Warehouse Compliance Lead

at  Sanofi US

EXPERIENCE:

• Established background and experience in production planning ideally in a pharma or GMP environment

SOFT SKILLS:

• Excellent accuracy and attention to detail
• Excellent communication and interpersonal skills
• Good Presentation skills
• Ability to cooperate with others at all levels of the organisation, across multi-sites and in a multinational environment
• Initiative – be able to work in a self-directed manner to see issues through to completion
• Highly motivated – ability to multi-task
• Adaptable and flexible as well as a pragmatically minded problem solver

TECHNICAL SKILLS:

• Extensive knowledge of cGMP and GDP in a regulated environment
• Specialist knowledge of training and quality systems in a regulated environment
• Knowledge of ERP – SAP
• Strong Excel and IT skills

EDUCATION:

• Degree level or above, APICs desirable

IF THIS OPPORTUNITY FITS YOUR EXPERIENCE AND HAS AROUSED YOUR INTEREST, WE ENCOURAGE YOU TO 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

• Raising and management of all Quality System processes including Change Controls, Deviations, Tasks, Quality Events etc.
• Driving of all Quality Metrics for the department
• Forward review of Quality Metrics to ensure no over-dues
• Active contribution to continuous improvement initiatives, for procedure efficency and simplification
• Ensure Training is fit for purpose and complies with all applicable legislative requirements
• Ensure effective co-ordination and support for external and internal audits for the department
• Perform critical / constructive review of procedures and practices
• Identify and lead projects to make step change improvements to the departments Quality
• Attend offline department meetings and be the voice of the department
• Actively contribute to continuous improvement initiatives utilising lean methodologies where appropriate
• Liaise with Quality Representative to support and improve RFT in the area and Always Audit Ready
• Ensure compliance to cGMP at all times