Description
Quality Project Specialist wanted for our Basel based client in the pharmaceutical sector.Your experience/skills:
- Apprenticeship degree or equivalent in manufacturing, laboratory or related discipline, relevant Bachelor degree is a plus
- 2+ years' working experience in a comparable line unit function like documentation, IT, manufacture, laboratory or packaging
- Competency of cGMPs as well as safety guidelines and environmental regulations
- Basic know-how of drug development
- Languages: fluent German and adequate English, both written and spoken
Your tasks:
- Maintaining GMP document management, including reviewing for SOP compliance
- Creating and completing GMP important documents in own area of responsibility, for example BRR sheets, CoCs, CoAs, SOPs and test scripts
- Identifying deficiencies and communicating them to supervisor along with suggesting actions as well as fixing simple defects
- Ensuring support for QA and process improvements, including relevant electronic systems and associates
- Acting as SME and contact person for the line unit
Start:
Duration: 12MM+
Location: Basel, Switzerland
Ref.Nr.: BH12073
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