Lab Technician

Job Role: Lab Technician – Advanced Therapeutics, Analytical Development

About the Role:
We are seeking a motivated and detail-oriented professional to join the Quality Control Development (QCD) team within Analytical Development. This role focuses on supporting release and stability testing, performing analytical and biological assays, and maintaining high-quality standards in a GMP-regulated environment. You will work closely with cross-functional teams to ensure reliable testing, accurate documentation, and smooth laboratory operations.

Key Responsibilities:

• Perform release and stability testing of GMP/TOX and clinical batches for Advanced Therapeutics products.

• Execute assay qualifications and routine analytical/biological assays such as UPLC/HPLC, ELISA, and PCR with a “first-time-right” approach.

• Culture and handle cells (e.g., A549, HEK293), including passaging and seeding.

• Maintain and document laboratory activities, including assay run sheets, digital ARS documents, laboratory notebooks, and equipment logbooks.

• Support process development testing in collaboration with the Development Department.

• Write, update, and maintain work instructions, test instructions, and equipment instructions.

• Ensure compliance with GMP quality standards and laboratory procedures.

• Collaborate with internal teams to ensure smooth laboratory operations and high-quality output.

Key Competencies:

• Flexible and adaptable, able to prioritize tasks in a dynamic laboratory environment.

• Strong attention to detail with a commitment to quality.

• Excellent communication skills in English and Dutch.

• Team player with accountability, ownership, and a positive “can-do” attitude.

• Experienced in working under GMP quality systems and following laboratory procedures.

Requirements:

• MBO or HBO level in life sciences.

• Minimum of 2 years of experience in a pharmaceutical or GMP-regulated laboratory environment.

• Experience with laboratory management systems.

• Affinity with performing assays under GMP conditions is highly desirable.

• Proficiency in documentation and laboratory record keeping.

Practical Info:

• Location: Leiden, The Netherlands

• Duration: Full-time

• Start Date: ASAP

• Work Model: Full-time, 40 hours per week

Interested or know someone who might be?
Send your CV or inquiries to e.cabral@panda-int.com to apply or learn more.