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Sobi

Medical Device und Pharmacovigilance Manager

RemoteGermany only
Published
Role
Operations
Experience
Mid
Employment
Full-time
Company size
Enterprise
Salary not disclosed
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Open to DE only. Set where you work from to check your eligibility.

No BS summary

Pharmacovigilance and medical device compliance manager based in Germany. Needs 3-5 years in pharmacovigilance, strong EU-GVP knowledge, and a pharmacy, medicine, natural sciences, or comparable degree. MDR/MPBetreibV and medical device vigilance knowledge is an advantage.

What you'll do

  • Managing and contributing to all pharmacovigilance (PV) activities
  • Maintaining and continuously improving a pharmacovigilance system
  • Supporting inspections by national regulatory authorities and providing the necessary support for global pharmacovigilance activities and other regulatory inspections
  • Establishing processes to ensure pharmacovigilance compliance, including documentation
  • Creating and maintaining PV SOPs and templates
  • Ensuring colleagues are trained on local and global SOPs and procedures
  • Performing reconciliation (line listing) of AE/SAE cases and complaints at the local level in accordance with Sobi AB/Akcea requirements; reviewing monthly ICSR compliance reports and preparing the local periodic check of Pharmalex performance
  • Reviewing potential late cases from ESPs and Sobi employees
  • Archiving, processing, and locally documenting all product complaints, as well as maintaining reconciliation lists (line listings) for AE/SAE cases
  • Collecting, processing, and reporting all drug safety information within the affiliate and to Sobi headquarters, including performing translations and quality checks of safety information as required
  • Coordinating requests for follow-up information related to all complaints
  • Training all colleagues/ESPs on pharmacovigilance
  • Overseeing and implementing pharmacovigilance requirements in third-party partner agreements, including distributors, medical information, clinical development, patient support programs, market research activities, social media, and other digital media activities
  • Documenting and managing PV-related deviations and CAPAs
  • Acting as the person responsible for medical device safety in accordance with §6 MPBetreibV (German Medical Devices Operator Ordinance)
  • Supporting regulatory matters related to medical devices in accordance with the MDR (Medical Device Regulation) and MPBetreibV
  • Responsibility for vigilance processes for medical devices
  • Creating, continuously updating, and reviewing relevant SOPs
  • Monitoring regulatory changes in medical device legislation
  • Collaborating with external notified bodies and authorities as required
  • Reviewing medical devices

What they require

  • Completed degree in pharmacy, medicine, natural sciences, or a comparable field of study.
  • 3-5 years of professional experience in pharmacovigilance.
  • Strong knowledge of EU Good Pharmacovigilance Practice (EU-GVP) requirements.
  • Preferred: Knowledge of the MDR/MPBetreibV and medical device vigilance is an advantage.
  • All Sobi employees need to demonstrate behaviors in line with Sobi's core values: Care, Ambition, Urgency, Ownership and Partnership.

Benefits

  • Competitive compensation for your work
  • Emphasis on work/life balance
  • Collaborative and team-oriented environment
  • Opportunities for professional growth
  • Diversity and Inclusion
  • Making a positive impact to help ultra-rare disease patients who are in need of life saving treatments
  • We offer a competitive benefits package, to support the health and happiness of our staff.

Sobi is a specialized biopharmaceutical company dedicated to developing and delivering innovative therapies to improve the lives of people who live with a rare disease.

🇸🇪 SwedenBiopharmaceuticalMid-size

What people say about this company

3.3/ 5

Salary not disclosed