Senior Deviation Management Specialist
Vor 7 Tagen
Leverage Your Expertise in GMP Compliance
As a global leader in healthcare manufacturing, we operate across five continents. We value talented people working together, devising ideas that help businesses to help people.
About the Job Description
- The Senior Deviation Management Specialist will oversee staffing, training and development through continuous learning.
- The role involves utilizing and allocating the resources of the team through cross-training/flexible resource planning.
- The successful candidate will work with Stakeholders to ensure cGMP compliance in all aspects of the GMP deliverables under its accountability.
- Collaboration with stakeholders and SMEs e.g., Ops BPEs, MSAT group, Engineering, QC is essential to bring about process robustness/improvements to routine manufacturing via CAPA strength.
- The specialist will be responsible for meeting deviations timelines to meet production and batch release schedules while ensuring investigation quality.
- Alignment and consistency from technical and quality perspectives in the different ops departments is crucial along with Ops Managers.
- Developing and managing information systems to monitor the efficiency and success of the implemented CAPAs and CRs is also key.
Key Requirements
- Strong leadership skills in team-based management.
- Effective communication and interpersonal skills.
- Analytical thinking and problem-solving skills are essential.
- Adaptability in dynamic work environments is crucial.
- Time management and organizational skills are vital.
- Familiarity with Microsoft Windows and Microsoft Office (Excel, Word, Project, PowerPoint) is required.
We strive to make a meaningful difference in the world through our work in life sciences.
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