Quality Technician

We are seeking a motivated Quality Technician to join a leading medical device manufacturing organisation operating within a highly regulated GMP environment. This is an excellent opportunity to become part of a quality-focused team, ensuring products meet the highest standards of safety, compliance, and performance.

The successful candidate will support quality assurance activities across incoming inspection, in-process and final product testing, quality documentation, and continuous improvement initiatives while ensuring compliance with industry regulations and internal quality systems.

Key Responsibilities

• Work collaboratively as part of the Quality Assurance team to achieve departmental quality objectives.
• Perform incoming material inspection and testing in accordance with approved specifications and procedures.
• Conduct in-process and final product inspections and testing to support product release.
• Support quality control, incoming quality assurance, and metrology activities as required.
• Ensure quality documentation is completed accurately, thoroughly, and in compliance with regulatory requirements.
• Escalate quality issues, deviations, or potential product concerns promptly to the appropriate stakeholders.
• Participate in internal quality audits and support audit readiness activities.
• Assist with change control activities, including review and update of quality system documentation.
• Prepare quality metrics and reports to support management review processes.
• Generate and maintain manufacturing batch records where required.
• Make disposition decisions for incoming materials in accordance with approved procedures.
• Maintain training compliance and adhere to all company policies and procedures.
• Contribute to continuous improvement initiatives focused on quality, safety, environmental performance, and operational efficiency.

Skills & Experience

Essential

• Previous experience working within a regulated manufacturing environment.
• Strong attention to detail with a commitment to quality and compliance.
• Excellent organisational and documentation skills.
• Good communication skills and the ability to work effectively within a cross-functional team.
• Ability to follow standard operating procedures and work within established quality systems.

Desirable

• Third-level qualification in a Science, Engineering, Quality, or related discipline.
• Experience within the medical device, pharmaceutical, biotechnology, or combination product industries.
• Experience working within a GMP-regulated environment.
• Familiarity with incoming inspection, quality control testing, batch record review, and quality documentation.
• Knowledge of ISO 13485, FDA, and cGMP requirements.
• Key Competencies
• High level of accuracy and attention to detail.
• Strong analytical and problem-solving skills.
• Ability to adapt to changing priorities and processes.
• Commitment to maintaining the highest quality and safety standards.
• Proactive approach to identifying and escalating quality concerns.
• Collaborative team player with a continuous improvement mindset.

For a confidential conversation about the role please apply for the role or contact Owen Clancy at oclancy@sterlingengineeringeu.com By applying to this job post you agree that Sterling Engineering may process your personal data for recruitment purpose.