Browse by job sector

CQV API Process System Owner

  1. Cork
  1. Contract
Competitive
  1. CAPEX Projects
12-09-2023
31978
Apply to this job Save job
CQV API Process System Owner – Pharmaceuticals - Ireland

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 a CQV API Process System Owner to work on an exciting capex project in Ireland on an initial 6-month contract.

Essential Duties and Responsibilities for this CQV API Process System Owner role include, but are not limited to, the following:
  • Ensure construction scope of works and timelines is agreed for their systems to support Green tag system turnover.
  • Familiarise themselves with their assigned systems such that they can assume ownership of all activities on their systems upon system transition from Construction at Green Tag.
  • Sign permits, as system owner, for all activities on their assigned systems during the CQV phase (incl. precommissioning).
  • Ensure pre-commissioning scope of works and timelines is agreed for their systems (e.g., loop check and calibration (E&I technicians), Automation engineers, M&P fitters).
  • Generate all verification documentation for their assigned systems, including RAMS (Risk Assessments / Method
  • Statements) for the verification activities.
  • Ensure that all materials (e.g., spares, consumables) and resources required to undertake commissioning & verification activities are available.
  • Approve SAT protocols for vendor skids within assigned systems.
  • Ensure vendors RAMS (Risk Assessments / Method Statements) are approved for works to proceed.
  • Execute the Verification documentation set for all assigned systems, in compliance with the schedule.
  • Attend Daily Whiteboard meetings (run by the Area CQV lead) and report status / progress, issues, escalations etc.
  • Provide routine updates on progress per system to facilitate project reporting, to the Project CQV Lead.
  • Facilitate system handover to end user using the SARR process and in compliance with the schedule.
Desirable Experience:
  • Minimum of 6 years relevant Process experience in engineering and commissioning activities within large scale
  • capital projects.
  • Small Molecule API experience will be a distinct advantage
  • Relevant experienced in leading teams in a high pace project environment.
  • Experience in use of Automation systems such as Delta V
  • Experience with managing complex projects and interfacing with existing operating facilities.
If this role is of interest, please apply now.

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.

To view Quanta's privacy policy, please visit our website
Apply to this job Save job
Save as a job alert
List #1

Similar Jobs

Programme Manager

Salary

Competitive

Location

Toulouse

Salary

Competitive

Sector

CAPEX Projects

Job type

Contract

Location

France

Description

Programme Manager – Pharmaceuticals – 12 Month Contract – Toulouse Our client, a global biotechnology organisation, is recruiting for a Programme Manager to join their greenfield, capital

Reference

29711

Expiry Date

01/01/0001

Caroline O’Sullivan

Author

Caroline O’Sullivan
Caroline O’Sullivan

Author

Caroline O’Sullivan
Read more
Read more
CQV Safety Advisor

Salary

Competitive

Location

Copenhagen

Salary

Competitive

Sector

CAPEX Projects

Job type

Contract

Location

Denmark

Description

CQV Safety Advisor - Pharmaceuticals - Denmark  Our client, a global CDMO in pharmaceutical manufacturing, is recruiting for a CQV Safety Advisor to join them on their new expansion project.

Reference

31892

Expiry Date

01/01/0001

Hannah Smith

Author

Hannah Smith
Hannah Smith

Author

Hannah Smith
Read more
Read more
Project Automation Engineer

Salary

Competitive

Location

Chicago

Salary

Competitive

Sector

CAPEX Projects

Job type

Contract

Location

Central

Description

Project Automation Engineer - Pharmaceuticals - Contract - Chicago Do you want to work with an exciting company who are an established market leader within their unique and niche field? We have a

Reference

30312

Expiry Date

01/01/0001

Dev Chauhan

Author

Dev Chauhan
Dev Chauhan

Author

Dev Chauhan
Read more
Read more

Insights

life sciences testing laboratory

Why you should work in Commissioning, Qualification and Validation
Read more

02/07/2023

Your next step as a Validation Engineer
Read more

07/20/2021

pharmaceutical factory construction

Working in an organisation from Start Up Phase

Read more

06/28/2021

VIEW ALL

Send us your CV

Our candidates are the cornerstone of our organisation and we are always looking to connect with new professionals who are seeking their next contract assignment or career opportunity.

Send your CV
Upload your CV