Validation coordination and Support to the QC virology team

Brabant Wallon  ‐ Onsite
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Keywords

Description

The company

The Harvey Nash Group was founded in the UK in 1988, and now has offices throughout Europe, America and Asia. The Harvey Nash Group is known for the thousands of successful assignments completed throughout the world.
From more than 39 offices, and with 5000 staff and associates, we offera unique range of consulting recruitment specialising in IT recruitment, benefits subcontracting and outsourcing services to ourclients. Our departments of Executive Search and Interim Management support our customers around the world by placing the senior managers essential to business growth and effective management.

For one of our clients, we're looking for a candidate, assuring the"Validation coordination and Support to the QC virology team"

FUNCTION DESCRIPTION

Provides support to the quality control (QC) virology team using technical and personal mastery, to provide accurate, compliant and ontime validation reports in accordance with GSK procedure and cGMP regulations (according Eur. Ph., CFR, OMS). You will work in a challenging network within QC Matrix organization and other GSK Bio departments. You will play a key tranversal role in the virology team to follow and maintain the status of quality in the organization and to meet our customer satisfaction

KEY RESPONSIBILITIES

- Writing of validation protocols and reports, procedure testing, taskforce report, request for change (method, biological material,transversal projects).
- Manage the datas needed for validation in collaboration with the virology team.
- Interact with the virology team to write procedure testing andassessment (risk assessment).
- Support and assures the efficiency of QC virology (delay validationreports, performance indicator, action plan).

PREREQUISITES

Education

- A university certificate with scientific orientation (Bio engineering, Biology, Biotechnology, Pharmacology).

Knowledge

- Bilingual French/English
- Strong knowledge of written and spoken French and English
- Good communication skills
- Ability to work under pressure due to the requested flexibility and reactivity of the activities
- Autonomous
- Ability to work in project teams in a multidisciplinary environment and a matricial organization

Experience

- At least 2 years in the pharmaceutical or biological field.
- Obligatory previous experience in one or more of the following areas: validation method (biology, pharmacology), cell culture, molecularbiology, bioassay cell culture (titration assay).
- Project management experience
- High c'GMP knowledge in pharmaceutical field.

TRAINING PERIOD

Training period: 2 months

Start date
15/1/13
Duration
6 months
From
Harvey Nash IT Recruitment Belgium
Published at
31.10.2012
Project ID:
441558
Contract type
Freelance
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