Shift Environmental Monitoring Scientist

Unfortunately, we are unable to offer visa sponsorship for this role.

Eurofins is currently recruiting for full time Environmental Monitoring Scientists based at our client site in Macclesfield, UK.

The successful candidates will provide expertise within the QC Microbiology testing section.

The candidates will have great organizational skills and proven ability to rapidly respond to technical challenges, great troubleshooting skills and operate in a flexible manner, exhibiting high energy, self-motivation and collaborative communication skills.

This role operates on a continuous 2 week rotating pattern of 11hour day shifts: -

Week One: Monday, Tuesday, Saturday and Sunday.

Week Two: Wednesday, Thursday and Friday.

Options for shifts 06:00 to 17:00 or 07:00 to 18:00 with breaks therein.

The primary purpose of this role is to support Environmental monitoring testing to assure suitability of client’s manufacturing facilities.

Job Responsibilities

• Aseptically collect Environmental Monitoring (EM) and cleaning validation samples at client’s facility using sampling protocols and associated documents.
• Ensure compliance with GMP policies and SOPs in a production environment
• Aseptically gown and work in sterile manufacturing areas
• Perform routine and non-routine QC testing such as Bioburden, Endotoxin, Concentration, and Conductivity
• Maintain and Ensure sample chain of custody using a LIMS system and perform all aspects of Sample management including aliquotting, storage, receipt, and testing.
• Review manufacturing schedule for dynamic environmental monitoring to ensure all samples are collected appropriately, and address problems where necessary
• Review and reconcile all environmental monitoring samples at the end of the production run to ensure all samples were appropriately taken, processed, and were within required limits
• Perform Laboratory and Equipment maintenance
• Participate in lean lab operation and continuous improvement programs to reduce operating costs
• Calculate, evaluate, review, and properly communicate data verbally and in written format
• To GMP review analytical data.
• To initiate and follow-up OOS results and action limits as per client procedures.