QC SPECIALIST FOR QUALITY CONTROL Are you passionate about quality control and do you like to be challenged? Then you may be the chemist with LC/GC/MS experience we’re looking for!

[xxxxx] 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 your 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 and techniques, e.g. LC, GC-FID, GC-MS and LC-MS. You will be responsible for ensuring that laboratory analyses are being performed according to relevant pharmacopoeias or QC procedures, and certifying that all handling of controlled substances, samples, and standards are performed in compliance with [xxxxx]’ Quality Management System (QMS). Your main tasks will include:

• Developing and maintain analytical methods that can either be based on pharmacopoeias or developed in house.

• Writing appropriate methods and approving of analytical data.

• Preparing protocols and reports to ensure validation or verification of methods.

• Giving the customers a superior service by ensuring close cooperation and transparency.

• Ensuring that methods are carried out according to current relevant standards and that analyses are being performed according to internal procedures

• Responsible for maintenance and periodic qualification of equipment.

• Work closely with the laboratory technicians and assist the broader laboratory operations, including equipment and method investigations and troubleshooting.

• Taking responsibility for change controls processes, deviation handling and for investigations related to your work.

• Collaborating with the Quality Assurance (QA) team when adapting and maintaining documentation, e.g., instruction and SOPs, equipment qualification protocols and relevant reports.

We need you to

• Be committed, structured and work focused on your tasks.

• Find daily operations exciting and be intellectually curious supporting troubleshooting.

• Ensure timely approval of analytical data and make sure to keep our customers satisfied

• Enjoy working in close cooperation with other technicians, microbiologists and chemists aiming to deliver the highest quality results.

• Thrive working in a GMP environment with high focus on robust operations

• Be a team player with a positive attitude and mindset.

Your background

• Relevant scientific education, such as a Master’s degree in Biomedicine, Molecular Biology, Biochemistry, Pharmacy, or equivalent.

• Strong understanding in chromatographic analytical techniques like LC, GC, and/or MS.

• Preferably experience/knowledge about GMP and pharmacopoeias.

• Preferably experience with the pharmaceutical industry or other relevant standards.

• Structured organizational skills and a strong attention to scientific details.

• Ability to read, write, and speak fluently in English.

Application

Applications are assessed continuously, and the position is to be filled as soon as possible. If you have any questions about the position, please contact: [xxxxx]
Kilde: [xxxxx]