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Manufacturing Specialist
full-timeVisp

Summary

Location

Visp

Type

full-time

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About this role

 

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 dedicated 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.

Due to the growth at our site in Visp, we are currently looking for several Manufacturing Specialists for our Ibex-facility. In this role, you will be responsible for performing operational activities of assigned manufacturing projects in specific areas (Up-stream or Down-stream processing).

Key responsibilities:

  • Complete manufacturing activities in either the Upstream Processing or Downstream Processing area according to cGMP guidelines, ensuring batch execution, evaluating test results, resolving issues, troubleshoot manufacturing equipment and make recommendations for resolution

  • Support the preparation of SHE (Safety, Health, environment), EM (Environmental Monitoring), operation and cleaning risk assessment for the assigned products and the implementation and control of defined measures

  • Assist document preparation (e.g. electronic batch records, SOPs) specific to the assigned production area

  • Review production documentation and work on deviations, change requests and implementation of CAPAs to ensure high-quality GMP standards

  • Engage in Capital investment projects for building and commissioning of new manufacturing units as manufacturing expert. Responsible for delivering all input required for the specific set-up, commissioning and qualification of the manufacturing suites and equipment

  • Responsible for the training of the manufacturing staff on specific equipment or standard operations

Key requirements:

  • Completed chemical / biopharmaceutical education or corresponding training qualification, Bachelor / Master's degree or equivalent experience in Biotechnology, Biology, Biochemical Engineering or related fields is an advantage

  • Sound knowledge of biotechnological processes either in the area of microbial and/or mammalian cultivation or protein purification

  • Excellent communication skills, great teammate, driven and solution-oriented

  • Fluency in English required, fluency in German is considered a plus

  • Open to work in shift (4-shift system)

  • Basic GMP understanding is a plus

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 meaningful 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 significant difference.

Other facts

Tech stack
Manufacturing,Biotechnology,Biochemical Engineering,Upstream Processing,Downstream Processing,GMP,Communication,Teamwork,Problem Solving,Training,Risk Assessment,Documentation,Capital Investment,Troubleshooting,Environmental Monitoring,Safety

About Lonza

Lonza is a pioneer and world leader in the CDMO industry, setting the pace with cutting-edge science, smart technology, and lean manufacturing. United by a common purpose, we turn our customers’ breakthrough innovations into viable therapies and manufacture the medicines of tomorrow.

Founded in Switzerland in 1897, our company is the first and original CDMO, and today we are more dynamic, agile and forward-focused than ever before. As one of the largest Western CDMOs, we bring together a global team of around 18,500 colleagues across five continents to deliver comprehensive, integrated solutions for our customers' complex needs.

For our customers and their patients, we bring quality, safety and reliability to bring life-enhancing and life-saving treatments to market at speed and at scale. For our colleagues, we strive to create a sense of belonging and inclusion where every person can thrive and bring their best.

Team size: 10,001+ employees
LinkedIn: Visit
Industry: Pharmaceutical Manufacturing
Founding Year: 1897

What you'll do

  • The Manufacturing Specialist will perform operational activities for assigned manufacturing projects in either Upstream or Downstream Processing areas. Responsibilities include ensuring batch execution, troubleshooting equipment, and supporting documentation preparation.

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Frequently Asked Questions

What does a Manufacturing Specialist do at Lonza?

As a Manufacturing Specialist at Lonza, you will: the Manufacturing Specialist will perform operational activities for assigned manufacturing projects in either Upstream or Downstream Processing areas. Responsibilities include ensuring batch execution, troubleshooting equipment, and supporting documentation preparation..

Why join Lonza as a Manufacturing Specialist?

Lonza is a leading Pharmaceutical Manufacturing company.

Is the Manufacturing Specialist position at Lonza remote?

The Manufacturing Specialist position at Lonza is based in Visp, Valais, Switzerland. Contact the company through Clera for specific work arrangement details.

How do I apply for the Manufacturing Specialist position at Lonza?

You can apply for the Manufacturing Specialist position at Lonza directly through Clera. Click the "Apply Now" button above to start your application. Clera's AI-powered platform will help match your profile with this opportunity and guide you through the application process. You can also learn more about Lonza on their website.