Browse by job sector

CQV Safety Advisor

  1. Denmark
  1. Contract
Competitive
  1. CAPEX Projects
29-08-2023
31892
Apply to this job Save job
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. Based in a charming Nordic location, this on a contractual basis, and will involve significantly growing the sites capacity for the manufacture of Biologics.

Reporting into the CQV Safety Lead, This individual will be responsible for the delivery of these activities on a complex Drug Substance manufacturing expansion project.

Responsibilities:
  • Working as part of a team of EHS advisors to ensure all aspects of commissioning safety on site.
  • Safety input into the CQV Process and all CQV Procedures, Plans, Test Scripts and IOC/IOQ Protocols.
  • Perform Safety Audit on all Vendors, pre-order, to ensure all Safety requirements are met.
  • Health and safety advice to Leads and Operatives on site.
  • Ensuring that the permit crossover process and permit co-ordination is as per company procedures.
  • Reviewing method statements, SPA’s and SOPs.
  • CQV Safety pre and post approval of all PSSR (Pre-safety and Start-up Review) and STW (Set to Work) documents.
  • Integral part of CQV Group perform pre Start-up Walk downs in Media, Cell Culture, Harvest, Purification, Column Packing and also Black and Clean Utilities. (CST,WFT,CCA, Lab Gases)
  • Perform P&ID Walk downs on all Process systems, both Equipment and Stick-built. 
  • Perform Weekly Audit’s on all systems in relation to Project Transition Procedure, to ensure Safety Tagging Process is being adhered to. (Green/Yellow and Blue Tag)
  • CQV Safety review of all CQV Boundaries and LOTO, prior to system start-up.
  • Review of all Safety Punch items, both at Mechanical Completion, Commissioning Completion and Final Blue Tag sign-off, prior to handover to Operations.  
  • Running HAZID workshops for CQV and Ops activities. Review and development of risk assessments for all CQV specific test and process activities. 
Requirements:
  • Degree Educated (BSc) or relevant field experience.
  • Minimum of 5 years’ experience supporting safety activities ideally within a complex CAPEX project environment.
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

Calibration Technician

Salary

Competitive

Location

Limerick

Salary

Competitive

Sector

CAPEX Projects

Job type

Contract

Location

Midlands (Ireland)

Description

Calibration Technician - Pharmaceuticals - 12-Month Contract - Limerick  Ireland is a hive of activity for the Life Sciences Sector at present with global players setting up new and expanding

Reference

32246

Expiry Date

01/01/0001

Christopher Hutchinson

Author

Christopher Hutchinson
Christopher Hutchinson

Author

Christopher Hutchinson
Read more
Read more
Process Maintenance Tech

Salary

Competitive

Location

Limerick

Salary

Competitive

Sector

CAPEX Projects

Job type

Contract

Location

Midlands (Ireland)

Description

Process Maintenance Tech - Pharmaceuticals - Limerick - 12-Month Contract  Ireland is a hive of activity for the Life Sciences Sector at present with global players setting up new and expanding

Reference

32245

Expiry Date

01/01/0001

Christopher Hutchinson

Author

Christopher Hutchinson
Christopher Hutchinson

Author

Christopher Hutchinson
Read more
Read more
Construction Manager

Salary

Competitive

Location

Dunkerque

Salary

Competitive

Sector

CAPEX Projects

Job type

Contract

Location

France

Description

Construction Manager - Pharmaceuticals - France - 12-Month Contract  Our client develops and delivers life changing medicines to millions of people globally and as part of their growth, they are

Reference

32238

Expiry Date

01/01/0001

Iain Bonner

Author

Iain Bonner
Iain Bonner

Author

Iain Bonner
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