Quality Control Analyst
3 weeks ago
RESPONSIBILITIES INCLUDE, BUT ARE NOT LIMITED TO:
• Perform efficient/reliable/high quality analytical testing in accordance with
USP/NF/EP/JP/FCC/etc. or customer supplied guidelines. Typical testing may include
Dissolution, Titration, Polarimetry, Loss on Drying, Viscosity, Residue on Ignition, Heavy Metal
Content, FTIR, HPLC, and GC, etc.
• Maintain accurate written records of all analysis performed.
• Accurately interpret and effectively communicate analytical results and issues.
• Schedule daily tasks in an organized and efficient manner.
• General knowledge of the use and operation of basic laboratory equipment.
• Calibrate and maintain lab equipment and instrumentation.
• Responsible for operating in a safe manner, must be familiar with basic laboratory and
chemical hygiene practices
• Become proficient in standard operating procedures and test methods.
• Ability to work in a “flow to the work” team environment.
• In combination with other lab personnel, be responsible for a clean and safe work
environment.
• Perform peer review of analytical testing and write up.
• Write SOPs on an as needed basis.
Essential Skills and Experience:
Education or Equivalent:
• Bachelors degree om Chemistry, Biology, Chemical Engineering or Life Sciences (preferred
Chemistry or Biology).
• Work Experience – 0-5 years in Quality, Laboratory, Clinical or Chemical manufacturing role
(including internships or co-op experience).
Knowledge/Skills Requirements:
• Ability to multi-task with high efficiency.
• Ability to work well under pressure and maintain efficiency.
• Ability to communicate effectively.
• Basic knowledge of lab safety and the ability to work safely with chemicals of varying potency.
• General computer literacy including use of Microsoft Word and Excel.
• Ability to perform analytical testing while standing for long periods of time
• Accurate testing on the first attempt under pressure of production details.
• Experience in the pharmaceutical industry preferred.
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