Specialist (m/w/d) MAH QA Compliance

Benefits

Parental leave

Not verified

Non-birth-parent leave

Not verified

Family-building benefits

• Fertility benefits: Not verified
• Adoption assistance: Not verified
• Surrogacy assistance: Not verified

Mental health support

Not verified

Relocation assistance

Not verified

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)

$81,444 U.S. median for this role

Projected growth (BLS Employment Projections)

+6.9% - Faster than average

Matched to SOC 29-1141 - Healthcare aggregate by role bucket.

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

Role

Role function

Healthcare 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

Not verified

Company

Company stage

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

Application

Cover letter

Not verified

Assessment

Not verified

Deadline

Not stated

Where they hire

State eligibility is not yet verified.

About this role

Specialist (m/w/d) MAH QA Compliance 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. Purpose of the function Ab sofort suchen wir für unseren Standort in Pfaffenhofen oder München eine/n engagierte/n Specialist (m/w/d) MAH QA Compliance Angaben zur Tätigkeit: Als Specialist (m/w/d) MAH QA Compliance unterstützen Sie das Team bei allen Qualitätssicherungsaktivitäten des MAH QA Teams mit Fokus auf folgende Bereiche: Eigenverantwortliche Prozessierung von pharmazeutisch-technischen Reklamationen (PTCs), Fälschungsverdachtsfällen und Fällen im Bereich Serialisierung im internationalen Umfeld. Dazu gehören u.a.: Aufnahme (Prüfen auf Minimalkriterien, Loggen, Kommunizieren) und Abschlussmitteilung von PTCs, Fälschungsverdachtsfällen und Fällen im Bereich Serialisierung in Trackwise (eQMS) im Austausch mit internationalen, externen und internen Stakeholdern Koordination der eingehenden Reklamationsmuster nach vorgegebenen Richtlinien Nachverfolgung der Untersuchungen und der festgelegten CAPAs zur Einhaltung inter

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