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Masterand (m/w/d) QA Operations

Daiichi Sankyo Company,Limited - Work Model Office Based Role (Daiichi Sankyo Europe) | Job Location (Country/Region)

Posted Jun 12, 2026

Benefits

Parental leave
Not verified
Non-birth-parent leave
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Family-building benefits
  • Fertility benefits: Not verified
  • Adoption assistance: Not verified
  • Surrogacy assistance: Not verified
Mental health support
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Relocation assistance
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Childcare support
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Learning budget
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Verification
Not verified checked Jun 7, 2026
Salary
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401(k) match
Reported from DOL Form 5500 industry filing (not employer-specific)

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Market context

U.S. role benchmark (BLS OEWS)
$61,842 U.S. median for this role
Projected growth (BLS Employment Projections)
+1.9% - Slower

Matched to SOC 11-1021 - Operations aggregate by role bucket.

Source: U.S. Bureau of Labor Statistics, OEWS, May 2024 and Employment Projections, 2024-2034.

Role

Role function
Operations From the posting source checked Jun 20, 2026
Seniority
Mid From the posting source checked Jun 20, 2026

Schedule

Shift type
Not verified
Weekend work
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Company

Company stage
Public-company From the posting source checked Jun 20, 2026

Application

Cover letter
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Assessment
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Deadline
Not stated

Where they hire

State eligibility is not yet verified.

About this role

Masterand (m/w/d) QA Operations Work Model Office Based Role (Daiichi Sankyo Europe) | Job Location (Country/Region) At Daiichi Sankyo, we are united by a single purpose, to improve lives around the world through innovative medicines. With a legacy of innovation since 1899, a presence in more than 30 countries, and more than 19,000 employees, we are advancing breakthrough therapies in oncology, cardiovascular disease, rare diseases, and immune disorders. Guided by our 2030 vision to "be an innovative global healthcare company contributing to the sustainable development of society", we are shaping a healthier, more hopeful future for patients, their families, and society. Title Assessment of Stakeholders and Concepts Involved in Establishing a New Manufacturing SiteBackground:Daiichi Sankyo Europe GmbH (DSE) is planning to build a greenfield Biological Drug Substance (DS) Production Facility. This ambitious project requires a well-defined responsibility landscape, particularly focusing on quality assurance and technology transfer perspectives, to ensure smooth and compliant site establishment.Objective:The Master's thesis aims to assess the stakeholders and key concepts involved in establishing a new manufacturing site. The focus will be on defining and mapping responsibilities from a quality and transfer perspective. Background: Daiichi Sankyo Europe GmbH (DSE) is planning to build a greenfield Biological Drug Substance (DS) Production Facility. This ambitious project requires a well-defined responsibility landscape, particularly focusing on quality assurance and technology transfer perspec

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