Analytical Technical Integrator

Bedrijfsnaam: -
Plaatsingsdatum: 09/02/2018
Standplaats: -

Functieomschrijving

SIRE Life Sciences® is the market leader in life science recruitment. We believe the recruitment market needs to gear up in technology and continues innovation. We like technology, in a life science 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!

THE COMPANY

Our client is a professional Pharmaceutical organization, based in Zuid-Holland Netherlands.

For our department we are currently seeking for a fulltime Analytical Technical Integrator (Project Manager Analytical Development)

ROLE DESCRIPTION

The Analytical Technical Integrator is part of the Analytical Development department (AD). AD is responsible for among other method development and validation, QC release and stability testing, outsourced testing, viral safety studies, and product characterization during the preclinical and clinical development phases until commercial launch of a vaccine.

RESPONSIBILITIES

- Developing analytical development strategies aligned with the CMC strategy;
- Representing the analytical department within the vaccine development organization and manage the planning and execution of analytical deliverables
- Coordinating project transfer between phases (early, late development and commercial launch);
- Accountable for the deliverables of the analytical department in the CMC project team;
- Work closely with team members in AD and other departments like CMC, QA, RA, drug substance/drug product development, external vendors, and strategic suppliers;
- Authoring documents/dossiers and support writing of regulatory submissions, amendments, annual reports, and agency responses.

REQUIREMENTS

- MS degree in chemistry, pharmacy or equivalent in life sciences. Advanced degree is preferred.
- A minimum of 6-8 years of experience within the pharmaceutical industry.
- In depth operating knowledge of functions involved in analytical within drug development/commercialization process.
- Project management
- Writing and communication skills

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

 

Aanbod/arbeidsvoorwaarden
-

Samenvatting

Plaatsingsdatum :
09/02/2018
Referentienummer :
91771
Standplaats :
-
Adres :
-
Postcode :
9723 HK
Opleidingsniveau :
WO
Uren :
Nader te bepalen
Dienstverband :
Vast
Werkervaring :
5 - 10 jaar
Contactgegevens :
bekijk