Vacant job

As a laboratory engineer at our site in Strängnäs, you will work with varied and stimulating tasks. The Strängnäs site is in an expansion phase with several ongoing projects, one of which is to increase QC capacity.

We manufacture penicillin products, and in our QC lab, analyses are performed on materials from the entire production chain, including raw materials, excipients, APIs, packaging materials, and finished products, as well as stability sample analysis. Our products reach customers and patients worldwide, and we strive to deliver the highest quality in everything we do.

You will be part of a growing team, currently consisting of 5 colleagues in the QC department. You will work together on daily analytical tasks using methods such as HPLC, GC, FTIR, Karl-Fisher, and various wet chemical methods. You will work in a GMP environment where we follow both internal analytical methods and pharmacopoeial analyses (PhEur/USP).

Your main responsibilities will include:

• Planning, conducting, and compiling analyses
• Reviewing and releasing analyses in LIMS
• Establishing and updating work instructions and checklists
• Participating in deviation investigations relevant to the area of responsibility
• Being responsible for analytical instruments
• Supporting ongoing projects with analysis execution and report preparation
• Participating in improvement work

We are looking for someone with a university degree in chemistry, biochemical analyst, or similar. You have experience working practically in a GMP environment and have worked with HPLC. Experience with GC and analysis work using pharmacopoeial methods is a plus. You have good knowledge of both Swedish and English, spoken and written.

As a person, you thrive in a fast-paced work environment, are flexible, solution-oriented, and meticulous. You work independently to plan, execute, and document your work, and you enjoy varied tasks and can re-prioritize your work when needed.

Does this sound like a job for you? We welcome your application as soon as possible! The last application date is 2025-04-15, but interviews will be conducted continuously, and the position may be filled before the application deadline. If you have questions about the position, please contact Quality Manager Sofia Eriksson at 08-6024432. Apply through the link. We do not accept applications via email or post.

Blue Wolf Capital Partners has acquired 7 former Recipharm sites, with the Strängnäs site being one of them, as well as Synerlab with 6 facilities in France and Spain. These organizations will be merged into a world-class CDMO organization, and the company name has not yet been launched but is expected to be announced shortly. The Strängnäs site has been manufacturing penicillin in various forms for its customers since the 1970s. Blue Wolf Capital Partners has development and manufacturing facilities in France, Spain, and Sweden, with its headquarters in London, UK.