Qualified Person (QP) / Team Lead
QTC Recruitment
Qualified Person (QP) / Team Lead
Samenvatting
Wat krijg je?
Wat ga je doen?
- Release manufactured radiopharmaceutical products timely
- Coach and develop QA specialists
- Investigate and resolve quality deviations
- Oversee validation and QMS activities
- Approve and review GMP documentation
Wat verwachten wij?
- Master in a scientific discipline, preferably Pharmacy
- Three years experience as QP or in QA
- Strong knowledge of GMP and pharmaceutical regulations
- Experience or ambition in leading a team
Volledige vacaturetekst
At this globally leading pharmaceutical site, you take the lead in ensuring the timely release of innovative radiopharmaceutical products that directly impact patients' lives. You combine batch release accountability with coaching a dedicated QA team in a fast-growing therapeutic field. Enjoy a culture of global recognition and 14 weeks of paid parental leave. Secure your role in the future of medicine.
For our client, a globally leading pharmaceutical organisation with a specialized radiopharmaceutical manufacturing site, we're looking to recruit a Qualified Person / QA Team Lead to ensure the timely and compliant release of radiopharmaceutical products and lead a team of QA specialists. This position is specifically interesting as you will combine your QP responsibility with a leadership role, in an innovative and fast-growing therapeutic field where reliable supply has a direct impact on patients.
This is how you will make the difference
- Release radiopharmaceutical products manufactured on site in a timely manner, in close partnership with Supply Chain
- Release batch analyses in line with the Marketing Authorisation, Directive 2001/83/EC and national regulations
- Lead, coach and develop a team of 4 to 6 QA specialists
- Ensure deviations, CAPAs, change controls and complaints are properly investigated, escalated and resolved
- Provide quality oversight of validation and qualification status, equipment, training and QMS activities
- Write, review and approve GMP documentation, including procedures, protocols and the Quality Manual
- Act as Subject Matter Expert during health authority inspections and internal and external audits
- Deputise for the Quality Operations Manager and provide shift or on-call support when required
What you bring
- Master's degree in a scientific discipline, preferably Pharmacy
- At least 3 years' experience as a QP or in a QA role within the pharmaceutical or biotechnology industry
- Strong knowledge of GMP and applicable European and Dutch pharmaceutical regulations
- Experience in, or a clear ambition for, leading and coaching a team
- An agile mindset focused on collaboration and continuous improvement
- Fluency in English, both written and spoken
- Willingness to provide shift or on-call support when needed
- Based within commuting distance of the site in the south of the Netherlands (relocation is not supported)
What's in it for you
- Competitive annual gross base salary, depending on experience and competencies
- Performance-based bonus
- Comprehensive benefits, including pension and insurance plans
- A minimum of 14 weeks' paid parental leave
- Access to wellbeing resources and global recognition programmes
- Leadership experience in a specialised, future-focused field
Over de werkgever
Zo werkt solliciteren
- Snel en eenvoudig via je mobiel
- Solliciteer in 1 minuut
- CV niet verplicht
- Volg je sollicitatie via Track & Trace
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