Downstream Operations Associate Specialist

more-jobs; Schachen; Vor Ort; CHF 65.000 - 90.000; Vollzeit

Zusammenfassung

more-jobs is seeking a Downstream Operations Associate Specialist (m/f/d) for a 12-month temporary assignment in the Greater Lucerne area, Switzerland. You will work hands-on in GMP manufacturing for early-phase biologics therapies, setting up and troubleshooting downstream processes, and ensuring GMP/EHS compliance.

Requirements include a life sciences background with 1–2 years in pharma/biotech, English fluency, and a collaborative, ownership-driven mindset.

Qualifikationen

• Educational background in life sciences with 1–2 years in pharma/biotech.
• Ability to stay composed and take ownership in GMP environments.
• Fluent in English; driving licence may be advantageous.

Aufgaben

• Set up, run and troubleshoot downstream processes in GMP-compliant operations.
• Uphold GMP and EHS standards in daily work.
• Draft and update SOPs and master batch records; review transfer docs.
• Manage materials using SAP ERP.
• Contribute to continuous improvement and tech roll-outs.
• Participate in sampling and on-call duties, including weekends.

Kenntnisse

Solution-oriented mindset

Ownership in GMP environment

Collaborative approach

English fluency

Ausbildung

Life sciences degree

Tools

SAP

Jobbeschreibung

Downstream Operations Associate Specialist (m/f/d)

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)
• Location: Greater Lucerne area, Switzerland
• 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 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
• A driving licence (category B) and access to a car is an advantage, to support on-call duties