QC Laboratory Technician Shift (Incoming QC)

at  Life Science Recruitment

QC Laboratory Technician Shift (Incoming QC)
RK21180
11 Months
Carlow
We’re currently recruiting for an exciting opportunity with an award-winning Pharmaceutical organization based in Carlow. This is an excellent position for anyone who is looking to join a leading multinational who are one of the best at what they do.

EDUCATION AND EXPERIENCE :

• Degree in Science, Engineering or similar
• 1 - 3 years’ experience in the Pharmaceutical, Biopharmaceuticals industry or a similar operating environment which includes experience in a Quality function.
• Previous Analytical Experience
• Knowledge of US and European cGMP guidelines, and other international regulatory requirements, as applicable to the site.
  If interested in this posting please feel free to contact Rachel Kent on +353 (0)87 427 8808 or rachel.kent@lifescience.ie for further information.

• 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/ rolling out accurate operational procedures, training materials and maintenance procedures for various Quality systems; ensure all work is carried out in line with same.
• Where applicable, review, approve and trend test results.
• 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 on a daily basis.
• Complete all documentation in compliance with GMP and GxP standards.
• Problem solving to get to root cause of issues.
• Provide support with audit/inspection requirements to ensure department compliance/readiness.
• Collaborating with others by sharing your skill-set and expertise
• Drive continuous improvement, perform root cause analysis on system failures e.g. FMEA, Fishbone diagrams, 5 why’s etc,
• Drive compliance with Global Policies, Procedures and Guidelines, regulatory requirements and execute current Good manufacturing Practices (cGMP) in the performance of day to day activities and all applicable job functions, including maintenance of accurate records.