Job Description
Company Description Efor Group is a global leader in Quality and Compliance for the Life Sciences industry, supporting pharmaceutical, biotech, and medtech organizations in securing production compliance and accelerating the launch of safe and effective therapies. Founded in 2013, the group has grown to 3,200 experts across four continents, partnering with many of the world's largest healthcare companies. Efor delivers recognized excellence in quality engineering and regulatory compliance, helping clients navigate complex technical and regulatory environments. The company's mission is to remove barriers so that innovation becomes accessible therapies, faster and safer, on a global scale. Efor offers an international, mission-driven environment for professionals who want to help transform healthcare.
- Support ongoing upstream process engineering and project activities for vaccine manufacturing facilities.
- Review and assess process flows, P&IDs, equipment design and process requirements to ensure alignment with manufacturing needs.
- Participate in P&ID shakedown and field verification, identifying discrepancies between design documentation and the installed process.
- Support identification and resolution of process, equipment and design gaps during project execution and plant readiness activities.
- Review upstream process parameters and provide recommendations for process parameter changes, operating ranges and process improvements, where required.
- Provide technical input into equipment and system design, including recommendations for modifications where the existing design does not adequately support the process.
- Work with Engineering and CQV teams to ensure that process requirements are adequately captured in commissioning and qualification activities.
- Support troubleshooting of process and equipment issues during commissioning, start-up and operational readiness.
- Participate in design reviews, technical discussions, risk assessments and process-related workshops.
- Review relevant engineering and process documentation, including P&IDs, process descriptions, equipment specifications, process flow diagrams and operating requirements.
- Support change control, deviation investigation and technical assessments related to upstream processing, where required.
- Coordinate with cross-functional stakeholders to ensure timely closure of identified process and design actions.
- Provide technical recommendations based on process requirements, GMP expectations, operational experience and manufacturing best practices.
- Support handover from project execution into manufacturing operations and ensure relevant process knowledge is effectively transferred.
More Info
Key Skills
GMP expectations
risk assessments
upstream process engineering
process flows
equipment and system design
manufacturing best practices
deviation investigation
commissioning and qualification activities
design gaps
process requirements
process parameters
process-related workshops
technical assessments
