Product Manager for Chemistry Manufacturing & Control (CMC) - Biologics and Vaccines
Budapest, Hungary Permanent Posted on Dec. 13, 2024 Closing on Jan. 12, 2025- Location: Budapest
- Flexible working: 60% home, 40% office
- Job type: Permanent, Full-time
About the job
Are you ready to shape the future of medicine? The race is on to speed up drug discovery and development to find answers for patients and their families. Your skills could be critical in helping our teams accelerate progress.
We are an innovative global healthcare company with one purpose: to chase the miracles of science to improve people’s lives. We’re also a company where you can flourish and grow your career, with countless opportunities to explore, make connections with people, and stretch the limits of what you thought was possible. Ready to get started?
Join us as Product Manager for Chemistry Manufacturing & Control (CMC) - Biologics and Vaccines and you will play a critical role in support and manage the regulatory activities associated with the Chemistry, Manufacturing and Controls for licensed and clinical biologic products. This position will provide input into the product strategy and to the direction provided to commercial and clinical teams. You will be responsible for assuring the established regulatory strategy is aligned with Health Authority requirements from a global perspective and that regulatory submissions are on time and with high quality. Additional duties include coordination with our global manufacturing sites, integration of regulatory strategy with those sites and communication to senior management, also provide support for other CMC projects.
Main Responsibilities:
- New applications for biologics:
- Plan/Prep/Submit/Review support for product dossiers
- CTA / IND preparation and maintenance
- License Maintenance:
- Recurrent filings: annual reports (US, Canadian NDC and YBPR, license and renewals)
- Site renewals (ex. Japan Accreditation)
- Post Approval Supplements:
- Regulatory strategy development
- Preparing / Authoring / Review of Submissions – US, EU and Rest of World (ROW)
- Technical Review of site supporting documents (CoA, declarations, SMF, MBR, SOPs)
- Notify Reg Ops for publishing and dispatch
- Response to Queries – US, EU and ROW
- Interaction / liaise with EMA and EU member state on CMC topics
- Change Controls:
- Change control assessments
- Initiate change in regulatory database and follow-up with local regulatory representatives on the assessments of the change
- Provide interpretive analyses regarding impact of complex regulatory guidance documents, regulations, or directives that impact company products and operations
About you:
Experience:
- +3 years regulatory experience or relevant industry experience
- Manufacturing, QA/QC experience
- Previous experience working in a fast-paced , matrix environment on multiple product lines
- Biological products, vaccines or small molecules experience is preferred
Soft skills:
- Excellent organizational and communication (written and verbal) skills
- Demonstrated ability to work successfully on project teams
Technical skills:
- Knowledge of FDA/EMA regulations is preferred
- Proficient in MS Word, Excel, PowerPoint, MS Project
Education:
- Minimum Bachelor’s degree in Life Sciences or related or equivalent
- RAC certification is desirable but not essential
Languages
- Strong command of spoken and written English is mandatory
Why choose us?
- Bring the miracles of science to life alongside a supportive, future-focused team in an international work environment
- Work from an "Office of the Year 2023" award winner with flexible home office policy
- Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact
- Take good care of yourself and your family, with a wide range of health and wellbeing benefits including high-quality healthcare, prevention and wellness programs and at least 14 weeks’ gender-neutral parental leave
- An individual and well-structured introduction and training of new employees and we will dedicate a Buddy for you to better navigate in your first weeks
- Join a great community & special events (Monthly Board Game Nights, Summer Events, Well-Being Lectures & Sport Clubs)
Pursueprogress, discoverextraordinary.
Better is out there. Better medications, better outcomes, better science. But progress doesn’t happen without people – people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let’s be those people.
At Sanofi, we provide equal opportunities to all regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, or gender identity.
Watch our ALL IN video and check out our Diversity Equity and Inclusion actions at sanofi.com!
Discover our Code of Conduct, that serves as the moral compass that guides us when chasing the miracles of science to improve people’s lives. Please ensure to have read this document before applying.
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Pursue progress. Discover extraordinary.
Progress doesn’t happen without people – people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. You can be one of those people. Chasing change, embracing new ideas and exploring all the opportunities we have to offer. Let’s pursue progress. And let’s discover extraordinary together.
At Sanofi, we provide equal opportunities to all regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, or gender identity.
Watch 'One day at Sanofi' and check out our Diversity Equity and Inclusion initiatives at sanofi.com
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