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Quality Control Consultant in the Pharmaceutical Industry

Randstad AB

49 days left
to apply for the job

Job Description

At Randstad Life Sciences, we are currently looking for someone who wants to work with quality assurance in the pharmaceutical industry for upcoming assignments. For this position, we are primarily seeking someone who wants to work with our clients in Strängnäs. As we have a broad client portfolio, we are constantly in need of expanding our consulting team, and if you are interested in working in laboratory quality control, you have come to the right place! 

 

As a consultant at Randstad Life Sciences, we are your employer, but you will have your daily workplace at one of our clients. Your consulting manager is always close at hand, both during and between assignments, to help you develop your career in the direction you dream of. As a consultant with us, you will receive a competitive salary, benefits, and collective agreement terms. We are attentive to your wishes regarding assignments and tasks, and with our broad client portfolio in Mälardalen, we will together adapt your continued career based on your skills, experience, and ambitions. You will be part of a larger consulting team within Life Sciences and have the opportunity to broaden your network and gain valuable experience from different workplaces.

Responsibilities

  • Perform quality control of incoming materials, packaging materials, media samples, in-process samples, and active pharmaceutical ingredients according to applicable methods/instructions.
  • Perform, evaluate, review analyses, and report results according to applicable methods/instructions, in line with departmental goals and production plans.
  • Be responsible for your part in ensuring the group delivers analysis results on time with good quality and EHS standards.
  • Actively contribute to a good working climate in the group and department.

Qualifications

  • University degree in chemistry or a related field.
  • Oral and written proficiency in Swedish and English is required.
  • Extensive experience in the pharmaceutical industry and work with cGMP, system knowledge, gLIMS, empower, and leadership experience.
  • Laboratory work in quality control in a cGMP-regulated environment.
  • Wet chemical (titration, gravimetry & colorimetry, ID analyses, and limit analyses), chromatographic (HPLC and GC), biochemical (absorbance measurements on proteins and coagulation, anticoagulation factors), and chemical analyses (Atomic Absorption, Kjeldahl, FTIR, TOC, density, UV-VIS).
  • Maintain and improve analytical methods/instruments and deviation management.
  • Pharmacopoeias.
  • Positive, driven, and enjoys working independently.
  • Ability to communicate well with others as collaboration with the group and other departments is part of the job.
  • The job requires accuracy, responsiveness, and initiative.

About the Company

Randstad

At Randstad, we know that everyone has a place in the job market. With operations across the country and in all areas of expertise, we help people find a job that feels right, where they have the opportunity to grow, develop, and reach their full potential.

With nearly 600,000 employees in 38 countries, Randstad is a world leader in HR services, aiming to become the world's leading and most appreciated partner in the job market. By combining our passion for people with the power of today’s technology, we help people and companies achieve their full potential. We call it Human Forward.

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