Associate Specialist Downstream Operations (m/w/d)

LHH; Luzern; Vor Ort; CHF 90.000 - 120.000; Vollzeit

Zusammenfassung

LHH is seeking an Associate Specialist Downstream Operations (m/w/d) for a leading biotechnology client in the greater Lucerne area to join their Schachen manufacturing team on site.

In this hands-on role, you will contribute to GMP manufacturing of innovative early-phase biologics, supporting downstream processing while upholding quality, compliance, and operational excellence. This is a 12-month, on-site contract at Schachen, five days a week.

Qualifikationen

• Bachelor's or Master's degree in Biotechnology, Life Sciences, Engineering, or a related discipline.
• 1–2 years of experience in pharmaceutical/biotechnology industry.
• Experience with biologics manufacturing in GMP environment; chromatography, virus filtration, UF/DF, formulation, fill/freeze would be advantageous.
• Experience with DeltaV and PAS-X is highly desirable.

Aufgaben

• Set up, execute, and troubleshoot downstream processes under GMP.
• Ensure GMP/EHS compliance and contribute to continuous improvement and tech transfer activities.
• Support sampling activities and occasionally weekend/on-call duties; typical schedule is not shift-based.

Kenntnisse

GMP experience

Problem solving

Cross-functional collaboration

Fluent German

Fluent English

Ausbildung

Bachelor's or Master's in Biotechnology/Life Sciences/Engineering

Tools

DeltaV

PAS-X

SAP

Jobbeschreibung

For one of our clients, a leading biotechnology company in the greater Lucerne area, we are currently seeking an Associate Specialist Downstream Operations (m/w/d) to join their manufacturing team in Schachen.

In this hands‑on role, you will contribute to the GMP manufacturing of innovative early‑phase clinical therapies, playing a key part in the production of biologics that support the development of next‑generation treatments. Working as part of a collaborative and highly skilled manufacturing team, you will support downstream processing activities while ensuring the highest standards of quality, compliance, and operational excellence.

This is an on‑site position requiring full‑time presence in Schachen to support manufacturing operations and facilitate close collaboration with cross‑functional teams.

Your Responsibilities:

• Set up, practical execution and troubleshooting of downstream processes under Good Manufacturing Practices (GMP)
• Knowledge of and compliance to GMP principles and EHS standards in the area of responsibility
• Involvement in continuous improvement efforts and support for the implementation of new technologies, including non‑GMP engineering runs or testing activities
• Creation and updates of SOPs and (electronic) master batch records. Technical review of various documentation related to process transfer and GMP manufacturing
• Material management using ERP systems (SAP)
• Participation in sampling activities (including occasional weekend work) or on‑call duties, as required by the process scheduling. Typical manufacturing activities do not include shift work.

Your profile:

• Bachelor's or Master's degree in Biotechnology, Life Sciences, Engineering, or a related discipline.
• Minimum of 1-2 years of experience in the pharmaceutical or biotechnology industry.
• Previous experience in biologics manufacturing within a GMP-regulated environment. Hands‑on experience with capture and polishing chromatography, virus filtration, UF/DF, formulation, fill, and freeze processes would be a strong advantage.
• Experience working with manufacturing automation systems such as DeltaV and electronic batch record systems such as PAS‑X is highly desirable.
• Strong problem‑solving skills with the ability to challenge existing approaches, explore innovative solutions, and continuously learn and improve.
• Ability to perform effectively under pressure in a complex GMP environment while taking ownership and accountability for assigned responsibilities.
• Flexible and collaborative mindset, with the ability to work effectively with internal and external stakeholders to achieve ambitious operational goals.
• Fluent communication skills in both German and English:
  • German: C1 level (written and spoken)
  • English: B2+ level (written and spoken)
• Residence within approximately 30 minutes commuting distance of Schachen (LU), or willingness to relocate.
• Valid Category B driving licence and access to a personal vehicle to support on‑call responsibilities.

Additional Information:

• This is a site-based role, 5 days per week.
• Location: Schachen
• Contract duration: This is a 12-month contract position, planned to start in September, with the possibility of extension.
• Type of employment: Temporary staffing