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Quality Manager

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The company

Our client is a professional organisation, based in Netherlands. .

Role description

In this role you will be responsible for the entire product group

Responsibilities

Monitoring and review of partners quality perform
CMO compliance through output from audits.
Identify and agree on improvement actions
Create, negotiate and maintain Quality Agreements
Review, evaluate, and contribute to investigation
Assess any change control
Review and evaluate complaints
Review and approve the product quality review
Review and analyse the trend associated to stability results
Review and approve protocol and validation report

Requirements

Scientific Degree with a professional qualification and QP status
Minimum of 10 years related pharmaceutical industry
Experience in CMOs management
Thorough working knowledge of regulatory requirements
Extensive knowledge of GMP
Experience in auditing in GMP/GDP/ISO environments
Experience with Regulatory and ISO inspections
Excellent verbal and written communication skills ability to present effectively to groups.

Other information

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


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SIRE Life Sciences®

Ref. nummer: 47932
Geplaatst door: SIRE Life Sciences®
Geplaatst op: 12-06-2019
Land: The Netherlands
Dienstverband: Permanent
Expertise: > 10 jaar
Locatie Type: Op locatie
Opleiding: PhD.
Taal: Engels
Sector: Pharmaceutical
Specialisatie: Quality

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Contact

SIRE Life Sciences B.V.

Mondriaan Tower
Amstelplein 52, 25th floor
1096 BC Amsterdam
+31 (0) 20 658 9800

SIRE Life Sciences Deutschland GmbH

Fünf Höfe
Theatinerstraße 11
80333 München
+49 (0) 89 3803 8966

SIRE Life Sciences UK

702 Howard House Dolphin Square
SW1V3PQ London
+44 7307 179882

SIRE Staffing Solutions B.V.

Keizersgracht 440A
1016 GD Amsterdam
+31 (0) 20 658 9804

SIRE Life Sciences Consultancy B.V.

Wetenschapsstraat 14B
1040 Bruxelles
+32 (0) 2 588 1277