making sure they are respected.What is more, Compliance Manager acting as Country Compliance Lead in Poland with responsibility for implementation and maintenance of compliance system in Poland, implementation of planned mandatory/statutory compliance system in Poland including creation of internal
pharmaceutical industry. Experience in CMC Regulatory, lifecycle management, interactions with Health Authorities, leading and managing regulatory teams.Strong understanding of and experience with global medical device-drug combination regulatory approvals;Business travel to be ~10-20% as required
to travel up to 25% of your time.- You have at least 8 years’ experience in the Pharmaceutical Industry in the manufacture and packaging of Pharmaceutical Drug Products (solids as well as sterile).- You have excellent verbal and written communication skills in English ...
quality support;- monitoring and reporting KPI's;- new product launches;- management of projects;- implementation of processes.Requirements- MSc or PhD in Life Sciences- 3+ years of experience in the Pharmaceutical industry in a (global) Quality role- Able to travel up to 10%- MS Office, SAP and eQMS-
nonstandard deliveries and network services. You are frequently in contact with representatives of several business areas to be able to determine the quality of the current service and to align the requirements for the future of the service. Reviews of the service are being led by the Service Delivery Manager
month) is expected. This means that although you will work with colleagues around the globe, travel is kept on family and environmentally friendly levels. What you'll need to succeed You have at least 3 years of audit or programmes/projects assurance experience, as well as you have audited large change
8 years commercial experience within the Medical Devices, Healthcare industry- International experience, with an existing network in Hospitals within Dutch, UK and the Nordics- Willing and able to travel 30% of the time- Commercial mindset- Knowledge/understanding of Medical Software is considered
generating business growth- Willing and able to travel frequently (50%) within Europe- Strong commercial mindset with great communicative skillsAre you interested and do want to apply for this role, please fill out your application via the apply button below and contact Frank Geerlofs ...
market segmentation, product/services development process, product/services road map planning, requirement definitions, customer communication and product/service life-cycle management- Willing and able to travel 30% internationally - Fluent in English- Entrepreneurial, adventurous personalityAre you
written communication in English, Dutch is a pré- Working knowledge of ICH/GCP regulations and clinical protocols- Experience in vendor- and site managementOther information- Ability to travel up to 10 - 20%- Accommodates a flexible work schedule according to clinical trial(s) priorities- Perform job
regulations for Quality Systems and Data Integrity- Capable of analyzing data to provide support of developing strategies for resolving compliance issues- Willing to travel (10%)- You have at least a Green Belt Six Sigma- Fluent in English (written/spoken)Heb je interesse en wil je meer weten over deze
7 years commercial experience within the Medical Devices, Healthcare industry- International experience, with an existing network in Hospitals within Dutch, UK and the Nordics- Willing and able to travel 30% of the time- Commercial mindset- Knowledge/understanding of Medical Software is considered