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Commissioning & Qualification Engineer

  1. Eastern Europe
Zagreb-dio
  1. Contract
Competitive
  1. CAPEX Projects
33610

This vacancy has now expired

Upstream C&Q Engineer - Pharma - Zagreb - 9-Month Contract 

Our client, One of the world’s largest pharmaceutical organisations is responsible for developing and manufacturing medicines and vaccines for a wide range of medical disciplines. They have been responsible for the development of many blockbuster drugs in both the USA and the EU and have a presence in the USA, EU and Asia-Pacific.

With continued organisational growth and a considerable amount of investment across the portfolio and capital programme they are seeking the expertise of Upstream C&Q Engineer.


Key Responsibilities:
  • Report to the commissioning Stream Lead
  • Prepare Commissioning Test Protocols / Verification Test Protocols using Design/Construction documentation such as P&IDs, Drawing, URSs, Risk assessment, Specifications, Vendor Turn Over Package….
  • Execute, Review and support vendor testing (e.g. SAT / CTP / VTP)
  • Initial system start-up activities inclusive of P&ID checks, utility energisation, motor checks, pressure service test.
  • Execute Delta V testing in accordance with approved Automation design and record test discrepancies for further analysis in accordance with project Engineering Change Controls procedures
  • Proficiency in Delta V commissioning of control modules, equipment modules, phases, synchronizations is desirable.
  • Documentation of the test results in the relevant test/Commissioning/Verification documents according to GDP
  • Participate to the daily morning meetings
  • Participate on Walk Down/Safety Walk Down and be responsible of the execution of safety measures

Requirements:
  • Bachelor of Science or similar qualification in Technical Field (engineering, life science, or equivalent) from accredited institution is advantageous.
  • Strong Pharmaceutical Process knowledge is desirable.
  • Minimum 5 years technical experience. 
  • Experience in a pharmaceutical / FDA-regulated manufacturing environment.  A solid working knowledge of cGMP and facility/equipment qualification requirements.
  • Experience with testing of automated manufacturing equipment / systems (e.g., Delta V / PLC-controlled equipment) is desirable.
  • Communication Skills: Excellent oral and written communication skills (English language), including presentations
  • Ability to write clearly, concisely, and persuasively in a professional environment and follow GEP / GMPs
  • Demonstrated ability to interact effectively with cross functional teams

If this sounds like the position for you then please apply today!

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