Browse by job sector

CQV CIP Engineer

  1. East Coast
North Carolina
  1. Contract
Competitive
  1. Commissioning, Qualification and Validation
22-04-2024
33357
Apply to this job Save job
CQV CIP Engineer - Pharmaceuticals - North Carolina - 15-Month Contract 

Our client, a global Pharmaceutical manufacturing organization are looking for a talented CQV CIP Engineer to join their expanding team. With continued organizational growth and considerable investment across their portfolio and capital programs this is an extremely exciting opportunity to contribute towards their brand-new manufacturing facility on the East Coast of the United States.


Main Responsibilities;
  • CQV Lead Engineer for all CIP Equipment in the DSM Buildings, initially responsible for review of all Design deliverables from engineering firm including Drawings, Datasheets, specifications and Engineering Lists.
  • Lead generation of all CQV CIP Documentation – FAT wraparounds, DQ, RTM, QRA, SAT/IOC and IOQ, including Final Reports.
  • Point CQV person for Vendor review for all CIP Vendor Packages.
  • CQV SME for all CIP Systems. Produce CIP Bridging to include all CCP, CQAs and worst case information of circuits.
  • Lead all circuit reviews for all CIP routes and circuits, working out “worst case” scenarios for testing and cleaning requirements.
  • Liaise with construction manager in relation to construction readiness and a schedule for all CIP systems, perform and lead all field walkdowns for all systems.
  • Lead CQV review, aligning with Transition Group in relation to review and approval of all Turnover Packages, both Vendor and Contractor Packages within the Process Equipment Support scope.
  • Liaise with CQV SWAT Team in relation to punchlist closure both pre-M/C and during the CQV execution phase for all Process Equipment Support systems.
  • Liaise with CQV PM and Lead Scheduler in relation to schedule creation and management for all CIP Systems, ensuring all correct predecessors and successors are in place.
  • Ensure Commissioning readiness of all CIP Systems to support Equipment Start-up and IOQ Testing.
  • Lead PSSR/STW field execution and guide CQV Team through Start-up exercise in a safe and controlled manner.
  • Lead CQV CIP Systems with EIDA / or Master Project Database equivalent system, ensure full traceability at all times for all systems.

Experience and contacts;
  • Minimum 10 years Equipment experience on Large Scale Biopharmaceutical Projects
  • SME on all CIP Systems, minimum 5 years
  • Working knowledge of ASTM E2500 / Leveraging Verification process
  • Experience with liaising with other departments and building PMs/leads
  • Minimum of 10years of Equipment experience including experience with design and construction projects for biopharmaceutical manufacturing facilities.
  • Minimum 5years experience on Equipment CQV Team
  • Experience with complex projects and working in or around operating facilities.
  • Ability to keep work pace and meet deadlines. Good organizing and planning skills.
  • Demonstrated proficiency communicating and collaborating at a variety of levels with customers, vendors, equipment suppliers and operations staff.
  • Proven success working well in a team environment with flexibility to react to changing business needs.

If this role is of interest to you, please apply now! 

 #LI-MC1
Apply to this job Save job
Save as a job alert
List #1

Similar Jobs

C&Q Lead – Buffer Prep

Salary

Competitive

Location

Cork

Salary

Competitive

Sector

Commissioning, Qualification and Validation

Job type

Contract

Location

Cork

Description

C&Q Lead - Buffer Prep - Pharmaceuticals - Cork - 12-Month Contract Located in Ireland, our Global pharmaceutical client is looking for C&Q Lead to join their state of the art pharmaceutical

Reference

32139

Expiry Date

01/01/0001

James Smithson

Author

James Smithson
James Smithson

Author

James Smithson
Read more
Read more
Cleaning Validation Engineer

Salary

Competitive

Location

Cork

Salary

Competitive

Sector

Commissioning, Qualification and Validation

Job type

Contract

Location

Cork

Description

Cleaning Validation Engineer   - Pharmaceuticals -  Cork -  12 Months  We have a great opportunity for Cleaning Validation Engineer to join our client, a research-based

Reference

33672

Expiry Date

01/01/0001

Andre Blanc

Author

Andre Blanc
Andre Blanc

Author

Andre Blanc
Read more
Read more
Cleaning Validation Specialist

Salary

Competitive

Location

Dublin

Salary

Competitive

Sector

Commissioning, Qualification and Validation

Job type

Contract

Location

Dublin

Description

Cleaning Validation Specialist - Pharmaceuticals - 12 Month Contract - Dublin Are you looking for the chance to join a life changing pharmaceutical organisation in their mission to continuously

Reference

30840

Expiry Date

01/01/0001

Tom Evans

Author

Tom Evans
Tom Evans

Author

Tom Evans
Read more
Read more

Insights

Day In the Life of a Commissioning Engineer

Day in the Life of a Commissioning Engineer

Read more

11/03/2023

life sciences testing laboratory

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

02/07/2023

engineer in white hard hat operating machinery

What is a Commissioning Engineer and why you should become one
Read more

01/26/2023

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