QUALITY CONTROL ANALYST HF

Job description

Entreprise:
Sanofi is a global life sciences company committed to improving access to healthcare and supporting the people we serve throughout the continuum of care. From prevention to treatment, Sanofi transforms scientific innovation into healthcare solutions, in human vaccines, rare diseases, multiple sclerosis, oncology, immunology, infectious diseases, diabetes and cardiovascular solutions and consumer healthcare. More than 110,000 people at Sanofi are dedicated to make a difference in patients’ daily life, wherever they live and enable them to enjoy a healthier life.
iMove, the Sanofi VIE Program, is available to citizens of the European Economic Area (EU + Norway, Liechtenstein and Iceland) aged between 18 and 28.
PLEASE NOTE that since this program is primarily an international development program, candidates cannot apply to a VIE assignment in their own country of citizenship.
PLEASE NOTE that applications that are only submitted in French cannot be considered by our non-French speaking partners at Sanofi worldwide.
Therefore, only applications that are submitted in English will be considered.
At Sanofi diversity and inclusion is foundational to how we operate and is embedded in our Core Values. We respect the diversity of our people, their backgrounds and experiences. We recognize to truly tap into the richness diversity brings we must lead with inclusion and have a workplace where those differences can thrive and be leveraged to empower the lives of our employees, patients and customers.
We are looking for a candidate for a VIE mission of:
Quality Control Analyst
- VIE Contract (W/M)
Responsibilities:
- Sampling and analyzing raw materials, drug substances and drug products
- Ensuring stability testing is initiated and completed within the required time frame
- Documenting analytical data and results according to cGMP (Current Good Manufacturing Practice)
- Collation of analytical data into release packs and generation of Certificate of Analysis as required
- Reviewing of raw data, where appropriate, ensuring all documented results are in accordance with the appropriate product/material specification and good documentation practice
- Being responsible for first line troubleshooting
- Cross value stream working to support the Quality Control function
- Training and supporting colleagues where appropriate
- Supporting projects on an as required basis
- May be required to support equipment requalification, calibrations, services etc.
- Ensuring that equipment is maintained and fit for purpose against site procedures before use
- Carrying out Risk/COSHH (Control of Substances Hazardous to Health) assessments and ensuring that the laboratory is maintained in a safe and tidy manner at all times
- Raising Events, CAPA's (Corrective and preventive actions) & Laboratory investigations immediately or within the required time frame from detection
- Taking responsibility for adhering to cGMP (Current Good Manufacturing Practice) requirements during all activities performed, and seek clarification of requirements when they are unclear
- Completing all corrective and preventative actions within the agreed timelines
- Maintaining core training and prior to conducting any activity ensure you are trained in the current version
- Being responsible for personal safety and that of others, reporting all accidents and unsafe acts and conditions
- Ensuring that the laboratory is maintained in a safe and tidy manner and recording all cleaning activities according to cGMP (Current Good Manufacturing Practice)
- Identifying and implementing improvements to ways of working with an aim to standardize each working week
Requirements:
- Education: Master degree in scientific field: Chemistry, Biochemistry, Biology, Pharma
- Experience: Laboratory experience and a working knowledge of laboratory health and safety is required
- Demonstrated ability to work consistently to quality policies and cGMP (Current Good Manufacturing Practice)
- Proven, sustained competence in analytical techniques and skills relevant to group
- Demonstrated ability to successfully manage own workload to meet departmental targets
- Soft skills: Act for Change, Strive for results, Cooperate Transversally, Commit to customers
- IT tools: LIMS system (Laboratory Information Management System) would be a plus
- Language: fluent English
Desirable skills:
- Root cause analysis and gap analysis skills