Plasma Fractionation Specialist


Strasbourg
Contract
Negotiable
Quality
CR/609221_1788940039
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

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.

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