Job Overview
The Quality Assurance Process Lead will be responsible for overseeing the review and approval of batch manufacturing documentation related to oral solid dose production. This involves ensuring that all documents are compliant with cGMP regulations and that quality systems are in place to prevent deviations.
This role requires strong leadership skills, excellent communication abilities, and a deep understanding of pharmaceutical industry regulations. The ideal candidate will have a degree in Chemistry/Analytical Science/Pharmaceutical Science or Forensic Science, with experience in quality assurance and process improvement.
Key Responsibilities:
* Lead the development and implementation of quality processes and procedures
* Conduct regular audits to ensure compliance with cGMP regulations
* Collaborate with cross-functional teams to identify and implement corrective actions
* Develop and maintain quality metrics and reporting
Required Skills and Qualifications:
* Strong background in quality assurance and process improvement
* Excellent communication and leadership skills
* Degree in Chemistry/Analytical Science/Pharmaceutical Science or Forensic Science
* Experience working in a fast-paced environment with multiple priorities
Benefits:
This is an exciting opportunity to join a dynamic team and make a meaningful contribution to the success of our organization. We offer a competitive salary and benefits package, as well as opportunities for professional growth and development.
What We Offer:
* A dynamic and supportive work environment
* Opportunities for career advancement and professional growth
* A competitive salary and benefits package
* Flexible work arrangements and work-life balance