Scope

The Knowledge Management (KM) Project Leader (PL) is the “engine” of the KM project at Quality Assistance.

The position reports to the Training Director.

Your mission

Establish and implement a strategy for collecting and channeling appropriate knowledge to the right people, in the right place, at the right time.

Encourage employees to use this knowledge in order to improve the performance of the company in terms of pharmaceutical, regulatory, scientific, technological and organizational « Excellence ».

In this context, the KMPL is responsible for managing the following processes:

  • creation and research of knowledge sharing methods

  • knowledge organization and retention

  • knowledge personalization

  • knowledge sharing

  • people integration within the company

The KM Project Leader is also responsible for:

  • monitoring technological innovation in the KM field

  • representing the Training Director during:

  • audits and visits of clients and regulatory authorities.

  • personnel training

Your profile

Master's deegree in Sciences (a Master's degree in Pharmaceutical Sciences is a plus).

  • Relevant experience in the pharmaceutical sector

  • Customer oriented with excellent communication and didactic skills

  • Autonomous, organized, rigorous, curious and creative

  • Good verbal and written communication in English (minimum B2 level)

Why join Quality Assistance?

We are a true career partner.

  • We accelerate people’s access to new medicines.

  • We offer an inspiring work-life balance in a human scale environmeant.

  • We care about mutual respect, assistance and communication.

  • We listen to your needs and your suggestions.

  • We offer a market-competitive remuneration package including numerous fringe benefits. 

Visit https://www.quality-assistance.com/quality-assistance/life-quality-assistance to learn more.

About Quality Assistance

Quality Assistance is a leading European Contract Research Organisation providing the pharmaceutical industry with all the analytical services required by EMA and FDA regulations for the development and marketing of innovative human medicinal products.

We assist our clients from candidate selection, through non-clinical and clinical studies, to marketing authorisation, using our state-of-the-art, product-dedicated expertise in analytical sciences. 

For each client project, we design customised solutions, define analytical protocols, develop and validate specific new analytical methods and perform characterisation, stability, pharmacokinetic, biomarker and immunogenicity studies as well as batch release testing, in order to evaluate the Quality, Safety and Efficacy of the given drugs.

The company holds a unique position on the market with all its laboratories on one site, 210 highly qualified professionals and over 35 years’ expertise at the forefront of analytical sciences.

The Quality Assistance environment is GMP, GLP and GCLP/GCP compliant.

Visit https://www.quality-assistance.com/quality-assistance/leading-analytical-cro to learn more.

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