Country: Hungary
Functional area: Quality Assurance & Quality Control
As a newly created position, our pharmaceutical manufacturing partner is in seach of a QRM & Audit Expert to join the company's quality organization to support and advise on internal quality processes and audits.
This mid-manager position (without direct subordinates) will actively cooperate with the site's quality, audit and production departments. As a member of the site quality board team this person will be responsible for:
Should you be interested please do not hesitate to submit your CV.
This mid-manager position (without direct subordinates) will actively cooperate with the site's quality, audit and production departments. As a member of the site quality board team this person will be responsible for:
- Developing long-term, sustainable strategic quality plans on company level (local)
- Managing risk assessment projects
- Defining CAPA plans and communication&follow up with the authorities
- Supervising the company's internal audit trainings
- Degree in Life Sciences: chemist, chemical engineer, biologist, bioengineer, pharmacist, etc.
- Solid background in pharmaceutical production environment as a quality professional
- Experience in manufacturing biological compounds / in aseptic production experienceis a plus
- Knowledge of GMP standards
- Fluent English and Hungarian knowledge
- Team-player and collaborator personality: ability to cooperate with cross-functional teams
Should you be interested please do not hesitate to submit your CV.
As a newly created position, our pharmaceutical manufacturing partner is in seach of a QRM & Audit Expert to join the company's quality organization to support and advise on internal quality processes and audits.
This mid-manager position (without direct subordinates) will actively cooperate with the site's quality, audit and production departments. As a member of the site quality board team this person will be responsible for:
- Developing long-term, sustainable strategic quality plans on company level (local)
- Managing risk assessment projects
- Defining CAPA plans and communication&follow up with the authorities
- Supervising the company's internal audit trainings
This is an exciting role for pharmaceutical manufacturing professionals with:
- Degree in Life Sciences: chemist, chemical engineer, biologist, bioengineer, pharmacist, etc.
- Solid background in pharmaceutical production environment as a quality professional
- Experience in manufacturing biological compounds / in aseptic production experience is a plus
- Knowledge of GMP standards
- Fluent English and Hungarian knowledge
- Team-player and collaborator personality: ability to cooperate with cross-functional teams
Should you be interested please do not hesitate to submit your CV.