Downstream Operations Associate Specialist (m/f/d)

nemensis ag; Schachen; Vor Ort; EUR 47.000 - 60.000; Vollzeit

Zusammenfassung

Nemesis AG is seeking a Downstream Operations Associate Specialist (m/f/d) for a temporary 12-month placement in the biopharmaceutical GMP manufacturing space in Germany. The role focuses on setting up and running downstream processes, ensuring GMP and EHS compliance, and contributing to early-phase therapeutic development.

You will draft SOPs, manage materials in SAP, and support continuous improvement, with English and German language fluency and a driving licence as assets; weekend/on-call

Qualifikationen

• Educational background with 1–2 years of professional pharma/biotech experience.
• Fluent in English and German.
• Willingness to work on-call including weekends.
• Driving licence (Class B) advantageous.

Aufgaben

• Set up, run and troubleshoot downstream processes under GMP.
• Uphold GMP principles and EHS standards.
• Draft and update SOPs and master batch records.
• Review transfer documentation from a technical perspective.
• Manage materials using SAP ERP.
• Support continuous improvement and implement new technologies, including non-GMP runs.
• Participate in sampling activities and on-call duties, including weekends.

Kenntnisse

Ownership mindset

Team collaboration

Bilingual English/German

Problem solving

Ausbildung

Educational background in pharma/biotech

Tools

SAP ERP

Jobbeschreibung

Downstream Operations Associate Specialist (m/f/d)

Turn cutting-edge biologics into life-changing therapies one batch at a time

Are you ready to get hands-on with GMP manufacturing for early-phase clinical therapies? As a Downstream Operations Associate Specialist (m/f/d), you'll be right at the heart of the action, helping bring next‑generation biologics from process to patient.

• Duration: 12 months (temporary assignment)
• Employment type: Temporary placement

About our client

For our client, an innovative company in the biopharmaceutical manufacturing sector, we are looking for a Downstream Operations Associate Specialist (m/f/d). The organisation specialises in the GMP‑compliant production of early‑phase clinical therapies and is known for pushing forward new technologies within biologics manufacturing.

Your responsibilities

• Set up, run and troubleshoot downstream processes in full compliance with Good Manufacturing Practice (GMP) standards
• Apply and uphold GMP principles and EHS standards consistently within your area of responsibility
• Draft and update SOPs and (electronic) master batch records, and review process‑transfer documentation from a technical perspective
• Manage materials using ERP systems (SAP)
• Contribute to continuous improvement initiatives and support the roll‑out of new technologies, including non‑GMP engineering runs and test activities
• Take part in sampling activities and on‑call duties as required by the production schedule, occasionally including weekend work

What you bring

• A relevant educational background paired with 1–2 years of professional experience in the pharmaceutical or biotech industry
• A solution‑oriented mindset, curiosity to keep learning, and the drive to continuously improve existing processes
• The ability to stay composed and take ownership in a demanding GMP environment
• A flexible, collaborative approach when working with internal and external stakeholders to reach ambitious goals
• Business fluency in English and German
• A driving licence (category B) and access to a car is an advantage, to support on‑call duties

What Nemesis AG offers you

• Nemesis AG is your specialised recruitment partner in the Life Sciences sector, based in Basel
• Comprehensive guidance and support throughout your application process from our consultants
• Access to a large network of clients and exciting positions across north‑western Switzerland
• A fast and straightforward way into your next role, thanks to individual coaching and advice during the application process