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Production Employee Bioindicators 100% (m/f/d)

SKAN AG

Employment type
Full-time
Workload
100%
Location
Allschwil
Company
SKAN AG, 4123 Allschwil
First posted
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Founded in 1968, SKAN is one of the pioneer companies in the specialized fields of cleanroom equipment and the development of isolators for the pharmaceutical industry. Innovative products, customer-specific solutions, and a high-performance service and support organization have made SKAN a market leader and an important partner to industry and research laboratories.

Production Employee Bioindicators 100% (m/f/d)

At a glance

The SKAN laboratory specializes in the manufacture and testing of bioindicators and is an important partner in questions regarding microbiological qualification processes. As part of our 6-member production team in the laboratory, you will work closely with your colleagues to reliably manufacture our world-renowned bioindicators.
The activity is strongly production-oriented and includes clearly defined, recurring work steps in compliance with our quality and GMP specifications. Carefulness, concentration, and a reliable way of working are particularly important. The tasks are partly routine and physically demanding - anyone who enjoys working in a structured and constant manner and maintaining the necessary accuracy and attention even during recurring activities will find a suitable environment here.
You will work closely with your colleagues and contribute directly to the quality of our products through your careful way of working. Experience in pharmaceutical production or in a laboratory is an advantage. However, particularly important to us are your willingness to learn our production processes, your sense of responsibility, as well as your calmness and reliability in everyday work.

Tasks

  • Manufacture of biological indicators including documentation of all work steps according to ISO and GMP guidelines
  • Independent and careful execution of individual production steps from preparation to the finished product
  • Preparation and provision of the required packaging and production materials
  • Execution of secondary packaging
  • Seamless and traceable documentation of all work steps according to GMP requirements
  • Compliance with hygiene, quality, and safety specifications throughout the entire production process
  • Ensuring a clean and GMP-compliant working environment
  • Support with general activities to maintain a structured and efficient production process

Hardskills

  • Completed training in the technical, scientific, or production technology field or comparable professional experience
  • At least 3 years of experience in production, ideally in the pharmaceutical industry or another GMP-regulated environment
  • GMP knowledge and experience with activities requiring documentation are an advantage
  • Experience in a microbiological or pharmaceutical environment is an advantage
  • Good German and English skills (B2)

Softskills

  • Willingness to take responsibility for your own tasks and to ensure a stable and reliable production process
  • High level of care and quality awareness, especially in complying with specified processes and work instructions
  • Perseverance and ability to concentrate during routine and recurring tasks
  • Physical resilience and willingness to work in a concentrated and careful manner even during long-lasting, partly repetitive activities
  • Teamwork and collegial behavior

We offer

  • An open and collegial corporate culture
  • Freedom for ideas
  • Participation in sports and leisure activities
  • Promotion through further training, especially at our SKAN Academy
  • Intensive and job-oriented induction
  • Short decision-making paths and flat hierarchies
  • Open communication policy
  • 5 weeks of vacation and the possibility of additional vacation days

Further information

We look forward to receiving your complete application documents (CV, diplomas, and work certificates), which you can submit directly via our career page.

For this vacancy, we rely on direct applications and do not work with external agencies. Submitted dossiers from agencies will not be processed.

If you have any questions, please contact Viviane Braxton.

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Posted 5 days ago

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