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QA Manager - Senior
Eingestellt von RM IT Professional Resources AG
Gesuchte Skills: Client, Support
Projektbeschreibung
QA Manager - Senior with profound GCP-knowledge wanted for our Zurich based client in the pharmaceutical sector.
YOUR EXPERIENCE/SKILLS:
- Bachelor's Degree in Biology, Nursing, Pharmacy, or in a related discipline with essential science knowledge to manage clinical trials and assure ethical treatment of subjects
- 10+ years' experience working in the pharmaceutical area in a GCP-related Quality environment with deep understanding of the medical impact of vaccines
- At least 7 years of indirect management level experience in GCP Quality Assurance including senior level project planning/budget management
- In-depth knowledge of the applicable GXP regulations, FDA Good Clinical Practices, ICH Guidelines, FDA Regulations and Guidance and Computer System Validation
- Excellent communication and presentation skills with the willingness to travel to various meeting or client sites (20% travel)
- Languages: fluent English both written and spoken, additional language knowledge is a plus
YOUR TASKS:
- Ensuring the development and implementation of strategies regarding the processes, procedures and quality standards required to maintain compliance to applicable regulations
- Analysing audit program results, quality issues and investigations in order to optimize regional operations and overall regional state of compliance
- Making sure that activities are conducted and reports are written according to applicable SOPs and regulations
- Supervising all GCP QA, PVQA, and GCLP QA activities including internal or external audit observations and development of adverse trends
- Identifying and mitigating GCP/PV/GCLP quality and compliance issues with potential impact across multiple compounds, sites, or functional groups within or outside of VBU
- Developing and presenting periodic reports for assigned project describing VBU compliance trends and identifying areas of potential risk to VBU senior management
START: ASAP
DURATION: 6MM+
LOCATION: Zurich, Switzerland
REF.NR.: BH11444
Does this sound like an interesting and challenging opportunity to you? Then take the next step by sending us your CV as a Word document and a contact telephone number.
DUE TO WORK PERMIT RESTRICTIONS WE CAN UNFORTUNATELY ONLY CONSIDER APPLICATIONS FROM EU OR SWISS CITIZENS AS WELL AS CURRENT WORK-PERMIT HOLDERS FOR SWITZERLAND.
GOING THE EXTRA MILE
NEW TO SWITZERLAND? In case of successful placement, we support you with:
- All administrative questions
- Finding an apartment
- Health - and social insurance
- Work permit and much more
YOUR EXPERIENCE/SKILLS:
- Bachelor's Degree in Biology, Nursing, Pharmacy, or in a related discipline with essential science knowledge to manage clinical trials and assure ethical treatment of subjects
- 10+ years' experience working in the pharmaceutical area in a GCP-related Quality environment with deep understanding of the medical impact of vaccines
- At least 7 years of indirect management level experience in GCP Quality Assurance including senior level project planning/budget management
- In-depth knowledge of the applicable GXP regulations, FDA Good Clinical Practices, ICH Guidelines, FDA Regulations and Guidance and Computer System Validation
- Excellent communication and presentation skills with the willingness to travel to various meeting or client sites (20% travel)
- Languages: fluent English both written and spoken, additional language knowledge is a plus
YOUR TASKS:
- Ensuring the development and implementation of strategies regarding the processes, procedures and quality standards required to maintain compliance to applicable regulations
- Analysing audit program results, quality issues and investigations in order to optimize regional operations and overall regional state of compliance
- Making sure that activities are conducted and reports are written according to applicable SOPs and regulations
- Supervising all GCP QA, PVQA, and GCLP QA activities including internal or external audit observations and development of adverse trends
- Identifying and mitigating GCP/PV/GCLP quality and compliance issues with potential impact across multiple compounds, sites, or functional groups within or outside of VBU
- Developing and presenting periodic reports for assigned project describing VBU compliance trends and identifying areas of potential risk to VBU senior management
START: ASAP
DURATION: 6MM+
LOCATION: Zurich, Switzerland
REF.NR.: BH11444
Does this sound like an interesting and challenging opportunity to you? Then take the next step by sending us your CV as a Word document and a contact telephone number.
DUE TO WORK PERMIT RESTRICTIONS WE CAN UNFORTUNATELY ONLY CONSIDER APPLICATIONS FROM EU OR SWISS CITIZENS AS WELL AS CURRENT WORK-PERMIT HOLDERS FOR SWITZERLAND.
GOING THE EXTRA MILE
NEW TO SWITZERLAND? In case of successful placement, we support you with:
- All administrative questions
- Finding an apartment
- Health - and social insurance
- Work permit and much more
Projektdetails
Geforderte Qualifikationen
-
Kategorie:
IT Entwicklung, Sonstiges