Plasma Fractionation Specialist

Strasbourg

Contract

Negotiable

Quality

CR/609221_1788940039

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

We are interested in professionals such as:

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.

FAQs

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