Regulatory Affairs PM

Join Our Team at Bonus BioGroup – Regulatory Affairs PM

About Us

Bonus BioGroup is a cutting-edge, clinical-stage biotechnology company applying innovative cell-based technologies to develop advanced therapies and tissue-engineered products. Our mission is to transform the future of medicine through science and innovation.

Position: Regulatory Affairs Project Manager

We are looking for a highly motivated and detail-oriented Regulatory Affairs Project Manager to join our Regulatory Affairs team. This is a unique opportunity to be part of a dynamic environment shaping the development and registration of breakthrough therapies.

Key Responsibilities

• Contribute to both global and local regulatory strategies and activities
• Collaborate cross-functionally with teams across the organization
• Support product development and regulatory registration processes
• Prepare and manage documents and submission packages for regulatory authorities
• Interpret and apply current regulatory requirements, guidelines, and standards
• Ensure company practices comply with evolving regulatory expectations

Qualifications & Requirements

• Ph.D. in a relevant scientific field (M.Sc. with strong experience will be considered)
• Background in the pharmaceutical or biotechnology industry – an advantage
• Strong scientific and analytical skills with a fast-learning curve
• Proven ability to work independently and meet deadlines with precision
• Excellent organizational and communication skills
• High attention to detail and ability to manage multiple tasks
• Fluent in English, both written and spoken
• Proficient in standard office and documentation software

Please reach us at: https://bonus-bio.com/  CV.Bonusbio@bonus-bio.com 

Additional Details

• Reports to: VP of Regulatory & Clinical Affairs
• Employment Type: Full-time, on-site
• Location: MATAM High-Tech Park, Haifa