GMP QC Lab Technician: Pharma Analyses & Data Integrity

Ekkiden; Lengnau BE; Vor Ort; CHF 90.000 - 150.000; Vollzeit

Benefits dieser Stelle

Health insurance (GEREP)

Meal vouchers (Swile card)

Zusammenfassung

Ekkiden is seeking a QC laboratory technician to join a pharmaceutical quality-control team in Switzerland. You will perform analyses on raw materials, intermediates and finished products under GMP, ensuring procedures and data integrity.

Responsibilities include physicochemical and microbiological analyses, documenting results, investigating OOS/OOT cases, and collaborating with QC, QA, production and engineering. German language skills required; French is a plus.

Qualifikationen

• Degree such as CFC laborantin(e) or bachelor/master in chemistry, biology, microbiology, pharmacy or equivalent qualification
• 5–10 years of experience in a pharmaceutical QC laboratory
• Experience in GMP environment
• Knowledge of GLP
• Knowledge of data integrity requirements
• Experience in managing OOS/OOT results
• German at operational/intermediate level; French is a plus
• Rigorous, autonomous and quality oriented
• Ability to work in a regulated and documented environment
• Good team spirit and communication skills

Aufgaben

• Perform QC analyses in compliance with GMP and internal procedures
• Carry out physicochemical analyses on pharmaceutical samples
• Perform microbiological analyses as needed
• Prepare samples, solutions, reagents and media
• Use and maintain laboratory equipment
• Investigate OOS/OOT results
• Document results in quality systems and files
• Ensure traceability and data integrity
• Participate in qualification, calibration and maintenance of equipment
• Draft/update laboratory documents and procedures
• Collaborate with QC, QA, production and engineering teams

Ausbildung

Bachelor's/Master's in chemistry, biology, microbiology, pharmacy or equivalent qualification

Jobbeschreibung

Ekkiden is seeking a QC laboratory technician to join a pharmaceutical quality-control team in Switzerland. You will perform analyses on raw materials, intermediates and finished products under GMP, ensuring procedures and data integrity.

Responsibilities include physicochemical and microbiological analyses, documenting results, investigating OOS/OOT cases, and collaborating with QC, QA, production and engineering. German language skills required; French is a plus.