QC Chemist - Tech Transfer

2021-11-11 18:37:462049-03-27Team Horizon
Job TypePermanent
AreaDublinDublinIreland
SectorLaboratory/Scientific
Start Date
AdvertiserMary King
Job Ref2240
Job Views181
Description

 QC Chemist, Tech Transfer – Team Horizon
 
We have an exciting opening on our client’s manufacturing facility in Dublin.You will be reporting to the QC Supervisor.
The QC Chemist as part of the technical transfer group is responsible for conducting testing to support the introduction of new products or assist in investigation analysis of existing products. This testing may include raw material, in process and finished product according to relevant SOPs.
 
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 under minimal supervision.
  • Complete all 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 fulfilment of production goals.
  • Participate in investigations and root cause analysis.
  • Author documents that ensure cGMP compliance, such as laboratory investigation, deviations, change controls, change notices, analytical test methods, method development/validation protocols and reports and method verification protocols and reports.
  • 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. 
  • Carry out and assist in the ongoing training of new and existing personnel, as appropriate.
  • Observe all safety and compliance procedures and actively highlight any safety concerns to help drive the reduction of accidents or near misses.
  • Minimum of a bachelor’s degree qualification in Chemistry or related Science.

 
What you need to apply:

  • 2+ years relevant laboratory experience in a cGMP environment.
  • Experience with method verification, validation, and transfer desirable.
  • Demonstrate knowledge of cGMP requirements and practices including knowledge of the USP and FDA Guidance Documents relating to the pharmaceutical Quality Control Laboratory.
  • Experience in method validation and or transfer desirable but not essential.
  • Demonstrate analytical competency in the use and troubleshooting/maintenance of common analytical instrumentation e.g., HPLC/UPLC, Dissolution, GC, FTIR, UV/Vis.
  • Demonstrated success in preparing and delivering presentations.
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