CQV Engineer
- Italy
- Contract
- Commissioning, Qualification and Validation
Do you want to work with an exciting company who are an established market leader within their niche field? We have a fantastic opportunity for C&Q Engineers to work on an exciting CAPEX project in central Europe.
CQV Engineer 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)
- Execute Delta V testing in accordance with approved Automation design and record test discrepancies for further analysis in accordance with DS3 Engineering Change Controls procedures
- 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)
- Initiate and support resolution of technical issues and escalate in case no solution is found
- Assess if commissioning/verification actions affect other discipline and escalate to the lead
- Coordinate field activities of vendors and contractors
- 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 3 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 (preferably English language), including presentations
- Ability to write clearly, concisely, and persuasively in a professional environment and follow GEP / GMPs
- EU right to work and able to travel for FAT’s
The candidate must have the rights to work in the location stated in the job advert.
Please note, Quanta part of QCS Staffing does not sponsor Visa applications.
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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
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
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
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