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Senior Director, Global Supplier Quality

Company: Danaher Corporation
Location: Sunnyvale
Posted on: April 5, 2021

Job Description:

Danaher Corporation Senior Director, Global Supplier Quality in Sunnyvale , California ESSENTIAL JOB RESPONSIBILITIES: Lead a high performing team and manage all aspects of supplier quality organization. Hiring, developing, coaching and mentoring staff including setting individual and team goals and conducting performance reviews. Responsible for all aspects of quality of supplied parts and services globally including #PL sites. Develop and deploy quality strategy, programs, and roadmap for contract manufactures, material suppliers and service providers such as third-party logistics services. Audit suppliers and contract manufacturers to ISO-9001, ISO13485, and applicable FDA requirements. Audits activities to include: Develop an audit plan, prepare audit reports, communicate findings, audit responses, compliance assessment including assessment of compliance risk. Accountable that the audit schedule and approved supplier list are maintained, and up-to-date ensuring supplier classifications are accurate. Accountable for the supplier compliance of: Audits, Supplier Quality Agreements (SQA), SCARs, Process Change Notifications (PCNs) and effective closure of audit non-conformances. Monitors and ensure compliance with company policies and procedures, as well as, global regulations and expectations (e.g. FDA, ISO, IVDD/IVDR, etc.). Assure all SQM related quality documentation and records are completed thoroughly and timely to maintain compliance. Monitor and report on meaningful SQM performance metrics as well as Supplier performance metrics. Collaborate with a cross-functional team to improve processes/share responsibilities to include leading a Supplier Review Board. Responsible for supplier performance and supplier process Capability Indices (Ppk's, Cpk's) Key liaison between Engineering, Purchasing, supplier Development and Suppliers during the product lifecycle stages. TRAINING RESPONSIBILITIES: (REQUIRED) Complete all assigned and required training satisfactorily and on time. For people managers, ensure your associates attend and complete all required trainings satisfactorily and on time. MINIMUM REQUIREMENTS: Education and Experience (in years): Bachelor's degree in field with 14+ years of related work experience OR Master's degree in field with 12+ years of related work experience 4+ years managing people Knowledge and skills: Significant Supplier Quality experience in medical devices or in-vitro diagnostics (IVD) industries with people management experience. In-depth knowledge Quality standards (GMP, ISO 9000, ISO13485, etc.) and experience in the medical device industry, knowledge of CFR 21 Part 820. Effective leadership skills and ability to influence department and peers, as well as be a team player. Excellent verbal & written communication skills (internal & external customers). Able to apply strategic thinking. Excellent attention to detail, flexible and adaptable to change. Able to operate under pressure, multitask, set priorities and meet deadlines. Must exhibit strong leadership skills, both with subordinates and peers, with emphasis on relationship development and implementation of company culture improvement initiatives. Must have excellent written and oral communication abilities including: The ability to present complex theoretical concepts and empirical scientific data effectively and concisely. The ability to articulate clearly and engage in dialogue with all levels within the organization. Must be able to influence with others in a fast-paced, cross-functional, matrixed organization. Strong analytical and technical skills. Motivated self-starter, capable of achieving objectives in a demanding environment. Extremely detail-oriented, accurate, and highly organized. Excellent problem-solving skills and judgement. Requires excellent interpersonal and communication skills. Ability to work well with people. Ability to interface successfully with various departments and be a part of their teams. Engage others, promote, and participate in Environmental, Health, and Safety initiatives, focusing on continuous improvement. Must be able to work on multiple projects simultaneously and demonstrate organizational, prioritization, and time management proficiencies. Willingness to think outside of the box and adapt best practices. PREFERRED REQUIREMENTS: Seven years of Department Leadership experience in managing both processes and resources. Experience in the medical device industry, knowledge of CFR 21 Part 820 (QSR), ISO 13485. A quality engineering certification from the American Society for Quality (ASQ), or other qualifying organizations. Examples include the CQE, CRE, CQA, etc. Certified in Lean manufacturing and/or Six Sigma. The statements in this description represent typical elements, criteria and general work performed. They are not intended to be an exhaustive list of all responsibilities, duties, and skills for this job. Danaher Corporation and all Danaher Companies are equal opportunity employers that evaluate qualified applicants without regard to race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law. The "EEO is the Law" poster is available here (http://www.dol.gov/ofccp/regs/compliance/posters/pdf/eeopost.pdf) .

Keywords: Danaher Corporation, Sunnyvale , Senior Director, Global Supplier Quality, Executive , Sunnyvale, California

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