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Quality Specialist
Eingestellt von Experis AG
Projektbeschreibung
QUALITY SPECIALIST
Are you a highly qualified Quality Specialist with experience within a pharmaceutical environment and looking for an exciting new opportunity with a market leading global company? If so, please have a look at the following details:
Experis IT Switzerland is currently on the search for a Quality Specialist to join one of their clients, a global and well renowned pharmaceutical company based in Basel.
YOUR RESPONSIBILITIES:
You as a Quality Specialist will implement the controlled document strategy for PDQ and the supported business partners, for all relevant regulatory compliance standards and processes related to clinical development and safety/pharmacovigilance:
- Slide knowledge of GCP, PV and regulatory requirements
- Customer focused approach, and highly effective teamwork and collaborations skills
- Ability to build and maintain good relationships with key business partners, ability for problem identification, ability to analyse and simplify complex systems
TO DELIVER THE BEST OUTPUT, IT'S NEEDED THAT YOU HAVE:
- 3-5 years' experience in the pharmaceutical industry, GxP regulated area
- Experienced in preparation, development and administration of GXP standards and processes
- Demonstration knowledge of GCP, Pharmacovigilance/drug safety and regulatory requirements, as well as analytical, organizational and planning skills
- Substantial knowledge of all services and activities provided by PDQ QS, Change Management expertise
If you are a dynamic and motivated Quality Specialist currently looking for a challenging new position that applies to your skills, then we look forward to receiving your application!
Don't hesitate and send us your CV today through the link in the advert. In case of any questions please contact Julie Mackerer.
Experis IT is Europe's leading IT&T recruitment agency.
Are you a highly qualified Quality Specialist with experience within a pharmaceutical environment and looking for an exciting new opportunity with a market leading global company? If so, please have a look at the following details:
Experis IT Switzerland is currently on the search for a Quality Specialist to join one of their clients, a global and well renowned pharmaceutical company based in Basel.
YOUR RESPONSIBILITIES:
You as a Quality Specialist will implement the controlled document strategy for PDQ and the supported business partners, for all relevant regulatory compliance standards and processes related to clinical development and safety/pharmacovigilance:
- Slide knowledge of GCP, PV and regulatory requirements
- Customer focused approach, and highly effective teamwork and collaborations skills
- Ability to build and maintain good relationships with key business partners, ability for problem identification, ability to analyse and simplify complex systems
TO DELIVER THE BEST OUTPUT, IT'S NEEDED THAT YOU HAVE:
- 3-5 years' experience in the pharmaceutical industry, GxP regulated area
- Experienced in preparation, development and administration of GXP standards and processes
- Demonstration knowledge of GCP, Pharmacovigilance/drug safety and regulatory requirements, as well as analytical, organizational and planning skills
- Substantial knowledge of all services and activities provided by PDQ QS, Change Management expertise
If you are a dynamic and motivated Quality Specialist currently looking for a challenging new position that applies to your skills, then we look forward to receiving your application!
Don't hesitate and send us your CV today through the link in the advert. In case of any questions please contact Julie Mackerer.
Experis IT is Europe's leading IT&T recruitment agency.
Projektdetails
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