LAB TECHNICIAN FOR QUALITY CONTROL IN MICROBIOLOGY
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Odense SØ
Are you passionate about quality control and do you like to be challenged by an exciting day? Then you may be the laboratory technician with microbiological experience we’re looking for!
is an advanced analytical laboratory providing research, development, and regulatory compliance services to pharmaceutical and biotechnology companies. Headquartered in Odense, Denmark, QNTM is dedicated to developing innovative analytical methods while maintaining the highest quality levels to forge new pharmaceutical industry standards. Our mission is to improve transparency and access to robust scientific analysis, working hand-in-hand with global drug producers, API manufacturers, and pharmaceutical industry stakeholders through analytical testing, contract research and clinical trial support.
The position:
Together with a team of technicians, microbiologists and chemists, you will be part of a dedicated Quality Control (QC) team that works with a variety of different analytical methods.
You will be responsible for ensuring that laboratory analyses are being performed according to relevant pharmacopeias or QC procedures, and certifying that all handling of narcotics, samples, and standards are performed in compliance with ’ Quality Management System (QMS).
Your main tasks will include:
· Planning and execution of microbiological analyses (e.g. TAMC, TYMC) in collaboration with your other colleagues in the microbiological team.
· Data processing and reporting
· Qualification and maintenance of analytical equipment
· Support in preparing and maintaining operating instructions and SOPs
· Practical tasks in the laboratory, such as contamination reduction and management, sterilization procedures etc.
· Maintain control of the documentation related to narcotic substances, both samples and standards
Assist in reviewing new and existing QC procedures, while collaborating closely with the microbiologists, other laboratory technicians in both chemistry and microbiology, chemists, and the Quality Assurance (QA) team when adapting and maintaining documentation, e.g. equipment qualification protocols, and suitability reports.
We need you to:
· Be committed, structured and work focused on your tasks
· Find daily operations exciting, and be intellectually curious
· Enjoy working in close cooperation with other technicians and microbiologists aiming to deliver the highest quality results
· Thrive working in a GMP environment with high focus on robust operations
· Take an interest in method development and improvement
· Be a team player with a positive attitude and mindset.
· Be open, flexible in your tasks and adaptable to business needs at work areas.
Your background
· Preferably experience working within a QC Lab in the pharmaceutical industry, or other relevant standards
· Strong understanding of and previous experience with aseptic techniques, microbiological identification and verification analyses
· Preferably experience/knowledge about GMP and pharmacopoeias
· Structured organizational skills and a strong attention to scientific details
· Ability to read, write, and speak fluently in English & Danish
Application
Applications are assessed continuously and positions are filled as soon as possible.
If you have any questions about the position, please contact:
Kilde:
is an advanced analytical laboratory providing research, development, and regulatory compliance services to pharmaceutical and biotechnology companies. Headquartered in Odense, Denmark, QNTM is dedicated to developing innovative analytical methods while maintaining the highest quality levels to forge new pharmaceutical industry standards. Our mission is to improve transparency and access to robust scientific analysis, working hand-in-hand with global drug producers, API manufacturers, and pharmaceutical industry stakeholders through analytical testing, contract research and clinical trial support.
The position:
Together with a team of technicians, microbiologists and chemists, you will be part of a dedicated Quality Control (QC) team that works with a variety of different analytical methods.
You will be responsible for ensuring that laboratory analyses are being performed according to relevant pharmacopeias or QC procedures, and certifying that all handling of narcotics, samples, and standards are performed in compliance with ’ Quality Management System (QMS).
Your main tasks will include:
· Planning and execution of microbiological analyses (e.g. TAMC, TYMC) in collaboration with your other colleagues in the microbiological team.
· Data processing and reporting
· Qualification and maintenance of analytical equipment
· Support in preparing and maintaining operating instructions and SOPs
· Practical tasks in the laboratory, such as contamination reduction and management, sterilization procedures etc.
· Maintain control of the documentation related to narcotic substances, both samples and standards
Assist in reviewing new and existing QC procedures, while collaborating closely with the microbiologists, other laboratory technicians in both chemistry and microbiology, chemists, and the Quality Assurance (QA) team when adapting and maintaining documentation, e.g. equipment qualification protocols, and suitability reports.
We need you to:
· Be committed, structured and work focused on your tasks
· Find daily operations exciting, and be intellectually curious
· Enjoy working in close cooperation with other technicians and microbiologists aiming to deliver the highest quality results
· Thrive working in a GMP environment with high focus on robust operations
· Take an interest in method development and improvement
· Be a team player with a positive attitude and mindset.
· Be open, flexible in your tasks and adaptable to business needs at work areas.
Your background
· Preferably experience working within a QC Lab in the pharmaceutical industry, or other relevant standards
· Strong understanding of and previous experience with aseptic techniques, microbiological identification and verification analyses
· Preferably experience/knowledge about GMP and pharmacopoeias
· Structured organizational skills and a strong attention to scientific details
· Ability to read, write, and speak fluently in English & Danish
Application
Applications are assessed continuously and positions are filled as soon as possible.
If you have any questions about the position, please contact:
Kilde:
Information og data
Denne ledige stilling har jobtypen "Laborant", og befinder sig i kategorien "Sundhed og forskning".
Arbejdsstedet er beliggende i Odense SØ.
Jobbet er oprettet på vores service den 4.9.2025, men kan have været deaktiveret og genaktiveret igen.
Dagligt opdateret: Dette job opdateres dagligt ud fra jobudbyderens hjemmeside via vores søgemaskineteknologi og er aktivt lige nu.
- Laborant
- Odense SØ
- Fredag den 31. oktober 2025
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