远程工作雷达

医疗器械与药物警戒经理

Medical Device und Pharmacovigilance Manager

其他未标注地域
公司Sobi
薪资未公开
工作地点Munich, BY, Germany
地域资格未标注地域
时区要求无特别要求
用工类型Full-time
发布时间2026-07-27
数据来源SmartRecruiters
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统计显示,女性和代表性不足的群体通常只在满足100%的资格要求时才会申请职位。Sobi鼓励你改变这一统计,并提交申请。很少有候选人完全符合所有要求。我们期待你的申请!
在Sobi,每个人都能带来独特的才能,作为团队的一员并产生影响。我们致力于开发和提供创新疗法,以改善患有罕见疾病患者的生活。我们的优势来自于我们的团队以及对患者的承诺。
在Sobi,我们的使命和文化让我们每天充满激情地来到工作岗位,但这里还有更多加入我们团队的理由:
· 为你的工作提供具有竞争力的薪酬
· 注重工作与生活的平衡
· 协作且以团队为导向的环境
· 职业发展的机会
· 多样性和包容性
· 积极影响,帮助急需救命治疗的超罕见疾病患者

该职位可在德国设立。
药理警戒与医疗器械合规经理的主要职责是建立、维护并持续发展公司的药理警戒体系。此外,该职位负责确保医疗器械的法规合规性,并作为药品和医疗器械法规之间的接口。
工作职责包括但不限于:
药理警戒(约60%)
· 管理并参与所有药理警戒(PV)活动
· 维护并持续改进药理警戒体系
· 支持国家监管机构的检查,并为全球药理警戒活动和其他监管检查提供必要的支持
· 建立流程以确保药理警戒合规性,包括文件记录
· 制定并维护PV标准操作程序(SOP)和模板
· 确保同事接受本地和全球SOP及程序的培训
· 按照Sobi AB/Akcea的要求,在本地层面进行不良事件/严重不良事件(AE/SAE)病例和投诉的核对(清单);审查月度ICSR合规报告,并准备本地 Pharmalex 表现的定期检查
· 审查来自ESP和Sobi员工的潜在晚期病例
· 归档、处理并本地记录所有产品投诉,同时维护AE/SAE病例的归档清单(清单)
· 收集、处理并报告所有

查看英文原文

Statistics show that women and underrepresented groups tend to apply to jobs only if they meet 100% of the qualifications. Sobi encourages you to change that statistic and apply. Rarely do candidates meet 100% of the qualifications. We look forward to your application!
At Sobi, each person brings their unique talents to work as a team and make a difference. We are dedicated to developing and delivering innovative therapies to improve the lives of people who live with a rare disease. Our edge comes from our team of people and our commitment to patients.
Here at Sobi, our mission and culture get us excited to come to work every day, but here are a few more reasons to join our team:
· 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

This position can be based in Germany.
The Manager, Pharmacovigilance & Medical Device Compliance is primarily responsible for establishing, maintaining, and continuously developing the company's pharmacovigilance system. In 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

  • 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.

All Sobi employees need to demonstrate behaviors in line with Sobi's 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 1,900 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, we’re ready to take on the world’s diseases, ailments and adversity. Our people believe they have the power to make a positive impact in others’ lives because that’s exactly what we do here. If you’re 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 can’t 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 talentacquisition@sobi.com.

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