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Production Associate, Bioindicators

 

Founded in 1968, SKAN is a pioneer in cleanroom equipment and the development of isolators for the pharmaceutical industry. Innovative products, tailor-made solutions and an effective service organization have made SKAN a market leader and a key partner to industry and research laboratories.

 

 

 

Overview

 

The SKAN Laboratory specializes in the production and testing of biological indicators (BIs) and is an important partner for microbiological qualification processes. As part of our six-person laboratory production team, you will work closely with your colleagues to reliably manufacture our internationally recognized biological indicators.

This position is highly production-focused and involves clearly defined, repetitive work steps carried out in accordance with our quality and GMP requirements. Attention to detail, concentration, and a reliable approach to work are essential. Some tasks are routine and physically demanding. This position is well suited to someone who enjoys working in a structured and consistent manner and who can maintain the required level of accuracy and attention even when performing repetitive tasks.

You will work closely with your colleagues and directly contribute to the quality of our products through your careful and dependable work. Previous experience in pharmaceutical manufacturing or a laboratory environment is an advantage. However, we place particular importance on your willingness to learn our production processes, your sense of responsibility, and your ability to remain calm and dependable in your day-to-day work.

 

 

Responsibilities

 

  • Manufacture biological indicators, including complete documentation of all work steps in accordance with ISO and GMP requirements
  • Independently and carefully perform individual production steps, from preparation through completion of the finished product
  • Prepare and provide the required packaging and production materials
  • Perform secondary packaging activities
  • Complete accurate, traceable, and comprehensive documentation of all work steps in accordance with GMP requirements
  • Comply with hygiene, quality, and safety requirements throughout the entire production process
  • Maintain a clean and GMP-compliant work environment
  • Support general activities that help maintain a structured and efficient production process

 

 

Hardskills

 

  • Completed training or education in a technical, scientific, or manufacturing-related field, or equivalent professional experience
  • At least 3 years of experience in manufacturing or production, ideally in the pharmaceutical industry or another GMP-regulated environment
  • Knowledge of GMP requirements and experience with documentation-related activities is a plus
  • Experience in a microbiological or pharmaceutical environment is a plus
  • Good German and English language skills (B2 level)

 

 

Softskills

 

  • Willingness to take responsibility for assigned tasks and contribute to a stable and reliable production process
  • Strong attention to detail and commitment to quality, particularly when following established processes and work instructions
  • Ability to maintain focus and consistency when performing routine and repetitive tasks
  • Physical stamina and willingness to remain focused and work carefully during extended periods of repetitive activity
  • Strong teamwork and a collaborative attitude

 

 

 

We offer you

 

  • An open and collaborative corporate culture
  • Freedom to contribute and develop ideas
  • Opportunities to participate in sports and social activities
  • Professional development and continuous learning opportunities, especially at our SKAN Academy
  • Comprehensive and career-focused onboarding
  • Quick decision-making paths and flat hierarchies
  • Transparent and open communication
  • 5 weeks of vacation, with the option to take additional leave

 

 

Additional information

 

We look forward to receiving your complete application documents (CV, diplomas and employment references) via our career page.
For this position, we are focusing on direct applications and are not working with external agencies. Any dossiers submitted by agencies will not be processed.

 

For questions please contact Viviane Braxton.

 

Apply now »