Bioprocess Specialst (m/w/d) DSP

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

Not verified

Learning budget

Not verified

Verification

Not verified checked Jun 7, 2026

Salary

Not verified

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

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

Bioprocess Specialst (m/w/d) DSP 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 Standort in Pfaffenhofen eine/n engagierte/n Bioprocess Specialst (m/w/d) DSP Angaben zur Tätigkeit: Zum aktuellen Zeitpunkt befindet sich das Projekt und die damit verbundenen Tätigkeiten in der Etablierungsphase: Etablierungsphase Sie sind verantwortlich für die Etablierung ausgewählter DSP-Prozessschritte mit Single Use Materialien, angefangen bei der unterstützenden Geräteinbetriebnahme und -qualifizierung (DQ/IQ/OQ) Planung und Umsetzung von Leistungsqualifizierungsaktivitäten (PQ, PPQ) Erstellung und Überprüfung von Risikoanalysen, Qualifizierungs- und weiteren GMP-Dokumenten Etablierung von GMP-gerechten Herstellanweisungen (Master Batch Records) Erstellen und Überarbeiten sowie Überprüfen von Rezepten/Methoden Ihr Zuständigkeitsbereich umfasst des Weiteren Tätigkeiten im Bereich Operational Readiness (u.a. Materialmanagement; Probenhandling; Environmental, Health and Sa

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