bioconductor. These are key in biotechnology, and having hands-on experience or at least familiarity can set you apart. Prepare to discuss any relevant projects you've worked on, especially if they involved data analysis or genomic research.
✨Show Your Teamwork Skills
Biotech often involves collaboration across multiple disciplines. Be ready to share stories that highlight your teamwork and communication skills, especially in research projects. Think about working with different teams at university or any internships – this is where you can show how well you fit into Moderna Therapeutics's culture.
✨Research Recent Biotech Innovations
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