Recruitment Consultant - Contracting Services
This organisation is a manufacturer, marketer, and distributor of veterinary pharmaceuticals and animal health products.
Responsibilities
1. Quality System Management
o Implement, maintain, and improve the Quality Management System (QMS) in accordance with GMP (Good Manufacturing Practices), VICH, FDA (21 CFR Part 210/211/226 for veterinary drugs), EMA, or WHO standards.
o Ensure compliance with Veterinary Medicinal Product Regulations and Good Distribution Practices (GDP).
2. Document Control
o Manage SOPs, batch records, specifications, and protocols.
o Ensure controlled distribution, versioning, review, and archiving of all QA documentation.
3. Batch Record Review and Product Release
o Review batch manufacturing and packaging records for accuracy and compliance.
o Approve and release raw materials, intermediates, and final products for distribution.
4. Deviation, CAPA, and non-conformance Management
o Initiate and track CAPAs (Corrective and Preventive Actions) and ensure timely closure.
Experience
* Bachelor's degree in a science related field.
* 2-3 years experience in a GMP environment.
* Knowledge of Good Manufacturing Practices (GMP) - especially veterinary GMPs.
* Knowledge of FDA (CVM), EMA, VICH, and USDA regulatory requirements.
* Knowledge of GLP, GDP, and ISO standards (e.g., ISO 9001).
* Knowledge of Quality Management Systems (QMS).
To discover more about this opportunity please apply online or contact Darragh on +353 879345234 for a confidential discussion.
Seniority level
* Entry level
Employment type
* Contract
Job function
* Quality Assurance
Industries
* Pharmaceutical Manufacturing
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