QA Specialist II-Raw Materials Compliance

About the role

QA Specialist II - Raw Materials Compliance Location: Portsmouth, NH (On-site) At Lonza, our greatest scientific solution is talented people working together to help improve lives around the world. As a QA Specialist II - Raw Materials Compliance, you will play a critical role in ensuring the quality, compliance, and availability of raw materials that support the manufacture of life-changing therapies.

This is an excellent opportunity for a quality professional who enjoys working cross-functionally, solving complex quality challenges, and influencing material compliance throughout the product lifecycle. You'll partner with Quality, Supply Chain, Logistics, Manufacturing Science & Technology (MSAT), and other stakeholders to help maintain uninterrupted operations while driving continuous improvement and inspection readiness.

What you will get An agile career and dynamic working culture Opportunities to expand your expertise in quality systems and raw material compliance Exposure to cross-functional teams across Quality, Supply Chain, Logistics, and Manufacturing A collaborative and quality-focused work environment Compensation programs that recognize high performance Medical, dental, and vision insurance Opportunities to grow and develop your career What you will do Perform quality release activities for raw materials by reviewing documentation, specifications, certificates, and test results Review supplier and manufacturer documentation to ensure accuracy, completeness, and compliance with approved requirements Provide guidance on GDP compliance, material receipt and disposition activities, inventory controls, and quality documentation practices Partner with QA, QC, Supply Chain, Logistics, and MSAT teams to resolve material-related issues and support timely material availability Support investigations, deviations, and quality events by providing expertise in raw material quality and compliance requirements Identify quality risks and process improvement opportunities while helping implement sustainable compliance solutions Develop and deliver training while providing support and guidance on raw material quality requirements to cross-functional stakeholders What we are looking for Bachelor's degree required; science or engineering background preferred Minimum 5 years of quality experience in a regulated industry Strong knowledge of cGMP, GDP, and quality system requirements Experience reviewing technical documentation, specifications, certificates, and quality records Strong attention to detail, organizational skills, and documentation review capabilities Proven problem-solving skills with the ability to identify quality risks and improvement opportunities Effective communication, collaboration, and stakeholder management skills in a regulated environment About Lonza 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. If you're ready to help turn our customers' breakthrough ideas into viable therapies, we look forward to welcoming you on board. Ready to shape the future of life sciences? Apply now.