Accounting Specialist | Mitarbeiter (m/w/d) im Rechnungswesen
URSAPHARM Arzneimittel GmbH
Job Summary
This role involves managing diverse accounting operations within a growing pharmaceutical company in Saarbrücken. On a day-to-day basis, you will be responsible for the verification, account assignment, and posting of business transactions across general and subsidiary ledgers. Key tasks include account reconciliation, master data maintenance, and processing payment transactions. You will also play a critical role in supporting monthly and annual financial statements, handling VAT returns, and coordinating with tax consultants and auditors. This position is ideal for a detail-oriented professional with a strong grasp of VAT law and MS Office. The role is particularly attractive as it offers a crisis-proof position within a modern family-owned business in the pharmaceutical industry, featuring an attractive salary based on the chemical industry collective agreement (Chemie-Tarifvertrag), a strong welcome culture, and long-term internal development opportunities.
Required Skills
Education
Completed vocational training as a Tax Assistant (Steuerfachangestellte/r), Industrial Clerk (Industriekaufmann/-frau), or a comparable commercial qualification.
Experience
- Professional experience in accounting or tax consultancy
- Experience in account reconciliation and posting business transactions
- Experience in preparing VAT returns and supporting financial audits
- Proven track record of working with MS Office applications
- Experience in the administrative and organizational management of financial data
Languages
Additional
- A valid identity document (ID copy) must be submitted with the application for identity verification purposes. This is a full-time position located in Saarbrücken. Applications must be submitted digitally.
More Jobs from URSAPHARM Arzneimittel GmbH
GMP Documentation Specialist | GMP Documentation Specialist (m/w/d) GMP-Compliance
May 7, 2026
As a GMP Documentation Specialist, you will play a vital role in managing the document lifecycle for...
Deputy Head of Manufacturing (Solid Dosage Forms) | Stellv. Herstellungsleitung (m/w/d) Feste Formen
May 7, 2026
As the Deputy Head of Manufacturing for Solid Dosage Forms, you will play a pivotal role in ensuring...
Technical Specialist, Qualification and Validation (GMP Compliance) | Technischer Mitarbeiter (m/w/d) Qualifizierung und Validierung, GMP-Compliance
May 7, 2026
As a Technical Specialist in Qualification and Validation, you will play a vital role in ensuring th...