Qualified Person QP

Cpl; Longford; On-site; EUR 50,000 - 70,000; Full time

Job summary

A leading consultancy company in Ireland is seeking an experienced Qualified Person to join their Quality Release Department. This permanent full-time role offers flexible working hours and emphasizes a healthy work-life balance. The ideal candidate will hold a BSc Degree, have Qualified Person status, and possess at least 2 years of experience in the pharmaceutical industry. Responsibilities include documentation review, quality investigations, and managing client projects.

Benefits

Flexible working hours

Supportive work environment

Qualifications

• Minimum 2 years experience in quality or production function within the pharmaceutical industry.
• Demonstrated self-starter with a proactive, hands-on approach.

Responsibilities

• Complete a range of activities within the Quality Release Department.
• Documentation review/control, deviation approval, material status assignment.
• Support for other Quality Systems activities relating to customer complaints.

Skills

Interpersonal skills

Decision-making

Teamwork

Communication

Education

Minimum of BSc Degree or equivalent

Qualified Person Status in accordance with EC Directives

Job description

Overview

Qualified Person – QP

On behalf of my client, a consultancy company for the Life Sciences industry we have a new role for a Qualified Person to join the team. We are seeking a highly experienced and driven Qualified Person to join the team. This is a permanent full-time opportunity. My client strongly believes that a supportive and healthy work life balance is critical for their team to be happy and successful, and so they offer truly flexible working hours as standard. This applies to both when and where you work, with autonomy and trust given to everyone in their team from day 1.

Your Role

To complete a range of activities as Qualified Person (QP) within the Quality Release Department relating to product release including, but not limited to:

• Documentation review/control, deviation approval, material status assignment/disposition
• Product stability OOT/OOS data investigations, quality defect reports and quality data performance reporting
• Support for other Quality Systems activities relating to customer complaints, product recalls, Annual Product Quality Reviews, the process change control and quality inspection systems
• To provide QP support for the business units and laboratories
• Nurture a continuously improving compliance culture within both the organisation and its clients.
• Manage personal client project assignments, including provision of Qualified Person support.

Your Qualifications

To succeed in this role, we imagine that you have the following qualifications:

• Minimum of BSc Degree or equivalent third level education
• Qualified Person Status in accordance with EC Directives
• Minimum 2 years, experience in quality or production function within the pharmaceutical industry

As a person you are a demonstrated self-starter with a proactive, hands-on approach, possessing excellent interpersonal, decision-making, teamwork, and communication skills.

For full details & Job Spec email your CV to [email protected] or call Tina at [phone]

Thornshaw Scientific is a division of the CPL Group www.thornshaw.com