Description
QA Manager wanted for our Basel based client in the pharmaceutical sector.Your experience/skills:
- BSc in science or a relevant discipline. MSc will be of advantage
- Background in compliance management along with 2+ years of working experience in QA
- Profound knowledge of cGMP, drug development, production and QA
- Sound scientific, technical and regulatory knowledge
- Experience in analyzing and evaluating GMP compliance
- Languages: fluent English both written and spoken, additional language would be an asset
Your tasks:
- Managing set of projects/processes, providing a discipline and /or supplying a service with a team of associates
- Evaluating and approving deliverables and related tools to ensure GMP compliance
- Supervising project related activities as well as assisting the team in evaluating of new QA tool
- Writing, reviewing and approving documents plus providing, inspecting and auditing activities
- Supporting TRD line functions in GMP compliance related issues in area of expertise
- Working on the improvement of internal and external guidelines regarding quality and safety
- Assisting the project management team in preparing PAI along with contributing to the internal compliance policy and regulations
Start: ASAP
Duration: 6MM++
Location: Basel, Switzerland
Ref.Nr.: BH11580
Does that sound interesting? Does that sound like a challenging opportunity to you? Then take the next step and send us your CV as a Word Document and a daytime 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