Quality Technical Services Manager - 12 month FTC

Life Science Recruitment; Dublin; On-site; EUR 60,000 - 80,000; Full time

Job summary

An innovative medical device company located in Dublin is seeking a Quality Technical Services Manager for a 12-month fixed term contract. In this onsite role, you will ensure smooth operations in manufacturing processes, lead continuous improvement initiatives, and maintain industry compliance. Ideal candidates have a bachelor's in Engineering or Science with over 6 years of relevant experience and strong leadership skills. A competitive salary and benefits package are offered.

Benefits

Competitive salary

12% bonus

Share options

Pension

Healthcare

Development opportunities

Qualifications

• 6+ years of experience in the medical device or highly regulated industry.
• Experience with audit management, process validation, CAPA systems, sterilization, and clean room environments.
• Ability to work independently and collaboratively.

Responsibilities

• Ensure efficient processes to support manufacturing and prevent disruptions.
• Lead procurement efforts for goods and services.
• Collaborate with leadership and manage specification changes.

Skills

Project management

Data analysis

Leadership

Communication

Interpersonal skills

Six Sigma

Education

Bachelor’s degree in Engineering or Science

Postgraduate qualification

Tools

Excel

Project

Minitab

Power BI

Job description

Quality Technical Services Manager - 12 month FTC

Job Title: Quality Technical Services Manager (1 year fixed term contract)

Location: Pottery Road, Dun Laoghaire, Dublin.

Benefits: Competitive salary, 12% bonus, Share options, Pension, Healthcare + excellent opportunity to develop your experience and career in an exciting company.

Company — For nearly 100 years, my client have been accelerating the journey to better diabetes care. With the creation of the first insulin delivery device, they have delivered an innovation that moved the management and treatment of diabetes forward.

Overview — In this role you will ensure the smooth operation of my client’s manufacturing processes, prevent disruptions, and lead continuous improvement initiatives. This role is key to maintaining equipment redundancy, validation, and maintenance, while also driving best‑in‑class laboratory practices and training programs. This is an onsite position and is a 1‑Year Fixed Term contract.

Responsibilities

• Ensure efficient processes to support manufacturing and prevent disruptions through managing equipment redundancy, validation, and best‑in‑class laboratory practices and training programs.
• Measure and communicate process efficiency and effectiveness, delivering improvement projects on time and within budget.
• Lead procurement efforts for goods and services, ensuring adherence to company policies.
• Facilitate technical problem‑solving, CAPA processes, and decision‑making within areas of responsibility.
• Co‑lead Quality Assurance initiatives, regulatory audits, and manage specification changes.
• Collaborate with leadership, offering guidance and solutions while ensuring alignment with Global Quality teams.
• Monitor team performance across key metrics (Safety, Quality, Delivery, Cost, People) and drive continuous improvement efforts.
• Oversee people management, including development, feedback, and performance evaluations.
• Stay current with industry trends to keep our practices competitive.
• Participate in the hiring process for critical roles and be a key member of the Site Quality Leadership team.

Qualifications

• Bachelor’s degree in Engineering or Science; postgraduate qualification preferred.
• 6+ years of experience in the medical device or highly regulated industry.
• Experience with audit management, process validation, CAPA systems, sterilization, and clean room environments.
• Strong project management and Six Sigma experience.
• Proficient in data analysis and reporting tools (Excel, Project, Minitab, Power BI).
• Excellent leadership, communication, and interpersonal skills, with the ability to work independently and collaboratively.

Does this sound like your next career move? To apply, forward your application to the link provided or contact me on 0870608656 [e-mail]