Sr Quality Engineer

• Lead, mentor, and develop a team of Supplier Quality Engineers, ensuring effective execution of supplier quality initiatives and audit programs.


• Allocate and prioritize team activities based on business requirements, risk assessments, and resource availability.


• Monitor team performance through defined KPIs, including audit closure timelines, supplier corrective action effectiveness, and supplier performance metrics.


• Provide technical guidance on quality methodologies such as FMEA, Statistical Process Control (SPC), Root Cause Analysis, DMAIC, and validation practices.


• Ensure alignment with global quality strategies, regulatory requirements, and organizational objectives.


• Conduct and oversee supplier audits, review audit reports, approve corrective action plans, and validate supplier qualification documentation.


• Drive standardization of supplier quality processes and maintain continuous audit readiness across operations.


• Facilitate team meetings, performance reviews, and knowledge-sharing initiatives to enhance capabilities and promote continuous learning.


• Collaborate with procurement, operations, research and development, and global quality teams to proactively resolve supplier-related quality issues.


• Serve as an escalation point for critical supplier quality concerns, ensuring timely resolution and stakeholder alignment.


• Promote a culture of compliance, accountability, teamwork, and continuous improvement across quality functions.

Requirements

• Bachelor's degree in Chemical Engineering, Biotechnology, Production Engineering, Pharmacy, or a related discipline; a Master's degree in Chemistry, Quality, Supply Chain Management, or related fields is advantageous.


• Minimum of 5 to 7 years of experience leading teams within Quality Assurance or Supplier Quality Assurance environments, preferably in chemical, pharmaceutical, or highly regulated industries.


• Lead Auditor certification in ISO 9001, ISO 13485, or other relevant quality standards.


• Extensive experience conducting ISO and GMP audits through both onsite and remote methodologies.


• Strong understanding of Lean methodologies and Six Sigma principles; Green Belt certification is considered an advantage.


• Hands-on experience with Root Cause Analysis tools, supplier quality management processes, and continuous improvement methodologies.


• Familiarity with SAP, electronic Quality Management Systems (eQMS), and data analytics tools.


• Excellent written and verbal communication skills with strong stakeholder management capabilities.


• Strong analytical and problem-solving abilities, with the capacity to balance strategic thinking and attention to detail.


• Ability to work independently and collaboratively within cross-functional and international environments.


• Strong documentation skills and the ability to effectively manage multiple priorities in fast-paced settings.


• High level of professionalism, confidentiality, adaptability, and commitment to continuous learning and innovation.

Benefits

• Opportunity to work within a globally recognized and innovation-driven organization operating across multiple industries and international markets.


• Exposure to meaningful projects that contribute to quality, sustainability, operational excellence, and customer impact.


• Collaborative and inclusive work environment that encourages professional growth and leadership development.


• Access to continuous learning opportunities, training programs, and career advancement initiatives.


• Opportunity to work alongside global teams and industry experts in highly regulated environments.


• Dynamic and fast-paced culture that values teamwork, accountability, and continuous improvement.


• Competitive compensation package and comprehensive employee benefits, aligned with local market practices.


• Exposure to cutting-edge quality systems, global best practices, and strategic supplier management initiatives.