Par Health is seeking a Principal Quality Engineer to oversee Quality Assurance management related to cGMP compliance and product release for pharmaceutical manufacturing. The ideal candidate will have strong leadership capabilities in quality systems and continuous improvement initiatives
Job Summary
Provides overall Quality Assurance (QA) management of the batch record review, manufacturing (current Good Manufacturing Practices) cGMP compliance, and product release functions for the manufacturing of pharmaceutical products.
Key leadership position within the Quality group, managing the QA team responsible for batch record review, product release, label issuance, sampling and sample management activities.
Provides expertise and guidance in interpreting governmental regulations, agency guidelines and internal polices to assure compliance and identifies, evaluates and remediates gaps as they pertain to data integrity.
Matching Summary
Match Score: 85
Par Health is seeking a Principal Quality Engineer to oversee Quality Assurance management related to cGMP compliance and product release for pharmaceutical manufacturing. The ideal candidate will have strong leadership capabilities in quality systems and continuous improvement initiatives.
Skills & Requirements
Must-have
batch record review
cGMP compliance
product release functions
quality systems
data integrity
pharmaceutical operations
Nice-to-have
continuous improvement
teamwork
accountability
elevating the essentials
Key Requirements
QA management experience
cGMP pharmaceutical experience
Experience with quality systems (exceptions, change controls, CAPA)
Experience with investigations (OOS, customer complaints)