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Documentation Expert
Pauwels Consulting
Anderlecht
Sur place
EUR 50 000 - 70 000
Plein temps
Aujourd’hui
Soyez parmi les premiers à postuler
Résumé du poste
A consulting firm in Brussels is seeking an experienced compliance manager to oversee projects aimed at enhancing processes in the pharmaceutical industry. Responsibilities include engaging stakeholders, standardizing procedures, and driving a compliance mindset throughout the organization. Ideal candidates have strong document and project management skills, alongside proficiency in English and French. This role requires being on-site at least three days per week.
Qualifications
5+ years of experience in a relevant field.
Strong expertise in document management and project management.
Experience in the pharmaceutical industry.
Excellent writing and communication skills.
Strong autonomy and leadership abilities.
Ability to engage stakeholders and drive change.
Familiarity with EDMS/ECMS systems is a plus.
Knowledge of GxP and healthcare compliance regulations.
Proficient in English and French.
Availability to be on-site at least 3 days/week.
Responsabilités
Take ownership of compliance projects to enhance processes.
Engage with departments to standardize compliance procedures.
Connect with healthcare stakeholders to understand practices.
Propose improvements for compliance documentation.
Collaborate with Talent team to identify impactful changes.
Promote compliance mindset across the organization.
Lead training initiatives for compliance standards.
Connaissances
Document management
Project management
Stakeholder engagement
Autonomy
Leadership
Communication
English proficiency
French proficiency
Description du poste
You take ownership of compliance projects aimed at enhancing processes.
You engage with various departments to standardize compliance procedures.
You proactively connect with healthcare stakeholders to understand current practices.
You propose simple and effective improvements to enhance compliance documentation.
You collaborate with the Talent team to identify impactful changes.
You promote a compliance mindset across the organization.
You lead training initiatives to ensure understanding and implementation of compliance standards.
Requirements
You have a minimum of 5 years of total experience in a relevant field.
You possess strong expertise in document management and project management.
You bring experience in the pharmaceutical industry.
You demonstrate excellent writing and communication skills.
You exhibit strong autonomy and leadership abilities.
You have a well-developed capacity to connect with stakeholders and drive change
Nice to have: Experience with EDMS/ECMS systems
Knowledge of GxP and healthcare compliance regulations
You are proficient in English and French.
You are available to be on-site at least 3 days/week.
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