Laboratory Analyst

While working under the direction of the Quality Control and Research & Development Manager, the selected candidate will be responsible to carry out analysis on raw materials and finished products, according to approved monographs and using various techniques including HPLC and GC.

The selected person will be expected to:

• Perform sample analysis according to established methods and procedures, and status labelling of raw materials, intermediate and finished products.
• Assist and support new and ongoing stability studies, analytical method validation studies, process validation studies and any R&D activities as required.
• Adhere to defined laboratory management systems such as sample registration and record of removal and/or entry of stability samples, etc.
• Assist in the day-to-day laboratory activities and operations in accordance with current Good Laboratory Practices.

The ideal candidates for above positions should be:

• In possession of a degree in Pharmacy, Chemistry, or a related science subject. Candidates having the BTEC National Diploma in Applied Science will also be considered.
• Although full training will be provided, the chosen candidates preferably must have a minimum of 2 years working experience in a pharmaceutical GMP environment.
• Have excellent organisation and communication skills
• Be able to work on own initiative, as well in a team and under pressure to meet pre-set deadlines.

If you are interested or know of someone that could be, kindly forward your CV in a word format to Krista Psaila on [email protected] or call on +356 27 204 518 for further information.
 
Should this position not be of interest to you, I am always on the look out for Accountants, Financial Controllers, Accounts Assistants, Web & Software Developers, Systems & Network Administrators and Graphic Designers. Get in touch with me by sending me your CV on [email protected]