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QC Specialist – GMP Lab – €55k

2 months ago

Odense, Denmark Blackswansexist Full time

We are seeking a QC Project Specialist to coordinate and manage quality control testing in our client’s advanced GMP lab. This is a brand new lab that started in 2024, so you can expect to work with the latest equipment.

The company provides laboratory testing services and, with the rapid growth of the pharmaceutical industry in Denmark, they have found a promising market. There is a high demand in the area for similar positions.

This would initially be a 12-month temporary position (maternity leave cover), but there is a good chance to transition into a permanent position afterward. English is the only required language, meaning we are open to candidates from within the EU/Schengen area considering a move to Denmark.

You will receive a formal employment contract directly with the client, including a base salary of around 55k euros annually (35k DKK per month), with the possibility of a higher salary for those with more experience. They can also assist with practical relocation matters.

This role involves performing analytical testing, method development, and ensuring compliance with GMP standards. You will also act as a project coordinator. More on that below.

Key Responsibilities:

  • Analytical Testing: Perform method development, validation, stability testing, and routine analysis using techniques like HPLC, GC, and UV-Vis.
  • Data Documentation: Keep accurate records of test results, ensuring compliance with GMP standards and regulatory requirements.
  • Method Development and Validation: Develop and implement new analytical methods to meet client and regulatory needs.
  • Equipment Maintenance: Qualify, validate, calibrate, and troubleshoot lab instruments to ensure efficiency and accuracy.
  • Compliance: Ensure all lab activities comply with GMP, FDA, and other regulations. Participate in quality audits.
  • Client Interaction: Communicate with clients about test results and analytical solutions, providing technical support.
  • Continuous Improvement: Identify and implement process improvements within the QC department.
  • Training: Support, train, and mentor QC staff on GMP standards and lab procedures.

Qualifications:

  • Education: Degree in Chemistry, Biology, Pharmaceutical Sciences, or related field; advanced degrees or certifications are a plus.
  • Experience: Minimum of 2 years in a GMP QC lab, preferably from a contract lab setting.
  • The ideal candidate should have expertise in analytical chemistry, microbiology, or pharmaceutical sciences with proficiency in HPLC, GC, UV-Vis, and/or other analytical techniques. Not every single one is required, but a background in this area is important given the hands-on nature of the position.
  • Fluency in English.

For more information, please reach out to Anders Sandberg at Black Swans Exist or apply directly with an attached CV by clicking the apply button.

Contact

If you want to hear more about this opportunity and the company, or if you have any questions regarding the position, please do not hesitate to contact us. If you wish to apply for the position, please send an updated version of your CV, together with your questions, and we will get in touch with you soon.

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