Scientist Analytical development strategies (ADS) PER.C6 management
Titel: Scientist Analytical development strategies (ADS) PER.C6 management
Werkgever: Hays
Plaats: Provincie Zuid-Holland
Provincie:
Locatie:
Provincie Zuid-Holland /
Omschrijving:
Your new company
Our client is a global vaccine company that focuses on the development, production and marketing of vaccines and recombinant proteins to prevent and combat infectious and other diseases. Within the company talented, entrepreneurial people are working in a dynamic culture in which innovation and a ‘can do’ state of mind are the central points. In order to strengthen our team we are continuously looking for enthusiastic, talented people who have the ambition to develop themselves and can be of value.
Department
The ‘Analytical Development’ department is part of the Process Development group and is responsible for developing methods that are required for analysis of virus and antibody products. Product analysis includes testing for quantity, potency, purity and identity, detailed structural characterization but also safety testing. In addition, the Analytical Development department performs formulation development and stability monitoring, as well as routine sample analysis to support other departments. Safety testing is part of product release testing to ascertain whether no contaminations are present in our product but also in our production cell banks. These test are performed at CROs but strategies to determine what to test are drafted within ADS and discussed and agreed in multidisciplinary teams.
Your new role
The successful candidate will be responsible for PER.C6 knowledge maintenance both internally and towards external licensees, Responsible for conducting tests at Contract Research labs using established methodology. Duties & Responsibilities: Plans and conducts experiments and analyzes and interprets the results. Keeps accurate records of work undertaken. Reviews reports for accuracy and completeness. Provides documentation to help supervisor with the preparation of technical reports, manuscripts, and other documents that record data or results. Communicates data to external parties when requested. Creates and updates and internet web page for both internal and external use regarding PER.C6.
What you'll need to succeed
You have a WO background and are familiar with GMP and/or GLP. You have experience in one or more of the following techniques: ELISA, qPCR, cell based assays. You have knowledge on webdesign and data acculation storage and presentation is a pre requisite. You have a good command of speaking and writing Dutch and English and have the ability to communicate effectively with investigational site staff, team members and functional manager. Last you need a positive attitude, enthusiasm and motivation.
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 Zuid-Holland /
Omschrijving:
Your new company
Our client is a global vaccine company that focuses on the development, production and marketing of vaccines and recombinant proteins to prevent and combat infectious and other diseases. Within the company talented, entrepreneurial people are working in a dynamic culture in which innovation and a ‘can do’ state of mind are the central points. In order to strengthen our team we are continuously looking for enthusiastic, talented people who have the ambition to develop themselves and can be of value.
Department
The ‘Analytical Development’ department is part of the Process Development group and is responsible for developing methods that are required for analysis of virus and antibody products. Product analysis includes testing for quantity, potency, purity and identity, detailed structural characterization but also safety testing. In addition, the Analytical Development department performs formulation development and stability monitoring, as well as routine sample analysis to support other departments. Safety testing is part of product release testing to ascertain whether no contaminations are present in our product but also in our production cell banks. These test are performed at CROs but strategies to determine what to test are drafted within ADS and discussed and agreed in multidisciplinary teams.
Your new role
The successful candidate will be responsible for PER.C6 knowledge maintenance both internally and towards external licensees, Responsible for conducting tests at Contract Research labs using established methodology. Duties & Responsibilities: Plans and conducts experiments and analyzes and interprets the results. Keeps accurate records of work undertaken. Reviews reports for accuracy and completeness. Provides documentation to help supervisor with the preparation of technical reports, manuscripts, and other documents that record data or results. Communicates data to external parties when requested. Creates and updates and internet web page for both internal and external use regarding PER.C6.
What you'll need to succeed
You have a WO background and are familiar with GMP and/or GLP. You have experience in one or more of the following techniques: ELISA, qPCR, cell based assays. You have knowledge on webdesign and data acculation storage and presentation is a pre requisite. You have a good command of speaking and writing Dutch and English and have the ability to communicate effectively with investigational site staff, team members and functional manager. Last you need a positive attitude, enthusiasm and motivation.
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".
