QC Specialist II-Laboratory Information

Lonza • Portsmouth, NH

1d • Onsite

About The Position

This role is based onsite in Portsmouth, New Hampshire. As a QC Specialist II – Laboratory Information, you will support quality control activities that help ensure safe, reliable medicines reach patients worldwide. You will work closely with cross-functional teams while contributing to continuous improvement and high GMP standards. 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. If you’re ready to help turn our customers’ breakthrough ideas into viable therapies, we look forward to welcoming you on board.

Requirements

• Experience working in a GMP laboratory environment, preferably within quality control
• An associate degree in science, or equivalent experience gained through work
• Strong attention to detail and the ability to follow procedures accurately
• Clear written and verbal communication skills
• Comfort working with documentation and regulated processes
• A collaborative mindset and willingness to support and train others
• The ability to manage tasks independently while prioritizing quality and safety

Nice To Haves

• Experience with shipment preparation, organization, and purchase order creation is preferred

Responsibilities

• Receive, store, and manage samples to ensure accurate tracking and proper storage conditions
• Coordinate and support shipments of samples to internal and external testing partners
• Prepare and maintain controlled documents, assay forms, and laboratory records
• Support cell bank vial receipt, shipment, and release activities
• Perform aseptic bulk dispensing for customer, stability, and final product samples
• Contribute to GMP documentation creation, review, and continuous improvement
• Support audit readiness and collaborate with teams to resolve quality or process issues

Benefits

• An agile career with opportunities to grow your expertise in quality control and laboratory operations
• A collaborative and inclusive workplace where your ideas are valued
• Competitive compensation programs that recognize performance and contribution
• Medical, dental, and vision insurance
• A culture that prioritizes safety, ethics, and quality
• The chance to contribute directly to therapies that improve lives

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Education Level: Associate degree