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Sanofi

Global pharma company; vaccines and R&D

Quality Graduate

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeWaterford, Ireland

About the Job

Requirements

  • Have graduated within the past two years or be due to graduate before 1 September 2027.
  • Hold a minimum 2.1 primary degree or a Master's degree in a relevant discipline such as Quality Assurance, Pharmaceutical Sciences, Biological Sciences, Chemistry, Biotechnology, Microbiology, Engineering, or a related Life Sciences field.
  • Have full, unrestricted right to work in Ireland.
  • Have strong analytical and problem-solving skills to assess risks and identify effective solutions.
  • Have communication and collaboration skills to work across diverse teams and stakeholders.
  • Have organisational and project management skills to manage multiple priorities in a fast-paced environment.
  • Have attention to detail and a commitment to quality, compliance, and continuous improvement.

Responsibilities

  • Support the Data Integrity Quality Improvement Programme through quality systems, documentation, and compliance activities.
  • Conduct routine Good Manufacturing Practice and data integrity checks, identify and address quality issues, and ensure proper documentation practices are followed.
  • Assist with technical writing, document management, Corrective and Preventive Action follow-up activities, and initiatives that strengthen inspection readiness and continuous improvement across the site.
  • Participate in internal audits and compliance assessments to identify opportunities for process improvements.
  • Support inspection readiness by reviewing documentation, tracking actions, and coordinating with operational teams.
  • Monitor Standard Operating Procedure compliance and contribute to initiatives that strengthen quality culture and regulatory adherence across the site.
  • Lead or support complex Corrective and Preventive Action investigations, identify root causes, and implement sustainable corrective actions.
  • Coordinate audit activities by working with stakeholders to prepare documentation, track commitments, and support successful outcomes.
  • Contribute to cross-site quality initiatives, including Quality Management System harmonisation projects, process improvements, or compliance enhancement programmes with regional or global impact.
  • Develop knowledge and practical skills in Quality Systems and Compliance to ensure products, processes, and quality systems meet regulatory and operational standards.
  • Develop understanding of quality management principles, regulatory requirements, Good Manufacturing Practice compliance, and Quality Management Systems within a highly regulated industry.
  • Build cross-functional collaboration, communication, project management, and stakeholder engagement skills through exposure to diverse teams and business processes.
  • Build expertise in risk assessment, problem-solving, root cause analysis, Corrective and Preventive Action management, auditing, and continuous improvement methodologies.

Desired Qualifications

  • Previous internship, placement, research, or work experience within a regulated industry such as pharmaceuticals, biotechnology, medical devices, or healthcare.
  • Knowledge of Quality Management Systems, Good Manufacturing Practice requirements, or regulatory compliance principles.
  • Experience participating in quality improvement, auditing, process improvement, or compliance-related projects.
  • Demonstrated leadership experience through academic, extracurricular, or professional activities.

About the Company

Sanofi

Global pharma company; vaccines and R&D

Sanofi is a global pharmaceutical and biotechnology company that develops, manufactures, and sells prescription medicines, over-the-counter products, and vaccines. Its products span immunology, oncology, rare diseases, and vaccines, addressing unmet medical needs through a strong focus on research and development. Sanofi's core product model relies on large-scale R&D, strategic partnerships, and licensing to bring new therapies to markets, with revenue generated from product sales and collaborations. The company differentiates itself by leveraging its global reach, diverse portfolio, and emphasis on patient-centric solutions, safety, and quality to navigate regulatory environments in developed and emerging markets. The company’s goal is to improve health outcomes and quality of life for people worldwide by delivering innovative treatments and vaccines that meet unmet medical needs.

Company size
10,001+
Company stage
IPO
Headquarters
Paris, France
Founded
1973

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