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QC Laboratory Technician

Quanta part of QCS Staffing

Leinster

On-site

EUR 30,000 - 45,000

Full time

14 days ago

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Job summary

A leading global pharmaceutical client seeks a QC Laboratory Technician for a state-of-the-art facility in Leinster, Ireland. As part of this role, you will contribute to quality assurance processes, ensuring compliance with health regulations and enhancing operational efficiency through collaborative teamwork. This is an excellent opportunity to join an innovative company focusing on vital oncology treatments with a supportive environment fostering continuous improvement.

Qualifications

  • 1-3 years’ experience in the pharmaceutical or biopharmaceutical industry.
  • Previous analytical experience preferred.
  • Ability to work independently with moderate guidance.

Responsibilities

  • Movement of materials and system transactions across QC labs.
  • Participate in writing and revising operational procedures.
  • Ensure compliance with GMP and GxP standards.

Skills

Strong communication
Interpersonal skills
Analytical experience
Problem solving
Continuous improvement

Tools

GLIMS
LIMS
SAP

Job description

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QC Laboratory Technician - Pharma - Carlow, Ireland - 11-Month+

With worldwide demand for their life-changing oncology treatment increasing; one of our global pharmaceutical clients is looking for a QC Laboratory Technician to join their team to support multiple capital projects taking place onsite in Leinster.

This is a fantastic opportunity to work on a state-of-the-art fill-finish facility and the company’s first stand-alone vaccine and biologics plant outside the US.

Role Summary:
  • Movement of materials across the network.
  • System transactions including movement and shipping of samples across QC labs within the network.
  • Knowledge and experience using systems such as GLIMS, LIMS, and SAP beneficial.
  • Inspection of primary packaging.
  • Participate in writing, revising, and rolling out accurate operational procedures, training materials, and maintenance procedures for various Quality systems; ensure all work is carried out in line with these standards.
  • Review, approve, and trend test results where applicable.
  • Peer review other analysts’ documentation, ensuring QC Right First Time KPIs are achieved.
  • Participate in QC daily meetings and ensure effective communication of testing progress, deviations, etc.
  • Ensure that all Quality Systems within the department are adhered to daily.
  • Complete all documentation in compliance with GMP and GxP standards.
  • Engage in problem solving to identify root causes of issues.
  • Support audit and inspection preparations to ensure department compliance/readiness.
  • Collaborate with team members by sharing expertise and skills.
  • Drive continuous improvement through root cause analysis methods such as FMEA, Fishbone diagrams, and 5 Whys.
  • Ensure compliance with global policies, procedures, guidelines, and regulatory requirements, and execute current Good Manufacturing Practices (cGMP) in daily activities and all applicable functions, including maintaining accurate records.
Experience, Knowledge & Skills:
  • 1-3 years’ experience in the pharmaceutical, biopharmaceuticals industry, or a similar operating environment with a focus on quality.
  • Previous analytical experience.
  • Ability to work independently and initiate improvement initiatives with moderate guidance.
  • Strong communication and interpersonal skills, with the ability to work across teams.

If this role interests you, please apply now!

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