Karo Healthcare Safety Specialist

11 hours ago


Stockholm, Stockholm, Sweden Karo Healthcare Full time

About Us

Karo Healthcare is a global leader in the consumer health industry, dedicated to empowering people to make informed health decisions. Our diverse portfolio encompasses over 80 brands across 7 categories, with operations in approximately 90 countries.

With a strong focus on innovation and customer satisfaction, we have established ourselves as a major player in the European consumer health market. As we continue to grow and expand our reach, we are committed to maintaining our core values of excellence, integrity, and customer-centricity.

Job Role

We are seeking a highly skilled Global Patient Safety Surveillance Specialist to join our team at our headquarters in Stockholm, Sweden. This role will be responsible for ensuring the safety and efficacy of our medicinal products throughout their lifecycle.

  • Develop and maintain a comprehensive understanding of medicinal product safety profiles and risk-benefit evaluations.
  • Guarantee high-quality activities are completed on time within Safety Surveillance & Risk Management.
  • Support the EU & UK QPPV/deputy in maintaining oversight of the PV system, particularly for Patient Safety surveillance activities.
  • Prepare and submit aggregate data, write, and review reports, such as PBRER, PSUR, DSUR, Addendum to Clinical overview, for Karo's medicinal products.
  • Collaborate in the development and maintenance of Risk Management Plans (RMPs) and risk minimisation measures.
  • Participate in signal validation and further signal assessment activities as applicable, and contribute to the Company Core Safety Information (CCSI) management.
  • Identify and communicate potential safety concerns within the Surveillance Team.
  • Contribute to the ongoing improvement of KARO's systems related to surveillance activities.

Key Responsibilities

The successful candidate will possess:

  • A Master's degree in Pharmacy, Medicine, or a related life science field.
  • At least 3 years of experience in Pharmacovigilance within the pharmaceutical industry.
  • Proficiency in Aggregated Reports and Signal Management.
  • Excellent oral and written communication skills in English.
  • Expertise in MS Office applications, including Word, Excel, and PowerPoint.
  • Experience with Veeva Vault Safety.
  • Knowledge of Pharmacovigilance Guidelines and Regulations.

What We Offer

As a member of our team, you will enjoy:

  • A dynamic and fast-paced business environment.
  • Flexible scheduling options, including hybrid work models.
  • Opportunities for growth and development in a rapidly expanding industry.
  • Responsibility for impactful projects with direct effects on customers and the industry.
  • A very positive work environment in an international and motivated team.


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