Senior Manager QA 100% (a) — Bachem AG
CHF 85'500 - 129'500
Bachem AG · Bubendorf (BL)
- Location
- Bubendorf
- Contract
- full-time
- Posted
- 49 days ago
SalaryCHF 85'500 - 129'500
Role overview
Mansioni Development and improvement of processes - take over a central role within the local unit when introducing a new global QMS system.
- Develop, optimize and unify GMP processes and concepts - Ensure that these processes are implemented easily and efficiently Implementation at the sites - Active support for local and global teams in the implementation and application of GMP processes and related systems.
- Practical cooperation (hands-on) on site Global/local projects
- Working in global projects in the field of GMP compliance
- Head of local projects in the field of GMP compliance Audit and inspections
- Support for government and customer audits Cooperation and reporting
- Ensure a holistic understanding of quality
- Creation and evaluation of quality indicators and reports (e.g.
QSMR, KPIs) - Focus on areas: Training, Document Management, Deviations, Complaints, Change Control and Audits
- Requisiti - Complete studies in the scientific or technical field (e.g.
pharmacy, chemistry, biotechnology)
- Multiannual professional experience in the pharmaceutical or chemical industry
- Of which at least 3 years in quality assurance
- Very good knowledge of GMP rules (EU and USA)
- Experience with complex, s
- Development and improvement of processes - take over a central role within the local unit when introducing a new global QMS system.
- Develop, optimize and unify GMP processes and concepts
- Complete studies in the scientific or technical field (e.g. pharmacy, chemistry, biotechnology)
- Multiannual professional experience in the pharmaceutical or chemical industry
Main responsibilities
- Development and improvement of processes - take over a central role within the local unit when introducing a new global QMS system.
- Develop, optimize and unify GMP processes and concepts
- Ensure that these processes are implemented easily and efficiently Implementation at the sites
Key requirements
- Complete studies in the scientific or technical field (e.g. pharmacy, chemistry, biotechnology)
- Multiannual professional experience in the pharmaceutical or chemical industry
- Of which at least 3 years in quality assurance
- Very good knowledge of GMP rules (EU and USA) Experience with complex, s
Application process
- Active support for local and global teams in the implementation and application of GMP processes and related systems.
- Practical cooperation (hands-on) on site Global/local projects
- Working in global projects in the field of GMP compliance
- Head of local projects in the field of GMP compliance Audit and inspections
- Support for government and customer audits Cooperation and reporting Ensure a holistic understanding of quality
- Creation and evaluation of quality indicators and reports (e.g. QSMR, KPIs)
- Focus on areas: Training, Document Management, Deviations, Complaints, Change Control and Audits
Additional details
- Mansioni Development and improvement of processes - take over a central role within the local unit when introducing a new global QMS system.
- Support for government and customer audits Cooperation and reporting Ensure a holistic understanding of quality
- Creation and evaluation of quality indicators and reports (e.g.
- Very good knowledge of GMP rules (EU and USA) Experience with complex, s
Notes and original content
- Support for government and customer audits Cooperation and reporting
- Ensure a holistic understanding of quality
- Very good knowledge of GMP rules (EU and USA)
- Experience with complex, s
