(Fixed-Term) Manufacturing Associate, Drug Substance - Shift Position
(Fixed-Term) Manufacturing Associate, Drug Substance - Shift Position
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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 leadingedge research development and manufacturing facility at Harwell as part of a longterm 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 lifesaving vaccines is a reality for all.
As a Manufacturing Associate at our Harwell site you will operate cuttingedge production equipment supporting the safe and effective manufacture of Modernas mRNA vaccines. Working in compliance with cGMP and health and safety regulations you will play a pivotal role in ensuring batch quality and process integrity. This position combines scientific and operational expertise with digital fluency requiring attention to detail rapid learning agility and collaborative teamwork. You will directly contribute to innovations and continuous improvement in a technologically advanced production environment central to Modernas mission to transform medicine.
Heres What Youll Do:
Your key responsibilities will be:
Operate and monitor production equipment while adhering to cGMP SOPs and health and safety procedures
Maintain a clean compliant and safe work environment through strict adherence to gowning and housekeeping standards
Execute operations and maintain accurate manufacturing documentation for batch disposition
Perform routine equipment maintenance such as lubrication filter changes and mechanical checks using handtools
Troubleshoot digital and equipmentrelated issues rapidly and efficiently
Keep training records and operational logs up to date ensuring full compliance
Work flexibly including offhours or overtime to support manufacturing schedules
Take part in deviation investigations (RCA) CAPA tasks and contribute to incident analyses
Collaborate closely with QA and other crossfunctional teams to meet production KPIs
Your responsibilities will also include:
Practicing and promoting safe work habits in alignment with Modernas safety culture
Proactively identifying and reporting safety or compliance concerns to leadership
Participating in multiple projects and continuous improvement initiatives
Applying lean tools and digital platforms to drive operational excellence
Engaging in a fastpaced matrixed work environment with agility and a problemsolving mindset
The key Moderna Mindsets youll need to succeed in the role:
We digitize everywhere possible using the power of code to maximize our impact on patients.
Your comfort in using digital tools and platforms will be essential in Modernas highly automated production environment. From troubleshooting to operational logging youll be expected to leverage technology to enhance efficiency and product integrity.We behave like owners. The solutions were building go beyond any job description.
In this role every team member is expected to step up with initiative and accountability. Youll own your area of operation and contribute beyond task execution seeking opportunities to improve workflows and patient outcomes through proactive problemsolving.
Heres What Youll Need:
1 years of experience in a GMP manufacturing environment
A university degree with a specialization in Pharmaceutical production technology or equivalent
This position is sitebased requiring you to be at Modernas site fulltime. This position is not eligible for remote work.
As part of Modernas commitment to workplace safety this role may require an enhanced preemployment check.
Heres What Youll Bring to the Table:
Experience with filtration and chromatography and cold chain management a plus
Experience in audit / inspection preparation understanding Health authority and regulatory guidelines
Ability to collaborate fluidly with peers leadership and crossfunctional support groups required
Excellent written oral communication and organizational skills required.
Ability to maintain attention to detail while executing multiple tasks with minimal supervision
Demonstrated commitment to Modernas values of Bold Collaborative Curious and Relentless embodying these values in the workplace
At Moderna we believe that when you feel your best you can do your best work. Thats why our global benefits and wellbeing resources are designed to support youat work at home and everywhere in between.
- Quality healthcare and insurance benefits
- Lifestyle Spending Accounts to create your own pathway to wellbeing
- 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 yearend shutdown
- Savingsandinvestments
- Locationspecific 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 worldclass 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 inperson culture is critical to our success. Moderna champions the significant benefits of inoffice collaboration by embracing a 70/30 work model. This 70% inoffice 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 smokefree alcoholfree and drugfree 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 nondiscrimination 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.
Were 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 .
#LIJP1Required Experience:
IC
Employment Type
Full-Time
