QC Program Coordinator Lvl ; CT

Job Title:

Quality Control Program Coordinator

Location:

Portsmouth, NH, (On-site) As a QC Program Coordinator, you'll be at the center of customer-facing quality initiatives, helping drive critical projects that support the development and manufacture of life-changing therapies. This is a unique opportunity to combine scientific knowledge, project leadership, and customer engagement while partnering with cross-functional teams to ensure deliverables are executed efficiently, compliance standards are met, and customer expectations are exceeded.

This role follows a Monday-Friday schedule from 8:00 AM to 4:30 PM.

• An agile career and dynamic working culture
• An inclusive and ethical workplace
• Compensation programs that recognize high performance
• Medical, dental, and vision insurance
• Opportunities to build customer-facing project management expertise
• Exposure to cross-functional teams across Quality, Manufacturing, and Program Management
• Career growth opportunities within a global life sciences organization

• Serve as the primary QC representative for assigned customer programs and quality-related initiatives
• Lead project meetings, track deliverables, and drive action items to successful completion
• Partner with customers and internal stakeholders to ensure quality commitments are met
• Coordinate quality activities involving investigations, deviations, CAPAs, and change controls
• Communicate project status, risks, and timelines to customers and leadership teams
• Collaborate with Manufacturing, QA, MSAT, and Program Management to support project objectives
• Support continuous improvement efforts that enhance quality, compliance, and customer satisfaction

• Bachelor's degree in a scientific discipline
• Experience working in a pharmaceutical, biotechnology, or other regulated environment
• Project management experience coordinating multiple priorities and stakeholders
• Strong communication skills with the ability to build relationships across teams and with customers
• Ability to organize, prioritize, and drive projects to completion in a fast-paced environment
• Problem-solving skills and the ability to make informed decisions using available data
• A collaborative mindset and commitment to quality, customer service, and continuous improvement

At Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together. Everyone’s ideas, big or small, have the potential to improve millions of lives, and that’s the kind of work we want you to be part of.

Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we offer equal employment opportunities to all qualified applicants regardless of race, religion, color, national origin, sex, sexual orientation, gender identity, age, disability, veteran status, or any other characteristic protected by law.

Ready to shape the future of life sciences?

Every day, our teams across the world work together to turn scientific breakthroughs into life-changing medicines that reach up to 100 million patients a year. Lonza is a place where people can make a unique impact, grow their careers and belong. You will feel at home at Lonza if you:

• Take ownership, step forward, and enjoy meaningful responsibility
• Love solving problems and thrive in a complex, fast-moving environment
• Are curious, always looking to learn and improve
• Work collaboratively, contributing to something bigger than yourself
• Are motivated to make a difference through work that impacts customers and their patients

We are a place of unique opportunity, where your ideas, expertise and ambition can make a real difference. Here, you will have the freedom to grow, the support to succeed and the chance to contribute to work that matters. We are the makers of the medicines of tomorrow.