Biotech Manufacturing Specialist (Upstream/Downstream)

Lonza Group Ltd.; Oberwallis; Vor Ort; CHF 85.000 - 120.000; Vollzeit

Zusammenfassung

Lonza Group Ltd. is expanding at its Visp site and seeks Manufacturing Specialists for Upstream or Downstream Processing. You will execute activities in line with cGMP, contribute to documentation, and support CAPAs and deviations with a focus on quality and compliance.

Requirements include a chemical/biopharmaceutical education, knowledge of biotechnological processes, strong communication, and a willingness to work a 4-shift system; English fluency is essential.

Qualifikationen

• Completed chemical/biopharmaceutical education or equivalent training.
• Bachelor or Master in Biotechnology, Biology, Biochemical Engineering or related disciplines is an advantage.
• Sound knowledge of biotechnological processes (microbial and/or mammalian cultivation or protein purification).
• Excellent communication skills, team player, driven and solution-oriented.
• Fluency in English required; German is a plus.
• Open to work in a 4-shift system.
• Basic GMP understanding is a plus.

Aufgaben

• Execute manufacturing activities in Upstream or Downstream Processing per cGMP guidelines; ensure batch execution and evaluate results.
• Support SHE, Environmental Monitoring, risk assessment and implementation of controls.
• Assist document preparation (batch records, SOPs) for the production area.
• Review production documentation; address deviations, change requests and CAPAs.
• Engage in Capital investment projects for building/commissioning of new units.
• Responsible for setup, commissioning and qualification inputs for manufacturing suites/equipment.
• Train manufacturing staff on equipment and standard operations.

Kenntnisse

English fluency

Team player

Problem solving

German language skills

Ausbildung

Bachelor/Master in Biotechnology

Jobbeschreibung

Lonza Group Ltd. is expanding at its Visp site and seeks Manufacturing Specialists for Upstream or Downstream Processing. You will execute activities in line with cGMP, contribute to documentation, and support CAPAs and deviations with a focus on quality and compliance.

Requirements include a chemical/biopharmaceutical education, knowledge of biotechnological processes, strong communication, and a willingness to work a 4-shift system; English fluency is essential.