Associate Specialist Downstream Operations

Job Opportunity: Associate Specialist Downstream Operations (m/w/d)

We are currently seeking an Associate Specialist Downstream Operations for one of our clients, a leading biotechnology company situated in the greater Lucerne area. This position is based in Schachen and is integral to their manufacturing team.

In this hands-on role, you will play a vital part in the GMP manufacturing of innovative early-phase clinical therapies, contributing to the production of biologics that advance next-generation treatments. By collaborating with a skilled manufacturing team, you will support downstream processing activities while upholding the highest standards of quality, compliance, and operational excellence.

Your Responsibilities:

• Set up, execute, and troubleshoot downstream processes under Good Manufacturing Practices (GMP).
• Demonstrate knowledge of and compliance with GMP principles and EHS standards within your area of responsibility.
• Engage in continuous improvement efforts and support the implementation of new technologies, including non-GMP engineering runs or testing activities.
• Create and update SOPs and (electronic) master batch records, and conduct technical reviews of various documentation related to process transfer and GMP manufacturing.
• Manage materials using ERP systems (SAP).
• Participate in sampling activities, including occasional weekend work or on-call duties, as required by 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.
• A minimum of 1-2 years of experience in the pharmaceutical or biotechnology industry.
• Prior experience in biologics manufacturing within a GMP-regulated environment is preferred.
• Hands-on experience with capture and polishing chromatography, virus filtration, UF/DF, formulation, fill, and freeze processes is a strong advantage.
• Experience working with manufacturing automation systems such as DeltaV and electronic batch record systems like PAS-X is highly desirable.
• Strong problem-solving skills with the ability to challenge existing approaches and explore innovative solutions.
• Capacity to perform effectively under pressure in a complex GMP environment while taking ownership of responsibilities.
• Flexible and collaborative mindset, effectively engaging with internal and external stakeholders to meet operational goals.
• Fluent communication skills in both German (C1 level) and English (B2+ level), both written and spoken.
• Residence within approximately 30 minutes commuting distance of Schachen, or willingness to relocate.
• Valid Category B driving license and access to a personal vehicle for on-call responsibilities.

Additional Information:

• This is a site-based role, requiring a full-time, 5-day work 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

Apply online using the form below. Only applications matching the job profile will be considered.