QC Specialist III- Raw Materials (Biotech)

Today, Lonza is a global leader in life sciences operating across three 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.

This is a remarkable opportunity to join Lonza AG as a QC Specialist III in our New Hampshire, USA location! This role has been crafted to support our ambitious growth and dedication to delivering world-class life sciences solutions. As part of our team with varied strengths, you will help us rigorously resolve and implement processes, ensuring flawless execution and compliance. The QC Raw Materials Specialist III is a pivotal project coordination role in the raw material release process, namely functioning to coordinate flow of raw materials through receipt, sampling, and testing to data authorization in preparation for release.

Key responsibilities:

• Support activities such as raw material sampling, testing decisions, sample distribution and data management in Laboratory Information Management Systems (LIMS) including but not limited to testing template creation and corrections requested from review.

• Prepare raw material packets that will be maintained through receipt to release and archiving.

• Assume responsibility for ancillary documentation support including but not limited to Raw Material Qualification Reports and Laboratory Investigations.

• Coordinate raw material testing externally- preparation of outsourcing paperwork.

• Maintain a working knowledge of SAP in order to execute procedural objectives.

• Apply Data Integrity principles in all aspects of work, in compliance with Lonza DI policies, guidelines and procedures.

• Perform other duties as assigned.

Key requirements:

• Associate degree or relevant experience with at least 2 years in regulated industry.

• Proven track record of collaborating effectively within diverse teams.

• Strong attention to detail and dedication to delivering high-quality results.

• Excellent problem-solving skills and the ability to handle sophisticated tasks.

• Effective communication abilities to convey information and collaborate with team members.

• Familiarity with regulatory standards and industry guidelines.

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.