Fixed-Term Manufacturing Associate - Shift Position
Fixed-Term Manufacturing Associate - 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 endeavor contributing to a future where access to lifesaving vaccines is a reality for all.
We are seeking a skilled Manufacturing Associate and digitally savvy Operator to join our mRNA vaccines production unit. The successful candidate will operate the production equipment in accordance to cGMP compliance as well as health and safety regulations. The role requires excellent technical skills a scientific way of thinking a rapid learning capacity for new technologies in mRNA and meticulousness.
The Manufacturing Associate will be expected to demonstrate digital proficiency be comfortable working in a highly technological environment where their participation in improvements and innovations will be regularly required.
This role is central to Modernas mission of producing safe effective vaccines and requires a balance of scientific understanding operational skills collaboration and digital acumen. The ideal candidate is a team player who will maintain meticulous attention to detail and participate actively to operational excellence in our fastpaced and dynamic environment.
Heres What Youll Do:
Your key responsibilities will be:
Adhering to Modernas safety procedures and maintaining housekeeping of assigned areas to ensure compliance and safety.
Executing operations activities according to current good manufacturing practices (cGMP) standard operating procedures and manufacturing documentation.
Collaborating closely with QA peers for timely closure of documentation related to commercial batch disposition.
Participating in investigations (RCA) and CAPA tasks to address deviations and compliance issues.
Utilizing performance tools in collaboration with the team to meet operational KPI objectives.
Responding to and troubleshooting routine equipment process and digital issues rapidly.
Your responsibilities will also include:
Proactively identifying and reporting compliance or health and safety issues to supervisors.
Keeping training records and documentation up to date.
Performing routine maintenance tasks (e.g. lubrication mechanical checks filter changes) using hand tools.
Flexibility to work offhours and overtime when necessary.
Contributing to multiple projects and continuous improvement initiatives in a fastpaced environment.
Collaborating effectively in a dynamic crossfunctional matrix environment.
The key Moderna Mindsets youll need to succeed in the role:
We pivot fearlessly: In this role flexibility and adaptability are key as you will need to adjust quickly to new technologies and challenges within the rapidly evolving field of mRNA production.
We push past possible: Success in this role requires a drive to overcome challenges and continuously seek improvement. The ability to move beyond comfort zones will be critical as you contribute to process innovations and operational excellence.
Heres What Youll Need:
3 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.
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
Modernas working hours and shift patterns are currently under review to best support the business when in 24/7 working operations. The below pattern will be used whilst Moderna are running manufacturing campaigns. Outside of this the shifts would then revert back to a more standard Monday to Friday operational model.
24 /7 Fixed shift Pattern:
What is a 223 work Schedule
The 223 or the Panama schedule is a slow rotation cycle of 28 days where each employee works in a 12 hour shift every day.
The schedule usually involves 4 teams who work for 2 days then get 2 rest days followed by 3 days of work.
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 modernatx/careers 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
