LIMS Labware Specialist

Pauwels Consulting; Waver; On-site; EUR 60,000 - 80,000; Full time

Job summary

Pauwels Consulting seeks a specialist to bridge laboratory operations and digital systems, translating analytical methods into digital logic and ensuring accuracy within a GMP quality control environment. You will configure and administer LIMS, manage method structures, and collaborate with lab teams to digitize manual processes.

Requirements include LabWare or LIMS experience, a BSc/MSc in Chemistry, Biology, Biotechnology, or Pharmacy, and fluent French with professional English.

Qualifications

• Experience with LabWare or other LIMS administration.
• Background in a quality control laboratory.
• Bachelor's or Master's in Chemistry, Biology, Biotechnology or Pharmacy.
• GMP environment experience.
• Fluent in French with professional English.

Responsibilities

• Translate analytical methods into computer logic for digital systems.
• Configure and administer LIMS to support quality control operations.
• Manage the structure of analytical methods including samples, tests, specifications, and calculations.
• Ensure digital methods are accurate and compliant within a regulatory framework.
• Collaborate with laboratory teams to digitize manual processes.

Skills

French fluency

English proficiency

Attention to detail

Education

Bachelor's or Master's in Chemistry/Biology/Biotechnology/Pharmacy

Tools

LabWare

LIMS administration

SAP QM

Job description

Our client, a leading organization in the life sciences sector, is looking for a specialist to bridge the gap between laboratory operations and digital systems. This role focuses on translating analytical methods into digital logic and ensuring technical accuracy within a quality control environment.

• Translate analytical methods into computer logic for digital systems.
• Configure and administer laboratory information management systems to support quality control operations.
• Manage the structure of analytical methods including samples, tests, specifications, and calculations.
• Ensure digital methods are accurate and compliant within a regulatory framework.
• Collaborate with laboratory teams to digitize manual processes.

• Experience with LabWare or other LIMS administration and configuration.
• Background in a quality control laboratory with an understanding of analytical method structures.
• Possess a Bachelor's or Master's degree in Chemistry, Biology, Biotechnology, or Pharmacy.
• You're rigorous and precise, particularly when working in a GMP environment.
• You are fluent in French with professional proficiency in English.

Nice to Haves

• Knowledge of GMP requirements, data integrity, and good documentation practices.
• Previous experience drafting technical documentation or performing dry-runs.
• Basic understanding of SAP QM, including inspection and sampling plans.

• Start date: ASAP.
• Contract: open to both permanent employees and freelancers.