Clean Utilities Commissioning & Qualification Engineer
- Worldwide
- Contract
- Commissioning, Qualification and Validation
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 Clean Utilities 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 energization, 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
- Check the availability of the accurate work permits (if required)
- Track issues and punch items
- Initiate and support resolution of technical issues and escalate in case no solution is found
- Document the daily progress
- Assess if commissioning/verification actions affect other discipline and escalate to the lead
- Coordinate field activities of vendors and contractors
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
- Proficient in manual tasks associated with equipment set up (tri- clamp, flange connections, manipulation of manual and automated valves, inline instruments, hose connections, vessel set ups etc.
If this sounds like the position for you then please apply today!
#LI-BP1
We have worked together with Quanta for seven years now and have always received a professional service. Quanta’s speciality certainly lies within their technical sourcing abilities and they have met our demanding requirements time and time again. Coupled with this are the integrity of Quanta’s people and their ability to deliver.
Global Pharmaceutical firm
I have always received a highly professional & personable service from the team at Quanta. They listen carefully to the specific requirements of available roles and work tirelessly to supply a pool of potential candidates and make the hiring and contract renewal process an easy activity to manage.
Global Pharmaceutical firm
Once again can I via you recognise the superb support I was given before, during and after this short contract. The support, was as usual professional and every friendly.
QA Specialist
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