Specialist 3, Quality Assurance Operations - LSA (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.

Join Lonza AG, a global leader in life sciences, as the Specialist 3, Quality Assurance Operations - LSA in New Hampshire, USA. This outstanding opportunity allows you to be part of an exceptionally dedicated team, driving world-class quality assurance operations. We are growing rapidly and need professionals who strive for flawless execution in all aspects of GMP operations.

Key responsibilities:

• Perform daily rotations through GMP operational areas, reviewing documentation and observing work habits.
• Provide direct mentoring and feedback on GMP and documentation behaviors.
• Conduct GMP training sessions to support work habits and knowledge.
• Offer GMP mentorship to Manufacturing for both routine and non-routine issues, handling complex problems independently.
• Respond to QA Hotline calls, making decisions from simple to complex, and advance issues to Senior management as necessary.
• Guide and support junior staff in compliant decision-making processes.
• Authorize the placement and removal of Quality Tag Outs.
• Act as the QA representative in meetings or project teams, making overarching decisions on behalf of the QA department.
• Assist in batch record issuance as necessary.
• Perform other duties as assigned.

Key requirements:

• Proven experience in Quality Assurance within a GMP environment.
• Strong ability to independently assess quality issues and determine appropriate actions.
• Outstanding problem-solving skills with the ability to handle complex issues.
• Experience in conducting training sessions and providing feedback.
• Competence in decision-making and dedication to compliance.
• Capability to serve as the QA representative in meetings and project teams.
• Excellent communication and collaboration skills.
• Ambitious and motivated to carry out effective quality assurance procedures.

If you are ambitious and ready to compete in a world-class environment, we encourage you to apply today! Your expertise will help build the future of life sciences at Lonza AG.

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.