Director Global Regulatory Affairs

BioNTech; City of London; On-site; GBP 60,000 - 80,000; Full time

Job summary

A leading biotechnology company is seeking a Director of Global Regulatory Affairs to lead oncology development projects. This role requires a university degree in natural sciences and over 9 years of regulatory affairs experience. Responsibilities include defining regulatory strategies and interacting with authorities. The company offers competitive remuneration and a commitment to a diverse and inclusive work environment.

Benefits

Competitive remuneration packages

Variety of benefits for diverse employee base

Qualifications

• 9+ years of experience in Regulatory Affairs in relevant roles.
• Experience in development of antibody- and ADC-based cancer therapies.
• Knowledge of multidisciplinary functions involved in drug development.

Responsibilities

• Act as Global Regulatory Lead for assigned development projects.
• Define the strategy for regulatory interactions with authorities.
• Coordinate preparation and reviewing of documents and dossiers.

Skills

Team-oriented mindset

Solution-oriented mindset

Business fluent English

Education

University degree in natural sciences

Job description

Director Global Regulatory Affairs (Oncology)

Mainz, Germany; London, United Kingdom; Munich, Germany | full time | Job ID:9340

You will act as the Global Regulatory Lead for assigned development projects by defining and executing the Regulatory Strategy including the Health Authority Interaction strategy and developing the storyline for regulatory applications and dossiers during product development up to marketing authorization (optional: act as US IND agent for assigned projects).

Your main responsibilities are:

• Act as Global Regulatory Lead for assigned development projects and define and execute the Regulatory Strategy from clinical development up to (including) marketing authorization.
• Define the strategy for regulatory interactions for the assigned projects. Plan, prepare and conduct interactions with national authorities and supra‑national agencies (e.g. MPA, PEI, EMA, FDA, as well as WHO when relevant) in the scope of product development incl. market authorization.
• Define the storyline for regulatory applications and dossiers through product development up to marketing authorization.
• Coordinate preparation, writing and reviewing of documents and dossiers (e.g. briefing books, IBs, BLA/MAA).
• Contribute to the setup, adjustment and continuous optimization of regulatory processes, systems and interfaces; represent GRA in cross‑functional initiatives for process improvement and with collaboration partners.
• Supervision of vendors active in regulatory affairs on behalf of BioNTech.
• Monitor changes and evolution in the regulatory landscape for relevant product and/or product classes; analyze the impact of new regulations on assigned projects; contribute to build transparent relationships with Regulatory agencies for the assigned projects.

What you have to offer:

• University degree in natural sciences (medicine, pharmacy, chemistry, biotechnology, biology or equivalent) followed by 9+ years of working experience in Regulatory Affairs in relevant roles/positions.
• Experience in the development of antibody‑ and ADC‑based cancer therapies; novel‑novel combination therapy and companion diagnostic development experience a plus.
• Team‑oriented and solution‑oriented mindset is expected.
• Experience in regulatory strategy planning and proven ability to plan, coordinate and lead activities.
• Knowledge of multidisciplinary functions involved in drug development.
• Business fluent English is a must.

BioNTech is committed to the wellbeing of our team members and offers a variety of benefits in support of our diverse employee base. We offer competitive remuneration packages which is determined by the specific role, location of employment and also the selected candidate’s qualifications and experience.

Note: The availability, eligibility and design of the listed benefits may vary depending on the location. The final requirements for the individual use of our benefits are based on the company's internal policies and applicable law.

How to apply:

Apply now by sending us your application documents including Curriculum Vitae, copy of ID, copies of degree certificates and professional certificates, motivation letter as well as your contact details via our online form.

Please note:

Only applications sent via our online form shall be considered. By submitting your application, you acknowledge that a background check will be conducted as part of the recruitment process in accordance with applicable laws and regulations. If you are considered for the position, BioNTech will conduct the background check through our service provider ‘HireRight’. You will be informed accordingly by your BioNTech‑Recruiter.

We are looking forward receiving your application.

BioNTech does not tolerate discrimination, favoritism or harassment based on gender, political views, religion or belief, nationality, ethnic or social origin, age, sexual orientation, marital status, disability, physical appearance, health status or any other physical or personal characteristics. BioNTech is committed to creating a diverse and inclusive work environment. We are proud to be an equal opportunity employer. The main thing is that you suit us, and we suit you!