QC Analyst

Job description

A leading Pharmaceutical is looking to grow their team of Lab Analysts in Sligo. Your new company is well recognised on the global Pharmaceutical scene and this is a great opportunity to join a great company.

As a Lab Analyst you will be responsible for: 

  • Maintain and comply with Laboratory Documentation and Computerized Systems Data Integrity requirements.
  • Understand Regulations and business processes required to maintain Laboratory Data Integrity
  • Responsible for housekeeping duties in the lab.
  • Responsible for the timely completion of chemical testing of raw material.
  • Ensure that all test equipment is used and maintained correctly.
  • Responsible for raising change requests and data verification as assigned.
  • Ensure all in process sampling and testing is completed in a timely manner.
  • Maintain up-to-date, complete and precise records of all tests performed.
  • Adhere to cGMP and GLP requirements.
  • Assist in the resolution of quality problems as required.
  • Developing and changing of in-house laboratory procedures as appropriate.
  • Aid in training of new analyst.
  • Supports the transfer of new products.
  • Adheres to and supports all EHS & E standards, procedures and policies 

To be considered for this role you must have previous expeirence with Lab Equiment operation in a GMP setting and be experienced in HPLC and/or GC.

If you are interseted in this role, apply now to be considered. Alternatively you can contact me via phone 014744692 or alternatively Connect with me on LinkedIn