QC Microbiologist Specialist

QC Microbiologist Specialist in Hoofddorp for a leading biopharmaceutical company, GMP microbiology lab role, temporary position.

Locatie
Hoofddorp
Sluitingsdatum

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Bekijk en reageer bij SIRE Life Sciences B.V. (externe link)

Eisen

  • Physically able to work in cleanroom and supporting areas, including lifting approximately 12 kg
  • Flexible and able to adapt priorities according to changing operational requirements
  • Practical experience with microbiological techniques such as air monitoring and surface monitoring
  • Experience with aseptic techniques and cleanroom operations
  • 0–4 years of experience in microbiology laboratory activities and/or environmental monitoring
  • Good working knowledge of MS Word, Excel, PowerPoint, and other relevant applications
  • Knowledge of GMP, regulatory requirements, and Quality Control processes
  • MLO level 3 or Bachelor's degree in Microbiology or a related scientific discipline
  • Strong interpersonal, verbal, and written communication skills in English
  • Able to work effectively in a collaborative and fast-paced environment
  • Comfortable working in cleanroom environments and following gowning procedures
Volledige omschrijving

The company is a leading international biopharmaceutical organisation focused on developing innovative therapies and advanced treatments for serious diseases. The organisation operates in a highly regulated environment where quality, scientific excellence, and patient safety are at the centre of its operations. As a QC Microbiology Analyst, you will join a professional Quality Control Microbiology team supporting laboratory testing and environmental monitoring within a highly regulated GMP environment.

Responsibilities: perform environmental monitoring of cleanrooms in accordance with approved procedures; perform microbiological assays, including sterility testing and plate reading; perform air and surface monitoring activities; accurately enter, review, and trend microbiological assay results and laboratory data; maintain accurate laboratory documentation in accordance with GMP requirements; perform routine maintenance of laboratory equipment and laboratory areas; follow applicable SOPs, GMP requirements, safety procedures, and quality standards; support departmental projects and continuous improvement initiatives; work collaboratively with Analysts, Senior Analysts, Lead Analysts, and other QC teams; support additional laboratory and departmental activities as required.

Requirements: MLO level 3 or Bachelor's degree in Microbiology or a related scientific discipline; 0–4 years of experience in microbiology laboratory activities and/or environmental monitoring; practical experience with microbiological techniques such as air monitoring and surface monitoring; experience with aseptic techniques and cleanroom operations; knowledge of GMP, regulatory requirements, and Quality Control processes; comfortable working in cleanroom environments and following gowning procedures; physically able to work in cleanroom and supporting areas, including lifting approximately 12 kg; good working knowledge of MS Word, Excel, PowerPoint, and other relevant applications; strong interpersonal, verbal, and written communication skills in English; able to work effectively in a collaborative and fast-paced environment; flexible and able to adapt priorities according to changing operational requirements.

Other information: if you are interested and want to apply, please submit your application via the apply button below and contact me.

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