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Quality & Compliance Manager Medical Affairs
View: 155
Update day: 26-03-2024
Category: Quality Assurance / Quality Control
Industry: Staffing Recruiting Biotechnology Pharmaceuticals
Position: Mid-Senior level
Job type: Full-time
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Job content
Do you have experience working in quality and clinical processes? Do you enjoy working in the medical device industry and are not afraid of taking on a new challenge?In this case, you should have a look at this opportunity!
Our client, a world leading medical device manufacturer in Zürich area is looking for a:
Quality & Compliance Manager Medical Affairs
(Permanent position - to start ASAP)
Your Responsibilities
- You will assure the compliance with guidelines, regulations and procedures in respect to clinical processes
- You will work on quality process management and contribute to harmonization of QMS within global environment
- You will perform quality checks internal and at the site
- You will be responsible for training and qualification activities in respect to Medical Affairs department and regions
- You will be performing and leading vendor qualifications/audits for external suppliers of clinical services
- You will act as an interface between MA and its external stakeholders in regards to quality aspects in medium to high complex questions
- You will be leading the execution of quality & compliance projects within the Medical Affairs department
Work experience:
- 3-5 years proven experience in the medical device and clinical/regulatory field (i.e. clinical studies, post market surveillance etc.)
- University or bachelor’s degree in scientific, medical field or law or equivalent experience and background in medical or pharmaceutical within clinical studies and regulatory field required
- Strong project and process management experience
- Knowledge/Expertise in ISO 14155, MDD, MDR, GDPR, 21 CFR relevant parts, ISO 14971
- Experience in (clinical) project work and experience as head of a work package within a project or programme
- Detail oriented and communicative team player with strong project management skills
- Strong self-starter and collaborator across all levels of the organization, within the business unit and with internal and external partners
- Fluent in German and English (written and spoken) Experience as an internal auditor/co-auditor
Do you have experience working in quality and clinical processes? Do you enjoy working in the medical device industry and are not afraid of taking on a new challenge?
In this case, you should have a look at this opportunity!
Our client, a world leading medical device manufacturer in Zürich area is looking for a:
Quality & Compliance Manager Medical Affairs
(Permanent position - to start ASAP)
Your Responsibilities
- You will assure the compliance with guidelines, regulations and procedures in respect to clinical processes
- You will work on quality process management and contribute to harmonization of QMS within global environment
- You will perform quality checks internal and at the site
- You will be responsible for training and qualification activities in respect to Medical Affairs department and regions
- You will be performing and leading vendor qualifications/audits for external suppliers of clinical services
- You will act as an interface between MA and its external stakeholders in regards to quality aspects in medium to high complex questions
- You will be leading the execution of quality & compliance projects within the Medical Affairs department
- 3-5 years proven experience in the medical device and clinical/regulatory field (i.e. clinical studies, post market surveillance etc.)
- Fluent in German and English (written and spoken) Experience as an internal auditor/co-auditor
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Deadline: 10-05-2024
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