Section Lead & Center of Excellence (CoE) Strategy Realization job opportunity at Roche.

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DateMore Than 30 Days Ago bot
Roche Section Lead & Center of Excellence (CoE) Strategy Realization
Experience: 6-years
Pattern: full-time
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degreeAssociate
loacation Basel, Switzerland
loacation Basel....Switzerland

At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters. The Position In Pharma Technical Development PTD, we collaborate to develop robust manufacturing processes and quality control systems to efficiently transform scientific ideas into products. We reliably deliver quality products to patients enrolled in clinical studies around the world. We excel in our work by creating an engaging and inclusive environment where everyone can bring their skills and talents to developing innovative medicines.   As a Section Lead & Center of Excellence (CoE) Strategy Realization in Drug Product Synthetic Molecules Parenterals, you are part of the Department “Pharmaceutical Development” in Pharma Technical Development (PTD) in Basel, Switzerland. The department Pharmaceutical Development is responsible for the development of parenteral drug products (Synthetic molecules and Biologics) from Phase 1 through Launch. Activities encompass formulation and manufacturing process development for parenteral drug products for all clinical stages and the market launch, the transfer of product and process to commercial manufacturing sites, commercial product support and line extension development.  The Opportunity This new leadership position is essential for the refinement of the DP SM Parenterals organization. The role is designed to bring clear focus and execution to formulation and process development strategies, while ensuring the team establishes and maintains the necessary capabilities and knowledge management to deliver a complex and growing SM parenterals portfolio. The successful candidate will be accountable for: Delivering Portfolio Strategy and Driving Scientific Excellence: Providing clear focus and execution on formulation and process development strategies to successfully deliver the complex and growing SM parenterals portfolio.  Act as a Pharmaceutical Development SPOC for the Research organizations and provide CMC risk assessment and mitigations for molecules entering the portfolio.  Leading, Developing, and Managing Capabilities: You will lead a team of four associate scientists, fostering a collaborative, supportive, and high-performing environment. You will take responsibility for lab equipment capabilities needed to deliver SM DP parenterals.   Ensuring E2E Connectivity and Strategic Influence: Working closely with cross-functional partners (Research organization, CMC experts, Pharmaceutical Development departments) to ensure End-to-End (E2E) connectivity.   CoE Strategy Realization and Unwavering Quality: Acting as the Team Lead & CoE Strategy realization , leading the team's operational focus and strategic direction toward meeting the CoE requirements. Ensure all experimental work in the laboratory adheres to stringent quality standards, maintaining data integrity for non-GMP data in close collaboration within Pharmaceutical Development and Partner functions (e.g. Analytical Development). Who you are You bring the following key skills, combining technical depth with leadership and strategic vision: Parenteral Expertise: Deep scientific expertise (Ph.D./Master's with 6 years of industry experience) in formulation and process development for parenteral dosage forms.   Team Leadership and Development: Proven ability to lead and inspire a scientific team, manage experimental work, and provide dedicated leadership support for people development and clear accountabilities   Regulatory and Quality Compliance (CMC): Direct experience in writing and reviewing regulatory CMC source and submission documents (e.g., NDA/CTA DP sections), with strong understanding of regulatory landscapes (e.g., ICH guidelines).   Strategic Problem-Solving: A proven team player with a problem-solving mindset and the ability to think end-to-end and globally, managing multiple parallel projects with a structured and rigorous approach.   Analytical methods:  Deep expertise in analytical methods to characterize liquid formulations for synthetic molecules Are you ready to make an impact? Please apply by submitting your updated CV and cover letter via our careers portal.     Who we are A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact. Let’s build a healthier future, together. Roche is an Equal Opportunity Employer.

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