Today, Lonza is a global leader in life sciences operating across five continents. While we work in science, there’s no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that’s the kind of work we want to be part of.
Are you prepared to advance your career and become a valuable member of an elite team? Lonza AG is seeking a highly dedicated R69736 Specialist 3, Quality Assurance Raw Materials - LSA to join our collaborative team in New Hampshire, USA!This crucial position has been built to support our ongoing growth and maintain the highest levels of quality assurance for raw materials!

KEY REQUIREMENTS:

• Proven expertise in quality assurance within the life sciences sector.
• Proven understanding of cGMP regulations and documentation.
• Proficiency in SAP and Trackwise systems.
• Outstanding attention to detail and organizational abilities.
• Ability to efficiently implement and balance multiple projects closely adhering to timelines.
• Effective communication and collaborative approach.
• A dedication to upholding the utmost standards of quality and compliance.
  Every day, Lonza’s products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically.
  People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference.
  Lonza is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a qualified individual with disability, protected veteran status, or any other characteristic protected by law

• Contact Lonza’s internal customers directly to acquire documentation needed for material evaluations and approval.
• Review cGMP documentation independently and provide approval for material assessments and release, including COA, internal and external test records, and BSE/TSE statements.
• Be responsible for material releases.
• Generate, revise, and/or approve material specifications.
• Conduct SAP transactions vital for material release along with other Quality responsibilities within SAP.
• Manage deviations and change controls as owner or QA approver in Trackwise system.
• Write and revise master documents such as Forms, Standard Operating Procedures (SOPs), and specifications.
• Maintain compliance with all required training and assist with the training of fellow analysts.
• Perform project-related tasks as assigned.
• Complete any other tasks as assigned.