Associate Director, Device Supplier Management

Position Overview – Basic Functions & Responsibility As a member of the Device Quality & Regulatory QMS group, the Associate Director will participate in and/or lead various initiatives in support of our QMS Purchasing Controls and Device Supplier Management objectives and build QMS capabilities that touch every aspect of our business processes, systems, and data. Primary Activities The Associate Director will collaborate and interact with cross‑function teams to identify opportunities for improvement and tackle challenges, balancing effective operations with transformative initiatives. The Associate Director, Quality System & Compliance will lead efforts to establish early commercialization Purchasing Controls processes and integrate the Device Supplier Management activities across MDCP programs and product lifecycle. Activities include supplier qualification & evaluation, documenting and maintenance of supplier quality agreements, supplier performance monitoring and re‑evaluation, participating in supplier audits, and addressing any quality and regulatory issues. This role aims to ensure compliance with MDCP current Good Manufacturing Practices (cGMPs), other Global Health Authority Regulations and our company’s requirements while driving continuous improvement in Device Supplier Quality Management. Accountable for other Quality Programs, as assigned. Works on all purchasing control phases for MDCP suppliers: planning, supplier evaluations/audits, supplier selection/qualification, quality agreements, supplier monitoring and re‑evaluation, maintenance, and sustainability. Develop and implement phase‑appropriate supplier controls for early commercialization to effectively support MDCP programs in Development. Supports Supplier Audits, as Medical Device SME. Partner with MDCP sites and internal stakeholders to support investigations related to supplier‑caused deviations and CAPAs. Integrate Purchasing Control Activities into Integrated Project Plan for each MDCP Program (with target dates) for execution. Support the development of our company’s supplier device specification based on intended use and user needs, including defining the list of requirements needed to be specified to supplier (quality, technical, commercial, supply) – shelf life, critical attributes, essential performance requirements, etc. Collaborate with Procurement for Device components, medical devices, and MDCPs to ensure all cGMP Purchasing Controls requirements are compliant. Participate on our teams supporting MDCP cGMP and quality issues related to pure Medical Devices and the device constituent part of a Combination Product. Manage activities within electronic computer systems, e.g., Material Management Systems (SAP), Document Management Systems (Veeva Vault), Supplier Management Systems, etc. Support MDCP sites with new/revised QMS Quality Standards and/or Global Procedures. Perform related duties, as assigned. Skills Preferred experience in the assessment of US FDA 21 CFR Part 4 and Part 820, EU MDR 2017/745, and ISO 13485:2016 for review of Quality Management System documents for the Quality Manual. Previous experience in Medical Device and/or Medical Device Combination Products E2E Supplier Quality Management activities and preferred supplier auditing experience. Must have strong knowledge of regulations listed above and be able to work in a team environment identifying gaps in the QMS documents. Working knowledge of the design, manufacture, packaging, purchasing, testing, release, storage, and distribution of medical devices and/or medical device combination products. Must be able to build relationships within a team environment. Experience using computer systems for Quality Management Systems. Must have working knowledge of regulatory expectations for the design, manufacture/packaging, and distribution of medical devices or medical device combination products with experience in quality assurance or regulatory oversight of these products. Experience authoring, reviewing and approving Quality Management System documents. Solid organizational skills including attention to detail and multi‑tasking skills. Effective people skills and ability to work collaboratively across diverse teams and networks, able to foster cooperation in others. Effective written and oral communicator, ability to speak up and contribute in a team forum. Qualifications B.S. and/or M.S. degree in an appropriate Science or Engineering discipline with a minimum of 8 years of experience with in‑depth knowledge of pharmaceutical, medical devices and/or medical device combination products with at least 4 years in Supplier Quality Management System/ Purchasing Controls and in managing external partners/suppliers. Required Skills Adaptability, Combination Products, Design Controls, Detail‑Oriented, Employee Training, GMP Auditing, GMP Compliance, GMP Guidelines, Good Manufacturing Practices (GMP), Influencing Skills, Manufacturing Processes, Medical Devices, Purchasing Management, Quality Management Systems (QMS), Regulatory Compliance, Risk Management, Strategic Planning, Supplier Quality Management, Supplier Relationship Management Location US And Puerto Rico Residents Only San Francisco Residents Only: We will consider qualified applicants with arrest and conviction records for employment in compliance with the San Francisco Fair Chance Ordinance. Los Angeles Residents Only: We will consider for employment all qualified applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles’ Fair Chance Initiative for Hiring Ordinance. Compensation and Benefits The salary range for this role is $129,000.00 – $203,100.00. The successful candidate will be eligible for an annual bonus and long‑term incentive, if applicable. We offer a comprehensive package of benefits including medical, dental, vision healthcare and other insurance benefits for employee and family, retirement benefits including 401(k), paid holidays, vacation, and compassionate and sick days. More information about benefits is available at EEO Disclaimer As an Equal Employment Opportunity Employer, we provide equal opportunities to all employees and applicants for employment and prohibit discrimination on the basis of race, color, age, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or other applicable legally protected characteristics. As a federal contractor, we comply with all affirmative action requirements for protected veterans and individuals with disabilities. For more information about personal rights under the U.S. Equal Opportunity Employment laws, visit EEOC Know Your Rights and EEOC GINA Supplement. We are proud to be a company that embraces the value of bringing together talented and committed people with diverse experiences, perspectives, skills and backgrounds. The fastest way to breakthrough innovation is when people with diverse ideas, broad experiences, backgrounds, and skills come together in an inclusive environment. #J-18808-Ljbffr Merck