C&Q Project Manager

Brussel  ‐ Onsite
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Keywords

Description

One of our clients, a multinational company in the pharmaceutical industry currently requires a Commissioning and Qualification Project Coordinator

Start: ASAP
Length: 10 weeks
Location: South of Brussels

Operations delivery is accountable for the performance of operations and/or support within the organisational division concerned.
Provide support to GSK Bio project team for C&Q coordination(FAT/SAT/IQ/OQ).

Description:

In the context of investments projects (new or upgrades) in vaccines production

- ensure proper execution of the GSK Biologicals C&Q methodology and application of cGMP
(Validation Master Plan, Design Qualification, Commissioning, Installation & Operational Qualification and Validation Reports).
- Follow and coordinate the commissioning and qualifications during aproject
- Review and ensure the compliance of the qualification protocols,review the commissioning and qualification raw data and finally approve the reports for conformance
- Must be able to advice the various actors in case of issues or deviations
- Has an expertise in all commissioning/qualification aspects of vaccine manufacturing such as qualifications of HVAC systems, Clean Utilities (Clean Compressed Air, Clean Steam, Purified Water,
Water For Injection, ...), autoclaves, analytical systems,CIP/SIP process, filling lines, bulk equipments (chromatographysystems, fermentor, ) and other equipment commonly used in vaccine manufacturing facilities and be able to manage most of these qualification aspects.
- Ensure that all GMP aspects are respected during the project.
- Able to manage the project respecting the established commissioning/qualification timelines and coordinate all actors (Contractors, Engineering, Users) to align them with the project planning.

Education:

Have a scientific degree (Chemistry, Biochemistry,) or equivalent by experience

Knowledge/Skills:

- Bilingual French/English (written and spoken)
- Good experience in managing qualifications projects
- Good understanding of the injectable manufacturing processes
- Knowledge in qualifications of HVAC systems, Clean Utilities (CleanCompressed Air, Clean Steam, Purified Water, Water For Injection, ...), autoclaves, analytical systems, CIP/SIP process, filling lines, bulk equipments (chromatography systems, fermentor, )
- Planning of activities
- Good skills and competencies level in C&Q activities: organization, understanding and implementation of C&Q practices inprojects, time schedule, team working,
- Coaching and communication skills
- Good knowledge in coordination of activities

Tags: Commissioning, Qualification, Project, Management, GMP, Calibrage, Mesure, CIP, SIP, HVAC, autoclave

Start date
ASAP
Duration
10 weeks
From
Harvey Nash IT Recruitment Belgium
Published at
08.11.2013
Project ID:
624539
Contract type
Freelance
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