Biotechnologist 1

Lonza; Slough; On-site; GBP 30,000 - 40,000; Full time

Job summary

Lonza is seeking a Biotechnologist 1 to join our Manufacturing team in Slough. In this role, you will be crucial in manufacturing drug substances under GMP standards. Ideal candidates will have experience in GMP environments and a commitment to safety and quality practices, contributing to the production of innovative pharmaceutical products.

Qualifications

• Experience in a GMP manufacturing environment required.
• Strong understanding of pharmaceutical equipment and multi-product operations.
• Ambitious approach with commitment to ongoing learning.

Responsibilities

• Operate and control pharmaceutical equipment and processes.
• Manufacture drug substances according to GMP standards.
• Engage in problem-solving and root cause analysis.

Skills

Problem-solving

Communication

Risk assessment

GMP documentation

Job description

Biotechnologist 1

Location: Slough, UK

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.

This is an outstanding opportunity to join Lonza AG as an R67861 Biotechnologist 1 in our dynamic Manufacturing team located in the United Kingdom. At Lonza, we are committed to ongoing growth and excellence, and this role is a critical part of our mission to produce elite pharmaceutical products. As a Biotechnologist, you will be at the forefront of innovation, helping to manufacture drug substances that have the potential to treat and save patients' lives!

Key responsibilities:

• Operate and control a variety of pharmaceutical equipment and processes.
• Manufacture drug substances according to GMP standards.
• Conduct risk assessments and participate in key safety training sessions.
• Apply and complete GMP documentation with precision.
• Understand and implement sampling methods and product testing applications.
• Actively communicate and collaborate with various functional areas to champion strong working relationships.
• Engage in problem-solving, root cause analysis, and resolution to ensure perfect operations.
• Gain exposure to the Lonza safety management system and quality management systems.
• Participate in significant technical training, including aseptic practices.

Key requirements:

• Confirmed experience in a GMP manufacturing environment.
• Strong understanding of pharmaceutical equipment and multi-product GMP facility operations.
• Excellent problem-solving skills with the ability to resolve root causes and implement effective solutions.
• Ability to closely adhere to safety and quality standards.
• Outstanding communication skills for effective collaboration across teams.
• Experience with risk assessments and safety management systems.
• Competence in using and completing GMP documentation accurately.
• Ambitious approach with a dedication to continuous learning and professional development.
• Knowledge of sampling methods and product testing.

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.