Pharmiweb ChannelsAll | PharmaCo | Clinical Research | R&D/BioTech | Sales/Mktg | Healthcare | Recruitment | Pharmacy | Medical Comms

Pharmiweb.com RSS Feed Pharmiweb.com RSS Feeds

Pharmiweb.com RSS Feed PharmiWeb Candidate Blog

Pharmiweb.com RSS Feed PharmiWeb Client Blog

Job Details

Quality Auditor GMP

Company: Planet Pharma Staffing Limited
Location:
Reference: ABQUAGMP
Closing Date: 22 Jan 17
Type: Contract
Salary (£): Negotiable
Benefits:

Job Summary:

If you would like to find out more information, please send a copy of your most up to date resume to Ashleigh Batchen at Planet Pharma: abatchen@planet-pharma.co.uk Or call on +44 (0) 203 868 1001

Requirements:

Job title: Quality Auditor

Location: Office-based in Boxmeer, The Netherlands

Contract length: 7 months

Start date: As soon as possible

FTE: 1.0

 

The primary purpose of the position is to ensure cGMP compliance for the specifically assigned Quality Systems.

 

Responsibilities:

  • Develop, improve, and maintain the assigned Quality Systems on system level. This includes areas of global and local Quality Management System (QMS) strategy.
  • Create an integral and thorough insight in the quality and compliance status of the site. With your deep understanding of all (quality) processes and all relevant guidelines you are acting as an expert for colleagues with less experience within their own discipline.
  • Ensure implementation of the Quality Strategy and you advise by giving direction to the departments and you ensure compliance in line with Global Policies.
  • As a liaison from the Site in Boxmeer, you are connected to Global Compliance Work Committees in line with assigned responsibilities. This will reflect into directions and results towards the QMS approach of Site in Boxmeer.
  • The coordination and execution of the internal and external audit program, monitoring and follow-up.
  • To maintain and support a supplier management system including auditing, Technical Quality Agreements, and supplier assessments according to plan.
  • The systems used are Trackwise, Supplier Transparency and ESAM

 

Requirements:

  • BSc degree or MSc degree
  • Minimal 5 years’ experience in a comparable function within Quality (Systems)
  • Minimal 10 years’ experience in the pharmaceutical industry is a preference
  • Experience within a (highly) regulated environment is necessary
  • Green Belt certification is a preference
  • Dutch and English language must be mastered. Dutch communication is of importance for the communication within the department and on the site.
  • Self-starting, can do attitude.
  • You promote and displays “Lean” behaviours and “Lean” culture and coach and develop your team.
  •  You lead by example and have developed project management skills.
  •  You are a proven team player
  • Eligible to work in the EU

Please note that this role is on a contract basis and is not permanent.

Apply for this job: Quality Auditor GMP

Contact Information:

Address:  Head Office
10 Greycoat Place, London,
SW1P 1SB
England
Tel:  +44 203 868 1000
Website:  Visit Our Web Site

Advertising
Share | | |
Site Map | Privacy & Security | Cookies | Terms and Conditions

PharmiWeb.com is Europe's leading industry-sponsored portal for the Pharmaceutical sector, providing the latest jobs, news, features and events listings.
The information provided on PharmiWeb.com is designed to support, not replace, the relationship that exists between a patient/site visitor and his/her physician.