Project manager (m/f) Trials coordination, Gaillard

Bayer is a global enterprise with core competencies in the Life Science fields of health care and agriculture. Its products and services are designed to benefit people and improve their quality of life. At Bayer you have the opportunity to be part of a culture where we value the passion of our employees to innovate and give them the power to change.

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)