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Société
Bayer AGLieu(x)
GaillardProject manager (m/f) Trials coordination, Gaillard
CDD
Ingénierie, Technique, Sciences, Santé
Offre archivée le 10/09/2018
Bayer AG
Bayer is an international group whose core businesses lie in the healthcare and agriculture sectors. At the intersection of chemistry and biology, Bayer helps to improve quality of life by offering products and services in human and plant health.
Your tasks and responsibilities
As a Project manager coordination of the trials, you will have the following tasks and responsibilities:
- Ensure and coordinate the ITC supplies of test samples (self-medication) of whom the international center of technical development has the responsibility for all kind of Bayer Consumer Care trials : preclinical, clinical, cosmetic and consumer trials to ensure the samples are distributed on time and with the required quality at the investigator centers
- Coordinate the activities related to the manufacturing, packing and labelling operations to ensure the tests samples are produced according to the cGMP and in accordance with the requirements of clinical Operations and/or Marketing
- Establish the required documentation with third parties (when operations are contracted out) ; Coordinate the teams in writing the manufacturing and labelling instructions for the internal operations in relation with the Galenic project managers and the Quality assurance
- Ensure the interface with clinical operations and/or Marketing Departments and with the Galenic project managers to plan and coordinate the activities above in an optimal way.
- Ensure the update and the creation of the Quality documents of its perimeters according to the Bayer Directives in collaboration with the Quality Insurance.
- Assist the Quality Inssurance in all internal and external audits related to defined activities and coordinate the relevant actions and follow under its responsibility.
Who you are
- You have achieved pharmacist studies or equivalent With a Master in Science or Formulation, you have at least one year experience in similar function or an experience within a Technical regulatory department or Quality assurance, preferably in the pharmaceutical industry.
- You have a good knowledge of GMP.
- You are organized, able to prioritize, and customer oriented. You also have good writing and communication skills.
- Rigor, integrity and team spirit are essential qualities to carry out your missions.
- A good English (oral and written) is required for this position (Frequent contacts with the international)
Apply
Offre archivée le 10/09/2018
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