jobid=A.0.0252
Job Role: Lab Technician
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/ +12 months
- 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.
