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.
