Quality Systems Specialist

Collins McNicholas Recruitment; Connacht; On-site; EUR 50,000 - 70,000; Full time

Job summary

A leading company in the MedTech sector is seeking a Quality Systems Specialist to join their QA team in County Mayo. The role involves enhancing Quality Management Systems, collaborating with various teams, and ensuring conformance to client requirements. Ideal candidates will have at least 3 years of experience in Quality Assurance within the pharmaceutical industry, a strong ability to communicate, and a detail-oriented approach. This is an exciting opportunity to contribute to life-saving therapies in a rapidly growing organization.

Qualifications

• Minimum 3 years of experience in the pharmaceutical industry.
• Strong communicator with clients.
• Adept at multi-tasking in a fast-paced environment.

Responsibilities

• Enhance Quality Management Systems supporting global pharma.
• Track and report key performance indicators.
• Manage Internal Audit program and corrective actions.

Skills

Communication

Attention to Detail

Problem Solving

Team Orientation

Self-Motivation

Results Driven

Education

Bachelor's degree in Science, Engineering or Business

Job description

Our client, based in Mayo, are an exciting scaling MedTech facility and are looking to grow their QA Team with a Quality Systems Specialist.

The Role:

As the Quality Systems Specialist. you will enhance their Quality Management Systems, thereby supporting global pharma in the production of life saving medicines and therapies. You will be responsible for ensuring that the QMS processes are efficiently maintained, and conform to internal and external client requirements, engaging cross functionally with exceptional SME team members to enhance our QMS and support our Client’s processes.

Responsibilities:

• Collaborate as a solution-oriented team member to work alongside the commercial and technical operations teams, delivering QA objectives to support business growth.
• Track and report metrics and key performance indicators for the Quality Management System.
• Collaborate with stakeholders to identify and support value-added improvements and key performance indicators.
• Review and follow-up on open actions related to Corrective and Preventative Actions (CAPA), Out of Specification (OOS) reports and Deviations.
• Support / host Client quality audits. Inclusive of addressing findings and required actions.
• Management of the Internal Audit program including coordinating audit schedules, reviewing findings, tracking corrective actions, and providing insights and initiatives to drive continuous improvement.
• Provide forward thinking innovative solutions and identify opportunities to add value to the teams’ deliverables.
• Assist in the development of appropriate systems and processes to ensure delivery of information across functions to support enhanced performance culture.
• Document Control - Site lead for managing our clients SOPs and Document Control.
• Manage quality training programs at Castlebar site to ensure these effectively mirror what is in place at HQ.
• Site lead for training compliance to SOPs.
• Other duties as required to support the growing Quality organisation.

Requirements:

• Minimum 3 years of professional experience in the pharmaceutical industry in Quality Assurance focused role.
• Adept at multi-tasking and working in a fast-paced environment.
• Strong, clear and concise communicator both internally and externally with pharmaceutical clients.
• Bachelor’s degree in science, engineering or business preferred.
• Willingness and availability to travel on company business.
• Team Oriented: Ability to integrate with the organizational Core Values, culture, and team climate.
• Detail Oriented: Ability to focus on the details yet understand the overall direction.
• Self-Motivated: Identifying what needs to be done and doing it before being asked or before the situation requires it.
• Results Driven: The ability to focus on the desired result of one’s own or one’s unit’s work, setting challenging goals, focusing effort on the goals, and meeting or exceeding them.

For more information and a confidential discussion on the role, please contactMichelle Mc Inerney.

[e-mail]

091 706717