Job Title:
Site Quality Director
Job Description:
We are seeking an experienced professional to lead our site quality management activities. This role will be responsible for ensuring compliance with regulatory requirements and industry standards.
Key Responsibilities:
* Assess product introductions and major capital projects for quality and validation considerations
* Collaborate with site and global functions to ensure compliant, on-time recommissioning and commercial supply of product
* Establish and maintain effective quality systems, managing quality methods, analytical testing, registration, and batch release
* Lead the development of compliant, robust, and lean quality management systems
* Recruit, train, and appraise quality management staff, ensuring ongoing development and succession planning
* Implement governance systems to monitor process performance and product quality
* Lead continuous improvement initiatives to enhance compliance, quality systems, and product lifecycle performance
Required Skills and Qualifications:
* 10+ years experience in a pharmaceutical manufacturing environment, including significant management roles
* Comprehensive knowledge of worldwide GMP regulations and expectations governing facilities, equipment, and procedures
* Demonstrated experience leading and driving results in continuous improvement projects
* Success in developing, implementing, and maintaining quality systems and standards at manufacturing site level
Benefits:
This role offers a unique opportunity to work in a dynamic and challenging environment. You will have the chance to develop your skills and expertise while contributing to the success of our organization.
Others:
This is a full-time position that requires strong leadership and communication skills. If you are a motivated and experienced professional looking for a new challenge, we encourage you to apply.