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    Manufacturing Senior Scientist - Oxford, Oxfordshire, United Kingdom - Moderna Therapeutics

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    Description
    Senior Scientist (Ligand Binding/HAI) page is loaded Senior Scientist (Ligand Binding/HAI)
    Apply locations Oxford - England Clinical Development time type Full time posted on Posted 2 Days Ago job requisition id R15277

    The Role:

    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.

    Our mission is to establish a leading-edge research, development, and manufacturing facility as 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.

    Moderna is seeking a talented, experienced, and motivated Senior Scientist to join the Immuno-Assays group to serve as a scientific expert and point of contact for the oversight of Immuno-Assay development, qualification/validation to support programs across multiple therapeutic areas.

    The Senior Scientist will lead a team in the design and execution of immunoassay development, qualification or validation, and the running of clinical samples to return high-quality data for clinical trials conducted by Moderna.

    Providing scientific strategies to implement new immune assays (MSD, ligand binding, Multi/single plex assays).
    Serving as a lead in the execution of multiple projects requiring immunoassay expertise.
    Demonstrating technical excellence and advancing high-quality scientific principles in immunoassays.
    Performing quality review of experimental reports and ensuring staff compliance with safety and regulatory guidelines.
    Researching scientific and technical literature to propose and implement innovative solutions applicable to the Laboratory.
    Assessing staff strengths and development needs, assigning projects accordingly.
    Identifying and resolving quality issues and performing quality review of study reports.

    Your role will require effectively managing multiple tasks and projects concurrently, ensuring the best outcomes through a comprehensive approach.

    Demonstrating the capacity to drive both strategy and execution, adapting swiftly to new data and changing priorities.
    2+ years in immunology or related field) or MSc with more than 4-6 years' experience in conducting assay validation in clinical Immunology under GLP/GCLP environment.

    A background in infections in diseases or oncology and experience with handling laboratory pathogens as containment level 3 is an advantage.

    Candidate will be curious in exploring new technology, bold in proposing creative experimental designs and ideas. Possess strong computational skills, preferably experienced with Word, Excel, Power Point, GraphPad Prism
    Knowledge of system software for data analysis and statistical analysis.
    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
    Generous paid time off, including vacation, bank holidays, volunteer days, sabbatical, and a discretionary year-end shutdown

    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.If you want to make a difference and join a team that is changing the future of medicine, we invite you to visit modernatx.

    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.

    Moderna is an E-Verify Employer in the United States. 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. Moderna is committed to offering reasonable accommodations to qualified job applicants with disabilities.

    Any applicant requiring an accommodation in connection with the hiring process and/or to perform the essential functions of the position for which the applicant has applied should make a request to the Talent Acquisition Partner or contact the Accommodations team at .

    Senior Scientist (Cell based)
    locations 2 Locations time type Full time posted on Posted 2 Days Ago Senior Scientist, LCMS
    locations 2 Locations time type Full time posted on Posted 2 Days Ago Principal Scientist Clinical Cytometry

    locations 2 Locations time type Full time posted on Posted 2 Days Ago At Moderna we are pioneering the development of a new class of drugs made of messenger RNA (mRNA).

    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.

    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

    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.

    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.

    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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