Location : Athens
Category : business support
Do you have experience in Quality Assurance or Regulatory Affairs 3 to 6 years in the pharmaceutical sector? Are you eager to take the next big step in your career as a ?
Are you self motivated, energized, and passionate? Do you think that this role of Quality Manager will give you the opportunity to grow professionally and personally?
Then our client may be seeking for you!
The Quality Manager who will successfully be chosen will be part of a multinational team with prospects for personal development.
Benefits include :
Pleasant and friendly working environment
Private health insurance
Mobile and laptop
This is a fantastic opportunity for a self motivated individual. As a Quality Manager, some of your main responsibilities are :
Ensure global quality practices are integrated in the affiliate to ensure compliance and safety obligations within company and local regulations
Responsibility for the maintenance of the GDP status in accordance with national, international and legal requirements.
Managing the lifecycle of Policies / SOPs / AIs / AFs at affiliates or within a global or local function.
Work with the affiliates management / corporate to ensure the proper support is provided for the local Quality organisation.
Develop, implement, communicate and maintain quality action plans to bring the company’s quality systems and policies into compliance with quality system requirements
Cooperate with purchasing department to establish quality requirements from external suppliers
Identify relevant quality-related training needs and delivering trainings as to ensure procedures are properly understood, carried out and evaluated
Ensure all QA deliverables are achieved in a compliant timely manner.
In order to be considered for this Quality Manager role, the requirements are :
Graduate degree, ideally in health related field, master degree will be an asset
3-6 years experience working in the pharmaceutical industry in a Quality Assurance position
Fluency in English
Experience interacting with regulatory bodies and third party organisations with respect to QA systems and regulatory inspection preparedness
Solid knowledge of relevant legal requirements of the global pharmaceutical industry, including the interpretation and practical application of applicable regulations
Good background knowledge of the pharmaceutical industry from a business and technical perspective
Project management skills & experience in project / change management
Must possess excellent interpersonal, verbal, and written communication skills
Self-motivated team player, encourage and support new ideas and act as a role model for others in driving the departmental / company vision.
If this sounds like you, we want to hear from you today!
Here's how to apply;
Apply online by clicking the Apply button
Upload your CV
For further info please send to
Please note that for transparency and equity reasons, only those applications made online via our site will be assessed.
After the screening of all the CVs received, we will only contact the candidates who meet the requirements of the job to arrange an interview.
All applications are considered strictly confidential.