Job description
We are seeking a Process Validation and Cleaning Specialist to join our team in the pharmaceuticals sector. The ideal candidate will have a minimum of 4 years of experience in process validation and cleaning within a regulated environment. This role is critical in ensuring that our manufacturing processes meet the highest standards of quality and compliance.
Key Responsibilities :
- Develop, execute, and manage process validation protocols and reports for pharmaceutical manufacturing processes.
- Oversee cleaning validation activities, ensuring compliance with regulatory requirements and industry standards.
- Collaborate with cross-functional teams, including manufacturing, quality assurance, and regulatory affairs, to ensure seamless validation processes.
- Conduct risk assessments and provide recommendations for process improvements and cleaning methodologies.
- Maintain accurate documentation of validation and cleaning activities, ensuring compliance with GMP and other regulatory standards.
- Stay informed about industry trends, regulatory changes, and best practices related to process validation and cleaning.
Qualifications :
Bachelor’s degree in Engineering, Life Sciences, or a related field.Minimum of 4 years of experience in process validation and cleaning in the pharmaceutical sector.Strong knowledge of regulatory requirements (FDA, EMA, etc.) and industry standards (GMP, ISO).Excellent analytical and problem-solving skills, with a keen attention to detail.Strong communication and interpersonal skills, with the ability to work effectively in a team environment.What We Offer :
Competitive salary and performance-based incentives.Comprehensive benefits package, including health insurance, retirement plans, and paid time off.Opportunities for professional development and career advancement.A collaborative and innovative work environment.