Senior Data & Technology Manager (all genders) - full-time/part-time at Merck KGaA
Darmstadt, , Germany -
Full Time


Start Date

Immediate

Expiry Date

03 Dec, 25

Salary

0.0

Posted On

04 Sep, 25

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Good communication skills

Industry

Information Technology/IT

Description

Job Id
291412
Darmstadt, Hessen, Germany
Job Type
full-time, part-time possible
Work Your Magic with us!
Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That’s why we are always looking for curious minds that see themselves imagining the unimaginable with us.
United As One for Patients, our purpose in Healthcare is to help create, improve and prolong lives. We develop medicines, intelligent devices and innovative technologies in therapeutic areas such as Oncology, Neurology and Fertility. Our teams work together across 6 continents with passion and relentless curiosity in order to help patients at every stage of life. Joining our Healthcare team is becoming part of a diverse, inclusive and flexible working culture, presenting great opportunities for personal development and career advancement across the globe.
Your role:
We are seeking a Senior Data & Technology Manager to focus on Safety Data Retrieval & Analysis while partnering with Regulatory Data Retrieval & Analytics. In this role, you will leverage your expertise in commercial pharmacovigilance (PV) systems and your strong knowledge of pharmacovigilance to drive the retrieval, analysis, and visualization of complex data. Your expertise will enable you to design, implement, and promote novel advanced analytical tools, building the next generation of safety capabilities by delivering value adding benefit risk information.

Key Responsibilities:

  • Maintain the validated state of the ArisGlobal commercial safety data warehouse (AWS/Snowflake).
  • Verify changes to reports through testing in non-production environments.
  • Oversee validation activities for new releases or change controls in compliance with GxP regulations.
  • Prepare for and support health authority audits and inspections.
  • Collaborate with the Qualified Person for Pharmacovigilance and her team to retrieve data from the safety database, ensuring compliant, high-quality analyses for Global Patient Safety.
  • Translate medical and scientific questions into robust technical solutions and act as the interface between operations, medical, and IT teams.
  • Specify and develop complex reports and dashboards using tools such as Snowflake, IBM Cognos, Python, and Tableau.
  • Drive continuous improvement and explore advanced technologies, including Snowflake features and knowledge graphs.

Who you are:

  • University degree in Data Science, Bioinformatics, Biostatistics, Computer Science, or Life Sciences.
  • Approximately five years of relevant working experience, particularly with BI/reporting tools and technologies (e.g., Python, Tableau, SQL, Cognos, Snowflake). Experience with knowledge graphs is a plus.
  • Proven pharmacovigilance knowledge and experience with commercial drug safety systems.
  • Strong sense of accountability and ownership, with a capacity for rapid learning.
  • Excellent project and vendor management skills.
  • Knowledge of GxP/GVP regulations and experience with test/validation management (HP ALM) of computerized systems.
  • Fluent in English; proficiency in German is a plus.
  • Excellent stakeholder communication skills, with the ability to translate scientific questions into technical requirements.
  • Ability to manage multiple projects simultaneously in a structured manner and build strong relationships within interdisciplinary teams.

What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We believe that this variety drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress!
and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!
US Equal Employment Opportunities
The Company is an Equal Employment Opportunity employer. No employee or applicant for employment will be discriminated against on the basis of race, color, religion, age, sex, sexual orientation, national origin, ancestry, disability, military or veteran status, genetic information, gender identity, transgender status, marital status, or any other classification protected by applicable federal, state, or local law. This policy of Equal Employment Opportunity applies to all policies and programs relating to recruitment and hiring, promotion, compensation, benefits, discipline, termination, and all other terms and conditions of employment. Any applicant or employee who believes they have been discriminated against by the Company or anyone acting on behalf of the Company must report any concerns to their Human Resources Business Partner, Legal, or Compliance immediately. The Company will not retaliate against any individual because they made a good faith report of discrimination.
Notice on Fraudulent Job Offers
Unfortunately, we are aware of third parties that pretend to represent our company offering unauthorized employment opportunities. If you think a fraudulent source is offering you a job, please have a look at the following information here.
Applicant Profile
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Responsibilities
  • Maintain the validated state of the ArisGlobal commercial safety data warehouse (AWS/Snowflake).
  • Verify changes to reports through testing in non-production environments.
  • Oversee validation activities for new releases or change controls in compliance with GxP regulations.
  • Prepare for and support health authority audits and inspections.
  • Collaborate with the Qualified Person for Pharmacovigilance and her team to retrieve data from the safety database, ensuring compliant, high-quality analyses for Global Patient Safety.
  • Translate medical and scientific questions into robust technical solutions and act as the interface between operations, medical, and IT teams.
  • Specify and develop complex reports and dashboards using tools such as Snowflake, IBM Cognos, Python, and Tableau.
  • Drive continuous improvement and explore advanced technologies, including Snowflake features and knowledge graphs
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