Specialist QA CSV (Computer System Validation) (m/w/d)
Simtra BioPharma Solutions · Halle, North Rhine-Westphalia, Germany
Posted 23 days ago
or apply directly on Simtra BioPharma Solutions's site. We never take the application ourselves.
Is this posting real?
- This role has been open
- 23 days Simtra BioPharma Solutions's roles stay open a median of 43 days
- Reposted
- No
- Salary listed
- No 3% of Simtra BioPharma Solutions's roles list one
- Ghost-job risk at Simtra BioPharma Solutions
- high 49 stale, 9 reposted of 103 open
- Hiring momentum
- 140 roles opened in the last 90 days ↑ up vs. the prior 90 days
- Last confirmed on the employer's board
- 2026-09-17
Measured from postings appearing on and disappearing from Simtra BioPharma Solutions's own greenhouse board since 2026-08-03. Full hiring picture for Simtra BioPharma Solutions.
About this role
In this role as a Specialist QA CSV, you will support the planning, execution, and continuous improvement of Computer System Validation (CSV) and Computer Software Assurance (CSA) in a GMP-regulated environment. Your responsibilities will include evaluating IT systems for validation relevance, coordinating CSV activities, reviewing documentation, and collaborating with various teams to ensure compliance and data integrity.
- benefits
- 5/5
- freshness
- 4/5
- career value
- 4/5
- role clarity
- 4/5
- pay transparency
- 0/5
Scored from the posting itself — how clearly the role is described, how much it says about pay and benefits, and how recently it was listed. Not a judgement of Simtra BioPharma Solutions as an employer.
What you need
- Abgeschlossenes Studium (Bachelor, Master, Diplom) mit einem naturwissenschaftlichem, technischem oder IT-nahem Hintergrund
- Idealerweise mindestens 2 Jahre Erfahrung im Bereich Datenmanagement, IT-Systeme, CSV/CSA in einem regulierten Umfeld
- Sehr gute Deutsch- und Englischkenntnisse in Wort und Schrift (mindestens B2-Niveau)
- Klare und proaktive Kommunikation, logische Denkweise sowie eine lösungsorientierte Arbeitsweise
Nice to have
- Erste Erfahrungen im GMP-Umfeld sind von Vorteil
- Kenntnisse der relevanten regulatorischen Vorgaben und Leitlinien
What you get
- Faire tarifgebundene Vergütung inkl. Sozialleistungen wie ein 13. Tarifgehalt, Urlaubsgeld, betriebliche Altersvorsorge und eine zusätzliche Pflegeversicherung
- Hauseigene moderne Kantine mit attraktiver Bezuschussung
- 30 Tage Urlaub plus Sonderurlaub
- Wochenarbeitszeit von 37,5 Stunden
- Job-Rad Leasing
- Corporate Benefits: Exklusive Rabatte für Mitarbeitende bei zahlreichen bekannten Marken
Worth weighing
- No salary listed
- The role requires a strong understanding of regulatory compliance in a GMP environment, which may be challenging for candidates without prior experience in this area.
Summarised from Simtra BioPharma Solutions's posting. Read the full original.
Listed by Simtra BioPharma Solutions on their greenhouse job board, last confirmed open on 2026-09-17. PitchMeAI is not the employer.
More roles at Simtra BioPharma Solutions
- Microbiology Supervisor, Quality Control Critical SystemsBloomington, Indiana, United States
- Teamleitung (m/w/d) Qualitätskontrolle Wareneingang und EndkontrolleHalle, North Rhine-Westphalia, Germany
- Sachbearbeiter (m/w/d) Produktionsdokumentation (in Teilzeit, 18,75 Stunden pro Woche)Halle, North Rhine-Westphalia, Germany
- Lead IT EngineerBloomington, Indiana, United States
- Quality Assurance Lead - Finishing (3rd Shift)Bloomington, Indiana, United States
- Sr. QA Inspector - Label Control (2nd Shift)Bloomington, Indiana, United States
- Sr. QA Inspector - Line Operations (3rd Shift)Bloomington, Indiana, United States
- Team Lead (m/w/d) QA Computer Systems Validation (CSV)Halle, North Rhine-Westphalia, Germany