43774 - QC Analyst

Orion Group Life Sciences are looking for 2 QC Analysts for our Multinational Pharmaceutical client based in Liverpool. One for initial 12-month contract and one for initial 6-month contract. This is an on-site position. 

Job Summary:

This role is for an Analyst within the Analytical and Raw materials laboratory, within Quality Control. It is a fast paced, high through put laboratory where compliance with health authority regulations and attention to detail is critical to support the vaccine manufactured onsite.

Responsibilities:

• Collection of samples from various manufacturing areas and receipt into the laboratory via GLIMs system.
• Work to a high level of cGMP and GDocP in order to maintain compliance and adherence to regulations.
• Perform analytical testing of raw materials, in process, finished product and utilities samples in accordance with relevant SOPs.
• Record and report laboratory analysis in a clear and concise manner ensuring compliance to regulations.
• Perform thorough peer review of analysis to ensure accuracy and adherence to GMP/GDocP.
• Instrument Maintenance and Calibration.
• Reagent and Standard Qualification.
• Escalation of issues to Team Co-Ordinator/Laboratory Manager and initiation of deviations in a timely manner.
• Escalate any OOS/OOE/OOT results to Team Co-Ordinator/Laboratory Manager as soon as practically possible.
• Initiate and perform laboratory investigations with discussion and collaboration with effected departments where necessary.
• Perform periodic reviews of SOPs.
• Completion of HSE risk assessments, periodic reviews and adherence.
• Archiving of laboratory documentation.
• Ordering of reagents and consumables.
• Ensuring a clean and safe workplace for all associates.
• Completion of training to maintain compliance.
• Participation in technical/validation studies where applicable.

Requirements:

• Educated to NVQ level 2 or equivalent in a relevant scientific discipline. Undergraduate (BSc) degree in Chemistry is preferred.
• Experience in the relevant testing discipline, ideally within the pharmaceutical industry having worked to cGMP standard.
• Minimum 1 year experience in Analytical Department.
• Previous experience of GLIMs is preferred.
• Sense of urgency.
• Attention to detail.
• Effective written and oral communication skills.
• Proficient use of Microsoft office e.g. outlook, Word, Excel and Powerpoint etc.

If you would like to have a confidential conversation regarding this opportunity please reach out to Tim Browaeys, tim.browaeys@orion-jobs.com or contact Tim on 0044 7593448607

#opportunity #multinational #pharmaceutical #quality #QC #analyst #samplecollection
#GLIMS #cGMP #GDocP #rawmaterialtesting #SOP’s #instrumentmaintenance # instrumentcalibration #analyticaldepartment


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