Specialist Manufacturing - Shift Position
Specialist Manufacturing - Shift Position
Employer Active
Job Alert
You will be updated with latest job alerts via email
Share
Job Alert
You will be updated with latest job alerts via email
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.
In this role you will be responsible for executing processing and combining mRNA and LMX/LNP for clinical pipeline products as well as commercial seasonal vaccines in a GMPregulated environment. You will act as a technical resource for the clinical and commercial drug substance manufacturing team applying fundamental and developing knowledge of bioprocess unit operations process engineering and digital systems.
This role requires participation in the development of operational procedures and training materials training of manufacturing associates technology transfer support and issue investigations while ensuring the progress monitoring of projects.
Heres What Youll Do
Your key responsibilities will be:
Ensuring compliance with GMP regulations guidelines and company policies.
Promoting safe work habits and adherence to safety procedures.
Executing tasks precisely as per Standard Operating Procedures (SOPs) and work instructions.
Maintaining Good Documentation Practices and Data Integrity for regulatory use.
Completing required training and requalification within the prescribed timelines.
Utilizing manufacturing support systems such as SAP VEEVA Delta V Syncade LIMS and CMMS.
Your responsibilities will also include:
Acting as a Qualified Trainer conducting OntheJob Training (OJT) for eBR review and unit operations.
Coaching the manufacturing team in process troubleshooting cGMPs and safety practices.
Supporting technology transfers crossfunctional projects and manufacturing operations.
Collaborating with process Subject Matter Experts (SMEs) to develop batch records SOPs and training materials.
Partnering with QA colleagues to ensure timely batch disposition deviation investigations and compliance reviews.
Managing equipment Out of Tolerance (OOT) responses and implementing CAPAs for deviations.
Leading change controls for team projects.
Handling purchasing and induction of simple equipment and tools.
Participating in equipment startup commissioning and validation activities.
The key Moderna Mindsets youll need to succeed in the role:
We behave like owners You will take responsibility for process troubleshooting and problemsolving ensuring that the solutions you implement improve operations beyond just your role. Your work will directly impact our ability to deliver highquality mRNA medicines efficiently and effectively.
We digitize everywhere possible As Moderna continues to push the boundaries of digital and automated manufacturing this role requires proficiency in digital systems such as SAP Delta V and LIMS ensuring seamless and data integrity in a highly regulated environment.
Heres What Youll Need Basic Qualifications)
STEM degree with 35 years industry experience or a Masters degree with 12 years industry experience
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 (Preferred Qualifications)
Strong understanding of GMP regulations.
A desire to make an impact as part of a highgrowth transformational company that is Bold Relentless Curious and Collaborative.
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:
Unclear Seniority
Employment Type
Full-Time
