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  1. Home
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  3. Goods And Materials Production
  4. Production Workers
  5. Manufacturing Operator
  6. operator – biotech production
Manufacturing Operator
operational

Operator – Biotech Production

Schachen, Lucerne
posted today
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Job details

Summary

  • Schachen, Lucerne
  • Temporary

Posted 24. july 2026

Reference number
25452
get in touch

we are here to help you with your questions.

M

Marta Tomczyk

+41 58 201 55 50

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randstad operational

randstad operational

We find, nurture, and connect uniquely skilled talent with employers when they need it, building successful teams that scale as their business grows while positioning individuals for rewarding careers and businesses for operational success.

Job details

For one of our clients, an international pharmaceutical company based in canton Lucerne, we are seeking a Biotech Production Operator.


General Information:
 

  • Start date: ASAP
  • Duration: 1 year
  • Extension: possible
  • Contract type: temporary contract via Randstad (employment)
  • Workplace: Schachen, Lucerne
  • Home office: not possible, 100% onsite
  • Workload: 100%

 

Tasks & Responsibilities:
...

 

  • Perform routine operator activities within the Weigh & Dispense (W&D) and Solution Supply Areas, in strict adherence to GMP and GDocP requirements 
  • Perform routine operational support activities within USP and DSP manufacturing areas 
  • Execute sampling activities in accordance with approved sampling plans, SOPs, and batch records 
  • Support equipment setup, preparation, and line clearance 
  • Assist with assembly and disassembly of single-use systems and process equipment 
  • Support equipment cleaning activities and ensure manufacturing room readiness 
  • Perform and support washer and autoclave activities in compliance with validated cycles and procedures 
  • Support calibration and routine maintenance activities 
  • Support material staging, transfers, inspection, and inventory checks 
  • Accurately complete GMP documentation (batch records, logbooks, electronic systems) 
  • Identify and escalate deviations, safety observations, and abnormal situations 
  • Support audits, inspections, and internal walkthroughs as required 


Your Profile:
 

  • Technical or scientific vocational training (e.g., Biotechnology, Chemistry, Lab Technician) 
  • Minimum 3 years GMP manufacturing experience (biotech/pharma preferred) 
  • Strong understanding of GDP and ALCOA+ principles 
  • High attention to detail and compliance mindset 
  • Experience working in cleanroom environments 
  • Hands-on experience with biotech equipment (single-use and stainless steel) 
  • Experience with sampling, material handling, and GMP documentation 
  • Fluent in German and English


Sounds interesting? Apply now – we’re looking forward to receiving your applications!

Show more

For one of our clients, an international pharmaceutical company based in canton Lucerne, we are seeking a Biotech Production Operator.


General Information:
 

  • Start date: ASAP
  • Duration: 1 year
  • Extension: possible
  • Contract type: temporary contract via Randstad (employment)
  • Workplace: Schachen, Lucerne
  • Home office: not possible, 100% onsite
  • Workload: 100%

 

Tasks & Responsibilities:
 

  • Perform routine operator activities within the Weigh & Dispense (W&D) and Solution Supply Areas, in strict adherence to GMP and GDocP requirements 
  • Perform routine operational support activities within USP and DSP manufacturing areas 
  • Execute sampling activities in accordance with approved sampling plans, SOPs, and batch records 
  • Support equipment setup, preparation, and line clearance 
  • Assist with assembly and disassembly of single-use systems and process equipment 
  • Support equipment cleaning activities and ensure manufacturing room readiness 
  • Perform and support washer and autoclave activities in compliance with validated cycles and procedures 
  • Support calibration and routine maintenance activities 
  • Support material staging, transfers, inspection, and inventory checks 
  • Accurately complete GMP documentation (batch records, logbooks, electronic systems) 
  • Identify and escalate deviations, safety observations, and abnormal situations 
  • Support audits, inspections, and internal walkthroughs as required 


...

Your Profile:
 

  • Technical or scientific vocational training (e.g., Biotechnology, Chemistry, Lab Technician) 
  • Minimum 3 years GMP manufacturing experience (biotech/pharma preferred) 
  • Strong understanding of GDP and ALCOA+ principles 
  • High attention to detail and compliance mindset 
  • Experience working in cleanroom environments 
  • Hands-on experience with biotech equipment (single-use and stainless steel) 
  • Experience with sampling, material handling, and GMP documentation 
  • Fluent in German and English


Sounds interesting? Apply now – we’re looking forward to receiving your applications!

Show more
    get in touch

    we are here to help you with your questions.

    M

    Marta Tomczyk

    +41 58 201 55 50

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