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Vigilance Specialist
Job Details - this job has expired, please see similar jobs below
Company develops products and services that make life easier for people with very personal and private medical conditions. In Szczecin we are Business Centre that is responsible for global financial operations, orders administration, HR and IT support, marketing & data analysis activities, and many others. If you have the right profile and the right amount of curiosity and ambition you can be a part of this exciting challenge. Curiosity works here!
About the department
The job is located in Company Business Centre in Szczecin, Poland. You will be a part of Quality Reporting team, a part of Global Operations Support department. The team consists of 7 highly skilled specialists, 4 working in Quality Reporting dedicated for Complaint, Nonconformities, Supplier Quality and Sustainability areas, 1 is Project Management Office Specialist and 2 are working in Vigilance area. You will support the Vigilance team within Post Market Surveillance & Quality Processes, a department within Global Quality & Regulatory Affairs located in Denmark. All your tasks and training will be coordinated from this team. The Danish team consists of 2 Vigilance specialists, which makes the Vigilance team 4 people in total.
Your new job in Company
Your main responsibilities will be to diligently investigate incidents and report to national competent authorities according to applicable regulatory guidelines and timelines. Furthermore, you will create PSUR and PMS reports, handle safety issues related to the use of our products and deliver vigilance data for the registration of products in new markets.
Your key responsibilities
Your main task is to be the specialist in handling vigilance cases, including investigating with colleagues in various parts of Company – for example Medical Affairs and Manufacturing Sites, and creating reports to authorities. Furthermore, you will:
• Interact with authorities to fulfill the regulatory requirements related to vigilance for Company products (e.g. reporting of serious incidents and Field Safety Corrective Actions)
• Effectively communicate vigilance regulatory requirements throughout Company
• Follow worldwide regulatory development of the vigilance framework
• Interact with stakeholders throughout Company and provide vigilance training for relevant Company departments and subsidiaries
Your qualifications
You have a degree in pharmacy, life science, public health, nursing or similar. Preferably, you have Vigilance or Regulatory experience from the medical device or pharma industry.
Furthermore, you:
• Are structured, disciplined and know how to drive a vigilance process forward
• Have the ability to keep the overview and be decisive even with several cases on-going at once
• Have knowledge of regulations, standards and guidelines within the medical device area e.g. MDR, ISO 13485, and FDA 21 CFR 820.30
• Have strong communication skills and are fluent in English – both verbal and written.
On a personal note you are a true team player with a positive and flexible mindset, who understands how to reach joint goals. You have a proactive mind-set and a constructive attitude to drive results combined with the ability to plan, execute and meet deadlines. You enjoy working with multiple tasks at the same time and are analytical and capable of digesting complex data without losing the overall picture.
We Offer:
- No probation period – long-term contract from the start
- Remote work possibility for those outside of Szczecin
- Challenging tasks and growth opportunities in a motivating work environment
- Gaining experience in an international organization
- Competitive salary with attractive benefit package
- Opportunity to use and develop foreign languages in daily work
- Fantastic work atmosphere full of respect and partnership
- Internal trainings
That's not all! We have even more for you!
- Modern workplace
- No dress code zone
- Delicious coffee and fresh fruits
- Private medical care
- Sports card
- Transportation co-funding
- Restaurant card
- Holiday bonus and occasional cards
Deadline Please apply with your English CV. We will contact candidates continuously and close the offer down once we find the best match to the team :)
#LI-Remote
#LI-Hybrid
Please apply by sending your application in English.
If you are curious like we are, and want to know more about our company go to Company website
Pursuing an ambitious growth agenda, Company develops and markets products and services that make life easier for people with intimate healthcare needs. Employing about 16.000 people and with products available in more than 143 countries, we are one of the world´s leading medical device companies. We are constantly growing our business and always looking for new ways to move forward – we explore, learn and look for new ways of doing things.
Company is committed to being an inclusive organization, where people bring their differences to work each day, fulfil their potential and have a strong sense of belonging because – and not despite – of their differences. We therefore encourage all qualified candidates to apply regardless of gender, age, race, nationality, ethnicity, sexual orientation, religious belief or physical ability.
Visit us on Company website.
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