Home » QA Specialist GMP

QA Specialist GMP at PHIBRO ANIMAL HEALTH CORP

Position QA Specialist GMP
Posted 20 Jul 2026
Expired 19 Aug 2026
Company PHIBRO ANIMAL HEALTH CORP
Location Sligo | IE
Job Type Full Time

Job Description:

Latest job information from PHIBRO ANIMAL HEALTH CORP for the position of QA Specialist GMP. If the QA Specialist GMP vacancy in Sligo matches your qualifications, please submit your latest application or CV directly through the updated Jobkos job portal.

Please note that applying for a job may not always be easy, as new candidates must meet certain qualifications and requirements set by the company. We hope the career opportunity at PHIBRO ANIMAL HEALTH CORP for the position of QA Specialist GMP below matches your qualifications.

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.

The QA Specialist GMP is an integral part of our Quality Assurance team based out of our Ireland - Sligo site.

PURPOSE

Provide dedicated Quality Assurance support to site project activities and strategic initiatives within the Sligo manufacturing facility.

Serve as the Quality representative for assigned project workstreams, ensuring GMP, regulatory, and Phibro quality requirements are incorporated throughout project execution.

Support qualification, validation, operational readiness, and continuous improvement activities impacting commercial vaccine manufacturing.

Partner with Manufacturing, QC, Engineering, Validation, Regulatory Affairs, Supply Chain, and project teams to ensure compliant and timely project delivery.

Ensure quality risks are identified, assessed, and managed throughout the project lifecycle while maintaining inspection readiness and site compliance.

KEY RESPONSIBILITIES
  • Serve as the QA representative for assigned site projects and strategic initiatives.
  • Ensure GMP and quality requirements are incorporated into project activities.
  • Participate in project governance, planning, and risk assessments.
  • Review and approve qualification and validation protocols and reports.
  • Provide QA oversight for facility, utility, equipment, computerized system, cleaning, and process qualification activities.
  • Support execution and closure of qualification and validation activities.
  • Support implementation and enhancement of site quality systems.
  • Ensure compliance with GMP, data integrity, and Phibro quality standards.
  • Support Veeva Vault, LIMS, and other quality systems required for project execution and operational readiness.
  • Review and approve project‑related GMP documentation.
  • Ensure quality documentation is complete, compliant, and inspection‑ready.
  • Support development of SOPs and operational quality procedures.
  • Partner with Engineering, TSA, Operations, Regulatory Affairs, and Project Management teams.
  • Provide quality guidance for change controls, deviations, investigations, and CAPA activities.
  • Support operational readiness and technology transfer initiatives.
  • Support facility GMP approval and regulatory inspection readiness activities.
  • Participate in audits, inspections, and regulatory responses as required.
  • Ensure compliance with applicable GMP, EHS, and company requirements.
  • Promote a strong quality culture throughout project execution.
KEY COMPETENCIES
  • Strong understanding of GMP compliance, quality systems, validation requirements, and manufacturing site quality standards.
  • Knowledge of facility, utility, equipment, computerized system, cleaning, and process qualification activities within a regulated manufacturing environment.
  • Ability to operate effectively in a site project environment with multiple stakeholders, deadlines, workstreams, and competing priorities.
  • Strong documentation review and technical writing skills, including protocols, reports, deviations, CAPAs, SOPs, and project documentation.
EDUCATION & EXPERIENCE

Essential

  • Third-level qualification in a scientific, engineering, quality, pharmaceutical, biotechnology, or related discipline.
  • Minimum 5 years' experience working in a GMP Quality environment, preferably within a manufacturing site.
  • Experience supporting qualification, validation, manufacturing readiness, technology transfer, or site improvement projects.
  • Working knowledge of GMP regulations, QMS, validation lifecycle, change control, deviations, CAPA and data integrity requirements.
  • Experience working within cross-functional teams in a regulated manufacturing environment.

Desired

  • Experience supporting regulatory inspections, audits & health authority interactions.

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: Quality Assurance

Location: Ireland - Sligo

Work Schedule: Monday - Friday (40 Hours)

#J-18808-Ljbffr

Job Info:

  • Company: PHIBRO ANIMAL HEALTH CORP
  • Position: QA Specialist GMP
  • Work Location: Sligo
  • Country: IE

How to Submit an Application:

After reading and understanding the criteria and minimum qualification requirements explained in the job information QA Specialist GMP at the office Sligo above, immediately complete the job application files such as a job application letter, CV, photocopy of diploma, transcript, and other supplements as explained above. Submit via the Next Page link below.

Next Page »

Similar Job Vacancies

  Job Search Agregator 2026
About Us
Privacy Policy
Disclaimer
Terms and Conditions
Contact Us
Submit XML Feed

© Jobkos

  By visiting the Jobkos website, viewing, accessing, or using any of the services or information created, collected, compiled, or submitted to Jobkos, you agree to be bound by the following Terms and Conditions of Service.
Created by Jobkos | | | |