Representative QA Operations (m/w/d) - Analytical & Quality Evaluation Research Laboratories

Benefits

Parental leave

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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

Representative QA Operations (m/w/d) - Analytical & Quality Evaluation Research Laboratories 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. Die Position Ab sofort suchen wir für unseren Daiichi Sankyo Europe Standort in Pfaffenhofen an der Ilm, eine engagierte Person die unser QA Operations Teams im Bereich AQERL unterstützt. Für diese Position setzen wir eine Bereitschaft zur täglichen persönlichen Anwesenheit an unserem Produktionsstandort in Pfaffenhofen an der Ilm voraus. Angaben zur Tätigkeit Überwachung der Einhaltung von GMP-Vorgaben und System-Compliance im Bereich Analytical & Quality Evaluation Research Laboratories (AQERL) Erstellung, Prüfung, Genehmigung und Freigabe von GMP-Dokumenten (SOPs, Risikoanalysen, Herstellanweisungen etc.) Unterstützung bei Bewertung und Bearbeitung von Abweichungen sowie abweichenden Prüfergebnissen Definition und Nachverfolgung von CAPAs (Corrective and Preventive Actions) Mitarbeit an Change Control Prozessen: Verfassen, Review, Definition und Nachverfolgung von Maßnahmen Durchführung von GMP-Schulungen im Fachbereich

Read the full description at careers.daiichisankyo.com. FewerJobs shows a preview and links to the original posting.