Quality Technical Services Manager

3 weeks ago

Dublin, Ireland TN Ireland Full time

Quality Technical Services Manager - South Dublin, Dublin

Client: ICDS Recruitment

Location: Dublin, Ireland

Job Category: Other

EU work permit required: Yes

Job Reference: af8498b6c030

Job Views: 57

Posted: 21.01.2025

Expiry Date: 07.03.2025

Job Description:

Quality Technical Services Manager - South Dublin

Ref No: AM18357

This is a 1 year fixed-term contract, on site.

We are seeking a dynamic and detail-oriented professional to ensure the smooth operation of the 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.

Key Responsibilities:
  1. Ensure efficient processes to support manufacturing and prevent disruptions through managing equipment redundancy, validation, and best in class laboratory practices and training programs.
  2. Measure and communicate process efficiency and effectiveness, delivering improvement projects on time and within budget.
  3. Lead procurement efforts for goods and services, ensuring adherence to company policies.
  4. Facilitate technical problem-solving, CAPA processes, and decision-making within areas of responsibility.
  5. Co-lead Quality Assurance initiatives, regulatory audits, and manage specification changes.
  6. Collaborate with leadership, offering guidance and solutions while ensuring alignment with Global Quality teams.
  7. Monitor team performance across key metrics (Safety, Quality, Delivery, Cost, People) and drive continuous improvement efforts.
  8. Oversee people management, including development, feedback, and performance evaluations.
  9. Stay current with industry trends to keep practices competitive.
  10. Participate in the hiring process for critical roles and be a key member of the Site Quality Leadership team.
Qualifications and Experience Requirements:
  1. Bachelor's degree in Engineering or Science; postgraduate qualification an advantage.
  2. At least 6 years' experience in the medical device or similar highly regulated industry.
  3. Experience with audit management, process validation, CAPA systems, sterilization, and clean room environments.
  4. Strong project management and Six Sigma experience.
  5. Proficient in data analysis and reporting tools (Excel, Project, Minitab, Power BI).
  6. Excellent leadership, communication, and interpersonal skills, with the ability to work independently and collaboratively.
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