1 job found in bulach, aargau

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    • bülach, aargau
    • contract
    Quality & Compliance Manager Medical AffairsDo 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 Your Profile : Work experience: 3-5 years proven experience in the medical device and clinical/regulatory field (i.e. clinical studies, post market surveillance etc.) Competencies & skills: 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  Languages: Fluent in German and English (written and spoken) Experience as an internal auditor/co-auditor Quality & Compliance Manager Medical AffairsDo 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  Your Profile : Work experience: 3-5 years proven experience in the medical device and clinical/regulatory field (i.e. clinical studies, post market surveillance etc.)  Competencies & skills: 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  Languages: Fluent in German and English (written and spoken) Experience as an internal auditor/co-auditor   
    Quality & Compliance Manager Medical AffairsDo 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 Your Profile : Work experience: 3-5 years proven experience in the medical device and clinical/regulatory field (i.e. clinical studies, post market surveillance etc.) Competencies & skills: 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  Languages: Fluent in German and English (written and spoken) Experience as an internal auditor/co-auditor Quality & Compliance Manager Medical AffairsDo 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  Your Profile : Work experience: 3-5 years proven experience in the medical device and clinical/regulatory field (i.e. clinical studies, post market surveillance etc.)  Competencies & skills: 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  Languages: Fluent in German and English (written and spoken) Experience as an internal auditor/co-auditor   

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