Analytical Development Technician – GMP Biochemistry

HAL Allergy Group; Leiden; On-site; EUR 42,000 - 56,000; Full time

Job summary

HAL Allergy is seeking a Technician Analytical Development to advance biochemical and immunological analytical methods. You will collaborate with Quality Control, Analytical Development, and Biochemistry to develop, validate, and implement methods that ensure product quality in a GMP environment.

You will perform ELISA, SDS-PAGE, potency assays, and protein assays, support method transfers to QC, and ensure robust documentation.

Qualifications

• Bachelor's degree in Biochemistry, Biology, Life Sciences, or equivalent.
• At least 3 years of relevant laboratory experience.
• Hands-on experience with ELISA, SDS-PAGE, potency assays, protein assays, and immunoblotting.
• Experience transferring analytical methods from development to Quality Control environments.
• Familiarity with GMP-regulated environments and quality systems.
• Strong analytical and problem-solving skills.
• Excellent communication and teamwork within multidisciplinary groups.

Responsibilities

• Develop, improve, qualify, and implement biochemical and immunological analytical methods.
• Support the transfer of analytical methods from development into routine QC.
• Quality Control testing.
• Perform laboratory assays including ELISA and SDS-PAGE.
• Execute potency assays and protein assays.
• Conduct immunoblotting where applicable.
• Troubleshoot analytical challenges and propose improvements.
• Ensure methods comply with GMP and regulatory guidelines.
• Accurately document, analyze, and report results.
• Support lab operations, including instrument maintenance and supply management.
• Collaborate with cross-functional teams to meet project goals.

Skills

ELISA

SDS-PAGE

Immunoassays

Protein assays

Immunoblotting

Method transfer

GMP familiarity

Documentation

Cross-functional teamwork

Education

Bachelor's degree in Biochemistry

Job description

HAL Allergy is seeking a Technician Analytical Development to advance biochemical and immunological analytical methods. You will collaborate with Quality Control, Analytical Development, and Biochemistry to develop, validate, and implement methods that ensure product quality in a GMP environment.

You will perform ELISA, SDS-PAGE, potency assays, and protein assays, support method transfers to QC, and ensure robust documentation.