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MES Expert Drug Product 80-100% (m/f/d)

Lonza -
Visp, VS

Soumettre votre candidature

Détails de l'emploi

Temps de travail : 90-100%
Il y a 14 jours

Avantages

Aide au déménagement

Qualifications

Anglais
Production
Allemand

Description complète du poste

The actual location of this job is in Visp, Switzerland. Relocation assistance is available for eligible candidates and their families, if needed.

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.

We are looking for a dedicated MES Drug Expert to join our team in Visp, Switzerland. If you're passionate about applying your expertise to optimize drug product manufacturing and truly make a difference, we encourage you to explore this opportunity.

What you will do:

Author and adapt MES/PCS Recipe based on the Drug Product Processes.
Responsible for defining the overall concept for MES recipes used in Drug Product Operations Visp to ensure an easy and fast creation as well as adaption.
Build and maintain relevant GMP documents (IQ, OQ, PQ etc.)
Provide front line MES support, working with the manufacturing teams (operators), plant engineers and QA operations.
Provide MES training for all end user.
Act as Subject Matter Expert during customer audits and visits, maintain MES at inspection readiness level and provides support where needed.
Lead process related investigations and critical deviations and assists in decision making on production issues.
Lead process changes, CAPAs, and CAPA efficiency checks related to process within required timelines and through GMP systems (e.g. Trackwise, MES, training, etc.)
Implements innovation and improvement projects comprising general manufacturing aspects for the production plant.

What we are looking for:

Studies in Pharmaceutical Technology/ Chemistry/ Pharmacy.
Experience in MES recipe authoring, preferably in Emerson Syncade.
Process knowledge in the area of sterile drug product is advantageous.
Knowledge of DeltaV is preferable.
Familiar with working in regulated environment, knowledge of cGMP, 21CRF part 11 and validation requirements.
Proficient in both German and English is an asset.
Familiarity with GMP requirements, quality procedures and SOP execution.
Good interpersonal skills and interaction with a variety of interfaces within the organization and on the shopfloor.
Structured, focused and well-organized working demeanor.
Motivated and driven; with a problem-solving attitude.

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.

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Je souhaite recevoir la dernière alerte Emploi pour les postes de ce type : associate manager, qa validation job

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