Browse by job sector

Senior Process Upstream Engineer

  1. Brussels
Brussels
  1. Contract
Competitive
  1. CAPEX Projects
34574

This vacancy has now expired

Senior Process Upstream Engineer - Brussels, Belgium - €80-90/hour 

We are looking for an experienced Senior C&Q Process Engineer for a fantastic 12 month contract based in Brussels.

You will be working with our client who are a global biopharmaceutical organisation committed to improving the lives of people afflicted with neurological and immunological disease.

This is a superb opportunity if you are looking to advance your career in the field with a supportive and innovative company that will put you first.


Responsibilities:
  • Accountable for the team Drafting or support the document drafting by a partner or supplier, coordinate review and approval of applicable C&Q documents (QRA/DV/RTM/FAT/SAT/IOV/VSR) following approved VMP and SLIA.
  • Act as C&Q Subject Matter Expert and Compliance. Ability to provide guidance/ manage supplier and all C&Q activities for the system(s), from design to field execution and to summary report approval.
  • Drive verification testing, protocol execution, walk-downs, verification of system drawings, design and operational testing and troubleshoot as required. Conduct deviation investigation and resolution for problems and issues encountered during field execution activities.
  • Responsible for the Planning, Tracking and Reporting of C&Q status and risks/issues for the selected system(s). Take appropriate corrective actions as required to ensure deadlines and milestones are achieved.
  • Accountable for the Review and acceptance by the team of turnover of equipment / system from construction group. Ensures Start-up of equipment/ system is completed in a safe and coordinated manner.
  • Generate and or review change controls related to C&Q and drive their closure in a timely manner
  • Ensures all personnel who perform C&Q activities for the system(s) have relevant training assigned.
  • Assist/ facilitate in the development of User Requirement Specifications (URS's) and Quality Risk Assessment for Equipment and Systems in scope.
 
Requirements:
  • 5+ years of hands-on, end to end experience with this equipment in International CAPEX C&Q
  • Extensive knowledge and demonstrated experience delivering Commissioning and Qualification for Pharmaceutical / Biotechnology projects including automation related aspects of equipment.
  • Experience with Post OQ activities is preferred.
  • Experience of sterile / biotech / single use equipment in the bio-pharmaceutical industry is preferred.
  • Experience with ISPE best practice / GAMP-5/ Anex 15 GMP EU/ ASTM E2500/ electronic execution
  • Knowledge of safety, GMP and environmental regulatory requirements
  • Be willing to Travel for FAT/SAT

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


 #LI-CB1
Save as a job alert
List #1

Similar Jobs

Full Stack Developer

Salary

€55 - €70 per annum

Location

County Dublin

Salary

up to £35,000

Sector

CAPEX Projects

Job type

Permanent

Location

North America

United States

Description

Full Stack Developer - Dublin, Ireland - Permanent We have an exciting job opportunity for a Full Stack Developer to join our client, one of Europe’s leading engineering experts and

Reference

36636

Expiry Date

01/01/0001

Mark Chaumeton

Author

Mark Chaumeton
Mark Chaumeton

Author

Mark Chaumeton
Read more
Read more
Electrical Lead

Salary

Competitive

Location

Munich

Salary

Competitive

Sector

CAPEX Projects

Job type

Permanent

Location

Germany

South Germany

Description

Electrical Lead - Munich, Germany - Permanent Our client is at the forefront of advancing health care. Their mission is to discover, develop, and deliver innovative care solutions that improve

Reference

36605

Expiry Date

01/01/0001

Peter Hallam

Author

Peter Hallam
Peter Hallam

Author

Peter Hallam
Read more
Read more
CQV PLC Support Engineer

Salary

Competitive

Location

North Carolina

Salary

Competitive

Sector

CAPEX Projects

Job type

Contract

Location

North America

United States

Description

CQV PLC Support Engineer - North Carolina, United States - 8 Months Rolling Contract Our client, a global pharmaceutical manufacturing organization are looking for a talented CQV PLC Support

Reference

36635

Expiry Date

01/01/0001

Mark Chaumeton

Author

Mark Chaumeton
Mark Chaumeton

Author

Mark Chaumeton
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