CMC Scientific Program Manager

Bedrijfsnaam: -
Plaatsingsdatum: 24/08/2018
Standplaats: -

Functieomschrijving

SIRE® is the market leader in Life Sciences recruitment. We believe the recruitment market needs to gear up in technology and continuous innovation. We like technology, in a Life Sciences market driven on science, we couldn’t stay behind; we drive Recruitment Science. Investing a majority of our turnover in technology enables us to use unique Resource Technologies. By using highly advanced algorithms, we enable our team of Resource & Data Strategists© to maintain the most advanced, detailed and complete Life Sciences network in Europe. This big data enables us to work Reverse Recruitment©: we first analyze the market in-depth before we go out to the market. Because we analyze the whole market, we can compare facts and data. This enables us to do Facts & Big Data Recruitment©, making sure we, or better yet, you find the right career!Our client is a professional Pharmaceutical and Biotechnology organisation, based in Netherlands.The CompanyOur client in the area of Weesp is producing raw materials for many medicines like laxatives, hormones and flu vaccin.

Role DescriptionYou will work within the CMC Scientific Program & Clinical Supply Management group. This group is responsible for all global projects on the field of product development. You are responsible for your own projects including budgets, timelines and delivering quality CMC files. You will guide the transmission of the production process from the development center to the production facilities.

Responsibilities- Responsible for your own team and their daily tasks and responsibilities
- Responsible for many processes:
raw material selection and availability, characterization of that raw material, purchases of comparators and reverse engineering, prototype development, including analytic methods development and validations.
- Planning and coordination of GMP production of clinical test material.
- Transfer production methods to factory, including upscaling and validation of production process.
- Drawing and assessing contracts with external parties

Requirements- PhD in Farmacie or (analytical) Chemistry
- minimum 5-10 years of experience within the pharmaceutical industry with production or development background
- Extensive experience in CMC drug development projects
- Experience in GMP guidelines
- Able to manage different projects in cross-functional teams
- willing to travel 10-25% of the time
- Excellent in Dutch and English language

Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Brwa Aziz.

 

Aanbod/arbeidsvoorwaarden
-

Samenvatting

Plaatsingsdatum :
24/08/2018
Referentienummer :
95115
Standplaats :
-
Adres :
-
Postcode :
9723 HK
Opleidingsniveau :
WO
Uren :
Nader te bepalen
Dienstverband :
Vast
Werkervaring :
5 - 10 jaar
Contactgegevens :
bekijk