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Analytical Compliance and Risk Program LeadUCB • bulle, freiburg, Switzerland
Analytical Compliance and Risk Program Lead

Analytical Compliance and Risk Program Lead

UCB • bulle, freiburg, Switzerland
Vor 20 Tagen
Stellenbeschreibung
ppWe are looking for an bAnalytical Compliance and Risk Program Lead /b who is bstrategic, collaborative, and quality-minded /b to join our team bAnalytical Industrialization Program / Industrialization Network Planning /b, based at our UCB campus located in bBraine-l’Alleud, Walloon Region, Belgium /b. /p h3About The Role /h3 pYou will lead a global analytical compliance and risk program that helps UCB anticipate regulatory expectations and strengthen analytical control strategies across the product lifecycle. You are going to shape governance, support consistent risk-based approaches, and ensure stakeholders have access to the right standards, processes, and training. In this role, you will help protect compliance across methods, specifications, stability, impurities, and analytical regulatory topics for commercial products and future lifecycle management activities. /p h3Who You Will Work With /h3 pYou will partner with cross-functional leaders across analytical, regulatory, quality, industrialization, and lifecycle management activities to balign expectations and accelerate decision-making /b. You will collaborate with subject matter experts, Corporate Process Owners, regulatory intelligence networks, and external industry groups to btranslate evolving expectations into practical standards /b. You will also represent UCB in expert forums and act as a trusted point of contact during audits, inspections, and regulatory discussions linked to analytical compliance. /p h3What You Will Do /h3 ul libChair /b the Analytical Compliance Risk core team and drive global alignment on priorities, decisions, and risk posture. /li liMaintain analytical compliance governance across methods, specifications, stability, impurities, and related regulatory topics. /li liAnticipate emerging risks through regulatory intelligence, benchmarking, and input from subject matter experts. /li liSecure compliant, consistent responses to pharmacopeial changes, monographs, audits, inspections, and authority questions. /li liCoach stakeholders and Corporate Process Owners on analytical compliance expectations, standards, and decision frameworks. /li liRepresent UCB in external expert groups and influence industry approaches to analytical compliance. /li /ul h3Interested? /h3 pFor this role, we are looking for the following education, experience, and skills: /p ul liYou hold a Bachelor’s, Master’s, or Ph.D. in a relevant scientific discipline. /li liYou bring at least 10 years of experience in the pharmaceutical or biotech industry. /li liYou have strong experience in analytical CMC and regulatory guideline implementation. /li liYou understand analytical control strategies, including methods, specifications, stability, impurities, and specification setting. /li liYou have experience with risk management and compliance in a global regulatory environment. /li liYou have supported audits, inspections, or responses to FDA, EMA, PMDA, or other health authorities. /li /ul h3What You Will Bring /h3 pThis is an opportunity to bshape enterprise standards, influence external thinking, and provide visible leadership /b in a role with direct impact on banalytical compliance, product quality, and regulatory confidence /b. For this role, we are looking for the following education, experience, and skills: /p ul liYou hold a Bachelor’s, Master’s, or Ph.D. in a relevant scientific discipline. /li liYou bring at least 10 years of experience in the pharmaceutical or biotech industry. /li liYou have strong experience in analytical CMC and regulatory guideline implementation. /li liYou understand analytical control strategies, including methods, specifications, stability, impurities and specification setting. /li liYou have experience with risk management and compliance in a global regulatory environment. /li liYou have supported audits, inspections, or responses to FDA, EMA, PMDA, or other health authorities. /li /ul pAre 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! /p h3About Us /h3 pUCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science. /p h3Why work with us? /h3 pAt 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 equal 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. /p pAt UCB, we’ve embraced a hybrid-first approach to work, bringing teams together in local hubs to foster collaborative curiosity. Unless expressly stated in the description or precluded by the nature of the position, roles are hybrid with 40% of your time spent in the office. /p pUCB is an equal opportunity employer. All employment decisions will be made without regard to any characteristic protected by applicable laws. /p pShould you require any adjustments to our process to assist you in demonstrating your strengths and capabilities contact us on Please note should your enquiry not relate to adjustments; we will not be able to support you through this channel. /p /p #J-18808-Ljbffr
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Analytical Compliance and Risk Program Lead • bulle, freiburg, Switzerland

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