Bioanalytical Scientist - GxP Lab, Data & Validation

Temp-Team Danmark

Halsnæs Kommune

On-site

DKK 420,000 - 560,000

Full time

14 days+

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Job summary

Unilabs Pharma Solutions is seeking a Biomedical Laboratory Scientist/Bioanalyst to join a highly skilled bioanalytical team in a commercial laboratory servicing the pharmaceutical industry. The role focuses on executing bioanalytical testing, method development, validation, and ensuring compliance with GxP standards in a regulated setting.

You will generate high-quality analytical data, maintain meticulous documentation, and support validation activities, CAPAs, and audits.

Qualifications

  • Degree as Biomedical Laboratory Scientist or equivalent.
  • 2–5 years of experience in pharma/biotech/CRO in a regulated laboratory.
  • Experience performing bioanalytical testing in a GxP-regulated environment.
  • Hands-on ELISA assay experience.
  • Fluent in Danish and English, both written and spoken.

Responsibilities

  • Perform routine and non-routine bioanalytical testing per approved methods and SOPs.
  • Execute ELISA-based assays with high accuracy and consistency.
  • Review data and documentation for completeness, accuracy and compliance.
  • Maintain, calibrate, troubleshoot and verify lab equipment to support efficient workflows.
  • Support method development, optimization, validation, transfer and continual improvement of analytical methods and lab processes.
  • Contribute to deviation investigations, change controls, CAPAs and audit readiness.

Skills

ELISA assays
Bioanalytical testing
Data integrity

Education

Biomedical Laboratory Scientist degree

Job description

Unilabs Pharma Solutions is seeking a Biomedical Laboratory Scientist/Bioanalyst to join a highly skilled bioanalytical team in a commercial laboratory servicing the pharmaceutical industry. The role focuses on executing bioanalytical testing, method development, validation, and ensuring compliance with GxP standards in a regulated setting.

You will generate high-quality analytical data, maintain meticulous documentation, and support validation activities, CAPAs, and audits.

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