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About the job:
We deliver 4.3 billion healthcare solutions to people every year, thanks to the flawless planning and meticulous eye for detail of our Manufacturing & Supply teams. With your talent and ambition, we can do even more to protect people from infectious diseases and bring hope to patients and their families.
Sanofi has added two new Modulus Facilities to our global industrial footprint. These production units represent the future of manufacturing. They allow us to increase our capacities while making production more flexible and respectful of the environment.
Fully digitalized, our Modulus Facilities will enable more responsive and flexible manufacturing across multiple vaccine and biological platforms including mRNA, while minimize our impact to the environment. These facilities will help improve people’s lives by giving them faster access to more treatments.
Main responsibilities:
- Ensuring all batch release activities comply with Good Manufacturing Practices (GMP).
- Perform disposition of drug substance for release
- Investigating and resolving any issues or deviations related to batch release (including temperature excursion evaluation per product in case distribution channel face an unusual event)
- Leading root cause analysis investigations for quality incidents and implementing preventive measures.
- Collaborating with regulatory support officer to ensure compliance with local and international regulations.
- Participating in Quality Alert/Product alert meetings and ensuring that investigation and actions taken during those meetings allow the decision for disposition of lots
- Point of contact within operational team for complaint investigation when needed on site (coordination of investigation report).
- Business Process Owner for annual product quality review
- Act as change control assessor and QA approver
- Implementing continuous improvement initiatives to enhance deviation investigation and progress monitoring process and effectiveness.
- Participating in internal and external audits and inspections.
Skills and Experiences
Experience
- At least 5 years of experience in a QA role within the pharmaceutical industry, with a focus on deviation management and batch release processes
- Strong knowledge of Good Manufacturing Practices (GMP) and quality assurance principles
Skills
- Capability to investigate and resolve issues or deviations efficiently.
- Ability to meticulously review batch release documentation to ensure accuracy and compliance with regulatory standards.
- Proficiency in analyzing performance metrics and identifying areas for improvement.
- Experience in managing multiple tasks and projects simultaneously
- Agility to work in an ambiguous start up environment
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, ability or gender identity.
Watch our ALL IN video and check out our Diversity Equity and Inclusion actions at sanofi.com!
