Manager II - IT Compliance Lead

At Bristol Myers Squibb, our employees often ask, “Who are you working for?”—a question that fuels collaboration, accountability, and urgency in our work. Our purpose-driven culture inspires us to discover, develop, and deliver innovative medicines to prevail over serious diseases. We offer uniquely interesting and meaningful work, opportunities for growth, and a supportive environment that values inclusion, wellbeing, flexibility, and comprehensive benefits. This is work that transforms the lives of patients, and the careers of those who do it. Integrated into the GPS IT Boudry department, Manager II - IT Compliance provides quality oversight on Boudry site IT systems and solutions through effective internal and cross-functional collaboration. Working location is Boudry, Switzerland. All activities will focus on the Boudry Manufacturing site facilities with potential cross-functional links with other Bristol-Myers Squibb sites. Drives risk-based activities, process improvements, and supports audits and remediation. Facilitates cross-functional collaboration, leads meetings on IT topics, and works independently across multidisciplinary teams to maintain continuous compliance and operational excellence. Duties/Responsibilities The accountability of the worker is the interpretation, implementation, and continuous monitoring of Company expectations to ensure robust quality systems and GMP compliance. Serves as the main point of contact between GPS IT Boudry team and QA Compliance team Communicate effectively on cross-departmental teams Promotes Quality Culture across all internal initiatives. Acts as a Quality Ambassador towards other functions and third parties to comply with BMS quality standards Has a comprehensive understanding of departmental goals, processes, and the ability to collaborate across functions. Ability to analyze and interpret data, identify gaps, and recommend solutions to support compliance, and regulatory objectives Oversee the strategy for Infrastructure qualification and GxP computerized systems, managing their lifecycle to ensure continuous compliance with regulatory and internal requirements. Supports Infrastructure integration on the Boudry site and ensure that the installation is compliant according to internal process. Assists the translation of compliance requirements into test conditions and expected results for application functionality, and acceptance testing (FAT, SAT, IQ, OQ, PQ) Supports or conducts deviation assessments and investigations pertaining to Information Technology. Proficient in writing reports/documents and presentations related to IT Compliance activities Manage local IT documentation, ensuring it stays aligned with the current state of IT systems and complies with both global and local requirements and quality standards. Provide training and serve as a mentor. Identifies, executes and leads process or system improvement projects Adopts a culture of ethics, leads by example and challenges non-compliance. Responsible for supporting site IT systems compliance, ensuring these are maintained in accordance with regulatory requirements (EU-GMP Annex 11 & 21-CFR part 11) and Computer System Validation (CSV) procedures. Oversees and defines quality expectations and provides support to the GPS IT department and 3rd parties to ensure effective implementation of systems that meet GMP requirements Anticipates and prioritize IT activities that support Quality Assurance based on risk-based approach Integrates risk management into the decision-making process for IT compliance activities. Supports Data Integrity program and remediation activities Facilitate meetings with business colleagues on IT topics Understands business objectives, processes, and strategies Able to work strategically and independently with internal and external groups on multiple simultaneous projects Qualifications Bachelor of Science degree required, minimum of 5-7 years of experience in the pharmaceutical or related industry Specific Knowledge, Skills, Abilities Pharmaceutical, Biotechnology, and Life Science industry experience is a must. 5 years’ experience in a similar role within pharmaceutical industry IT technical knowledge such as Operating System, Infrastructure and Networking and Systems. Broad working knowledge of Quality Management Systems Knowledge of GxP systems (MES, LIMS…) Education/Experience/ Licenses/Certifications University degree in Quality, Engineering, Sciences or another relevant discipline Expert in Computer System Validation (CSV) Deep knowledge of 21-CFR Part 11, EudraLex, MHRA Experience in Data Integrity requirements Fully operational in English, French language a strong plus Works independently or with minimal supervision. Autonomous in analysis, problem solving and achieving deliverables Exceptional Oral and Written communication Analytical and structured working style; strong attention to detail Ability to effectively work as part of a multidisciplinary, international team Hands-on personality We hire for skills and capabilities, not just credentials – if this role excites you, but doesn’t perfectly match your resume, we encourage you to apply anyway. How We Work Where you work matters – because collaboration, innovation and patient impact happen in many settings. Our roles are structured across four work models: site-essential, site-by-design, field-based and remote-by-design. The model assigned to this role is based on its core responsibilities. Learn more at . Supporting People with Disabilities BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to . Visit to access our complete Equal Employment Opportunity statement. 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