
Validation Supervisor
Greetings! At PPD-Pharmaceutical Product Development, we are seeking a highly motivated and experienced Validation Supervisor to join our dynamic team. As a global leader in contract research organization, we provide innovative solutions to advance clinical research and bring life-changing therapies to market. As a Validation Supervisor, you will play a crucial role in ensuring the quality, accuracy, and compliance of our pharmaceutical products. Your expertise and leadership will be instrumental in maintaining our reputation for delivering high-quality services to our clients. If you have a strong background in validation, a passion for quality assurance, and the drive to exceed expectations, we invite you to apply for this exciting opportunity. Join us in our mission to improve the lives of patients worldwide through groundbreaking research and development.
- Develop and maintain validation protocols and procedures for all pharmaceutical products in accordance with regulatory requirements.
- Oversee and manage a team of validation technicians, providing guidance, training, and support to ensure quality and compliance.
- Review and approve validation documentation, including protocols, reports, and change controls.
- Collaborate with cross-functional teams, including production, quality control, and regulatory affairs, to ensure timely completion of validation activities.
- Conduct risk assessments and implement risk-based validation strategies to ensure efficient and effective validation processes.
- Perform gap analyses and identify areas for improvement in validation processes and procedures.
- Stay up-to-date with industry best practices, regulatory guidelines, and changes in validation requirements.
- Manage validation projects, including timelines, budgets, and resources, to ensure successful completion.
- Lead investigations into validation deviations and implement corrective and preventive actions.
- Participate in regulatory inspections and audits, providing support and documentation as needed.
- Communicate validation status, issues, and concerns to upper management and stakeholders.
- Foster a culture of quality and compliance within the validation team and across the organization.
- Mentor and develop team members, providing opportunities for growth and advancement.
- Identify and implement process improvements to increase efficiency, reduce costs, and improve quality.
- Act as a subject matter expert on validation and provide guidance and training to other departments as needed.
Bachelor's Or Master's Degree In A Science-Related Field, Such As Chemistry Or Biology.
Minimum Of 5 Years Of Experience In Validation Within The Pharmaceutical Industry.
Strong Knowledge Of Current Industry Regulations And Guidelines, Including Fda And Ich Guidelines.
Experience Managing And Leading A Team Of Validation Professionals.
Excellent Communication And Organizational Skills, With The Ability To Effectively Collaborate With Cross-Functional Teams And Present To Clients And Regulatory Agencies.
Process Improvement
Project Management
Data Analysis
Quality Control
Team Leadership
Risk assessment
Interpersonal Communication
Audit management
Regulatory compliance
Problem-Solving
Gmp Standards
Communication
Emotional Intelligence
Leadership
Time management
Interpersonal Skills
creativity
Organization
Teamwork
Adaptability
Problem-Solving
According to JobzMall, the average salary range for a Validation Supervisor in Cincinnati, OH, USA is between $70,000 and $110,000 per year. This range can vary depending on the specific industry, company, and level of experience of the individual. Factors such as additional certifications and education may also impact the salary range.
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PPD, Inc. is a global contract research organization providing comprehensive, integrated drug development, laboratory and lifecycle management services.

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