Join a global leader in biopharma as a QC Technical Specialist, focusing on lab quality and compliance. This role offers a chance to be a Subject Matter Authority for cGMP inspections, driving continuous improvement and ensuring cGMP and LEAN excellence. You'll lead deviation management, support New Product Introductions, and act as a technical system owner. Benefit from a hybrid working model, blending on-site and remote flexibility, while championing safety and reliability. Uncover the reasons why this position could elevate your career.

Over het bedrijf

Panda International

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QC Technical Specialist – Lab Quality & Compliance

For our client – a global leader in biopharma, based at the Leiden site in the Netherlands –I am looking for a Technical Specialist to support the lab’s Medium and High quality & compliance activities. This is a unique opportunity to act as Subject Matter Authority for cGMP inspections, drive continuous improvement and ensure the team maintains cGMP and LEAN excellence.

Key responsibilities:

Lead deviation management: investigate non-conformances and coordinate corrective/preventive actions.
Create, review and update lab documentation, including supporting materials for New Product Introductions (NPIs).
Provide technical support to the lab and services group; liaise with local and global stakeholders.
Serve as technical system owner for analytical equipment—ensure qualification, calibration and maintenance.
Act as Subject Matter Authority during audits and inspections, interfacing with regulatory bodies.
Lead and drive LEAN based continuous improvement projects to enhance lab performance and compliance.
Champion safety, compliance and reliability; maintain an audit?ready environment.
Communicate effectively with team members and cross-functional partners to build credibility and trust.

Key requirements:

Bachelor’s degree (HLO) or higher in Life Sciences, Molecular Biology or a related field.
Excellent written and oral communication skills in English; Dutch strongly preferred.
Proven ability to work independently and collaboratively within cross?functional teams.
Experience with microbiological techniques (bioburden, endotoxin, sterility) is preferred.
Strong analytical thinking and technical problem solving skills.
Previous GMP experience is a plus.

Practicalities:

Location: Leiden, the Netherlands
Contract Duration: 12 months with high chance of extension
Start Date: ASAP
Working Model: 40 hours/week, hybrid (on-site plus remote flexibility)
Languages: English required; Dutch strongly preferred

Sound interesting?
Send your CV to Khanyi Mabena at via de button "Solliciteer nu" op deze pagina. or reach out directly at +31 2020 44502.

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