11776141 – QA Specialist External Quality- Dublin Contractor

Purpose

The QA Specialist for External Quality will be responsible, with management support, for providing oversight of quality activities associated with drug substance, drug product, and finished product manufacturing processes to contract manufacturing organizations. The Specialist contributes and guides the completion of milestones associated with specific projects and supports ongoing quality assurance responsibilities in support of Contract Manufacturing oversight and quality systems including Change Control, Deviations, and CAPA’s. Acts independently to determine methods and procedures on new assignments and provides guidance to lower-level personnel. Performs’ all responsibilities in accordance with company policies, procedures, and regulations.

Responsibilities

• Serve as Quality Assurance support and SME for Drug Substance, Drug Product, and Finished product manufacturing maintaining knowledge of industry standards and regulatory requirements to ensure all drug manufacturing, storage, and shipping activities are compliant.
• Providing oversight of GMP systems completed by CMO’s and External Supply Chain function related to Drug Substance, Drug Product, and Finished Product.
• Provides oversight to continuous quality system improvements and supports implementing improvements at CMO’s in compliance, Preventive Maintenance, Deviation Management, and Change Control Programs as they impact the company.
• Works closely to build relationships with contract manufacturers’ quality personnel.
• Works closely with internal cross-functional impacted areas, such as External Plant Operations, CMO Management, CMC/Regulatory Affairs, and Technical Services to resolve open issues in a timely manner resulting from record reviews and deviation events.
• Responsible for reviewing contractor documents i.e., Batch records, deviations, and change controls to ensure that they comply with company procedures and meet company standards.
• Approve company-specific standard operating procedures and controlled documents issued by contract manufacturing organisations.
• Support contract manufacturing organisation audits, including pre-approval inspections, as necessary.
• Develop and issue quality metrics pertaining to the process quality activities.
• Trends and analyses quality aspects of technical transfer activities to measure key performance indicators, identifies areas for continuous process improvements and risk mitigation, compiles and presents analyses at Quarterly Management Review meetings, proposes and leads team implementation of appropriate CAPA.
• Reviews and assesses deviations; includes performing risk assessments, participating in root cause analysis investigations, tracking, follow-up, and reporting/trending.
• Review Corrective and Preventive Actions (CAPA); includes tracking, follow-up, and reporting/trending, and evaluating CAPA for effectiveness.
• Represents Quality Assurance to guide various projects and technical meetings, as needed.
• Responsible for documenting and reporting compliance issues to management.
• Any other duties as required by management.

Minimum Qualifications and Experience

• Bachelor’s degree required; preference is given to candidates with advanced degrees; 2 or more years cGMP experience preferred; consideration will be given to other relevant experience and education.
• Must have experience/knowledge of drug substance, drug product, and finished product manufacturing processes in a cGMP environment.
• Must have detailed knowledge of industry best practice and current regulatory expectations concerning drug substance, drug product, and finished product manufacturing. Minimum of 2-5 years’ GMP related experience in biopharmaceutical/pharmaceutical or related industry
• Experience working with contract manufacturing organisations.
• Ability to provide project leadership and guide successful completion of Quality projects.
• Excellent written and verbal communication and negotiating skills.
• Risk assessment and risk management
• Ability to exercise judgment with defined procedures and practices to determine appropriate action.
• Ability to prioritize daily activities in order to meet internal and external customer needs on time of established timelines in a fast-paced environment.
• Ability to monitor and report on assigned tasks, goals, and objectives.

Note: This role requires 20% travel