About Phibro Animal Health Corporation
Phibro Animal Health Corporation is a publicly traded organization with a rich history spanning nearly 100 years of service. The Company is a global manufacturer of medicated feed additives, feed ingredients, advanced nutrition solutions, vaccines, and specialty chemicals for various industrial markets. Phibro’s revenues are in excess of $820 million and are supported by over 1500 employees worldwide.
The QA Associate (Document Control) is an integral part of our Manufacturing team based out of our Ireland - Sligo site.
Position Details
Responsible for delivery of quality assurance activities to ensure product is manufactured in accordance with GMP and Regulatory requirements. This key role is an individual contributor role whereby the individual must be a self-starter with professional and academic experience in QA. This key role involves collaboration with other departments such as Quality Control, Manufacturing, Engineering, and Technical Services.
Principle Responsibilities
1. Manage the GxP Document Management system as per site procedures.
2. Manage the Training Management system as per site procedures.
3. Support and/or manage assigned areas of the Quality Management System (QMS) including Deviation, Change Control, and CAPA management systems; Internal/External audits; Customer Complaints; Vendor Management; review/approval Manufacturing Batch Records and assessment/approval and release of production materials.
4. Generate, review, and approve SOP's/other documentation as applicable to your area of responsibility to ensure compliance with GMP and regulatory requirements.
5. Manage the reference and retention sample program.
6. QC Support including review and approval of QC testing documentation.
7. Issuance and retrieval of batch records and protocols, logbooks.
8. Review and approval of Batch Processing Records.
9. Review and approval of validation protocols/reports and related documentation to ensure compliance with current EU regulatory expectations and site procedures.
10. Support QA activities in project work-streams involving cross-functional, multidepartment teams including Operations, Quality Control, Quality Assurance, Engineering, and others.
11. Support audits and inspections.
12. Actively contribute to continuous improvement activities.
13. Other duties as assigned.
Education /Experience
Third level qualification in a Biological/Pharmaceutical science discipline with a minimum of 3 years’ experience working in a GMP Quality Environment.
Phibro is an Equal Opportunity Employer
All qualified applicants will receive consideration for employment without regard to race, national origin, gender, age, religion, disability, sexual orientation, gender identity, veteran status, marital status, or any other characteristics protected by law.
Business Unit: Animal Health & Mineral Nutrition
Division: Animal Health & Nutrition
Department: Manufacturing
Location: Ireland - Sligo
Work Schedule: Monday - Friday (40 Hours)
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