Quality Engineer II-III, Quality Assurance

MedPharm•Durham, NC

13d•Onsite

About The Position

Quality Engineer II-III, Quality Assurance is responsible for designing, implementing, and maintaining the Quality Management System across the manufacturing lifecycle. This role supports process validation; root-cause investigations for deviations; oversees Corrective and Preventive Actions; and ensures compliance with current Good Manufacturing Practices. This position is responsible for monitoring and control the quality processes supporting incoming, in-process and final disposition including batch record review and release for GMP, clinical, and commercial programs through broad knowledge of GLP/GMP manufacturing theories and principles. This position works closely with other functional areas of the Company to release raw materials, per agreed upon timelines. Additional areas of responsibility include QA oversight of operational metrics and supporting client and internal auditing activities. The Quality Engineer II-III, Quality Assurance shall adhere to the Company’s quality system including but not limited to the applicable standards, policies and procedures in the areas of responsibility defined in this job description.

Requirements

B.A. / B.S. in a Engineering discipline, or equivalent experience preferred
Quality Assurance experience in the pharmaceutical industry for 5 +years
Knowledge of Pharmaceutical Quality Management Systems requirements and execution
Demonstrated proficiency in written, verbal and face-to-face communication to effectively present information to internal and external customers
Ability to successfully manage multiple tasks and multifunctional resources concurrently while maintaining high attention to detail while responding to rapidly changing priorities and aggressive deadlines
Technically capable of identifying root cause of a problem, offering potential solutions, and engaging with others to resolve the problem
Produces consistent, high quality and quantity of outputs and meaningful results that contribute to the agency mission and strategic goal. Is efficient in producing results that are delivered on time or before.
Ability to work independently and as part of a team
Expertise in MS Office (Excel, Word, Outlook, Project) and Adobe Pro

Responsibilities

Ensure all production practices strictly align with FDA 21 CFR Parts 210/211, ICH Q10, and global cGMP standards.
Quality Assurance review and approval of validation protocols (IQ/OQ/PQ) for manufacturing equipment, facilities, utilities, and analytical laboratory software.
Support investigation of manufacturing deviations and out-of-specification (OOS) results using root-cause analysis tools like 5 Whys and Fishbone diagrams.
Quality Assurance review and approval of manufacturing documentation, including specifications, batch records, and batch release.
Support Quality Risk Management (QRM) initiatives utilizing Failure Mode and Effects Analysis (FMEA) to minimize patient and product risk.
Evaluate and approve change controls for processes, materials, or equipment to ensure they do not negatively impact product quality.
Conduct routine internal audits and manage readiness documentation for external regulatory agency inspections.
Partner with procurement to audit third-party raw material suppliers and manage external quality issues.
Oversee the quality management processes ensuring that client requirements, specifications, and regulatory requirements are met by the Operations Unit.
Collaborate with cross-functional teams, including production, engineering, supply chain, and customer service, to address quality issues and drive continuous improvement initiatives.
Analyze quality data and performance metrics to identify trends, root causes of defects, and opportunities for process optimization.
Partner with Operations supporting closure of Quality Events and quality improvement plans when needed.
Conduct regular audits to monitor compliance with quality standards and identify areas for improvement.
Routinely draft and revise standard operating procedures and QA review of master batch records.
Leads internal and supports external audits in accordance with Company procedures and schedules. Develop reports of audit findings and communicate these to the relevant project team and to Company management.