Analytical Development Technician - GMP Biotech Lab

HAL Allergy International; Leiden; Remote; EUR 38,000 - 60,000; Full time

Benefits offered by this job

30 leave days

Pension and health insurance

Dynamic HQ in Leiden

Job summary

HAL Allergy is seeking a Technician Analytical Development in Leiden to develop, optimize, validate and implement biochemical and immunological analytical methods that ensure product quality.

You will collaborate with Quality Control, Analytical Development and Biochemistry teams, transfer methods to QC, perform ELISA, SDS-PAGE, potency and protein assays, and support GMP-compliant laboratory operations in a dynamic biopharmaceutical environment.

Qualifications

• Bachelor's degree in Biochemistry, Biology, Life Sciences, or related field.
• Minimum 3 years of laboratory experience.
• Hands-on experience with ELISA, SDS-PAGE, potency assays and immunoblotting.
• Experience with transferring analytical methods to QC and GMP environments.

Responsibilities

• Develop, optimize, validate, and implement analytical methods for quality products.
• Support the transfer of analytical methods from development to routine QC.
• Conduct Quality Control testing and report results.
• Perform ELISA, SDS-PAGE, potency and protein assays, and immunoblotting.
• Ensure GMP compliance and proper documentation of experiments.
• Maintain instruments and collaborate with cross-functional teams.

Skills

Analytical method development

Biochemistry knowledge

GMP knowledge

Regulatory compliance

Team collaboration

Education

Bachelor's degree in Biochemistry or Life Sciences

Tools

ELISA

SDS-PAGE

Immunoblotting

Protein assays

Job description

HAL Allergy is seeking a Technician Analytical Development in Leiden to develop, optimize, validate and implement biochemical and immunological analytical methods that ensure product quality.

You will collaborate with Quality Control, Analytical Development and Biochemistry teams, transfer methods to QC, perform ELISA, SDS-PAGE, potency and protein assays, and support GMP-compliant laboratory operations in a dynamic biopharmaceutical environment.