Quality Assurance QA Specialist

2 weeks ago

Västerås, Västmanland, Sweden QIAGEN Full time

At the heart of QIAGEN's business is a vision to make improvements in life possible.

We are on an exciting mission to make a real difference in science and healthcare. We are still the entrepreneurial company we started out as and have today achieved a size where we can bring our full power to many initiatives and to our presence across the globe. Our most valuable asset are our employees – more than 6000 in over 35 locations around the world. Our ambition is to ensure we have outstanding and passionate people working in the best teams and we are constantly looking for new talent to join us. There are few players who have shaped the world of modern science and healthcare as much as QIAGEN, and we have only just started. If you are looking to advance your career, are seeking new challenges and opportunities, enjoy working in dynamic, international and diverse teams and want to make a real impact on people's lives, then QIAGEN is where you need to be.

QIAGEN DNA Synthesis AB in Sweden, has produced high quality synthetic DNA for diagnostic purposes for more than 30 years. We are situated in Västerås and have around 100 employees. We apply the medical device directives, ISO13485 (EU) and 21CFR820 (USA) and our production is carried out in accordance with GMP.

Join us. At QIAGEN, you make a difference every day.

Position Description

Please submit your application in English.

An exciting opportunity has arisen in our Quality Assurance team for a motivated individual with a positive outlook to join our diverse team. As a QA Specialist, you will join a team of eight motivated and highly educated colleagues focusing on product compliance as well as continuous improvement projects. This is a dynamic role involving lots of cross functional interactions and the opportunity to be involved in shaping the organization and making positive changes.

Key Responsibilities:
  • Batch record review and product release of our oligonucleotide products produced onsite
  • Document control and risk analyses
  • Handling of deviations, CAPAs and change requests
  • Data analysis to identify areas for improvement in the quality system
  • Reporting of quality metrics and performance to management
  • Working cross functionally with colleagues from other departments on improvement projects
Position Requirements
  • Degree qualified in a relevant subject.
  • Work experience in a regulated environment - experience in a QA role and/or working under GMP or ISO13485 would be beneficial.
  • Knowledge of tools, methods, and concepts of Quality Assurance as well as regulatory standards.
  • Good communication skills, both verbal and written. Fluent English and Swedish essential.
  • A people oriented person with excellent communication skills and a collaborative nature.
  • High attention to detail with excellent data collection and analysis skills.
What we offer

At the heart of QIAGEN are our people who drive our success. We act with passion, always challenging the status quo to drive innovation and continuous improvement. We inspire with our leadership and make an impact with our actions. We create a collaborative, safe and engaging workplace which forms the basis for high performing individuals and teams. We drive accountability and entrepreneurial decision-making and want you to excel your growth and shape the future of QIAGEN.

We offer:

  • Possibility to develop in an international company
  • Extra pension benefit
  • Health contribution (2500 SEK/year)
  • Volunteering day
  • Opportunity to join internal QIAGEN communities
  • Performance related bonus

QIAGEN is committed to creating a diverse environment and is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, sex, age, national origin, religion, sexual orientation, gender identity, status as a veteran, or disability.

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