3M has a long-standing reputation as a company committed to innovation. We provide the freedom to explore and encourage curiosity and creativity. We gain new insight from diverse thinking, and take risks on new ideas. Here, you can apply your talent in bold ways that matter.

• Proven category leadership
• Exposure to attractive end-markets
• Innovation mindset driving improved patient outcomes
• Collaborative customer relationships
• Deep global regulatory experience
• Operational excellence and strong cash flow
• Strong sales growth and profitability with significant recurring sales

• Ensure implementation, monitoring and improving local Quality Management System (QMS) with regulatory compliance across the company in alignment with Healthcare Business Group corporate quality standards and country regulatory requirements
• Prepare, review, update, track implement and monitor compliance of standard operating procedures
• Support Quality team in deployment of corporate policy to country local QMS
• Work closely with cross-functional teams in overseeing and providing regulatory/compliance guidance on operational activities (including customer complaints handling and supplier/subcon management)
• Support audit(s) activities including internal audit, external audit, supplier audit and regulatory audit
• Participate in CAPA board meeting to ensure corrective and preventive action is meeting corporate and country regulatory requirements.
• Ensure timely follow-up, execution, completion of necessary action and review effectiveness of CAPA. Support quality compliance improvement programs/projects
• Work closely with Management team to improve internal control and governance practices to enhance the effectiveness and efficiency of the operations and process to ensure compliance
• Serve as the point of the contact in the country on quality compliance matter
• Conduct and support training activities to cross-functional team in the country in alignment with corporate QMS requirements
• Support regional Quality Compliance leader to drive and implement any improvement project in country
• Issue CAPA based on audit findings and follow up through until closure
• Ensure CAPA effectiveness Conduct and support activity related to Field Corrective Action (FCA).
• Ensure timely follow-up, execution and completion of necessary action
• Plan and conduct audit(s) on subcon activity regularly to ensure effectiveness of QMS
• Identify requirements and establish the process for Issue Review and Escalation to division
• Leads the Identify and Assess steps within the Issue Review portion of this process.
• Responsible for documentation and obtaining approvals of the Issue Review Document
• Responsible for the investigation in issue review
• Support SEA country compliance specialist in daily operation
• Other such duties that may be determined by management.

• Bachelor's degree or higher in Pharmaceutical, Pharmacy or Science or equivalent
• Minimum 5-10 years of experience in Quality function in a private, public, government or military environment
• Has analytical skill, able to interpret information and data for routine operational needs.
• Certified ISO 13485 or GDPMDS internal auditor is preferred
• Experience with project management is preferred

Learn more about 3M's creative solutions to the world's problems at www.3M.com or on Twitter @3M. Our approach to flexibility is called Work Your Way, which puts employees first and drives well-being in ways that enable 3M's business and performance goals. You have flexibility in where and when work gets done. It all depends on where and when you can do your best work.