What are the responsibilities and job description for the Manufacturing Process Improvement Director position at Avantor?
Job Description:
Avantor is a leading provider of products and services to the life sciences industry. As a Quality Engineer Lead, you will lead efforts in site quality assurance programs and improvement activities to ensure regulatory compliance with cGMPs, ICHQ7, IPEC guidelines, ISO regulations, and FDA requirements. Your key responsibilities will include identifying and implementing programs to ensure regulatory compliance, supporting CAPA, cGMP, Complaint Investigation and Response, ISO System, Stability, SPC, and Validation systems.
Requirements:
Avantor is a leading provider of products and services to the life sciences industry. As a Quality Engineer Lead, you will lead efforts in site quality assurance programs and improvement activities to ensure regulatory compliance with cGMPs, ICHQ7, IPEC guidelines, ISO regulations, and FDA requirements. Your key responsibilities will include identifying and implementing programs to ensure regulatory compliance, supporting CAPA, cGMP, Complaint Investigation and Response, ISO System, Stability, SPC, and Validation systems.
Requirements:
- Bachelor's Degree in chemistry or a related field.
- Minimum of five years of experience in quality engineering or a related role.
- Experience working within pharmaceutical, biotechnology, and/or chemical environments.
- Excellent writing and presentation skills.
- Demonstrated familiarity with chemical nomenclature and Quality Control testing and methods.
- Excellent organization and project management skills.
- Ability to interface effectively with people at all levels of the organization.
