A growing pharmaceutical group of companies, part of an international corporation, specialized in the production of APIs and finished dosage forms is working alongside GRS Malta to recruit a Quality Control Laboratory Analyst. The selected candidate will be responsible for the analysis of incoming raw materials, Active Pharmaceutical Ingredient and Finished Dosage Form according to GMP Principles.
If you are in possession of a Diploma or a Degree in Chemistry or related scientific subject, and hold an EU citizenship and available immediately for employment, send your CV today for this Malta based role.
MAIN DUTIES AND RESPONSIBILITIES
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Sampling, analysing, and reporting the quality of raw materials, APIs and Finished Dosage Form products.
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Compiling and interpreting test results.
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Performing equipment calibration and confirmatory analysis.
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Carrying out documentation and standard operation reviews and other tasks relating to
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Quality Control in the pharmaceutical industry.
CANDIDATE PROFILE
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Holder of EU citizenship already residing in Malta and available immediately for employment.
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In possession of a Diploma or a Degree in Chemistry or related scientific subject.
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Ideally experienced with working in a pharmaceutical environment.
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Extremely organised and possess excellent communications skills.
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Able to work on two shifts: morning/ afternoon.
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Able to think critically and a good problem solver.
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Able to work independently as well as in a team environment.
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Self-motivated and have excellent attention to detail.
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Results oriented and will display an attitude that reflects our Company values.
COMPANY BENEFITS
Due to the high volume of applications we receive at GRS Recruitment, only shortlisted candidates will be responded to.
To apply for this position, please email your CV to
Michelle Cooper, michelle@grsrecruitment.com quoting the above job reference or call +356 216 80 800