2027 Spring Co Op Site Management Operations
Sanofi
About the Role
- Join Sanofi for a Spring Co-op in the Biologics Drug Product Development Group, supporting the US Vaccine R&D Site Operations team.
- Assist Site Management Operations Leads with day-to-day site activities, operational initiatives, and cross-functional projects.
- Opportunity to gain hands-on experience in a dynamic, GxP-regulated environment.
- Duration: 4 to 6 months.
- Location: Waltham, MA.
Key Responsibilities
Operational Support
- Assist with tracking and coordinating ongoing site activities, action items, and deliverables.
- Support the preparation and maintenance of site operational dashboards, metrics, and KPI reports.
- Monitor and follow up on open action items, corrective actions, and site commitments.
Data Analysis & Reporting
- Collect, compile, and analyze operational data to identify trends, gaps, and opportunities for improvement.
- Prepare summaries, presentations, and reports for site leadership and cross-functional stakeholders.
- Support the development and maintenance of tracking tools (Excel, SharePoint, Power BI, or equivalent).
Process Documentation
- Assist in drafting, reviewing, and updating Standard Operating Procedures (SOPs), work instructions, and process maps.
Project Coordination
- Provide coordination support for site improvement initiatives, capital projects, and operational change management activities.
- Track project milestones, timelines, and resource needs; flag risks or delays.
- Assist in preparing project charters, status updates, and stakeholder communications.
Facilities & Equipment Group Support
- Assist with equipment maintenance tracking and scheduling.
- Support facility maintenance coordination by helping to organize work orders and maintenance requests.
- Help maintain equipment inventory and asset management records.
- Assist with facility compliance documentation, including calibration records and qualification documentation.
- Support preventive maintenance (PM) programs.
Cross-Functional Collaboration
- Participate in cross-functional meetings with R&D, Engineering, Facilities, Supply Chain, and Regulatory Affairs teams.
- Serve as a liaison for information gathering and communication between site functions and Operations Leads.
- Support the planning and execution of site events.
Qualifications
Basic Qualifications
- Currently enrolled in an accredited bachelor's or master's degree program in:
- Life Sciences (Biology, Microbiology, Biochemistry, or related)
- Chemical, Biochemical, or Engineering
- Pharmaceutical Sciences
- Operations Management, Supply Chain, or Business Administration
- Environmental Health & Safety or related discipline.
- Must be permanently authorized to work in the U.S. without requiring future employment visa sponsorship.
- Must be enrolled in an accredited college or university throughout the duration of the co-op/internship.
- Must be able to relocate to the office location and work 40 hours/week, Monday to Friday for the full duration.
Preferred Qualifications
- Strong organizational skills with the ability to manage multiple priorities.
- Proficiency in Microsoft Office Suite (Excel, Power BI/data visualization tools, PowerPoint, Word, Outlook); SharePoint experience is a plus.
- Excellent written and verbal communication skills.
- Analytical mindset with attention to detail and data accuracy.
- Ability to work both independently and collaboratively.
- Demonstrated ability to maintain confidentiality.
- Prior internship, co-op, or research experience in a pharmaceutical, biotech, or regulated manufacturing environment.
- Experience with data visualization tools (Power BI, Tableau) or project management platforms (Smartsheet, MS Project).
- Knowledge of Lean, Six Sigma, or continuous improvement methodologies.
Compensation
- Hourly rate: $27.00 - $47.00.