(Junior) Post-Market Surveillance Manager (mIfId)
at Miltenyi Biotec
5BG, Nordrhein-Westfalen, Germany -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 30 Jan, 2025 | Not Specified | 01 Nov, 2024 | N/A | English,It,Working Environment,Powerpoint,Documentation,Databases,Life Sciences | No | No |
Required Visa Status:
Citizen | GC |
US Citizen | Student Visa |
H1B | CPT |
OPT | H4 Spouse of H1B |
GC Green Card |
Employment Type:
Full Time | Part Time |
Permanent | Independent - 1099 |
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Contract to Hire – Corp 2 Corp |
Description:
JOIN US
For 35 years, we have been developing innovative medical devices to empower biomedical research and advance medical treatments. This is how we are pushing the boundaries of cell and gene therapy and personalized medicine.
To realize our vision, we combine sophisticated research with advanced engineering solutions in agile software development, data science, the Internet of things, artificial intelligence, and connectivity. Today, more than 4,800 experts from over 50 countries contribute to breakthrough innovations and sustainable success.
Job Description
- You will join our team responsible for the post-market surveillance (PMS) of our clinical products (medical devices, in vitro diagnostics and GMP products) and perform organizational and administrative tasks to manage PMS data.
- You will be responsible for the management of PMS data collected from various sources (e.g. feedback, complaints, databases) for products on the market, as well as the identification of any further assessment needs.
- To evaluate the PMS data, you will initiate and document interdisciplinary and cross-departmental product and market monitoring meetings. Your objective is to identify the necessary corrective actions and to continuously improve our products to ensure a consistently high level of safety and performance.
- You will work closely with several other departments, in particular Clinical Evaluation, Risk Management, Marketing, Quality Assurance and Regulatory Affairs.
- You will collect and process post-marketing information in a dedicated database. The system-supported creation of the resulting reports as quality documents rounds off your varied area of responsibility.
QUALIFICATIONS
- You have successfully completed your studies, preferably in the field of life sciences or engineering, or have a comparable qualification. It is preferable that you have already gained professional experience in a regulated environment.
- You are a team player with experience of working in an interdisciplinary environment and can demonstrate an ability to bring together disparate elements in a goal-oriented manner.
- You are proficient in MS Excel, Word and PowerPoint and have experience of working with IT data processing tools. You have a comprehensive understanding of databases and are adept at working with large amounts of data. You work accurately with databases and the creation of documents, which is an inherent aspect of your role.
- You will thrive in an organized and independent working environment. Your proficiency in English allows you to comprehend information and documentation in English, and to produce reports on the results.
Additional Information
CONTACT US
If you have the skills and qualifications for this position, please use the link to send us your details (application letter, curriculum vitae, references and certificates). Please give us some idea of when you can start and the kind of salary you are looking for, outlining the reasons you have made this application
Responsibilities:
Please refer the Job description for details
REQUIREMENT SUMMARY
Min:N/AMax:5.0 year(s)
Pharmaceuticals
Clinical Pharmacy
Graduate
Proficient
1
51429 Bergisch Gladbach, Germany