Product Quality Manager - GMP/BGE/Documentation/SAP (m/f) 100%

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Beschreibung

Product Quality Manager - GMP/BGE/Documentation/SAP (m/f) 100% Lucerne

Role Purpose:
For our client, a renowned pharmaceutical company in Switzerland, we are looking for a Product Quality Manager with practical experience in regulated or GMP compliant environment.

Responsibilities:
- Q-Review on regulatory completeness/correctness of Device History Records (DHR) of semi-finished and finished products according to Roles and Responsibilities
- Release of BGE products
- Ensure that product-related deviations are checked and closed
- Responsible for Good Documentation Practice Training and Compliance within the company
- Leading and / or supporting special projects or initiatives in the area of quality and business partners if requiredsss
- Execute usage decision in SAP after variances, changes, rework, or disconnection
- Ensuring and advising on compliance with regulatory requirements for standard and GMP-compliant production and its documentation
- Collaboration in the creation of statistics for production monitoring, such as error statistics and quarterly reports
- Permanent optimization of the workflow to increase quality and efficiency

Required Skills:
- Practical experience in a regulated or GMP compliant environment
- Experience with internal or external interfaces
- Practical experience in a quality environment
- Medical devices or pharmaceutical experience preferred
- Technical or scientific understanding
- Good knowledge with Theoretical GMP
- Good communication and expression skills
- HF/Bachelor's degree or completed education

Languages:
- Fluency in German.
- English Advanced.

Reference No.: 918706NC
Role: - Product Quality Manager
Domain: Medical
Location: Lucerne und region, Switzerland
Workload: 100%
Start Date: ASAP
Duration: 12 Months (Strong possibility of Extension)

Should you find yourself suitable for this position then please send us your complete CV using the link in this advert. If the position is not a perfect match and you wish to receive other opportunities directly, you can send us your CV anyway via this advert or to jobs[at]itcag[dot]com.

Contact us for further information regarding our company, our positions or our attractive payroll-only-program: .

About us:
ITech Consult is a certified ISO 9001:2015 Swiss company with offices also located in Germany and Ireland. ITech Consult is specialised in delivering IT candidates for contract work. We were founded in 1997 by IT professionals; hence we well understand what it means to be professionally supported in your search for a new project and being employed.
Start
10/2019
Dauer
12 Months+
(Verlängerung möglich)
Von
ITech Consult AG
Eingestellt
30.10.2019
Projekt-ID:
1841722
Vertragsart
Freiberuflich
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