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QA/QC Manager
Eingestellt von RM IT Professional Resources AG
Gesuchte Skills: Support, Client
Projektbeschreibung
QA/QC Manager wanted for our Basel based client in the pharmaceutical sector.
YOUR EXPERIENCE/SKILLS:
- University degree in Pharmacy, Biochemistry, Chemistry or related science
- 5+ years' working experience in the pharmaceutical industry in compliance with QC, method development, validation or stability testing
- Expertise in cGMP as well as regulatory requirements, ICH guidelines and risk management
- Profound background in project management
- Languages: fluent English both written and spoken
YOUR TASKS:
- Defining and implementing business processes and SOPs for a robust Quality System within External Supply affecting the laboratory activities, such as maintenance of testing monographs and management of changes
- Supporting implementation of guidelines and qualification process at external partners and suppliers
- Conducting programs and initiatives for implementing changes as well as supporting Tech Transfer assessments for analytical method transfers
- Interpreting stability data, analysing trends and providing scientifically sound conclusions for assignment and monitoring support of product shelf life, packaging and transport categories and storage conditions
- Defining studies needed for change support and supporting assessments of analytical Change Control records for acceptability
START: ASAP
DURATION: 12MM+
LOCATION: Basel, Switzerland
REF.NR.: BH11900
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:
- University degree in Pharmacy, Biochemistry, Chemistry or related science
- 5+ years' working experience in the pharmaceutical industry in compliance with QC, method development, validation or stability testing
- Expertise in cGMP as well as regulatory requirements, ICH guidelines and risk management
- Profound background in project management
- Languages: fluent English both written and spoken
YOUR TASKS:
- Defining and implementing business processes and SOPs for a robust Quality System within External Supply affecting the laboratory activities, such as maintenance of testing monographs and management of changes
- Supporting implementation of guidelines and qualification process at external partners and suppliers
- Conducting programs and initiatives for implementing changes as well as supporting Tech Transfer assessments for analytical method transfers
- Interpreting stability data, analysing trends and providing scientifically sound conclusions for assignment and monitoring support of product shelf life, packaging and transport categories and storage conditions
- Defining studies needed for change support and supporting assessments of analytical Change Control records for acceptability
START: ASAP
DURATION: 12MM+
LOCATION: Basel, Switzerland
REF.NR.: BH11900
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
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Kategorie:
IT Entwicklung, Sonstiges