For our client, an international company based in Bern, we are looking for a Senior Quality Engineer.
General Information:
- Start date: ASAP
- Duration: 1 year contract
- Extension: possible (to be discussed)
- Workplace: Bern
- Workload: 100%
- Home office: max. 2 days per week (possibly less at the beginning)
- Working hours: standard
Tasks and Responsibilities:
- Create impact assessments, investigation reports and risk files.
- Owning, shaping and managing quality tasks: CAPA and NC ownership and investigation documentation, Audit front room support, Quality database support (COMET).
- Keep track on due dates and writes investigation reports with a
- best-in-class quality.
- Create storylines for audit front rooms.
- Can defend his work in front of an auditor.
- Manage individuals on their deliverables.
- Keep track on ongoing changes within the department.
- Support the department leader on quality actions.
- Working with engineers and equipment owners as well as external providers to be compliant within our processes.
- Support manufacturing plant excellence at the site by providing guidance.
- Technical optimization of processes and systems / improvement measures.
- Work in close collaboration with department manager on timeline & deliverables.
- Managing and shaping internal processes.
- Close cooperation with internal departments.
Your profile:
- Educational background (preferably master's diploma) in mechanical, electrical, industrial, chemical or equivalent fields.
- Experience in GMP quality systems (preferably in pharma industry)
- Audit front room experience
- Aware of maintenance management, GMP practices
- Excellent oral and written communication skills at different hierarchical levels
- Fluent English and German is a must
- Ability to work in a matrix organization
- Ability to lead without direct management responsibility
- Excellent analytical skills
- Flexible and proactive, willing to work onsite
For our client, an international company based in Bern, we are looking for a Senior Quality Engineer.
General Information:
- Start date: ASAP
- Duration: 1 year contract
- Extension: possible (to be discussed)
- Workplace: Bern
- Workload: 100%
- Home office: max. 2 days per week (possibly less at the beginning)
- Working hours: standard
Tasks and Responsibilities:
- Create impact assessments, investigation reports and risk files.
- Owning, shaping and managing quality tasks: CAPA and NC ownership and investigation documentation, Audit front room support, Quality database support (COMET).
- Keep track on due dates and writes investigation reports with a
- best-in-class quality.
- Create storylines for audit front rooms.
- Can defend his work in front of an auditor.
- Manage individuals on their deliverables.
- Keep track on ongoing changes within the department.
- Support the department leader on quality actions.
- Working with engineers and equipment owners as well as external providers to be compliant within our processes.
- Support manufacturing plant excellence at the site by providing guidance.
- Technical optimization of processes and systems / improvement measures.
- Work in close collaboration with department manager on timeline & deliverables.
- Managing and shaping internal processes.
- Close cooperation with internal departments.
Your profile:
- Educational background (preferably master's diploma) in mechanical, electrical, industrial, chemical or equivalent fields.
- Experience in GMP quality systems (preferably in pharma industry)
- Audit front room experience
- Aware of maintenance management, GMP practices
- Excellent oral and written communication skills at different hierarchical levels
- Fluent English and German is a must
- Ability to work in a matrix organization
- Ability to lead without direct management responsibility
- Excellent analytical skills
- Flexible and proactive, willing to work onsite