We are seeking a dedicated Quality Compliance Officer to support quality assurance activities, maintain the Quality Management System (QMS), and ensure compliance with pharmaceutical regulations at our client's facility in Co.Westmeath.This is an excellent opportunity for someone with a background in quality compliance to join a dynamic and growing team. This is a permanent position offering hybrid working.
Key Responsibilities:
Manage change control, complaints, and CAPA (Corrective and Preventive Actions).
Maintain and oversee QMS processes in line with company procedures.
Conduct and support quality tasks such as internal audits, document control, and reporting of quality indicators.
Investigate deviations, ensure root causes are identified, and verify corrective actions for effectiveness.
Monitor the performance of contract manufacturers and laboratories for GMP/GDP compliance.
Review records to ensure completeness and adherence to regulations.
Qualifications and Experience:
Bachelor’s degree in Life Sciences, Biomedical, or a related field (or equivalent work experience).
Minimum 2 years of experience in quality compliance within the pharmaceutical industry.
Strong knowledge of cGMP, 21 CFR Part 211, and pharmaceutical regulations.
Proficiency in MS Office.
Skills and Attributes:
Excellent organizational and planning skills.
Ability to manage multiple responsibilities in a fast-paced environment.
Effective verbal, written, and interpersonal communication skills.
Collaborative mindset with the ability to work independently when required.
For a confidential discussion about this opportunity please contact Ranait Coughlan
ranait.coughlan@collinsmcnicholas.ie
(090) 6450664 (01) 66 200 88