Onsite QC Specialist - Pharmaceutical Packaging & Materials

Lonza; Basel; Vor Ort; Vertraulich; Vollzeit

Benefits dieser Stelle

Competitive hourly rate

Zusammenfassung

Lonza in Basel is seeking an experienced Quality Control professional to perform analytical testing on packaging materials, raw materials and consumables to ensure compliance with cGMP and safety standards for patient therapies. This onsite role starts in September/October 2026.

You will collaborate with QA, Supply Chain and Operations to maintain timelines, author QC documentation, and drive improvements in laboratory efficiency while upholding strict documentation practices.

Qualifikationen

• Completed vocational training as a Laboratory Technician with 4+ years of QC experience in a cGMP environment.
• Solid practical experience in analytical testing of raw materials, excipients, and consumables (e.g., wet chemistry, FTIR, or physical/chemical assays).
• Sound working knowledge of cGMP regulations, pharmacopeial standards, and quality control systems.

Aufgaben

• Perform analytical testing of primary packaging materials, raw materials, and consumables per cGMP guidelines.
• Execute investigations for out-of-spec results and support troubleshooting.
• Support analytical method implementation, qualification, verification, and validation activities.
• Author, review, and update QC-related documentation including SOPs and lab records.
• Liaise with suppliers and external labs to obtain and verify CoAs and GMP documentation.
• Collaborate cross-functionally with QA, Supply Chain, and Operations to maintain timelines and compliance.
• Drive continuous improvement across laboratory operations.

Kenntnisse

QC testing

cGMP knowledge

Analytical testing

Documentation practices

Lab investigations

Cross-functional collaboration

English communication

Ausbildung

Laboratory Technician training

Bachelor's degree in Chemistry

Master's degree in Chemistry

Tools

FTIR

HPLC

Jobbeschreibung

Lonza in Basel is seeking an experienced Quality Control professional to perform analytical testing on packaging materials, raw materials and consumables to ensure compliance with cGMP and safety standards for patient therapies. This onsite role starts in September/October 2026.

You will collaborate with QA, Supply Chain and Operations to maintain timelines, author QC documentation, and drive improvements in laboratory efficiency while upholding strict documentation practices.