Analytical Sciences Analyst

at  Sanofi US

EXPERIENCE:

• Experience in a laboratory environment – ideally part of which would be in the pharma or biopharma sector.

TECHNICAL AND SOFT SKILLS:

• Experience in leading people or projects.
• Operational experience of quality laboratories in a fast-moving manufacturing environment.
• Knowledge of quality management systems, pharmaceutical manufacturing operations, requirements for cGLP, pharmacopeial methods and stability
• Knowledge of relevant quality / compliance regulations
• Ability to manage projects to plan and budget
• Good communication and facilitator skills
• Ability to work independently
• Flexibility, drive, and innovation, eagerness to learn new techniques
• Dedication to adherence to business needs
• Effective collaboration with other functions and AST team

EDUCATION:

• Degree in Science (Chemistry or Biochemistry preferred)

IF THE DESCRIPTION FITS YOUR EXPERIENCE AND SPARKS YOUR INTEREST, PLEASE APPLY SO WE CAN GET IN CONTACT WITH YOU!

Discover our Code of Conduct, that serves as the moral compass that guides us when chasing the miracles of science to improve people’s lives. Please ensure to have read this document, before applying.
Better is out there. Better medications, better outcomes, better science. But progress doesn’t happen without people – people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let’s be those people.
At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, or gender identity.
Pursue Progress, Discover Extraordinary

• Participate in delivery of analytical projects as pertaining to business needs. Cooperation in development, qualification, and method optimisation for the projects.
• Participate in analytical and functional method improvements, manage and give update on ongoing activities.
• Ensure current Good Laboratory Practices cGLP is adhered to in all areas of work.
• Create and maintain safe work environment and report any unsafe conditions observed in the workplace.
• Provide analytical chemistry expertise and support to AST-MSAT and the Site activities.
• Effective interaction with other departments on matters related to ongoing projects. In particular, close contact maintained with Quality Assurance, Quality Control, Manufacturing, Engineering and Program Leads.
• Participate in method transfer activities.
• Provide update on the ongoing projects and identify improvements when needed.
• Bring innovative ideas and actively research for improvements around the analytical space.
• Support other functions in investigations, troubleshooting, as required.
• Assist with training of the analyst in areas of expertise and knowledge and in new methods, and techniques.
• Update the AST Team Leader on potential problems and highlight improvements where possible by use of the normal communication means.
• Ensure all quality documents and records are complete and current.
• Ensure laboratory areas meet current Good Laboratory Practices (cGLP) requirements.
• Ensure relevant procedures are correctly defined and followed.
• Ensure that critical chemical testing and related equipment meets current validation requirements (IQ/OQ/PQ) where required.
• Ensure safety & compliance standards are maintained to the highest standards.
• Maintain internal / external audit ready standards.
• Maintain training compliance.
• Maintain Good Documentation Practices (GDP) at all times including laboratory notebooks and analytical reports.
• Ensure compliance to current Good manufacturing Practices (cGMP) at all times.