Quality Control Laboratory Technician

As our new Quality Control Laboratory Technician, you will perform analytical testing of raw materials, in-process samples, stability samples, and finished products to verify compliance with established specifications and quality standards. You will work with a range of analytical techniques and laboratory instrumentation while supporting investigations, stability programs, method verification activities, and continuous improvement initiatives across the site.

This is an excellent opportunity for a laboratory professional who enjoys hands-on analytical work and wants to contribute to a modern manufacturing environment with high standards for quality, compliance, and continuous improvement.

Perform testing of raw materials, in-process control, and finished product samples to verify compliance with established specifications.

Conduct analytical testing using techniques such as HPLC, IR, Karl Fischer, TLC, and other approved test methods.

Investigate Out-of-Specification Out-of-Trend and atypical results in accordance with approved procedures.

Perform stability testing and maintain accurate stability study records.

Record and review analytical results in compliance with established procedure and data integrity requirements.

Maintain and calibrate QC laboratory instruments

Participate in interlaboratory comparison studies, proficiency testing programs, and method verification activities.

Perform routine laboratory housekeeping and ensure compliance with safety, quality, and environmental requirements.

Carry out special projects and actively participate in cross-functional teams, continuous improvement initiatives, and site development activities.

Minimum 2 years of experience in an analytical laboratory or process laboratory, preferably within industrial manufacturing, pharmaceutical, biotechnology, food, or chemical process industries.

Hands-on experience with Liquide Chromatography (HPLC) and wet chemistry analyses is essential. Experience with Gas Chromatography (GC) is considered an advantage. Experience with Chromatography Data Systems or chromatography management software is considered an advantage.

Knowledge of laboratory quality systems, ISO 17025, or similar regulated environments is preferred.

Strong troubleshooting and problem-solving skills, with the ability to investigate analytical issues, OOS, OOT, and non-conforming results.

Fluent in English, both written and spoken. Knowledge of Norwegian or another Scandinavian language is considered an advantage.

Able to work independently while collaborating effectively within a team environment.

Reliable and committed to delivering accurate, high-quality work.

A strong communicator who can effectively share findings, issues, and recommendations with relevant stakeholders.

Flexible and adaptable, with the ability to manage changing priorities and support different activities as needed.

The opportunity to work in a modern, well-equipped ISO/IEC 17025 accredited laboratory with advanced analytical instrumentation.

Collaboration with experienced and knowledgeable colleagues in a supportive and international work environment.

Participation in exciting projects and initiatives that contribute to the growth and success of the site.