QC Compliance Specialist

www.recruitireland.com - jobboard; Limerick; On-site; EUR 60,000 - 80,000; Full time

Job summary

A multinational biopharmaceutical company in Limerick is seeking a QC Compliance Specialist. You'll manage projects for quality compliance and support the implementation of GMP standards. The ideal candidate will have a Bachelor’s degree in a science-related field and over 5 years of relevant experience. This is a full-time onsite role with an initial 12-month contract.

Qualifications

• 5+ years’ relevant experience in quality compliance.
• Knowledge of GMP practices is highly desirable.

Responsibilities

• Manage projects to improve quality and compliance standards.
• Implement and maintain quality compliance systems and processes.
• Support colleagues with documentation and compliance issues.

Skills

Attention to detail

Documentation practices

Knowledge of GxP regulations

Quality management systems

Education

Bachelor’s degree in a science-related subject

Job description

A QC Compliance Specialist is required by CareerWise Recruitment for our multinational biopharmaceutical client in Limerick for a full‑time onsite, initial 12‑month contract role.

The QC Compliance Specialist will join a team responsible for Good Manufacturing Practice (GMP) quality compliance and audit readiness, within a manufacturing facility.

THE ROLE

• Manage and support projects and initiatives aimed at identifying opportunities for improvement in quality and compliance standards
• Implementing, monitoring, maintaining, and improving the systems and processes used for quality compliance
• Roll out of site quality initiatives
• Supporting departmental colleagues and partnering lines with guidance on documentation, compliance issues and systems support
• Working proactively to ensure delivery of on‑time high quality records, investigations, and associated actions
• Monitoring metrics and trends to improve compliance standards that will meet internal and external auditor expectations
• Lead and support quality‑based investigations and associated action outcomes, including on‑time completion
• Complete documentation updates associated with change requests, manufacturing, and cleaning to ensure compliance with global regulatory agencies and quality standards

REQUIREMENTS

• A Bachelor’s degree in a science‑related subject (Micro/Chemistry/Biochemistry or equivalent preferred)
• 5+ years’ relevant experience
• Good attention to detail and good documentation practices
• Knowledge of current Good Manufacturing Practices and the applicable GxP regulations and standards (highly desirable)
• Experience in quality management systems

Please call Laura Gallagher today for further information on 087-4526468 or email: [e-mail]