Bioprocess Engineer Role Dublin

Process Engineer

  • Posted Sep 16, 2022
  • Dublin
  • Contract
  • BBBH25765


LSC have a great contract opportunity for a Process Engineer to a leading biotech company based in Dublin.
If you have a minimum of 5 years' (for MSc) or 7 years' (for BSc) directly related experience in academia, pharmaceutical or biotechnology company and are ready for your next challenge, this could be the perfect project for you!


ABOUT THE PROJECT - KEY RESPONSIBILITIES:

  • Supporting experimental design, execution, data analysis and interpretation.
  • Interpreting trends observed in commercial process monitoring (e.g., proactive process analysis (PPA), continued process verification (CPV), statistical process control (SPC) multivariate analyses (MVDA), and for further technical investigations and process changes that seek to drive improvements to yield and/or robustness.
  • Supporting deviation management.
  • Supporting change control prioritization and implementation.
  • Authoring and reviewing of batch documentation, technical reports and global regulatory submissions.
  • Supporting multidisciplinary teams (manufacturing science and technology, quality, analytics, regulatory) for process improvement and troubleshooting with end-to-end product focus.
  • Applying LeanSixSigma tools by:
  • Securing continuity of an appropriate LSS/CEM level of knowledge.
  • Facilitating problem solving & risk assessment (FMEA) projects/meetings.
  • Making problems visible and strive for continuous improvement.
  • Lead and support various manufacturing science and technology organizational initiatives as needed (examples include safety, financial forecasting, work standardization, etc).
  • Maintain continuous focus on quality and safety compliance and unflinching focus on the customer.


ABOUT YOU - ARE YOUR SKILLS A MATCH?

  • Experience with upstream cell culture and/or downstream purification of biological molecules. Experience with technology transfer, regulatory filing, and commercial drug substance manufacturing of biologics is a plus.
  • Technical operations experience in the drug substance manufacture of biological molecules at commercial-scale.
  • Prior experience in drug substance process development, process characterisation studies, process performance qualification and validation, site readiness, batch record reviews, authoring regulatory CTD sections and/or working with external contract organisation for development and/or manufacturing.
  • Working knowledge of statistical methods for DOE design and data analysis (e.g., JMP or Design Expert software) .
  • Working knowledge of statistical process control (SPC), multivariate analysis (MVDA).


Note: Are you currently eligible to work in Ireland? As this is a contract opportunity you will need to hold a Stamp 1G/Stamp 4 visa to apply!
Apply via this advert or contact Peter Cronin on 021-4777329 if you have any more questions about this Process Engineer opportunity!

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