Head of Supplier Quality Management

Note: This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US. Your Role Lead the governance of the SQM system to ensure compliance with cGxP regulations, applicable ICH and ISO guidelines/standards, and Merck and LS standards and procedures Serve as a technical authority in drug regulations and industry standards specifically related to supplier quality to ensure consistency in interpretation of cGxPs throughout the business Develop and execute strategic plans to improve supplier quality and costs on a global basis Identify strategic initiatives to drive continuous improvement opportunities within the SQM system and harmonize procedures across sites globally to enhance efficiency Leverage close collaboration across different geographies (US, EU, UK, APAC) and proactively seek support from key stakeholders to obtain the required input and alignment with Quality strategies Responsible for ensuring compliance to regulatory standards in the conduct and reporting of work performed Create, manage, and drive effective plans to improve the culture of quality with defined actions, timelines, and KPI reporting to BioReliance CTS leadership, Quality and site leadership, or other Merck stakeholders as required Manage supplier quality resources in the areas of strategic sourcing, new product development, and at key suppliers ensuring the assessment, qualification, and approval process for suppliers are based on risk, QMS capabilities, and technical competence Provide oversight for supplier qualification activities including scheduling, planning, and conduct of supplier audits and participate in development and negotiation of Quality Agreements Manage supplier nonconformance, investigations, and corrective actions and preventive actions (CAPA) to resolve quality issues Evaluate supplier-initiated change notifications and conduct risk assessments for materials and services Collaborate, identify, and implement risk-based strategies to identify, assess, and mitigate QMS risks across the organization Participate in site readiness activities and provide SQM support in managing client audits, internal audits, and regulatory inspections Advocate and drive standardization of quality approaches and procedures across the global quality framework where appropriate Participate in or lead other activities as required by Senior Management. Financial Dimension Manage resource and financial planning to ensure alignment with business needs and quality requirements. Management of People Recruit, lead, train, and develop a high performing team to respond to business demands while ensuring compliance to quality and regulatory requirements Responsible for day-to-day management, setting objectives, coaching, developing employees, performance appraisal, and recommending employee compensation Actively manage the performance and development of teams using available tools and procedures, ensuring all team members have appropriate goals and objectives set. Who You Are Minimum Qualifications: Bachelor’s degree in a scientific discipline; advanced degree preferred Quality certification in auditing or a Quality related discipline 8+ years working in a cGMP/GLP environment/FDA/EMA regulated industry such as pharmaceutical and biopharmaceutical, devices and diagnostics and a track record of quality improvement and execution 5+ years of leadership in Quality Assurance in Bio/Pharmaceutical or Life Sciences industry Strong relationship building and negotiation strategies, ability to influence, network, drive and manage change. Previous experience in a client facing Quality role is preferred Working knowledge of 21 CFR 210 & 211, EU GMP, MHRA GLP & GMP, OECD GLP, ICH Q7, ISO 9001, and other applicable regulations, standards, and guidelines Expertise in managing and leading the transformation of SQM or other quality systems Experience with regulated products or services across different geographies preferred Experience as a SQM subject matter expert and/or as a host during regulatory inspections and as a certified lead auditor for customer or client audits Preferred Qualifications Fluent in both written and spoken English Excellent leadership & management skills Excellent communication, interpersonal & conflict resolution skills Excellent working knowledge of implementing, managing & applying QMS in a US/EU/APAC GxP environment Leadership experience in building and/or enhancing an SQM system Direct experience in communicating with regulatory authorities preferred Leadership skills in managing change, attracting/developing talent, and coupling high performance standards with soft skills Experience of managing a global operation preferred Pay and Benefits Pay Range for this position: $133,900-$220,900 The offer range represents the anticipated low and high end of the base pay compensation for this position. The actual compensation offered will be determined by factors such as location, level of experience, education, skills, and other job-related factors. Position may be eligible for sales or performance-based bonuses. Benefits offered by the Company include health insurance, paid time off (PTO), retirement contributions, and other perquisites. What we offer We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We believe that this variety drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress! #J-18808-Ljbffr MilliporeSigma