Jobs at Sanofi

The Site Project Lead manages new production introduction projects, ensuring operational readiness and alignment with site and global stakeholders. Responsibilities include project planning, execution, risk management, and compliance oversight in line with pharmaceutical regulations.

Support site Quality Systems and Compliance by assisting QMS implementation, digital documentation (electronic logbooks/forms), document archival/destruction, Quality Culture and Data Integrity programs, tracking quality gaps/actions and site quality projects, and supporting inspection readiness logistics.

Support the procurement team with vendor management, supplier evaluation, spend consolidation, sourcing research, report and dashboard preparation, meeting representation, and procurement administrative tasks.

Support HSE fieldwork, compliance, environmental reporting, training, and documentation. Conduct ATEX compliance surveys, produce waste/energy/water/cooling reports, assist safety and process-safety initiatives, create a safety induction video, perform ISO14001:2026 gap assessments, and deliver at least one HSE improvement project.

Participate in routine cGMP manufacturing across Upstream, Downstream, or Central Manufacturing Services. Operate and monitor equipment and digital/automation systems, maintain documentation and audit readiness, support batch records, deviations and change control, and contribute to continuous improvement initiatives within a 12-hour rotating shift.

Provide Tier 3 multi-disciplinary project support, feasibility input, and third-party coordination; act as technical liaison between Manufacturing and Engineering for complex troubleshooting, commissioning, and process improvements; support system lifecycle, handovers, and root-cause investigations in a GxP biopharmaceutical manufacturing environment.

The Supply Chain Intern will support the team with data-driven insights, improve logistics processes, and manage supply planning data. They will collaborate with various functional teams and engage in designing reporting metrics and dashboards.

Lead Engineering & Maintenance compliance activities to ensure GMP/GxP inspection readiness. Manage deviations, CAPAs, change controls, audits, investigations, and continuous improvement. Collaborate with Quality, Validation, and Engineering to strengthen quality systems, review procedures, train staff, and support reliable biologics manufacturing operations.

Support automation engineers in manufacturing operations by collecting and analyzing process and alarm data, performing root-cause analysis, improving documentation (change controls, drawings), identifying critical spare parts, and assisting with daily team tasks and metric updates.

Lead site engineering and Tier‑3 capital projects (<€5M), driving project selection, feasibility, execution (design, procurement, construction, C&Q), compliance with GMP/FDA, process engineering support, contractor management, continuous improvement, and staffing and development of the site engineering/project team while integrating global projects.

Lead and oversee internal and external communication strategies, manage corporate messaging, media relations, and stakeholder communications, ensuring alignment with global communication objectives and local market needs.

Support QC laboratory operations including equipment maintenance, cleaning, calibration, inventory and waste management. Assist with lab housekeeping, staging reagents and consumables, contract lab coordination, and continuous improvement activities while learning GMP/GLP, documentation and QC workflows.

The Associate Engineer supports upstream biopharmaceutical manufacturing operations by monitoring processes, ensuring compliance with GMP, and contributing to continuous improvement efforts.

Serve as site QC digital key user and SME for Labware LIMS. Deploy and validate QC digital solutions, maintain master data and access, train and support end users, lead equipment qualification and maintenance, investigate QC events, execute CAPAs, support method validation and reviews, and ensure cGMP/data integrity compliance.

The Scientist II in MSAT designs and executes laboratory studies for manufacturing support and process improvement, with strong emphasis on upstream operations and technology transfer.

Maintain and optimize DeltaV-based automation and control systems in a GMP-regulated pharmaceutical site. Troubleshoot complex automation issues, support CSV and lifecycle documentation, deploy IoT/data-collection devices for digital manufacturing, and drive system upgrades, CAPAs, change controls and continuous improvement while ensuring regulatory compliance and data integrity.

The Specialist II will provide Quality oversight for GMP operations, ensure compliance with global standards, support digital initiatives, and lead quality improvements during manufacturing operations.

The Supervisor, Manufacturing leads the startup and operations in bioprocess manufacturing, ensuring compliance, team management, and continuous improvements.

The Reliability and Methods Engineer enhances reliability and maintenance of GMP systems, develops strategies, audits compliance, supports maintenance planning and leads improvement actions.

Support material release performance and data analysis, assist quality walkdowns and shop-floor oversight, collect and analyze production/QC quality data, monitor deviation/CAPA/change control metrics, and contribute to investigations and corrective actions.