Lab Technician GMP

randstad professional; Leiden; Sur place; EUR 39 000 - 56 000; Plein temps

Avantages offerts par ce poste

Project allowance 4%

Holiday pay 8%

Travel allowance

Pension scheme

Home workplace budget

Randstad Academy access

Onboarding program

Networking events

Résumé du poste

Randstad Professional seeks a Senior QC Technician to join the Testing Operations team within Analytical Development. You will independently execute critical quality control and stability studies for clinical and toxicological batches, ensuring data reliability and GMP compliance.

In a close-knit group of about twelve analysts, you will advance routine testing workflows, perform ELISA and (q)PCR, and apply HPLC/UPLC techniques.

Qualifications

• MBO/HBO Life Sciences degree required; Master’s ok if motivated for bench work.
• 2–3 years GMP-lab experience mandatory.
• Practical ELISA, (q)PCR, and/or HPLC/UPLC experience.
• Cell culture experience is a strong advantage.
• Strong English communication; Dutch optional.

Responsabilités

• Independently perform release and stability testing under GMP.
• Conduct bio-analytical and physicochemical assays (ELISA and PCR).
• Apply chromatographic methods (HPLC/UPLC).
• Carry out cell culture activities (passaging, seeding).
• Execute assay qualifications/validations in GMP lab.

Connaissances

GMP knowledge

Bio-analytical assays

ELISA

(q)PCR

HPLC/UPLC

Cell culture

LIMS

First-Time-Right mindset

English communication

Formation

MBO/HBO Life Sciences

Outils

ELISA

PCR

HPLC

UPLC

Description du poste

Job Description:

Apply your GMP expertise where it matters most. Within Analytical Development, you independently execute critical quality control and stability studies supporting clinical and toxicological batches. Make an immediate impact within a driven, expanding team of analytical professionals.

As a Senior QC Technician, you strengthen the Testing Operations team within Strategic Operations. Working in a close-knit group of approximately twelve analysts, you secure reliable data and compliance for innovative pharmaceutical products. Leveraging your background, you uphold strict GMP standards and elevate routine testing workflows.

Your key responsibilities:

• Independently execute release and stability testing under GMP quality standards with a First-Time-Right mindset.
• Perform bio-analytical and physicochemical assays, including ELISA and (q)PCR.
• Apply chromatographic techniques such as HPLC and UPLC.
• Carry out cell culture activities, including cell passaging and seeding.
• Execute assay qualifications and validations within a GMP-qualified laboratory setting.

Functie-eisen

• An MBO or HBO degree in a Life Sciences discipline (e.g., Biochemistry, Biotechnology, Microbiology, or Analytical Chemistry). (Candidates with a Master's degree are open to consideration provided there is a clear and sustained motivation for purely operational, routine bench work).
• A minimum of 2 to 3 years of hands-on experience in a GMP-regulated laboratory environment (mandatory requirement).
• Practical experience with ELISA, (q)PCR, and/or HPLC/UPLC. Experience with cell culturing is a strong advantage.
• Languages: Strong communication skills in English (verbal and written). (Dutch is optional and not required)

Competenties

• Ownership & Initiative: Proactive mindset; you see what needs to be done and take responsibility for your tasks.
• Flexibility & Prioritization: Daily planning can shift; you keep a clear overview and prioritize effectively under pressure.
• Curiosity & Attention to Detail: Eager to learn new assays and committed to working with high accuracy and compliance
• Experience with assay qualifications/validations and laboratory management systems (e.g., LIMS) is a plus.

Arbeidsvoorwaarden

• A contract for a year of 40 hours per week (with possibility tot extend)
• A monthly project allowance 4% of your salary
• 25 holiday days.
• 8% Holiday Pay
• A travel allowance 0.21per KM or NS BusinessCard
• A good pension scheme (flexsecurity)
• Extra allowances for a home workplace budget E750.-
• A training budget, coaching, an onboarding program, and unlimited access to the Randstad Academy with over 3,000 courses and trainings
• Networking events and knowledge sessions,

This position has no work from home possibility. 100% on-site.

Bedrijfsinformatie

This international pharmaceutical and innovative healthcare company focuses on developing and delivering high-quality medical solutions and medicines. Within a dynamic, fast-changing campus environment, diverse disciplines and quality levels collaborate closely to translate scientific innovations into impactful healthcare. The organization upholds the highest standards for safety, health, environment, and quality (EHS&S and GMP). Driven by a strong quality mindset and continuous focus on process improvement, the company ensures a reliable and safe infrastructure where both internal experts and external facility partners collaborate to deliver sustainable, efficient campus facilities.

About the client:

You will work within the Analytical Development department of a leading pharmaceutical organization. The Testing Operations team (part of Strategic Operations) fosters a collaborative, quality-focused culture centered on professional standards and continuous improvement.

About Randstad Professional:

Randstad Professional acts as your career partner and mentor. We connect ambitious bachelor's and master's graduates with top-tier players across the Life Sciences industry. In addition to securing an assignment that aligns with your goals, we provide personalized coaching, active career guidance, and access to industry-specific training via the Randstad Academy to keep your career moving forward.