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QC Specialist I/II


Become a member of the BioNTech Family!

Based in Cambridge, MA and Gaithersburg, MD. We are committed to improving the health of people worldwide with our fundamental research and our work in the area of development of immunotherapies utilizing the full potential of the immune system to fight cancer, infectious diseases and other serious diseases. We believe in scientific rigor, innovation and passion as driving forces. BioNTech was founded by scientists and physicians to translate science into survival by combining fundamental research and operational excellence.

With decades of deep immunology expertise and experience in developing and optimizing mRNA as part of its broad suite of novel technologies, the company is working with the global community to defeat life-threatening and serious diseases such as cancer, COVID-19, malaria and tuberculosis. The first ever approved mRNA vaccine was created in the labs of BioNTech in Mainz, Germany. A fully integrated immunotherapy powerhouse. We remain focused on bringing our broad pipeline of next-generation immunotherapies and vaccines to people around the world to address cancer, infectious diseases, as well as a growing list of other medical conditions. To accomplish this, we continue to be deeply rooted in science and academic research while also having built a fully integrated, global immunotherapy company with cGMP and GMP manufacturing facilities anchored around deep expertise in immunology and complemented by an expanding set of capabilities.

 

 

QC Specialist I/II 

 

Primary responsibilities include:

  • Execute analytical methods/SOPs and operate equipment and instruments supporting ELISA, qPCR, ddPCR assays, cell bioassays and Flow Cytometry.
  • Support technical transfer of analytical methods, including comparability testing and co-qualification.
  • Support quality system records, including deviations, lab investigations, OOS, CAPA and change control. 
  • Support QC equipment qualification for new lab equipment and perform routine maintenance of lab equipment and lab spaces.
  • Support review of QC documentation and logbooks.
  • Revise, and review SOPs, technical protocols, and technical reports.
  • Support QC training activities.
  • Support inspection readiness activities.
  • Lead and participate on teams to support new processes and improve existing processes in the QC labs.
  • Lead and support LEAN and 5S efforts as required.
  • Perform other duties as required, including ad-hoc projects to support site and QC team objectives.

 

What you have to offer. 
Requirements:

  • Master’s or Bachelor’s degree in sciences and
    • Level I:  0-2 plus years of experience in a GMP/QC lab setting
    • Level II:  2-4 plus years of experience in a GMP/QC lab setting
  • Experience with safe lab practices and the handling of biological material
  • Strong attention to detail and the ability to work cross-functionally
  • Excellent communication and organizational skills
  • The position will start as five eight-hour days but will move to four ten-hour days.

 

Preferred Requirements and skills:

  • Preferred knowledge of GMPs, GDPs, SOPs and Quality Control processes within a regulated QC laboratory.
  • Preferred knowledge of compendia and regulatory requirements for QC testing and validation pertaining to the pharmaceutical industry.
  • Familiar with analytical techniques such as Flow Cytometry, ELISA, PCR, cell bioassays and other applicable methods to the testing of biopharmaceuticals.
  • Familiar with requirements and strategies to support technology (tech) transfer of analytical methods.
  • Preferred knowledge of Quality Systems, including deviations, CAPA, change control, and document management systems.
  • Excellent interpersonal, verbal and written communication skills are essential in this collaborative work environment.
  • Comfortable in a fast-paced environment with minimal direction and able to adjust workload based upon multiple projects and changing priorities.
  • Proficient in MS Word, Excel, Power Point and other applications. 

 

 

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Benefits for you:
 

BioNTech US is committed to employee wellbeing and offers best-in-class benefits & HR programs to support an inclusive & diverse workforce. 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, Critical Illness Insurance

  • Pre-tax HSA & FSA, DCRA Spending Accounts

  • Employee Assistance & Concierge Program (EAP) available 24/7

  • Parental and Childbirth Leave & Family Planning Assistance

  • Sitterstream: Virtual Tutoring & Childcare Membership

  • Paid Time Off: Vacation, Sick, Bereavement, Holidays (including Floating) & Year-End U.S. Shutdown.

  • 401(K) Plan with Company Match

  • Tuition Reimbursement & Student Loan Assistance Programs

  • Wellbeing Incentive Platforms & Incentives

  • Professional Development Programs

  • Commuting Allowance and subsidized parking

  • Discounted Home, Auto & Pet Insurance

 

…and more! More details to be shared.


 

BioNTech is an equal opportunity employer and complies with all applicable federal, state, and local fair employment practices laws. BioNTech does not tolerate discrimination against employees or applicants because of race, color, religion, creed, national origin or ancestry, ethnicity, sex (including gender, pregnancy, sexual orientation, and gender identity), age, physical or mental disability, citizenship, past, current, or prospective service in the uniformed services, genetic information, or any other characteristic protected under applicable federal, state, or local law.

If you are unable or limited in your ability to use or access BioNTech’s online application tools due to a disability, you can request reasonable accommodations by calling 1-857-228-6231or by e-mailing jobs@biontech.de. Thank you for your interest in BioNTech.

 

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