QC Chemist - Rapidly GROWING CHEMICALS MANUFACTURER

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Brand new role - QC Chemist required for a leading fine chemicals manufacturer based in the Teesside/Middlesbrough area.

Job Opportunity – QC Chemist

Company: Multinational fine chemicals manufacturer, that supplies its products to some of the leading brands across the globe.  The company is now in stage of investment into people and facilities and has very ambitious growth plan.

Hours of work: 8am to 4pm, Monday to Friday (some flexibility if required) + Overtime which can be days and nights to cover holidays etc.  (shift premiums will apply)

Why join?  

• Variety of work including QC and QA
• Great salary and benefits 
• Joining the company at a time of rapid growth and investment.
• Working with an international company which offers training and career development.
• Established team to learn and gain experience from.

Location:  Teesside/Middlesbrough.

NB - own transport is desirable due to location.

Duration: Permanent

Salary: Up to £35k depending on your skills and experience (Overtime paid for shift working 

You  will be involved in:

• Testing of raw materials, in-process and final products to ensure that they are manufactured correctly.
• Use of analytical systems such as GLC and GCMS along with bench chemistry techniques.
• Updating technical documents including CofAs and SOPs.
• Helping with audits and other admin duties as required.
• Ensure that the testing done is carried out to the required standard (GMP, GLP, MHRA etc) and equipment is calibrated correctly,

What do you need to be considered?

You will need:

• Degree or equivalent experience in science-based subject, ideally Chemistry.
• Working knowledge of GLC or GCMS instrumentation (Other chromatography experience will be considered) and bench/wet chemistry techniques.
• Minimum of 1 years experience working in a commercial laboratory either via industrial placement or work experience.
• Experience of working in a regulated environment working to one of the following standards ISO, UKAS, GMP, GLP, FDA, MHRA.
• Prior experience in auditing, writing documents and updating SOPs is desirable.