Senior C&Q Engineer
- Belgium, Brussels
- Contract
- CAPEX Projects
We are looking for an experienced Senior C&Q Engineer for a fantastic 6 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.
- Extensive hands-on, end to end experience with this equipment in International CAPEX C&Q.
- Technical qualification at third level or equivalent in Engineering. English is must.
- Extensive knowledge and demonstrated experience delivering Commissioning and Qualification for Pharmaceutical / Biotechnology projects including automation related aspects of equipment.
- Strong understanding of a risk-based approach
- Experience with Post OQ activities is preferred.
- Experience of sterile / biotech / single use equipment in the bio-pharmaceutical industry is preferred.
- Knowledge of safety, GMP and environmental regulatory requirements.
- Ability to make decision under pressure and demonstrated strong Communication/ Leadership skills.
- Demonstrated ability to collaborate with senior stakeholders to achieve optimal outcomes.
#LI-CB1
We have worked together with QCS Staffing for seven years now and have always received a professional service. QCS Staffing'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 QCS Staffing'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 QCS Staffing. 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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