QC Bioanalytics Intern: ELISA & qPCR in GMP Lab

Lonza

Lavamünd

Vor Ort

Vertraulich

Vollzeit

Vor 5 Tagen
Sei unter den ersten Bewerbenden
Bewerbungsgenerator

Eine maßgeschneiderte Bewerbung für diese Stelle — ein maßgeschneiderter Lebenslauf und ein Anschreiben, die genau zur Stellenanzeige passen.

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Benefits dieser Stelle

Agile career
Inclusive workplace
Compensation programs
Benefits by role/location

Zusammenfassung

Lonza Visp invites you to join the QC Bioanalytics internship to gain hands-on experience in a GMP-regulated laboratory. You will support routine analyses with ELISA and qPCR, and help document results and write work instructions.

This fully site-based role offers close collaboration with a dynamic team, exposure to quality control operations, and a practical introduction to pharmaceutical manufacturing, with a focus on accuracy, safety, and compliance.

Qualifikationen

  • GMP-regulated environment experience is an asset.
  • Completed vocational training in biology or related field.
  • Experience with ELISA or qPCR is advantageous.
  • Independent, responsible, and precise with good teamwork.

Aufgaben

  • Carrying out routine analysis with a focus on ELISA and qPCR, in compliance with GMP and safety guidelines
  • Method implementation, validation and method transfer
  • Administrative activities, such as documenting the results and creating work instructions
  • Support laboratory maintenance (responsibility for equipment) and ensure that the laboratory is clean and tidy

Kenntnisse

Teamwork
Independent work
Communication

Ausbildung

Biology Laboratory Technician vocational training
Bachelor's degree in Biology

Tools

ELISA
qPCR

Jobbeschreibung

Lonza Visp invites you to join the QC Bioanalytics internship to gain hands-on experience in a GMP-regulated laboratory. You will support routine analyses with ELISA and qPCR, and help document results and write work instructions.

This fully site-based role offers close collaboration with a dynamic team, exposure to quality control operations, and a practical introduction to pharmaceutical manufacturing, with a focus on accuracy, safety, and compliance.

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