Pharmaceutical Formulation Manager M/F
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As a global leader in animal health, Ceva Animal Health believes our success is linked to our passionate people researching, developing , producing and supplying innovative health solutions for all animals, which contributes to the future of our diverse planet.
We are committed to ensuring the highest possible level of care and well-being for farm animals (poultry, pigs, ruminants), companion animals (dogs and cats) and wildlife.
Indeed, Our “Together, Beyond Animal Health” vision emphasizes that the health and wellbeing of people, animals and our planet are totally interlinked. More than ever, Ceva is committed to a "One Health" approach.
As part of our “Diversity, Equity and Inclusion” policy, Ceva Animal Heath is committed to the employment of people with disabilities and will make reasonable accommodations throughout the interview process to ensure an inclusive and accessible experience for all applicants. To request an accommodation, please contact a member of the Ceva Talent Acquisition team.
Your
missions :
We are looking for a Pharmaceutical Formulation Manager M/F for our Beaucouzé campus. The position is available as soon as possible on a permanent contract (CDI).
MAIN RESPONSIBILITIES:
In accordance with GMP and procedures, the incumbent will organise the activities of the PFS department (preparation/formulation/distribution/packaging of ATUs/autovaccines/APSA). This position will ensure that costs are kept within budget and that production is completed as quickly as possible. You will supervise and manage the continuous improvement processes within the department.
SECONDARY RESPONSIBILITIES:
-> Leads or participates in cross-functional projects as needed.
-> Partially backs up the Production Director during his/her absences.
MAIN PURPOSES OF THE POSITION:
-> Supervises, organises and carries out, where necessary, MSFP activities in order to meet production schedule objectives.
-> Ensures that staff training/certification is monitored.
-> Supervises, organises and carries out, where necessary, IPCs.
-> Ensure GMP quality within the scope of the position.
-> Ensure that documentation is kept up to date.
-> Anticipate needs (equipment, materials, staff, projects, CAPEX).
-> Supervise and lead continuous improvement initiatives.
-> Supervise and lead cross-functional projects as needed.
-> Participate in internal and external audits and inspections
The job holder organises production within their scope.
In the event of non-compliance, report the incident in the system and alert the Production Director and Quality Assurance.
The job holder proposes solutions to guarantee compliance.
Your
profile :
You have a Master's degree or engineering degree in health, pharmaceuticals or biology/microbiology.
You already have one or more significant management experiences in the pharmaceutical sector. You demonstrate rigour, responsiveness, reliability, adaptability and commitment on a daily basis.
You demonstrate positivity on a daily basis and know how to adapt to a changing environment, and you are ready to support a growing company.
A good level of English may be an advantage for the position in question.
