Project Quality Lead Development Quality

Hessen  ‐ Vor Ort
Dieses Projekt ist archiviert und leider nicht (mehr) aktiv.
Sie finden vakante Projekte hier in unserer Projektbörse.

Beschreibung

Project Quality Lead Development Quality

You will be the primary contact for quality issues in projects/products as member of product development teams.

You will provide global quality oversight for projects/products in scope by ensuring application of GMP requirements.

You support the preparation and ensure the execution of Quality activities integrated in CMC development plans, e.g. elements of QbD, GATE.

You prepare and communicate lessons learnt to MSQ and development network and ensure risk assessments are performed at appropriate stages of development and for decision making on issues arising.

You will support the timely preparation and completion of GMP documentation, operational sites in preparation of PAIs, quality management of CMOs used in development.

In your role you furthermore support and involve QPs in timely manner providing information on quality issues/topics needed for QP release.

Skills:

Drug product Process Validation - 5 years minimum

GMP in development and routine manufacturing - 5 years minimum

Product & Process development & Validation - 5 years minimum

Quality by design - 5 years minimum

Risk assessment - 5 years minimum

Languages:

English - business fluent

German - nice to have

If you are interested do not hesitate to contact me!

Marcel Otto Recruitment Consultant Pharma / Medical Devices / Contract Division

Real Life Sciences

Ein Geschäftszweig der SThree GmbH Goetheplatz 5-7, 60313, Frankfurt

T:

E:

Global Village:

www.realstaffing.com

Mehr Informationen über Real Staffing erhalten Sie unter www.realstaffing.com/de
Start
08/2016
Von
Real Staffing
Eingestellt
12.08.2016
Projekt-ID:
1184716
Vertragsart
Freiberuflich
Um sich auf dieses Projekt zu bewerben müssen Sie sich einloggen.
Registrieren