Senior QC Scientist – LC-MS/HPLC Method Expert

Lonza Group Ltd.

Geleen

On-site

EUR 54,000 - 76,000

Full time

14 days+
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Job summary

Lonza Group Ltd. Geleen, Netherlands, is seeking a QC Technical Expert for a 12-month fixed-term contract. The role requires applying scientific skills to support quality control activities and drive improvements across QC processes.

You will work hands-on with LC-MS and HPLC methods within GMP environments, contribute to method validation and document control, and collaborate with manufacturing and audits to ensure product quality and safety.

Qualifications

  • Hands-on experience of 5+ years in QC laboratory or related role in pharma/biotech.
  • Extensive knowledge of LC-MS and HPLC-based methods and related techniques.
  • Subject Matter Expert in QC assays including LC-MS and HPLC.
  • Experience in Analytical Method Validation.
  • Capable trainer and regular trainer to QC team members.

Responsibilities

  • Represent the QC department in Quality Control topics with manufacturing collaboration.
  • Provide expert advice and propose improvements.
  • Participate in gap assessment, transfer, validation and implementation of new QC methods and equipment.
  • Write, review, and approve quality documents (SOPs, stability protocols, reports, quality instructions).
  • Draft and review method validation protocols and reports per regulatory guidelines.
  • Participate in execution of method validation activities.
  • Generate, review and approve QC documents; act as expert during audits.

Skills

QC Laboratory
LC-MS expertise
HPLC expertise
Analytical Method Validation
Training & Mentoring

Tools

LC-MS systems
HPLC systems
ELISA
UV-Vis

Job description

Lonza Group Ltd. Geleen, Netherlands, is seeking a QC Technical Expert for a 12-month fixed-term contract. The role requires applying scientific skills to support quality control activities and drive improvements across QC processes.

You will work hands-on with LC-MS and HPLC methods within GMP environments, contribute to method validation and document control, and collaborate with manufacturing and audits to ensure product quality and safety.

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