QC Separation Analyst

at  Life Science Recruitment

Cork, County Cork, Ireland -

Start DateExpiry DateSalaryPosted OnExperienceSkillsTelecommuteSponsor Visa
Immediate13 Jul, 2024Not Specified14 Apr, 20242 year(s) or aboveCapillary Electrophoresis,Pharmaceutical IndustryNoNo
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Description:

We’re currently recruiting for an exciting opportunity with an award-winning Pharmaceutical organization based in Cork. This is an excellent position for anyone who is looking to join a leading multinational who are one of the best at what they do.

EDUCATION & EXPERIENCE

  • BSc (Honors) in a scientific/technical discipline.
  • 2 years’ experience in a QC laboratory-testing environment within the biological and/or pharmaceutical industry.
  • HPLC, Capillary Electrophoresis, UPLC/ Mass Spec experience
    If interested in this posting please feel free to contact Sean McCarthy on +353 (0)87 798 8480 or sean.mccarthy@lifescience.ie for further information.

Responsibilities:

  • Achieves a high level of competency in laboratory methods and procedures to support in process and release testing of biotechnology products.
  • Review and approval of laboratory test results.
  • Performs analytical testing activities in relation to method validation and technical transfer activities to ensure that all methods meet ICH, USP and EP guidelines.
  • Executes validation, operation, maintenance, calibration and troubleshooting of equipment and it’s associated software.
  • Write/executes reports and reviews IQ/OQ and PQ protocols to ensure that all relevant equipment is qualified for cGMP use.
  • Ensures that all testing is completed, reviewed and approved within agreed turnaround times.
  • Ensures QC activities are carried out in compliance with product license commitments, cGMP and company quality standards.
  • Trains other QC analysts in laboratory methods and procedures when required.
  • Writes/updates and reviews TMs, SOPs and WIs as required.
  • Writes and reviews invalid assays, non-conformances and deviations as required.
  • Actively participates in JSI lean initiatives such as Kaizen, 6S and Gemba.
  • Is an active member of the QC group and provide assistance with other group activities as required.
  • Communicates relevant issues to the QC Team Leader promptly.
  • Maintains and develops knowledge of analytical technology as well as cGMP standards.


REQUIREMENT SUMMARY

Min:2.0Max:7.0 year(s)

Pharmaceuticals

Pharma / Biotech / Healthcare / Medical / R&D

Clinical Pharmacy

BSc

Proficient

1

Cork, County Cork, Ireland