TASKS & RESPONSABILITIES

In the context of investments projects (new or upgrades) in vaccines production, ensure proper execution of C&Q; methodology and application of cGMP (Validation Master Plan, Design Qualification, Commissioning, Installation & Operational Qualification and Validation Reports).

- Follow and coordinate the commissioning and qualifications during a project.
- Review and ensure the compliance of the qualification protocols, review the commissioning and qualification raw data and finally approve the reports for conformance.
- Must be able to advice the various actors in case of issues or deviations .
- Has an expertise in all commissioning / qualification aspects of vaccine manufacturing such as qualifications of HVAC systems, Clean Utilities (Clean Compressed Air, Clean Steam, Purified Water, Water For Injection, ...), autoclaves, analytical systems, CIP/SIP process, filling lines, bulk equipments other equipment commonly used in vaccine manufacturing facilities and be able to manage most of these qualification aspects.
- Ensure that all GMP aspects are respected during the project.




- Able to manage the project respecting the established commissioning / qualification timelines and coordinate all actors (Contractors, Engineering, Users) to align them with the project planning.

YOUR PROFIL

- Have already demonstrated success in C&Q; coordination in projects
- Over 3 years’ experience in C&Q; in pharmaceutical area
- Bilingual French/English (written and spoken)
- Good experience in managing qualifications projects
- Good understanding of the injectable manufacturing processes
- Knowledge in qualifications of HVAC systems, Clean Utilities (Clean Compressed Air, Clean Steam, Purified Water, Water For Injection, ...), autoclaves, analytical systems, CIP/SIP process, filling lines, bulk equipments (chromatography systems, fermentor, …)
- Planning of activities
- Good expertise in GMP Practices (V cycle, …)
- Ability to work under heavy pressure due to the requested flexibility and reactivity of the activities
- Ability to work in project teams in a multidisciplinary environment and a matricial organization
- Quality oriented

📌 C&q engineer pharma h-f (España)
🏢 EFOR
📍 España