Senior Manager, Corporate Quality Auditor

Work Your Magic with us!  

Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us.  

Task and Profile of the Position

• Assess the level of quality and compliance of suppliers in APAC/Greater China Region vs. applicable contractual agreements, company standards, regulatory requirements and business needs 
• Assess the level of quality and compliance of Merck business units / ES sites QMS on assigned internal audit program
• Identify and alert the Corporate Management of business threats and risks
• Support the stakeholders with risks management and CAPA plan establishment
• Support the maintenance of the SQQA workflow / eSQA system improvement and network based in APAC/China to manage the suppliers
• Lead or support the assigned management tasks/project for achieving the organizational objectives 

Responsibilities of the Position

• Timely schedule and execute audits as per approved SQ-QA Audit plan
• Deliver audit findings to auditee’s management in a constructive yet firm manner
• Report in timely manner reliable assessment of the applicable ISO/GxP/Merck quality requirement compliance level of processes, tools, quality systems, and resources of suppliers
• Report in timely manner reliable assessment of the applicable ISO/GxP/Merck quality standards compliance level of processes, tools, quality systems, and resources of Merck organizations according to internal audit plan
• Issue reports in English according to the established SQ-QA standard
• Alert immediately the Management of any critical or compromising audit finding in an expert manner
• Support the stakeholder in the establishment of a technically sound CAPA plan, and to follow up on CAPA until completion and close-out of the audit
• Produce reports on quality/trends/indicators on the basis of audit findings

Who You Are:

Education

• Life Science degree, Chemistry, Chemical Engineering,Master Degree would be a plus
• Chinese mother language
• Fluency in English is a must

Professional Experience

• Minimum 10 years solid experience in Electronics materials, Pharmaceutical materials, intermediates (Excipient, API, Food, Cosmetics etc.), manufacturing of pharmaceutical products.
• A minimum of 5 years in auditing
• Solid Quality Assurance understanding and experience in an Electronics or Life Science or regulated HealthCare environment is a must
• Demonstrated success records in independent auditing
• Solid management experience of Supplier Quality management function is a plus
• Position specific knowledge and competencies
• Assertiveness and strong skills: ability to interact constructively with management and functions
• Strong verbal and written communication skills,
• Result-oriented
• Excellent time management and organizational skills
• Ability to maintain effectiveness when experiencing major changes in work tasks or work environment
• High sense of confidentiality and ethics

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!

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!