Plasma Fractionation Specialist

Overview

We are seeking an experienced pharmaceutical professional with direct plasma fractionation manufacturing experience to support ongoing operations and project activities at a pharmaceutical site in Strasbourg. The role is open to candidates from a range of backgrounds, including Process Engineering, CQV, Manufacturing, Production, Validation, and Technical Operations. The key requirement is hands-on experience within a plasma fractionation environment. This is a site-based contract position requiring practical GMP manufacturing knowledge and the ability to work effectively across multidisciplinary teams. Please note: Candidates must have previous hands-on experience working in a plasma fractionation facility. Experience in general pharmaceutical manufacturing alone will not be sufficient for this position.

Responsibilities

• Support manufacturing and operational activities within a plasma fractionation facility.
• Provide technical expertise across process, production, engineering, qualification, or validation activities as required.
• Work closely with operations, quality, engineering, and project teams to ensure efficient execution of site objectives.
• Assist with troubleshooting, process optimisation, and continuous improvement initiatives.
• Support commissioning, qualification, validation, or process implementation activities where applicable.
• Ensure all activities comply with GMP requirements and site procedures.
• Contribute to the preparation, review, and execution of technical documentation and reports.
• Participate in project execution and site-based operational support activities.

Requirements

Essential

• Direct experience working within a plasma fractionation manufacturing environment.
• Pharmaceutical or biopharmaceutical industry experience.
• Strong understanding of GMP-regulated operations.
• Ability to work full-time on-site in Strasbourg.
• Experience supporting manufacturing, engineering, CQV, validation, production, or technical operations activities.

Preferred

• French language skills.
• Experience with plasma-derived medicinal products (PDMPs).
• Previous contract or project-based pharmaceutical experience.
• Exposure to commissioning, qualification, validation, process engineering, or manufacturing support activities.

Candidate Backgrounds Considered

• Process Engineers
• CQV Engineers
• Manufacturing Specialists
• Manufacturing Engineers
• Production Engineers
• Validation Engineers
• Technical Operations Specialists
• Process Specialists

The job title is flexible. Direct plasma fractionation experience is the critical requirement.