Quality Compliance Specialist

RT Lane Ltd Recruitment; Swords; On-site; CAD 60,000 - 100,000; Full time

Job summary

An established industry player is seeking a motivated QC Specialist for an exciting 11-month contract role. This position involves ensuring the integrity and compliance of the Quality Management System within a dynamic pharmaceutical environment. As part of a high-performing team, you will manage deviation and change control metrics, support regulatory inspections, and contribute to continuous improvement efforts. The ideal candidate will have extensive experience in Quality Control and a strong understanding of relevant guidelines and regulations. If you are passionate about quality and compliance and eager to make a meaningful impact, this opportunity is perfect for you.

Benefits

Paid Holidays

Qualifications

• 4+ years in Quality Control or Pharmaceutical Operations required.
• Strong knowledge of Quality and Compliance Guidelines essential.

Responsibilities

• Manage Deviation, CAPA, and Change Control metrics daily.
• Support compliance inspections and manage recalls as needed.

Skills

Good Documentation Practices

Quality systems

Pharmaceutical quality

GMP

CAPA

cGMP

Interpersonal skills

Root cause analysis

Change control management

Deviation management

Education

Bachelor’s degree in Chemistry, Biology, Microbiology, Automation, Engineering

Job description

R.T. Lane Recruitment are currently recruiting for a QC Specialist – release of Incoming goods to work with a Pharmaceutical Company in North Dublin.

This is an 11-month contract with strong potential for extension.

Please note that candidates must hold the correct working visa for Ireland as my client cannot offer visa assistance and must be already residing in Ireland.

Roles and Responsibilities:

• The main areas of expertise are, but not limited to, specific tasks and roles such as: deviation management, change control management, quality systems management, document / SOP management, data integrity management, GMP training & knowledge management.
• Ensure the health & well-being of the Quality Management system at the site to ensure timely actions are taken to meet compliance & production needs.
• Serve as support for metrics management for site deviation management and change control systems.
• Support the review and approval of site deviation and investigations reports.
• Support maintenance of the site master file and site manufacturing license and variations, as required.
• Ensure root causes have been identified and corrective action implemented and can demonstrate basic knowledge of six sigma, LEAN, and root cause analysis tools used for identifying and correcting deviations.
• Day to day management of Deviation, CAPA and Change Control, QRM metrics.
• Support Regulatory and Compliance Inspections at the site, as required.
• Support for management of recalls, as required.

What skills you will need:

• Minimum of 4 years’ experience in Quality Control, Quality Assurance or Pharmaceutical, Vaccine or Biological Operations or Technical Operations.
• Motivated to be an inspiring member of a high performing team.
• Excellent interpersonal skills: communication, decision making, people influencing skills.
• Ability to interact with multiple stakeholders.
• Desire to continuously learn, improve and develop.
• Excellent knowledge of relevant Quality and Compliance Guidelines (cGMP, Auditing, Quality Management Systems, Quality Agreements, Regulatory Affairs, Training) and respective regulations.
• Experience with new product introductions and/or process qualification/technology transfer.
• Bachelor’s degree (or higher) in Chemistry, Biology, Microbiology, Automation, Engineering, or equivalent.

For more information or a full Job Description please contact – Michelle Power, R.T. Lane Recruitment.

Skills:
Good Documentation Practices, Quality systems, Pharmaceutical quality, GMP, CAPA, cGMP

Benefits:
Paid Holidays