Senior Quality Engineer *

  • Gaithersburg, Maryland
  • Work experience
  • Quality Management, Quality Assurance
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Senior Quality Engineer*

Become Part of the BioNTech Family.

This position is based in Gaithersburg, MD at our newly formed clinical manufacturing site for BioNTech US. Together with the BioNTech US North American Headquarters in Cambridge, MA, both the Gaithersburg and Cambridge sites are an important part of our global effort to pioneer the development of next-generation immuno-oncology therapies that expects to experience significant growth in the near future. BioNTech US is a subsidiary of BioNTech SE with a strong foundation in Europe and a focus on the development of novel neoantigen-targeted T cell therapies, complementing BioNTech’s highly innovative scientific approach and diversified pipeline of transformative cancer medicines. As a key research and clinical development hub, BioNTech US will enable BioNTech’s growing presence in the US.

BioNTech is seeking an experienced, collaborative, and self-driven Senior Quality Engineer with focus on Quality Risk Management. This position has the responsibility to support, facilitate, or lead the Quality Risk Management program at BioNTech’s center of excellence for clinical Cell-Therapy manufacturing operations in Gaithersburg, MD. The Quality Engineer will serve as the Risk Management subject matter expert for the site, as well as a liaison with corporate Quality.

Here, you’ll achieve greatness.

 Responsibilities for the Senior Quality Engineer include:

·        Provide in-depth understanding and application of pharmaceutical quality risk management           practices and phase appropriate approaches within GMP manufacturing, GMP Facilities, and           GMP Quality Control.
·        Demonstrate knowledge of pharmaceutical relevant standards, principles and best practices.
·        Lead and guide cross functional teams in the use of available QRM tools, including HACCP ,           FMEA, PHA, , RR&F.
·        Collaborate with other departments (e.g. quality control, quality assurance, manufacturing,           facilities, product development,) to complete risk assessments. Leads teams in identifying             mitigations and ensuring traceability of identified mitigations.
·        Lead data analytics program for the site, including evaluation of product data (e.g. process           and/or product changes, deviations, CAPAs, complaints, etc.) for their impact to the current           quality risk management files.
·        Author and review quality risk management plans, reports, and risk assessments and                   supporting technical documents such as validation documentation and change control.
·        Provides training and guidance for risk management processes including suitable methods             for documentation.
·        Ensure that all procedures and work instructions for the Risk Management Program are                 followed at the site level.
·        Support maintenance of the the site quality risk registry.
·        Ensure periodic reviews of Risk Management Reports are performed according to schedule.
·        Report status and progress of quality risk management activities or projects to                             management. Track, review and report metric information.
         Support site Quality Engineering efforts and perform other duties as assigned


What you have to offer.

  • Minimum requirements; Bachelor’s OR Master’s Degree Degree and 4 plus years’ experience working in a Quality Engineering function within a pharmaceutical or FDA regulated environment

    Preferred Qualifications:
    ·        Knowledge of global regulatory agencies’ requirements for Quality Risk                       Management and Quality Systems (ICH Q9, GAMP5, 21CFR 11/210/211, etc.).
    ·        Demonstrated completion of risk assessments supporting GMP and Cell Therapy           applications.
    ·        Manage and follow-up on several projects and activities running in parallel.
    ·        Demonstrated and effective written and verbal communication skills.
    ·        Excellent technical writing experience in a regulatory environment. Must be                 detail oriented and exhibit a high degree of flexibility and initiative.
    ·        Ability to function efficiently in a diverse, fast paced, changing environment.
    ·        Must be able to work independently as well as part of a team.
    ·        Ability to think critically, and utilize troubleshooting and problem-solving skills.
    ·        Cell Therapy experience is a plus.

Benefits for you.

BioNTech US is committed to the well being of our team members and offers a variety of benefits supporting our diverse employee base. Salaried/Position-Targeted Hourly Employees working 30+ hours per week are eligible for our comprehensive benefits package. Benefits include but are not limited to:
  • Medical, Dental and Vision Insurance
  • Life, AD&D, STD and LTD Insurance
  • HSA & FSA Spending Accounts
  • Health & Wellness, including free onsite gym access
  • Adoption & Surrogacy Assistance
  • Vacation and Unlimited Sick Time
  • Holidays and Floating Holidays, including discretionary winter shutdown
  • 401(K) Plan with Significant Company Match
  • Tuition Reimbursement and Professional Development
  • Commuting Assistance and free onsite parking
  • Discounted Home and Auto Insurance
  • Pet Insurance
Plus more benefits that will be shared upon hire!

Have we kindled your pioneering spirit?

Then apply now for our location Cambridge (Boston) and simply send us your application documents using our online form.

For those who require assistance due to disability, or have questions prior to applying, please email

*BioNTech does not differentiate on the basis of gender, race or ethnicity, religion, color, sexual orientation or identity, disability, age and other protected statuses as given by applicable law. We are committed to creating a diverse environment and are proud to be an equal opportunity employer. Most important – it’s a match!