External Collaboration Expert
vor 4 Wochen
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.The PositionOur 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.The OpportunityLead the PTDC Analytical Outsourcing Strategy to support safe, cost-effective, and efficient external testing activities for direct materials, APIs, and Drug Products, ensuring full compliance with current Good Manufacturing Practices (cGMP) and Roche’s quality policies.Provide matrix leadership by guiding all PTDC-A professionals involved in external testing and coordinating activities to ensure seamless collaboration and high-quality results.Serve as the key contact for all analytical outsourcing within PTDC, working closely with cross-functional partners to develop and execute a cohesive, overall outsourcing strategy.Develop, implement, and roll out cGMP-compliant and non-GMP business processes for testing, and support audits and Health Authority inspections related to external testing topics.Define and monitor key performance indicators (KPIs) to track the performance of Contract Lab Organizations (CLOs) and Contract Development and Manufacturing Organizations (CDMOs), and define necessary actions to optimize performance.Continuously identify new externalization opportunities and scout for suitable CLOs, balancing cost, capabilities, and capacity to build strategic partnerships.Embody PT lean leadership principles, fostering a continuous improvement mindset and acting as a visible change agent to promote flexible and open-minded approaches to new opportunities.Actively contribute to strategic goal setting, hiring, and onboarding of new colleagues, while promoting a positive safety culture and proactive problem prevention.Who you areYou have a PhD or Master's degree in organic chemistry, analytical chemistry, pharmacy, or a related scientific field, or a Bachelor’s degree with significant relevant experience.You bring at least 10 years of experience in the pharmaceutical industry, with a minimum of 5 years in a leadership position (people or matrix leadership), and substantial experience working with external partners in a cGMP environment.You have a solid understanding of analytical chemistry, particularly synthetic molecules testing using techniques like HPLC, GC, dissolution, and titrations.You possess excellent knowledge of cGMP regulations and have proven experience with GMP inspections.You have strong negotiation skills and the ability to build and maintain excellent collaborative relationships with CDMOs and CLOs.You are comfortable with frequent changes and can manage parallel activities with full autonomy, drive, and ownership.You have solid project management skills, a systems-thinking approach, and a continuous improvement mindset.Ready to bring your unique qualities to Roche and make an impact? Apply now and join us in our mission to shape the future of healthcare.Who we areA 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. #J-18808-Ljbffr
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External Collaboration Expert
Vor 6 Tagen
Basel, Basel-Stadt, Schweiz Roche Vollzeit CHF 80'000 - CHF 120'000 pro JahrJOB DESCRIPTION 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...
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External Collaboration Expert
vor 4 Wochen
Basel, Schweiz F. Hoffmann-La Roche AG VollzeitAt 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...
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External Collaboration Expert
vor 4 Wochen
Basel, Schweiz Roche VollzeitAt 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...
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External Quality Operation Manager
vor 2 Wochen
Basel, Schweiz Sobi Vollzeit**Company Description** **_ At Sobi, each person brings their unique talents to work as a team and make a difference. We are dedicated to developing and delivering innovative therapies to improve the lives of people who live with a rare disease. Our edge comes from our team of people and our commitment to patients. Here at Sobi, our mission and culture get...
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Analytical Subject Matter Expert
vor 1 Tag
Basel, Schweiz Sobi Vollzeit**Key Responsibilities/Scope of the Job** **Shared responsibilities**: - Act as analytical lead when appropriate for managing analytical projects under his/her responsibility - Cross functional interaction/collaboration within Sobi organization. - Interaction/collaboration with CDMOs/CLOs as required by the projects. - Act as a technical expert for...
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Ewm and Tm Expert
Vor 7 Tagen
Basel, Schweiz Coopers Group AG VollzeitEWM and TM Expert For our Pharma client in the Basel area, we are currently looking for a EWM and TM Expert **Tasks & Responsibilities**: - Single point of contact for functional topics within the LAL system (in SAP EWM and/or SAP TM module) - Initiate and coordinate collaboration with Business, implementation partner and developer on functional design...
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QA Expert
vor 1 Woche
Basel, Schweiz Takeda Pharmaceutical Vollzeit**Takeda Neuchâtel** **Site de Production Biotech | Biotech Manufacturing Site** Takeda is an industry-leading, global pharmaceutical company with an unwavering dedication to putting patients at the center of everything we do. We live our values of Takeda-ism - Integrity, Fairness, Honesty, and Perseverance - and are united by our mission to strive...
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Api Operations Manager
vor 1 Woche
Basel, Schweiz Elanco VollzeitEducation : EQUIVALENTEXPERIENCE **As a leading global animal health company, Elanco delivers innovative products and services to improve the health of pets and farm animals around the world because we believe making animals' lives better, makes life better. Since 1954, we have provided solutions that support veterinarians, farmers and pet owners to advance...
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Quality Assurance Expert
vor 2 Wochen
Basel, Schweiz Takeda Pharmaceutical VollzeitTakeda is an industry-leading, global pharmaceutical company with an unwavering dedication to putting patients at the center of everything we do. We live our values of Takeda-ism - Integrity, Fairness, Honesty, and Perseverance - and are united by our mission to strive towards Better Health and a Brighter Future for people worldwide through leading...
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Expert Regulatory Writer
vor 1 Tag
Basel, Schweiz Novartis Vollzeit500! The number of regulatory documents we authored last year. As an Expert Regulatory Writer you will develop documents which cover all Novartis therapeutic areas and therapies, ranging from Phase I to IV Clinical Study Reports to regulatory submission documents (e.g. Clinical Summaries, Clinical Overview, Briefing Books, answers to Health Authority...