Director of Quality Control
QTC Recruitment
Director of Quality Control
Samenvatting
Wat krijg je?
Wat ga je doen?
- Eindverantwoordelijkheid dragen voor Site Quality Control
- Optreden als Systeemeigenaar voor Laboratoriumcontroles
- Naleving van GMP- en EHS-eisen waarborgen
- Stabiliteitsprogramma's voor grote moleculen beheren
- Doorlooptijden van testen en vrijgave beheren
Wat verwachten wij?
- Master in een wetenschappelijke of technische discipline
- 10 tot 15 jaar senior leidinggevende ervaring
- Ervaring met aansturen van laboratorium- of kwaliteitsteams
- Kennis van FDA, EMA en GMP-richtlijnen
Volledige vacaturetekst
As Director Quality Control for this global biopharmaceutical manufacturer, you take ownership of a strategically critical QC function. You lead a complex biologics manufacturing network with the autonomy to shape systems and people. Besides a competitive bonus, you benefit from unique perks like twelve weeks of parental leave and extensive well-being programs. Ready to define the vision for this high-performing laboratory? Dive into the details and lead the way in quality excellence.
For our client, a global biopharmaceutical manufacturer recognised for its leadership in large molecule medicines, we're looking to recruit a Director Quality Control to lead and elevate the Quality Control organisation supporting a complex biologics manufacturing network. This position is specifically interesting as you will take ownership of a strategically critical QC function, with the mandate and autonomy to shape its direction, systems and people at director level.
This is how you will make the difference
- Full quality accountability for the Site Quality Control department, including release, stability, raw material,microbiological and environmental testing;
- System Owner for Laboratory Controls;
- Ensure compliance with GMP, EHS and SOX requirements across all QC activities;
- Ensure full alignment of Site Quality Control with registered dossiers for Large Molecule products;
- Provide governance to Large Molecule stability programs across all development phases;
- Manage testing and release lead times to secure timely product disposition;
- Hold budget responsibility for CAPEX, headcount, CIP and departmental expenses;
- Act as the department's spokesperson during regulatory audits and inspections.
What you bring
- Master's degree in a scientific or technical discipline;
- 10-15 years' experience in a senior leadership role within the biological and/or pharmaceutical industry;
- Proven experience managing people and building laboratory or quality teams;
- Working knowledge of FDA/EMA regulatory frameworks and GMP requirements applicable to biologics;
- Experience supporting an adjacent functional area (e.g. R&D, Manufacturing, Engineering, EHS or Technical Services) is a plus;
- Strong written and verbal communication skills, with a collaborative, open leadership style;
- Fluent in English;
- Demonstrated strategic thinking, with the ability to define and drive a vision for the function.
What's in it for you
- A director-level role with full ownership of a Quality Control organisation;
- A competitive base salary complemented by an annual bonus tied to individual and company performance;
- Generous vacation entitlement and parental leave of at least 12 weeks;
- Bereavement, caregiver and volunteer leave;
- Well-being reimbursement and programs supporting financial, physical and mental health;
- Service anniversary and recognition awards;
- Participation in company insurance plans, subject to plan terms;
- A genuinely strategic mandate, with direct visibility to senior site and quality leadership.
Over de werkgever
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