Analytical Scientist – 23-Month On-Site Contract (Ireland)

Sanofi Group

Munster

On-site

EUR 55,000 - 73,000

Full time

9 days ago

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Job summary

Waterford, Ireland-based Sanofi is seeking an Analytical Scientist for a 23-month fixed-term contract. You will drive analytical development, handle LCM projects, and collaborate with MSAT, Quality, Operations and Regulatory to ensure product quality attributes are met.

The role emphasizes daily execution, project reporting, and cross-site collaboration, with on-site duties in Waterford. A degree in Biologics or Chemistry and strong GMP experience are required.

Qualifications

  • Degree in Biologics or Chemistry or related discipline.
  • Experience leading analytical development projects (design, transfer, qualification).
  • Knowledge of lyophilisation (Lyo) and mAbs sterile fill/finish context.
  • Experience developing and implementing analytical control strategies.
  • Experience providing technical support for GMP activities.

Responsibilities

  • Specialist in critical process parameters and product quality attributes.
  • Key team member for analytical development and analytical/product Life Cycle Management projects.
  • Work with Autonomous Production Units to support analytical LCM execution daily/weekly.
  • Report on assigned analytical projects' progress and seek site-performance improvements.
  • Collaborate with MSAT, Quality, Operations, Validation, Regulatory and program leads.
  • Interact with sister sites through various projects/forums.
  • Support CI boosters for MSAT-Analytical and QC as required.

Skills

Analytical development
Transfer projects
LCM, QC, QA support
Project reporting
Cross-functional collaboration
Analytical method design

Education

Biologics or Chemistry degree (NFQ 7/8)

Job description

Waterford, Ireland-based Sanofi is seeking an Analytical Scientist for a 23-month fixed-term contract. You will drive analytical development, handle LCM projects, and collaborate with MSAT, Quality, Operations and Regulatory to ensure product quality attributes are met.

The role emphasizes daily execution, project reporting, and cross-site collaboration, with on-site duties in Waterford. A degree in Biologics or Chemistry and strong GMP experience are required.

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