QC Chemist /Lab Analyst (HPLC/GC)

2022-01-11 09:41:392049-06-11Team Horizon
Job TypePermanent
AreaDublinDublinIreland
SectorLaboratory/Scientific
Start Date
AdvertiserMary King
Job Ref2311
Job Views1586
Description
 
Team Horizon currently has an exciting opening for a QC Chemist to work on our client’s manufacturing facility. This is a permanent role and you will be part of the team in Clonshaugh, Dublin. You will have the chance to improve laboratory testing and equipment therefore you will need really strong scientific methods and techniques skills.
 
Why you should apply:
  • Our client has developed a stand-out culture of innovation, inclusion and development, and consistently features as a great place to work.
  • The role is generously compensated, and attracts a competitive base salary and highly attractive benefits package.
  • Excellent career progression opportunities.
 
What you will bedoing:
  • Conduct chemical and physical laboratory tests and analyze raw materials, intermediates, and final product to ensure compliance with standards.
  • Complete all testing, including special project / protocol testing in a timely manner that supports established production targets and SLAs. 
  • Maintain data integrity and ensure compliance with FDA, GLP, QSR and cGMP regulations, as well as with company SOPs and specifications. 
  • Observe established escalation process for laboratory issues that impact established production-related Service Level Agreements (SLAs) and/or the fulfillment of production goals.
  • Participate in deviation investigations. 
  • Author documents that ensure cGMP compliance, such as laboratory investigation, deviations, change controls, change notices, analytical test methods; analytical test method development reports; method validation protocols; method transfer protocols and reports; method verifications protocols and reports; and instrumentation qualification documentation (URS/IQ/OQ/PQ).
  • Seek process innovation and continuous process improvement and perform quality improvement initiatives in the laboratory to meet site production goals. 
  • Support and adhere to established processes and productivity targets.
  • Recognize and report to immediate supervisor any issues or deviations from accepted standards.
  • Provide status updates on own activities and productivity challenges according to defined procedures.
  • Complete and conform to all training requirements for job role, including company-required and job role-specific training. 
What you need to apply:
  • A third level qualification in Chemistry or related Science, preferably a bachelor’s degree with 6 months + GMP experience with relevant Quality Control experience. 
  • Experience in pharmaceutical manufacturing facility.
  • Demonstrate knowledge of cGMP requirements and practices including extensive knowledge of the USP and FDA Guidance Documents relating to the pharmaceutical Quality Control Laboratory.
  • Demonstrate competency in the operation, calibration and qualification of common analytical instrumentation e.g., HPLC, Dissolution, GC, FTIR, Electro Chemistry (DME), UV/Vis and other USP instrumental and Wet chemistry technologies used in pharmaceutical Quality Control Laboratory.
  • Demonstrate strong analytical laboratory skills and laboratory troubleshooting abilities.
  • Demonstrated success in making effective and persuasive presentations on complex topics to upper management.
 
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