GRA Labeling Officer
Titel: GRA Labeling Officer
Werkgever: Hays
Plaats: Provincie Noord-Brabant
Provincie:
Locatie:
Provincie Noord-Brabant /
Omschrijving:
Your new company
Global data management and labeling is part of global regulatory affairs AH. This department is responsible for the entire regulatory data and document infrastructure electronic publishing of registration dossiers and management of the related labeling for the AH product portfolio. Global data and labeling management AH is looking for a Regulatory affairs labelling officer
Your new role
Responsible for guarding the uniformity of country-specific product labeling, achieving deadlines, target dates and internal and external communication. You will Coordinate and implement a new and revised product labeling in line with regulatory product files. Also you will be responsible for the correct and timely control of the art-work design department (internal and/or external). Next to this you will be collecting all necessary information for the preparation of new product labeling, such as technical specifications, design specifications, registration requirements and texts. Your responsibility for proper phasing of the modified materials and control of phasing out of the existing packaging materials. You will maintain contacts with all major stakeholder e.g. Local Companies, packaging sites, Regulatory Affairs, Supply Chain Dept., Area Management, external printing, QA. Finally you will be responsible for correct/complete intake of the documents and procedure that trigger initiation of introductions / changes
What you'll need to succeed
A Bachelor degree is required Preferably gained work experience in Regulatory, QA or Supply Chain Department within the pharmaceutical industry; Preferably experience working with an artwork/document management system Preferably experience with GMP guidelines within the pharmaceutical industry; Good communication skills. Team Player Fluent English (speaking, reading and writing) Service minded Accurate and efficient
What you need to do now
If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now.
If this job isn't quite right for you but you are looking for a new position, please contact us for a confidential discussion on your career.
Interesse?
Stuur ons dan je CV en motivatie toe door te klikken op onderstaande knop "Reageer op deze vacature".
Provincie Noord-Brabant /
Omschrijving:
Your new company
Global data management and labeling is part of global regulatory affairs AH. This department is responsible for the entire regulatory data and document infrastructure electronic publishing of registration dossiers and management of the related labeling for the AH product portfolio. Global data and labeling management AH is looking for a Regulatory affairs labelling officer
Your new role
Responsible for guarding the uniformity of country-specific product labeling, achieving deadlines, target dates and internal and external communication. You will Coordinate and implement a new and revised product labeling in line with regulatory product files. Also you will be responsible for the correct and timely control of the art-work design department (internal and/or external). Next to this you will be collecting all necessary information for the preparation of new product labeling, such as technical specifications, design specifications, registration requirements and texts. Your responsibility for proper phasing of the modified materials and control of phasing out of the existing packaging materials. You will maintain contacts with all major stakeholder e.g. Local Companies, packaging sites, Regulatory Affairs, Supply Chain Dept., Area Management, external printing, QA. Finally you will be responsible for correct/complete intake of the documents and procedure that trigger initiation of introductions / changes
What you'll need to succeed
A Bachelor degree is required Preferably gained work experience in Regulatory, QA or Supply Chain Department within the pharmaceutical industry; Preferably experience working with an artwork/document management system Preferably experience with GMP guidelines within the pharmaceutical industry; Good communication skills. Team Player Fluent English (speaking, reading and writing) Service minded Accurate and efficient
What you need to do now
If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now.
If this job isn't quite right for you but you are looking for a new position, please contact us for a confidential discussion on your career.
Interesse?
Stuur ons dan je CV en motivatie toe door te klikken op onderstaande knop "Reageer op deze vacature".
