Direct message the job poster from Phibro Animal Health
Regional Human Resources Generalist at Phibro Animal Health
About Phibro Animal Health Corporation
Phibro Animal Health Corporation is a publicly traded, global organization with a rich history in animal health and nutrition as a manufacturer and marketer of medicated feed additives, vaccines, nutritional specialty products, and mineral nutrition. We strive to be a trusted partner with livestock producers, farmers, veterinarians, and consumers who raise or care for farm and companion animals by providing solutions to help them maintain and enhance the health of their animals.
Phibro is a diversified company in manufacturing and marketing products for ethanol performance, microbials for plants, home and industrial applications, and specialty chemicals for various industrial markets. In addition to, Phibro’s revenues are in excess of $1 billion and are supported by over 2,300 employees worldwide.
At Phibro, people are our greatest asset. We strive to develop a diverse workforce that fosters an environment where people feel supported in openly sharing their creativity and skills that allows them to be the most successful that they can be.
If you are interested in working for Phibro and feel that you do not meet all qualifications, we encourage you to apply as you might be the right candidate for this role or other positions.
The QA Associate is an integral part of our Quality Assurance team based out of our Ireland - Sligo site.
The QA Associate (Document Control) is an integral part of our Manufacturing team based out of our Ireland - Sligo site.
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.
Key Responsibilities:
* Manage the GxP Document Management system as per site procedures
* Manage the Training Management system as per site procedures
* 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.
* Generate, review, and approve SOP's/other documentation as applicable to your area of responsibility to ensure compliance with GMP and regulatory requirements.
* Manage the reference and retention sample program
* QC Support including review and approval of QC testing documentation
* Issuance and retrieval of batch records and protocols, logbooks
* Review and approval of Batch Processing Records
* Review and approval of validation protocols/ reports and related documentation to ensure compliance with current EU regulatory expectations and site procedures.
* Support QA activities in project work-streams involving cross-functional, multidepartment teams including Operations, Quality Control, Quality Assurance, Engineering, and others
* Support audits and inspections
* Actively contribute to continuous improvement activities
* Other duties as assigned
Job Specific Technical, Functional and Professional Competencies:
* Strong understanding of GMP compliance and quality standards
* Excellent attention to detail and significant document review experience essential
* Excellent technical writing skills including deviation reports and SOPs
* Effective time management and multi-tasking skills
* Demonstrate ability to drive the completion of tasks, trouble shooting skills and excellent attention to detail
* Proficient in written and spoken English
Essential Education and Experience:
Third level qualification in a Biological/Pharmaceutical science discipline with a minimum of 3 years’ experience working in a in a GMP Quality Environment.
To learn more about Phibro Animal Health's competitive benefits package, please click here: Phibro Benefits .
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
Department: Quality Assurance
Location: Ireland - Sligo
Work Schedule: Monday - Friday (39 Hours)
Seniority level
* Seniority level
Mid-Senior level
Employment type
* Employment type
Full-time
Job function
* Job function
Quality Assurance
* Industries
Pharmaceutical Manufacturing
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