(Junior) Vigilance Specialist

Miejsce pracy: Szczecin

Coloplast develops products and services that make life easier for people with very personal and private medical conditions. In Szczecin we have our Business Centre that works with global financial operations, orders administration, HR and IT support, Legal & Business Ethics, marketing & data analysis activities, QA 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 Coloplast 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 9 highly skilled specialists, 4 working in Quality Reporting dedicated for Complaint, Nonconformities, Supplier Quality and Sustainability areas, 1 is Project Management Office Specialist and 4 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 6 people in total.

About the job
(Junior)Vigilance Specialist is responsible for independently managing vigilance cases from intake through investigation and reporting. This includes assessing reportability, preparing and submitting regulatory reports to competent authorities, and contributing to post-market surveillance activities such as trend analysis and CAPA. Role involves cross-functional collaboration to ensure timely and compliant vigilance handling.

Responsibilities:

Verify and manage Vigilance Review Required (VRR) complaints.
Conduct Adverse Event Reporting (AER) and ensure timely submission to the competent authorities.
Perform trend analyses and provide insights to product owners to drive continuous improvement.
Contribute to the preparation and maintenance of periodic reports (PSUR, PMSR, PRER), ensuring alignment with regulatory expectations and product performance data.
Support the creation, maintenance, and review of Post-Market Surveillance (PMS) Plans, ensuring consistency with product risk profiles and regulatory requirements; document all updates in the change control system in accordance with internal procedures.
Assist in the assessment, documentation, and regulatory communication of Field Safety Corrective Actions (FSCA) and product recalls, in alignment with internal procedures and applicable regulatory requirements.
Contribute to product risk reassessments.
Develop and update relevant PMS procedures (including Vigilance) in a timely manner.
Complete Vigilance Profile Reports (VPR) as requested by Regulatory Affairs

Requirements:

You have a degree in pharmacy, life science, public health, nursing or similar and you have Vigilance or Regulatory experience from the medical device or pharma industry working with VRR complaints.

Furthermore, you:

Have solid understanding of medical device regulations and vigilance processes.
Have solid knowledge of medical terminology and/or clinical documentation.
Have knowledge of relevant standards and legislation (ISO13485, Medical Device Regulation, FDA-part 820, Health Canada Device regulations, Japanese QMS for Devices) with special focus on regulations for Vigilance.
Have experience with Regulatory Reporting and Vigilance platforms.

We are looking for a detail-oriented professional with strong analytical and problem-solving skills, fluent in English and confident in presenting vigilance topics in cross-functional settings. The ideal candidate is proactive, self-driven, and able to manage multiple vigilance cases independently while collaborating effectively with internal and external stakeholders. A commitment to quality, compliance, and continuous improvement is essential, along with an interest in leveraging new technologies such as AI and Microsoft 365 tools. Familiarity with data visualization platforms like Power BI will be a strong advantage.

We offer:

No probation period – long-term contract from the start.
Hybrid or remote type of work.
Flexible working hours, Mon-Fri.
International work environment with Scandinavian culture.
Opportunity to use and develop foreign languages in daily work.
Fantastic work atmosphere full of respect and partnership.
Internal trainings.
Great company events.
Sports card.
Private medical care.
Restaurant card.
Holiday bonus and occasional cards.

Thats not all! We have even more for you:

Modern workplace.
No dress code zone.
Delicious coffee and fresh fruits.
Transportation co-funding.

If you are curious like we are, and want to know more about our company go to https://www.coloplast.com/

Pursuing an ambitious growth agenda, Coloplast 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.

Coloplast 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.

By clicking the "Apply" or "Apply Now" button or by sending a recruitment application otherwise to Coloplast Business Centre Sp. z o.o., you agree for processing of your personal data for recruitment purposes in accordance with art. 6 par. 1 point b and f of the Regulation (EU) 2016/679 of the European Parliament and of the Council of 27 April 2016 on the protection of natural persons with regard to the processing of personal data and of the free movement of such data, and repealing Directive 95/46/EC (General Data Protection Regulation). You also agree to the processing of personal data included in the application form for future recruitments by Coloplast Business Center Sp. z o.o.
The administrator of personal data is Coloplast Business Center Sp. z o.o . with registered office in Szczecin, ul. Piastów 30, 70-064 Szczecin; contact to the Data Protection Officer: dataprotectionoffice@coloplast.com.
In addition, we would like to inform that:
Your personal data will be processed up to six months from the completion of the recruitment process.
You have the right to request access to your personal data, its rectification, erasure or limitation of processing and the right to object to processing, as well as the right to data portability.
You have the right to withdraw your consent at any time. The above does not affect the lawfulness of processing which was carried out on the basis of your consent before it was withdrawn.
You have the right to lodge a complaint with a supervisory authority - the President of the Office for Personal Data Protection.
Providing your personal data by yourself is voluntary, but necessary to participate in the recruitment process.
Decisions regarding the recruitment and selection process will not be taken in an automated manner.

P	W	Ś	C	P	S	N
		1	2	3	4	5
6	7	8	9	10	11	12
13	14	15	16	17	18	19
20	21	22	23	24	25	26
27	28	29	30	31

Pracownik Biurowy

Praca: (Junior) Vigilance Specialist

Specjalista ds. Nadzoru nad Wyrobami Medycznymi

RA Business Partner

Specjalista / Starszy Specjalista w Dziale Realizacji Kontroli w Terenowym Wydziale Kontroli III w Departamencie Kontroli

Specjalista / Starszy Specjalista w Dziale Realizacji Kontroli w Terenowym Wydziale Kontroli IV w Departamencie Kontroli

Backoffice-Mitarbeiter/in mit Deutsch und Englisch

Specjalista ds. Sourcingu & Administracji z językiem niemieckim

Młodszy Specjalista ds. Rekrutacji Niemieckojęzycznej

Doradca ds. obsługi klienta z językiem niemieckim

Kasjer / Kasjerka

Specjalista ds. Wsparcia Zespołu Protetycznego

Młodszy Specjalista ds. Telefonicznej Obsługi Pacjenta

Pracownik biurowy

Szukaj pracy