Senior C&Q Engineer – Vaccine GMP Projects Lead

EFOR; Wallonië; On-site; EUR 65,000 - 90,000; Full time

Job summary

EFOR Belgium seeks an experienced C&Q specialist for vaccine manufacturing projects, ensuring proper execution of C&Q methodology and cGMP throughout the program.

You will coordinate commissioning and qualifications, review protocols, approve reports, and advise on deviations while working with HVAC, Clean Utilities, autoclaves, CIP/SIP, filling lines, and bulk equipment to ensure GMP compliance.

Qualifications

• Over 3 years’ experience in C&Q in pharmaceutical area.
• 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 equipment(s).
• Planning of activities and schedules for qualification campaigns.
• Strong GMP knowledge and ability to work under pressure and meet timelines.
• Experience coordinating contractors, engineering teams and users within projects.

Responsibilities

• Follow and coordinate the commissioning and qualifications during a project.
• Review and ensure the compliance of the qualification protocols, review the qualification data and approve the reports for conformance.
• Advise the various actors in case of issues or deviations and guide resolution.

Skills

C&Q in pharma

Project management

GMP practices

Multidisciplinary teamwork

French/English bilingual

Job description

EFOR Belgium seeks an experienced C&Q specialist for vaccine manufacturing projects, ensuring proper execution of C&Q methodology and cGMP throughout the program.

You will coordinate commissioning and qualifications, review protocols, approve reports, and advise on deviations while working with HVAC, Clean Utilities, autoclaves, CIP/SIP, filling lines, and bulk equipment to ensure GMP compliance.