Regulatory Cmc Scientist

1 week ago

Toronto, Canada UCB S.A. Full time

**Make your mark for patients**

We are looking for a **Regulatory CMC Scientist - Biologics** to join us in our **Global Regulatory** team, based in any of our **Brussels** (Belgium), **Monheim** (Germany), **Slough** (UK), **Raleigh** or **Atlanta** (US) or **Toronto** (Canada) offices.

As a **Regulatory CMC Scientist - Biotech products,** you will have the following responsibilities:

- Define the strategy, planning and preparation (writing and review) of CMC submission documentation for regulatory submissions from a global/regional perspective to achieve timely approvals to meet business needs.
- Provide regulatory CMC leadership on the cross functional sub teams (Global Regulatory Affairs (GRA) Teams and Supply & Technology Solutions (S&TS) Teams) and advise on best practices and/or supports Commercial Teams, as assigned by the GRA-CMC&Devices Leadership Team.
- Contribute and ensure adequate provision of regulatory CMC input to all Health Authority (HA) interactions on CMC matters in all regions
- Ensures effective communication of CMC regulatory strategy, risks, and overall plan to GRA Teams, S&TS Teams and Development and Commercial Teams
- Highlights anticipated and ongoing critical issues arising through the product life cycle in a timely manner to GRA-CMC & Devices LT to enable communication to key stakeholders (including S&TS Teams, GRA Teams, PV solution teams)
- Lead or provide input to internal regulatory business initiatives and/or cross functional work streams as assigned by the GRA Leadership Team

Interested? For this position you’ll need the following **education**, **experience** and **skills**:

- Bachelor’s degree, Master’s preferred in a relevant life science or business-related discipline
- Significant relevant experience in the pharmaceutical industry preferably in Regulatory Affairs CMC and/or in pharmaceutical manufacturing, analytical development, and quality assurance/control or related technical field, or a regulatory authority in a CMC review capacity
- Proven track record of successful authoring and contribution to delivering CMC sections of marketing authorisations for new biological and/or chemical entities
- Knowledge of GMP requirements and standard systems (e.g. change management systems and tools)
- Demonstrated competence in contributing on cross-functional teams and operating within a matrix organisational structure
- Effective interpersonal, presentation and communication skills with established internal and external stakeholders
- Proven leadership, problem-solving ability, flexibility, influence, and effective teamwork skills.

RANDATUCB

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you

**About us**
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are around 8,500 people in all four corners of the globe, inspired by patients and driven by science.

**Why work for us?**
At UCB, we don’t just complete tasks, we create value. We aren’t afraid to push forward, collaborate, and innovate to make our mark for patients. We have a caring, supportive culture where everyone feels included, respected and has equitable opportunities to do their best work. We ‘go beyond’ to create value for our patients, and always with a human focus, whether that’s on our patients, our employees or our planet. Working for us, you will discover a place where you can grow, and have the freedom to carve your own career path to achieve your full potential.

**Learn more** about sustainability at UCB and how it is integrated into our business approach.

UCB and its subsidiaries encourage diversity and inclusion in the workplace; we are an Equal Opportunity Employer. We do not discriminate on the basis of race/colour/religion/sex/national origin/veteran/disability/age/sexual orientation/gender identity.

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