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Anlaytical Expert
Eingestellt von Harvey Nash IT Recruitment Switzerland
Gesuchte Skills: Support, Client, Network
Projektbeschreibung
For our client in Basel we are looking for an ANALYTICAL EXPERT for one year contract.
Place: Basel
Workload: 100%
Duration: ASAP- 30.06.2018
Job description:
. Design, plan, perform, interpret and report results of scientific experiments for the preparation and timely delivery of drug substances (DS) and drug products (DP).
. Responsible for analytical methods development, validation, stability and release testing and transfer activities of drug substance and formulated drug product.
. Contribute to the overall analytical project strategy
. Write analytical documents (eg Analytical methods, Validation reports, Stability reports)
. Ensures GMP compliance for all GMP relevant analytical activities of assigned projects in alignment with regulations and network decisions.
. Author, reviewer and approver of GMP relevant documents (eg analytical methods, raw data, SOPs, qualification reports for analytical instruments, etc.)
. Review analytical batch records according to SOPs
. Support defining the analytical strategy of development projects (proposes specifications, re-test dates, storage conditions, and/or batch release decision according to analytical results, SOPs).
. Support identifies scientific, technological and GMP issues and proposes solutions to relevant persons in the analytical project team.
. Demonstrate cost awareness in all assigned projects and/or networks.
For more information, please contact:
Anna Chmura
(see below)
Place: Basel
Workload: 100%
Duration: ASAP- 30.06.2018
Job description:
. Design, plan, perform, interpret and report results of scientific experiments for the preparation and timely delivery of drug substances (DS) and drug products (DP).
. Responsible for analytical methods development, validation, stability and release testing and transfer activities of drug substance and formulated drug product.
. Contribute to the overall analytical project strategy
. Write analytical documents (eg Analytical methods, Validation reports, Stability reports)
. Ensures GMP compliance for all GMP relevant analytical activities of assigned projects in alignment with regulations and network decisions.
. Author, reviewer and approver of GMP relevant documents (eg analytical methods, raw data, SOPs, qualification reports for analytical instruments, etc.)
. Review analytical batch records according to SOPs
. Support defining the analytical strategy of development projects (proposes specifications, re-test dates, storage conditions, and/or batch release decision according to analytical results, SOPs).
. Support identifies scientific, technological and GMP issues and proposes solutions to relevant persons in the analytical project team.
. Demonstrate cost awareness in all assigned projects and/or networks.
For more information, please contact:
Anna Chmura
(see below)
Projektdetails
Geforderte Qualifikationen
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Kategorie:
IT Entwicklung, Sonstiges