Qualifications

• Bachelor's degree in Engineering, Life Sciences, Quality, Computer Science, or related field.
• 8+ years of experience in pharmaceuticals, biotechnology, medical devices, or regulated manufacturing.
• 3+ years of experience leading validation, quality, compliance, or lifecycle management programs.
• Strong knowledge of GMP regulations and validation lifecycle principles.
• Experience managing multidisciplinary technical teams.
• Excellent written and verbal communication skills.
• Strong organizational, planning, and leadership abilities.

Responsibilities

• Serve as the primary client interface for validation lifecycle and periodic review programs.
• Develop and manage execution plans, schedules, and staffing plans.
• Lead program meetings, status updates, and performance reviews.
• Monitor program metrics and key performance indicators.
• Ensure timely execution and completion of review activities and deliverables.
• Oversee quality and consistency of validation documentation.
• Support development and updates of Validation Master Plans (VMPs).
• Coordinate activities across various workstreams.
• Identify risks, issues, and develop mitigation strategies.
• Provide technical leadership and mentorship to project team members.
• Ensure compliance with GMP requirements and quality standards.
• Perform validation activities to support program objectives.

Benefits

• Access to continuous professional development and training.
• Opportunity to work on diverse validation projects.
• Collaborative and supportive team environment.
• Exposure to cutting-edge technologies in regulated industries.