Senior Quality Systems Specialist
Senior Quality Systems Specialist voor een farmaceutische opdrachtgever in Hoofddorp, tijdelijke aanstelling.
- Locatie
- Hoofddorp
- Werkvorm
- op locatie
- Sluitingsdatum
Bekijk en reageer bij SIRE Life Sciences B.V. (externe link)
Alle 2 publicaties en brokers
Eisen
- Pragmatic and structured approach to quality and compliance
- Strong knowledge of GMP, EU GMP, and ICH Q10 requirements
- Proven experience with Change Control, Deviations, CAPA, and MRB processes
- Strong communication, stakeholder management, and organizational skills
- Experience in Drug Substance and/or Drug Product environments
- 5+ years of Quality Assurance experience within a GMP environment
Wensen
- Knowledge of aseptic manufacturing and/or ATMP environments is an advantage
- ASQ, Lean Six Sigma, or similar certification is a plus
- Familiarity with Power BI, Power Automate, Smartsheet, and MS Office is desirable
Volledige omschrijving
The Company: Our client is a global leader in advanced cell therapy, specializing in developing and delivering cutting-edge treatments for patients with serious illnesses. The organization operates state-of-the-art manufacturing facilities and follows the highest GMP standards to ensure quality and safety.
Role Description: As a Senior Quality Systems Specialist, you are responsible for governing and improving key GMP Quality Systems, ensuring processes remain compliant, robust, and inspection-ready. You will work closely with Quality, Operations, and cross-functional stakeholders at site and cross-site level.
Responsibilities: Manage and support Quality Systems including Change Control, Deviations, CAPA, and MRB. Maintain and improve quality procedures and coordinate site training. Monitor compliance, quality metrics, and management review inputs. Identify and manage quality risks in line with EU GMP, ICH Q10, and internal policies. Chair or support multidisciplinary quality boards and committees. Support audits and regulatory inspections, including preparation and follow-up.
Review and approve quality documentation, changes, deviations, and CAPAs. Drive continuous improvement of quality processes, reporting, and automation. Provide backup support to the Quality Systems Lead/Manager when required.
Requirements: 5+ years of Quality Assurance experience within a GMP environment. Strong knowledge of GMP, EU GMP, and ICH Q10 requirements. Proven experience with Change Control, Deviations, CAPA, and MRB processes. Experience in Drug Substance and/or Drug Product environments. Strong communication, stakeholder management, and organizational skills. Pragmatic and structured approach to quality and compliance. Knowledge of aseptic manufacturing and/or ATMP environments is an advantage.
ASQ, Lean Six Sigma, or similar certification is a plus. Familiarity with Power BI, Power Automate, Smartsheet, and MS Office is desirable.
Other Information: If you are interested and want to apply, please submit your application via the apply button below and contact me.
Je CV en reacties
Voeg een CV toe om de eisen naast jouw ervaring te bekijken.
Je reageert zelf bij de bron. Leg hieronder vast wanneer je je reactie hebt verstuurd.
Bewaar de broker en datum in Mijn reacties.