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Senior Compliance Validator
2 weeks ago
Job Description:
Oversight of all quality management aspects is crucial in our organization. To achieve this, we are looking for an Associate Director who can drive the validation process from planning to reporting. The successful candidate will ensure adherence to validation SOP/work procedures during application development and alignment of project outputs with quality standards through coordination with project managers and teams.
The ideal candidate should have a minimum of 10 years' experience in Quality Management within Pharma or regulated industry. They should be able to manage GxP/non GxP projects from requirement definition to retirement, with a strong focus on innovative validation strategies for business initiatives.
Responsibilities:
- Drive the validation process from planning to reporting.
- Evaluate data and QM processes to identify improvements for efficiency and accuracy.
- Manage change control process for tool updates and deployments while driving continuous improvements in validation and quality workflows.
- Support in audits and inspections to ensure adherence to compliance regulations and industry standards.
Requirements:
- Minimum 10 years' experience in Quality Management within Pharma or regulated industry.
- Proven experience in managing GxP/non GxP projects from requirement definition to retirement.
- Strong leadership skills with the ability to drive a team towards meeting quality standards.
- High attention to detail with the ability to identify potential risks or issues.
Benefits:
- Opportunity to work on high-profile projects.
- Collaborative and dynamic work environment.
- Competitive compensation package.
Preferred Qualifications:
- Working experience in all lifecycle stages of IT systems (including System retirement) is preferred.
- Ability to drive innovative validation strategies for business initiatives.
