Production Operator (m/f/d)

Client Overview

Our client is a premier global biotechnology organization located in the greater Lucerne area, renowned for its state-of-the-art biologics manufacturing facility in Schachen. This innovative site focuses on the development and production of biologic drug substances, playing a pivotal role in cutting-edge clinical programs and technology innovation initiatives. The organization is dedicated to delivering high-quality medicines through the application of advanced manufacturing technologies and a robust culture of quality and compliance.

Key Responsibilities

• Execute routine operator activities within Weigh & Dispense (W&D) and Solution Supply areas.
• Support operational functions within Upstream Processing (USP) and Downstream Processing (DSP) manufacturing areas.
• Conduct sampling activities in accordance with approved sampling plans, Standard Operating Procedures (SOPs), and batch records.
• Assist with the setup, preparation, and line clearance of equipment.
• Participate in the assembly and disassembly of single-use systems and process equipment.
• Ensure cleanliness of equipment and readiness of manufacturing environments.
• Support washer and autoclave operations according to validated procedures.
• Assist with routine maintenance and calibration of equipment.
• Manage material staging, transfers, inspections, and inventory checks.
• Complete GMP documentation, batch records, logbooks, and electronic systems accurately.
• Identify and escalate deviations, safety observations, and abnormal situations.
• Support audits, inspections, and internal walkthroughs as necessary.

Preferred Qualifications

• Technical or scientific vocational training in Biotechnology, Chemistry, Laboratory Technician, Chemical Operator, or a related field.
• A minimum of 3 years of experience in GMP manufacturing, ideally within biotech or pharmaceutical settings.
• Comprehensive understanding of Good Documentation Practices (GDP) and ALCOA+ principles.
• Experience working in cleanroom environments.
• Hands-on experience with biotech equipment, including both single-use and stainless-steel systems.
• Proficiency in sampling, material handling, and GMP documentation.
• Exceptional attention to detail and a strong compliance-oriented mindset.
• Professional communication skills in both German and English.

Additional Details

Location: Lucerne Area

Contract Duration: 12-month contract position starting October 2026

Employment Type: Temporary Staffing

Work Model: 100% Onsite

Working Hours: 40 hours per week