Opella is the self-care challenger with the purest and third-largest portfolio in the Over-The-Counter (OTC) & Vitamins, Minerals & Supplements (VMS) market globally.
Our mission: to bring health in people's hands by making self-care as simple as it should be for over half a billion consumers worldwide.
At the core of this mission is our 100+ loved brands, our 11,000-strong global team, our 13 best-in-class manufacturing sites and four specialized science and innovation development centers.
Headquartered in France, Opella is the proud maker of many of the world's most loved brands, including Allegra, Buscopan, Doliprane, Dulcolax, Enterogermina, Essentiale and Mucosolvan.
B Corp certified in multiple markets, we are active players in the journey towards healthier people and planet. Find out more about our mission to bring health in your hands at www.opella.com.
JOB SIZE / CONTEXT:
Ensure the analytical realization related to the various missions of the Compiègne Development Center:
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New Product Development
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Maintenance of existing products
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Innovation
In a GMP Pharmaceutical or Dietary Supplements environment.
MAIN MISSIONS OF THE POSITION:
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Prepares and carries out analytical work according to the protocols defined in collaboration with the project manager. Presents the results of the work and reports all the analysis data in the corresponding monitoring documents (laboratory notebooks, study reports, etc.) by checking their accuracy. Writes the documentation required for projects (protocols, methods, reports, etc.). Offers a critical analysis of the results transmitted.
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Respects deadlines and expectations for the smooth progress of projects and alerts quickly in case of difficulties. Makes available and shares the information necessary for the progress of the project. Communicates the progress of the actions for which he is responsible to the project team. Informs the project team member of drifts and difficulties.
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Ensures the maintenance of the premises/laboratories/equipment under his/her responsibility. Ensures the assembly, dismantling, cleaning of equipment and maintenance operations under his responsibility. Ensures the management and supply: materials, consumables, reagents,...
REQUIRED SKILLS
Education or professional experience:
Bac+2, Bac+3 Diploma in Quality Control, Chemistry, with minimum experience of 2 to 3 years in analytical development
Technical skills:
Knowledge of physico-chemical analysis techniques
Knowledge of validation of analytical methods (good knowledge of ICH and EMEA standards)
Mastery of office automation tools
Knowledge of technical English
Behavioural skills:
Organisation, rigor, methodical
Autonomy
Communication, listening, motivation
Pursue progress, discover extraordinary
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!
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What We Do
We are Sanofi, an innovative global healthcare company. We chase the miracles of science to improve people’s lives.
Our team, across some 100 countries, is dedicated to transforming the practice of medicine by working to turn the impossible into the possible. We provide potentially life-changing treatment options and life-saving vaccine protection to millions of people globally, while putting sustainability and social responsibility at the center of our ambitions.
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