Manufacturing Associate, Drug Substance, Day Shift - Oxford, United Kingdom - Moderna
Description
We are excited to announce that we are expanding our team and have multiple positions available for this role - join us in shaping the future*
The Role:Joining Moderna offers the unique opportunity to be part of a pioneering team that's revolutionizing medicine through mRNA technology with a diverse pipeline of development programs across various diseases.
As an employee, you'll be part of a continually growing organization working alongside exceptional colleagues and strategic partners worldwide, contributing to global health initiatives.
Moderna's 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.
Moderna's strategic partnership with the UK Government is exemplified by our innovative presence at Harwell.Our mission is to establish a leading-edge research, development, and manufacturing facility, 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 and NHS partners across the UK.
We're looking for global experts eager to join us in this endeavor, contributing to a future where access to life-saving vaccines is a reality for all.
As a Manufacturing Associate in the Drug Substance division at Moderna's Manufacturing Site in the UK, you will play a crucial role in the production of mRNA vaccines.
You'll be an integral part of a team dedicated to producing safe and effective vaccines, upholding strict cGMP compliance and contributing to operational excellence in a dynamic, technology-driven environment.
Here's What You'll Do:
Within 3 Months, You Will
Master safe work practices and adhere to Moderna's safety procedures and guidelines.
Get accustomed to gowning procedures and maintain housekeeping standards in your assigned area.
Begin participating in incident investigations and CAPA tasks.
Within 6 Months, You Will
Execute operational activities with adherence to cGMP, SOPs, and manufacturing documentation.
Collaborate closely with QA for documentation closure needed for commercial batch disposition.
Engage in troubleshooting routine equipment, process, and digital issues promptly.
Within 12 Months, You Will
Actively participate in investigations of deviations and CAPA tasks.
Maintain training records and associated documentation.
Contribute to continuous improvement projects, demonstrating agility and adaptability in a fast-paced environment.
Here's What You'll Bring to the Table:
Typically, 3-5+ years of experience in a GMP manufacturing environment
A College degree with a specialization in Pharmaceutical production technology or equivalent
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 cross-functional support groups required
Excellent written, oral communication, and organizational skills required.
Ability to maintain attention to detail while executing multiple tasks with mínimal supervision
Demonstrated commitment to Moderna's values of Bold, Collaborative, Curious, and Relentless, embodying these values in the workplace
Moderna offers personalized benefit programs and well-being resources as unique as our global workforce so employees can do their best work.
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, and a discretionary year-end shutdown
Educational resources
Savings and investments
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.
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 BiophaMore jobs from Moderna
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