Analytical QC Lab Technician — Pharma & GMP

Vantive; Medolla; In loco; EUR 35.000 - 50.000; Tempo pieno

Descrizione del lavoro

Vantive is seeking a Laboratory Technician for our Medolla plant to perform analytical work in the chemical and microbiological lab. You will execute analyses, document controls, validate methods, and generate data-driven reports for quality assurance.

Requirements include a degree in scientific disciplines, a state exam, at least two years' QC/chemical lab experience in pharma, and knowledge of ISO/GMP. English communication is required. On-site role with potential process improvements.

Competenze

• Degree in scientific disciplines (e.g., Pharmacy, CTF or chemistry).
• State examination for the practice of the profession (Pharmacy, Chemist).
• At least two years’ experience in Quality Control or chemical laboratory in medical/pharmaceutical settings.
• Knowledge of ISO and GMP regulations; instrumentation and laboratory analysis.
• Good written and verbal communication in English.

Mansioni

• Execute laboratory analysis.
• Document chemical controls on raw materials, water, materials, semi-finished and finished products.
• Validate analytical methods and instruments; write validation protocols and method reports.
• Collect chemical data for statistical processing and prepare trends/reports.
• Ensure environmental controls to maintain clean room standards.
• Manage internal procedures.

Conoscenze

Problem-solving

Independent work

English communication

Formazione

Degree in scientific disciplines (Pharmacy, CTF, chemistry)

State examination for the practice of the profession

Strumenti

LIMS

Descrizione del lavoro

Vantive is seeking a Laboratory Technician for our Medolla plant to perform analytical work in the chemical and microbiological lab. You will execute analyses, document controls, validate methods, and generate data-driven reports for quality assurance.

Requirements include a degree in scientific disciplines, a state exam, at least two years' QC/chemical lab experience in pharma, and knowledge of ISO/GMP. English communication is required. On-site role with potential process improvements.