Supervisor Quality Engineering
About The Position
Be a part of a revolutionary change! At Philip Morris International (PMI), we’ve chosen to do something incredible. We’re totally transforming our business and building our future on one clear purpose – to deliver a smoke-free future. With huge change, comes huge opportunity. So, if you join us, you’ll enjoy the freedom to dream up and deliver better, brighter solutions and the space to move your career forward in endlessly different directions. Our success depends on people who are committed to our purpose and have an appetite for progress. Your “Day-to-Day” Lead day-to-day Quality Engineering activities ensuring manufacturing processes, equipment, and systems comply with PMI standards. Coordinate validation, change management, and risk assessment activities across operations. Guide engineers and project teams in qualification and validation activities. Maintain accurate manufacturing specifications and documentation. Drive continuous improvement actions that enhance process capability and quality performance. Investigate deviations and material-related issues, implementing corrective and preventive actions. Support DIM-related trials and collaborate with central teams on material improvements. Develop, coach, and mentor the Quality Engineering team to ensure high performance. Ensure validation and quality documentation is complete, accurate, and audit-ready. Who We Are PMI is a global leader undergoing a historic transformation toward a smoke-free future. We are focused on innovation, sustainability, and building world-class manufacturing and quality systems. Our teams collaborate across functions and geographies to deliver products that meet the highest quality, safety, and regulatory expectations. Who We Are Looking For We are seeking a strong Quality Engineering leader with deep technical knowledge, strong communication skills, and the ability to guide teams through complex validation and change management processes.
Requirements
- Master’s degree in Chemistry, Biological Sciences, Physical Sciences, Engineering, or equivalent through demonstrated experience.
- 5+ years in Quality Engineering within tobacco, food, pharmaceutical, or FMCG industries.
- Expertise in product/process qualification and analytical evaluation.
- Strong data interpretation and reporting skills.
- Project Management and Change Management capability.
- Excellent understanding of ISO, GMP, GCP, ICH, GLP, and related standards.
Nice To Haves
- Experience with FDA inspections is considered an asset.
Responsibilities
- Lead day-to-day Quality Engineering activities ensuring manufacturing processes, equipment, and systems comply with PMI standards.
- Coordinate validation, change management, and risk assessment activities across operations.
- Guide engineers and project teams in qualification and validation activities.
- Maintain accurate manufacturing specifications and documentation.
- Drive continuous improvement actions that enhance process capability and quality performance.
- Investigate deviations and material-related issues, implementing corrective and preventive actions.
- Support DIM-related trials and collaborate with central teams on material improvements.
- Develop, coach, and mentor the Quality Engineering team to ensure high performance.
- Ensure validation and quality documentation is complete, accurate, and audit-ready.
Benefits
- We offer a competitive base salary, annual bonus (applicable based on level of position), great medical, dental and vision coverage, 401k with a generous company match, incredible wellness benefits, commuter benefits, pet insurance, generous PTO, and much more!
- We have implemented Smart Work, a hybrid model of working that promotes flexibility in the workplace.
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What This Job Offers
Job Type
Full-time
Career Level
Manager
