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Materials Analyst – Pharmaceuticals

Permanent, Shift Based (Mon-Fri, Day Shifts)

Paying up to £26,000 +  shift allowance + benefits

Based in North London

Do you have experience within science, and an interest in working with samples for the pharmaceutical industry?

Would you like to work for a reputable scientific organisation, making a direct difference to patients’ lives across the globe?

My client, a leader in delivering high quality, processed biological materials is seeking a Materials Analyst – Pharmaceuticals to join their growing team in London. In this role you will be responsible for testing samples, including raw materials, using testing and inspection methods in line with company Standard Operating Procedures (SOP’s) and Good Manufacturing Practice (GMP).

Key responsibilities of the Materials Analyst – Pharmaceuticals include:

Inspection and release of materials, including raw materials and packaging, in line with company polices, SOP’s and GMP.

Ensure results are reported in a timely manner, within appropriate systems e.g. LIMS.

Preparation of laboratory reagents and controls, for use in sampling activities and experiments.

Support the overall smooth running of the function, including general housekeeping activities and equipment calibration and validation.

Report any Quality Assurance (QA) incidents e.g. non-conformities and deviations. Supporting with investigations and resolutions e.g. change controls and CAPA’s.

Follow Health and Safety (H&S) policies and procedures, raising concerns or potential risks to management within the organisation.

To be considered for the Materials Analyst – Pharmaceuticals, you will need the following skills and experience:

A background within science, minimum of a STEM A-Level (or equivalent), with a passion for working within science in the pharmaceutical industry.

Hands on experience within industry e.g. materials testing, pharmaceutical manufacturing / production or a scientific warehouse would be strongly advantageous.

Knowledge of Health and Safety guidelines and procedures. Beneficial: Within a laboratory and/or warehouse environment.

A technical mindset, so able to develop skills within equipment calibration and validation activities.

An understanding of Good Manufacturing Practice (GMP) would be highly advantageous.

Strong communication skills, so able to cross functionally communicate with internal departments and teams.

Experience of working collaboratively, whilst also being self-motivated when working independently within a laboratory environment.

This is an excellent opportunity to take the next step in your career within a reputable and growing Pharmaceutical organisation.

Please apply online or contact Katie-May Kress at CY Partners for more information.

Keywords: “Materials Analyst, Materials Analysis, Chemist, Chemistry, Quality, Quality Control, Raw Materials, Packaging, Materials, Warehouse, Good Manufacturing Practice, GMP, SOP, LIMS, Pharmaceutical, Biopharmaceutical, London, North London”

The recruiter has stated that all applicants for this job should be able to prove that they are legally entitled to work in the UK. CY Partners Recruitment Ltd, trading as CY Partners is an Employment Business/Agency