QC Technician - Pharmaceutical Company / England

I am currently recruiting for a pharmacutical company going through an exiting new expansion, they are looking to expand their team and bring on new talent this role would be perfect for a recent graduate or someone with industry experience:

Job Summary…

A crucial part of the pharmaceutical production process is undertaken by the Quality Control Department, which performs chemical and biochemical testing to ensure that the manufactured product is safe, efficacious and fit for patient use as a pharmaceutical material. The QC Technician is primarily responsible for ensuring the day to day running of the QC Analytical laboratories with daily tasks including ordering consumables, maintaining stock lists, calibration activities, waste disposal and housekeeping within QC Analytical.

The post holder will be required to work shift rotation. This rotation includes 2 weeks out of 8 weeks where the shift is 2-10pm and potential weekend working (schedule dependent).

We are looking for…

A full time, permanent QC Technician to maintain the laboratories day to day. The ideal candidate will have at least 2 A-levels in numerate / science subjects. (A degree in Chemistry, Biochemistry or related subject is desirable). Candidates with a working knowledge / experience of a regulated or cGMP environment are desirable. Other key skills include the ability to work to deadlines, organization skills and good computer literacy.

The post holder will...

• Carry out stock checks for Laboratory and reagents
• Place orders for routine orders and one-off items
• Maintain stock lists
• Receive and book in delivered consumables and reagents
• Removal of out of date materials and waste from the QC laboratories
• Assist with housekeeping in Analytical QC
• Disposal of toxic, hazardous and non- hazardous waste generated within Analytical QC
• Calibration and scheduled maintenance of analytical equipment
• Routine QC testing
• To ensure GMP documentation practices are followed when completing the necessary documentation
• Undertake work in accordance with Porton Biopharma’s Code of Safety Practice and Quality Systems
• Maintain training records
• Assist with sample receipt and booking samples in to the QC department

For more information apply and you will be promptly contacted