Dieses Jobangebot ist archiviert und steht nicht mehr zur Verfügung.
Vakante Jobangebote finden Sie unter Projekte.
Vakante Jobangebote finden Sie unter Projekte.
QA/QC Expert
Eingestellt von Harvey Nash IT Recruitment Switzerland
Gesuchte Skills: Client
Projektbeschreibung
For our client in BASEL we are looking for a QA/QC EXPERT for a 12-MONTH contract.
DURATION: 2018-01-03 TILL 2018-12-31
LOCATION: BASEL
WORKLOAD: 100%
MAJOR ACCOUNTABILITIES:
- Maintains and builds contacts with external experts, eg GQO, TRD, RegCMC, SCM, HSE etc. and ensures fast and direct communication channels
- Provides scientific and technical expertise on QA/QC procedures within ChemOps CH and to other organizations
- Maintains and adheres to cGMP, SOPs, Rolling Review, CAPA
- Prepares, participates in and conducts authority inspections and audits
- Ensure uniform GMP standards through regular exchange with central QA function
- Initiate revision, validation and improvement of GMP documents eg testing monographs, SOP's, qualification and validation documents
- Provide input to health authority requests
- Manage investigations regarding product quality (eg OOS/OOE, deviations, customer complaints)
- Procures validation support; supports launches
- Local and global project participation or lead
- Maintains state-of-the-art knowledge of Health Authority requirements, trends, technologies, processes and systems.
IDEAL BACKGROUND:
- University or academic degree in Chemistry, Biology, Pharmacy or equivalent
- Fluent German and English
- Experience in chemical/pharmaceutical industry is an advantage
- General IT-knowledge
For any further details please contact Beata Arciszewsk.
DURATION: 2018-01-03 TILL 2018-12-31
LOCATION: BASEL
WORKLOAD: 100%
MAJOR ACCOUNTABILITIES:
- Maintains and builds contacts with external experts, eg GQO, TRD, RegCMC, SCM, HSE etc. and ensures fast and direct communication channels
- Provides scientific and technical expertise on QA/QC procedures within ChemOps CH and to other organizations
- Maintains and adheres to cGMP, SOPs, Rolling Review, CAPA
- Prepares, participates in and conducts authority inspections and audits
- Ensure uniform GMP standards through regular exchange with central QA function
- Initiate revision, validation and improvement of GMP documents eg testing monographs, SOP's, qualification and validation documents
- Provide input to health authority requests
- Manage investigations regarding product quality (eg OOS/OOE, deviations, customer complaints)
- Procures validation support; supports launches
- Local and global project participation or lead
- Maintains state-of-the-art knowledge of Health Authority requirements, trends, technologies, processes and systems.
IDEAL BACKGROUND:
- University or academic degree in Chemistry, Biology, Pharmacy or equivalent
- Fluent German and English
- Experience in chemical/pharmaceutical industry is an advantage
- General IT-knowledge
For any further details please contact Beata Arciszewsk.
Projektdetails
Geforderte Qualifikationen
-
Kategorie:
IT Entwicklung