Senior Manager, Clinical Quality Assurance Compliance (Remote)
BioNTech SE
We guide you through the promising world of immunotherapies. Find info on basic research and new developments of new treatment options.
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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.
Senior Manager, Clinical Quality Assurance Compliance (Remote)
The Senior Manager Clinical QA Compliance position supports and oversees the proactive and risk-based Quality Strategy implementation in the clinical development activities within a specific portfolio.
Provide quality oversight in the following areas
• Support and collaborate with key stakeholders in a study team to ensure that risks are detected and remediated.
• Provide guidance to day-to-day questions arising from Clinical trial deliverables.
• Interact with CROs to ensure adequate quality oversight on clinical activities.
• Provide guidance to Clinical Development Operations to support initiatives relevant to outsourced activities.
• Support inspection preparation activities in collaboration with other QA functions.
• Provide support for audits and inspections, as well as, follow-up activities including CAPA preparation.
What you have to offer
• At least 3-5 years of experience in Good Clinical Practice (GCP) and/or Quality Assurance Environment in Pharmaceutical Clinical Development or Clinical Research Organization.
• Knowledge of worldwide regulations (including FDA, EMA) related to clinical development and post approval.
• An academic degree in Life Science
Benefits for you:
BioNTech USis 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
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 subsidized 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 locationCambridge (Boston)and simply send us your application documents using our online form.
*BioNTech does not tolerate discrimination, favoritism, or harassment based on gender, political opinion, religion or belief, nationality, ethnic or social origin, age, sexual orientation, marital status, disability, physical appearance, health status or any other aspect of personal status. We are committed to creating a diverse and inclusive environment and are proud to be an equal opportunity employer. Most important – it’s a match!
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