Sr. Engineer I, Drug Product, Ms&T

Sr. Engineer I, Drug Product, MS&T page is loaded Sr. Engineer I, Drug Product, MS&T Apply locations Madrid - Spain Drug Manufacturing time type Full time posted on Posted 2 Days Ago job requisition id R15861 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 is solidifying its footprint within our international centre for analytical excellence in Madrid, a city known for its rich scientific heritage. This facility, the largest such center outside the United States, exemplifies our commitment to solidifying our manufacturing network and advancing our promising mRNA product portfolio. We're looking for talents who can contribute to our innovative research and development efforts.
This Sr. Engineer position is part of the Drug Product (DP) Moderna's Manufacturing Science and Technology (MST) team, tasked with technical support of GMP operations across international and US sites. Working under the guidance of the Director, you will play a crucial role in liaising with DP Contract Manufacturing Organizations (CMOs) and Moderna sites to drive forward the portfolio of projects and initiatives supporting commercial lifecycle management, technology transfer, and drug product technologies.
Here's What You'll Bring to the Table: Your key responsibilities will be: Supporting continuous improvement initiatives and complex technical projects for DP and Aseptic manufacturing operations globally.
Collaborating with Moderna's DP Operations to establish robust and compliant manufacturing performance at drug product CMOs.
Partnering with Technical development to investigate and resolve complex manufacturing issues at CMOs.
Your responsibilities will also include: Writing or revising the appropriate GMP documentations.
Automating, visualizing, and analyzing QC data and metrics, identifying trends and patterns, analyzing causality, formulating improvement proposals, and converting the insights with business teams to actions and plans for measurable business improvements.
Representing MST as a subject matter expert (SME) on DP manufacturing data analysis with Digital, Operations, and Technical Development teams.
Contributing to our process data management and overall knowledge management strategy.
The key Moderna Mindsets you'll need to succeed in the role: Prioritize the platform: Your work prioritizes our platform of mRNA technology, ensuring that every effort is aimed at enhancing our capability to deliver outstanding results.
Act with dynamic range: You'll need the ability to drive both strategy and execution simultaneously, adapting to new data and changing contexts swiftly and effectively.
Here's What You'll Need ( Basic Qualifications) MS or equivalent in a scientific, engineering or mathematical discipline with 5+ years' experience in the pharmaceutical industry, Ph.D level with 0+ years' experience. BS applicants with 8+ years' relevant experience will also be considered.
Proficiency in English required
Good communication skills (verbal and written) to collaborate with other CMC team members and managers in a dynamic, cross-functional matrix environment
Prior experience in aseptic manufacturing
Prior experience with DP operations and/or and Laboratory Instruments
Prior experience working in a GMP environment.
Technical agility. The capability to manage, and work with, diverse technical teams.
The ability to collaborate effectively in a dynamic, cross-functional matrix environment.
This position is site-based, requiring you to be at Moderna's site full-time. This position is not eligible for remote work.
Here's What You'll Bring to the Table (Preferred Qualifications) Preferred: Strong experience in creating statistical analysis models. Use of statistical programs for DOE analyses, multivariate analysis, and statistical process control.
Subject matter expertise on statistical best practices
A desire to make an impact as part of a high-growth, transformational company that is Bold, Relentless, Curious, and Collaborative. Moderna offers personalized benefit programs and well-being resources as unique as our global workforce so employees can do their best work. We recognize and appreciate your diverse needs and interests and do our best to support you at work and at home with:
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.
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 employment opportunity 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 also consider qualified applicants regardless of criminal histories, consistent with legal requirements.
Belonging, Inclusion, and Diversity are critical to the success of our company and our impact on society. We're focused on attracting, retaining, developing, and advancing our employees and believe that by cultivating diverse experiences, backgrounds, and ideas, we can provide an environment where every employee is able to contribute their best.
Moderna is committed to offering reasonable accommodations 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 ****** .
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At Moderna we are pioneering the development of a new class of drugs made of messenger RNA (mRNA). This novel drug platform builds on the discovery that modified mRNA can direct the body's cellular machinery to produce nearly any protein of interest, from native proteins to antibodies and other entirely novel protein constructs that can have therapeutic activity inside and outside of cells.
We have a clear mission to propel the field of mRNA science forward and deliver new medicines to patients and a unique vision for how to achieve this mission.
Our Mission: To deliver on the promise of transformative messenger RNA (mRNA) science to bring new medicines to patients.
Our Vision: To unlock the potential of mRNA by establishing an ecosystem of teams and partners that will work together to develop the broadest possible array of drugs, across diverse therapeutic areas and routes of administration, for serious diseases that are not treatable today.
Third Party Staffing Agencies M oderna does not accept unsolicited resumes from any source other than directly from candidates. For the protection of all parties involved in the recruiting process, resumes will only be accepted from recruiters/agencies if a signed agreement is in place at the inception of the recruiting effort and authorized for a specified position. Unsolicited resumes sent to Moderna from recruiters/agencies do not constitute any type of relationship between the recruiter/agency and Moderna and do not obligate Moderna to pay fees if we hire from those resumes.
Reasonable Accommodation Notice Moderna will make reasonable accommodations for qualified individuals with known disabilities, in accordance with applicable law.Applicants with disabilities may be entitled to reasonable accommodation under the terms of the Americans with Disabilities Act and certain state or local laws. Please inform the company's personnel representative by calling 617-460-9346 or emailing ****** if you need assistance completing any forms or to otherwise participate in the application process.Examples of reasonable accommodation include making a change to the application process or work procedures, providing documents in an alternate format, using a sign language interpreter, or using specialized equipment.
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