Original Beschreibung
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# GRCD-0, Senior Manager Global Regulatory Affairs CMC
Work Your Magic with us!
Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us.
United As One for Patients, our purpose in Healthcare is to help create, improve and prolong lives. We develop medicines, intelligent devices and innovative technologies in therapeutic areas such as Oncology, Neurology and Fertility. Our teams work together across 6 continents with passion and relentless curiosity in order to help patients at every stage of life. Joining our Healthcare team is becoming part of a diverse, inclusive and flexible working culture, presenting great opportunities for personal development and career advancement across the globe.
**Your role:**
You are responsible for driving all CMC Regulatory activities for assigned large molecules (biotech) commercial products and projects worldwide. In this role you develop, author and own the relevant Global Regulatory CMC Life Cycle Strategy and all CMC Dossier types, such as NDAs/MAAs, variations, amendments, renewals, annual reports, and answers to health authority questions.
You serve as the contact point for CMC Regulatory topics and act as liaison in-between technical CMC-, quality-, supply- and Regulatory Affairs functions and provide strategic support and advice to the CMC team, the Global Regulatory Strategy Team (GRST), the Global Product Supply Team (GPST), and other cross-functional project teams (e.g. Tech Transfer Project Team). Upon collecting and interpreting country-specific regulatory CMC requirements you translate them into deliverables. You plan and align CMC Regulatory activities and develop submission roll-out and implementation plans, in close collaboration with key stakeholders.
You are the expert for CMC regulations, guidance, regulatory trends and competitive environment, including accelerated pathways, and CMC innovations and lead and participate in internal and cross-functional, international initiatives.
**Who you are:**
* University degree in Life Sciences such as Biochemistry, Biotechnology or a related discipline (minimum MSc or equivalent degree), higher degree preferable (e.g. PhD in a scientific discipline)
* 4 to 9 years of CMC regulatory and/or CMC technical experience within the pharmaceutical / biotech industry (e.g. in regulatory affairs, quality control, analytical development or manufacturing / process development)
* Ability to develop and prepare successful regulatory CMC strategies for variations, renewals, or new registrations (new MAAs)
* Experience in preparation and management of regulatory CMC documentation, such as a full international submission (new product application) or complex variations
* Practical experience in one of the following areas: manufacturing process development, technical transfers, validation or analytical development, control strategies
* Sound understanding and in-depth knowledge of global pharmaceutical legislation
* Ability to work in teams, good interpersonal skills
* Assertive, proactive, flexible, speak up personality
* Ability to think strategically
* Excellent written and spoken communication skills in English (knowledge of other European languages such as French, Italian or German is an asset)
**What we offer:** We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We believe that this variety drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress!
Job Requisition ID:
289651
Location:
Eysins
Career Level:
D - Professional (4-9 years)
Working time model:
Full-time, Part-time possible
**North America Disclosure**
The Company is committed to accessibility in its workplaces, including during the job application process. Applicants who may require accommodation during the application process should speak with our Candidate Services team at 844-655-6466 from 8:00am to 5:30pm ET Monday through Friday. If you are a resident of a Connecticut or Colorado, you are eligible to receive additional information about the compensation and benefits, which we will provide upon request. You may contact 855 444 5678 from 8:00am to 5:30pm ET Monday through Friday, for assistance.
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