Senior QC Scientist — Build & Validate a New Lab (Relocation Supported)

Lonza; Stein (AR); Vor Ort; Vertraulich; Vollzeit

Benefits dieser Stelle

Agile culture

Inclusive workplace

Performance pay

Lifestyle benefits

Zusammenfassung

Lonza in Stein, Switzerland seeks a Quality Control professional to join a site-based team responsible for release and stability testing of Drug Products. You will execute and review physico-chemical and biochemical assays, support method validation and transfers, and maintain GDP and 6S standards in a fast-paced lab environment.

Ideal candidates have solid GMP QC experience, hands-on ELISA/HPLC/iCIEF skills, and a background in Analytical Chemistry or related fields.

Qualifikationen

• Solid work experience in Quality Control within GMP environments.
• Hands-on experience with ELISA, HPLC or iCIEF (multiple methods preferred).
• Experience in analytical method validation and transfer is a plus.
• Apprenticeship as Lab technician or degree in Analytical Chemistry/Biochemistry/Pharmaceutical Sciences.
• Knowledge of LIMS, Tiamo or CDS ( Empower/Chromeleon ).
• Fluent in English; German is an asset.
• Ability to work independently in a dynamic, fast-paced project environment.

Aufgaben

• Release of medicines by executing and reviewing physico-chemical and biochemical tests under cGMP.
• Document assay execution following Good Documentation Practices (GDP).
• Perform operational lab tasks: mobile phase prep, equipment calibration, 6S, consumables management.
• Support validation and transfer activities for new projects.
• Contribute to investigations and troubleshooting.
• Assist in authoring cGMP documents and quality records (SOPs, CAPA, OOE/OOS).

Kenntnisse

Quality Control experience

cGMP

Documentation & GDP

6S / housekeeping

Independent work

Ausbildung

Lab technician apprenticeship or degree in Analytical Chemistry/Pharmaceutical Sciences

Tools

ELISA

HPLC

iCIEF

Jobbeschreibung

Lonza in Stein, Switzerland seeks a Quality Control professional to join a site-based team responsible for release and stability testing of Drug Products. You will execute and review physico-chemical and biochemical assays, support method validation and transfers, and maintain GDP and 6S standards in a fast-paced lab environment.

Ideal candidates have solid GMP QC experience, hands-on ELISA/HPLC/iCIEF skills, and a background in Analytical Chemistry or related fields.