Manager Pharmacovigilance and Medical Device Regulations

This position can be based in Germany.

The Manager Pharmacovigilance & Medical Device Compliance is primarily responsible for establishing maintaining and continuously developing the companys pharmacovigilance addition the role is responsible for ensuring compliance with regulatory requirements for medical devices and serves as the interface between pharmaceutical and medical device regulations.

Job responsibilities include but are not limited to:

Pharmacovigilance (approx. 60%)

• 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

Medical Devices (approx. 40%)

• 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

Qualifications :

• 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.
• Knowledge of the MDR/MPBetreibV and medical device vigilance is an advantage.

Additional Information :

All Sobi employees need to demonstrate behaviors in line with Sobis core values: Care Ambition Urgency Ownership and Partnership. Are you ready to be on the Sobi team Come join a culture that empowers every person to be the person that makes a difference for rare disease.

Why Join Us

We are a global company with over 1900 employees in more than 30 countries and are committed to the societies where we operate. With a deeply skilled management team directing our day-to-day wins and a Board with a stellar track record were ready to take on the worlds diseases ailments and adversity. Our people believe they have the power to make a positive impact in others lives because thats exactly what we do here. If youre seeking a career that taps into your talents in a way that makes the world a better healthier place we just may have a job for you.

We know our employees are our most valuable asset and our culture conveys that. We offer a competitive benefits package to support the health and happiness of our staff.

Sobi Culture

At Sobi we refuse to accept the status quo. This is because we have witnessed first-hand the challenges facing those affected by rare diseases and have used this knowledge to shape our business to find new ways of helping them.

As a specialized biopharmaceutical company we are dedicated to rare diseases. And we see this focus as a strength. By effectively turning our research into ground-breaking treatments we help make medicine more accessible and open up more possibilities for patients and more opportunities for those caring for them. This has been our approach since day one but we know we cant change the world of rare diseases on our own. Accomplishing this requires strong partnerships with patients partners and stakeholders across the entire value chain. Together we define how our business can create solutions that serve the needs of those affected by rare diseases while facilitating sustainable growth.

An Equal Opportunity Employer

Sobi is an Equal Opportunity Employer and prohibits discrimination and harassment of any kind. All employment decisions at Sobi are based on business needs job requirements and individual qualifications without regard to race color religion or belief national social or ethnic origin sex (including pregnancy) age physical mental or sensory disability HIV Status sexual orientation gender identity protected veterans and/or expression marital civil union or domestic partnership status past or present military service family medical history or genetic information family or parental status or any other status or protected groups by the laws or regulations in the locations where we operate.

Sobi is an affirmative action and equal opportunity employer. Disabled/Veterans. If you are a qualified individual with a disability or a disabled veteran you may request a reasonable accommodation if you are unable or limited in your ability to use or access this website to apply for a vacancy as a result of your disability. You can request reasonable accommodations by sending an email to

Remote Work :

Yes

Employment Type :

Full-time

Experience: years
Vacancy: 1