Responsibilities
- Execute and ensure effective implementation of Global Quality Assurance processes across Biopharma sites, with a strong focus on packaging activities and final product release.
- Provide operational general support to site Quality teams to ensure consistent application of QA processes, standards, and requirements.
- Coordinate and support the management of quality incidents, deviations, investigations and CAPAs.
- Support and monitor batch release processes, collaborating with Supply, Logistics, and other stakeholders to facilitate product flow and ensure timely release.
- Perform oversight of Quality Systems, identifying risks and proactively escalating critical issues to Senior Management when required.
- Coordinate and contribute to global Quality projects and initiatives, ensuring execution, follow‑up and delivery of defined objectives.
- Support internal and external audits and regulatory inspections, ensuring proper preparation, execution and follow‑up of actions.
- Collect, analyze and monitor Quality Metrics and KPIs, preparing reports and trend analyses to support data‑driven decisions.
- Promote harmonization, consistency and best practices across Biopharma sites, fostering a culture of continuous improvement and compliance.
- Supervise and coordinate Quality teams, supporting capability development, knowledge sharing and operational alignment across sites.
- Stay informed of applicable regulatory requirements and quality standards, supporting their correct and timely implementation.
Qualifications
- Bachelor’s Degree in Health Sciences or a related field.
- 5-10 years of experience in Quality Assurance within the pharmaceutical or biopharmaceutical industry.
- Analytical and problem‑solving abilities.
- Excellent written and verbal communication skills.
- Experience in project management.
- Ability to facilitate change.
- Developes collaborative working relationships.
- Good understanding of regulatory requirements and quality standards relevant to Biological products.
- International experience.
- Willingness to travel internationally as needed.
- Ambitious, results‑oriented, business‑minded person.
Benefits
- Contract of Employment: Permanent position.
- Flexibility for U Program: Hybrid Model.
- Flexible schedule: Monday‑Thursday 7‑10 to 16‑19h and Friday 8‑15h (with the same flexible start time).
- Location: Spain.
Grifols is an equal opportunity employer.
We believe in diverse talent and want to remove any barriers that may hinder your participation. If you require any adjustments in our selection process, please let us know.
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