Lund University, Faculty of Medicine, Dept of Laboratory Medicine, Lund

Lund University was founded in 1666 and is repeatedly ranked among the world’s top universities. The University has around 47 000 students and more than 8 800 staff based in Lund, Helsingborg and Malmö. We are united in our efforts to understand, explain and improve our world and the human condition.

Lund University welcomes applicants with diverse backgrounds and experiences. We regard gender equality and diversity as a strength and an asset.

The Research Group
The Center for Translational Genomics (CTG) is a prioritized research infrastructure at the Faculty of Medicine, Lund University, part of the Clinical Genomics platform at SciLifeLab. The platform aims to offer translational and clinical researchers access to state-of-the-art methods in genomics and transcriptomics (e.g. WGS, RNA-seq and new single cell analyses) and to quickly translate new research findings into improved clinical utility in close collaboration with the regional healthcare. Locally, this is performed through close interactions with the Section for Molecular Diagnostics at Region Skåne. Within CTG, there is great expertise in Next Generation Sequencing (NGS) technologies, bioinformatics and several different disease areas, and seen from both a national and international perspective, the unit is at the technological forefront with access to very powerful sequencing instruments (e.g.Illumina NovaSeq 6000). For data processing, the center uses a dedicated high-performance computing cluster at Lund University.

At the national level, CTG and Clinical Genomics Lund are also involved in a Swedish initiative for precision medicine; Genomic Medicine Sweden, where the development of new methods for tomorrow's research and diagnostics is coordinated with the corresponding large-scale sequencing facilities at the country's other university hospitals.

We are now looking for a driven, curious, and thorough person, who wants to contribute to front-line research based on advanced genomic methods. The employment is a permanent full-time position with the desired start date of January 1, 2022, or by agreement. Probationary employment of 6 months may be applied.

Work duties and area of expertise
You will be part of a lab team of 5-6 people, within which you will primarily focus on services to research projects in need of different single cell sequencing-based interrogation methods (currently 10X Genomics and Takara iCell8cx-based). In addition to laboratory work, key duties in the position include customer contact and consultation as well as various administrative tasks (see below).

The main tasks include:

  • project planning and execution of established methods within CTG's single cell analysis-based services (e.g. mRNA, CITE-seq, ATAC-seq). Practical lab works also includes receiving samples, preparation and pooling of NGS libraries and sequencing, especially on the Illumina platform
  • making project-specific cost calculations for service projects based on established templates
  • customer contact and consultation in connection with standard service projects
  • participating in laboratory development of new single cell sequencing-based methods
  • documenting and streamlining of laboratory workflows
  • various administrative tasks, e.g. ordering reagents and laboratory accessories

Qualifications
The position requires:

  • Adequate University degree, e.g. bachelor's degree as a biomedical analyst or master's degree in molecular biology, biomedicine or equivalent
  • > 2 years of documented practical experience in molecular biologiy (e.g. extraction of DNA/RNA, PCR-based methods, Sanger sequencing and/or NGS)
  • Experience in preparing NGS libraries
  • Experience in sequencing NGS libraries on the Illumina sequencing platform
  • Ability to quickly understand different scientific needs and to discuss these with researchers, e.g. related to standard services or development of new methods
  • Excellent abilities to quickly learn new methods and establish new protocols
  • Excellent oral and written communication skills in English

Great emphasis will be placed on personal suitability. The tasks require that you are structured and have an excellent ability to prioritize at work. The work is very team-based - both internally and externally - and therefore requires very good communication and collaboration skills. In addition, you need to have the ability to work independently. We are looking for you who are unpretentious and have a service-oriented approach.

The following are desired for the position:

  • PhD in a relevant field (e.g. genomics or genetics)
  • > 1 year of practical experience in single cell sequencing technologies (e.g. from 10X Genomics, SmartSeq2 or Takara iCell8cx protocols) and/or relevant tissue-based analysis
  • > 2 years practical experience of methods based on NGS (library preparation and/or sequencing)
  • Experience in one or several of the following techniques/areas; cell culture, fixation of tissue and cells, and microscopy (e.g. FISH or RNA scope)
  • Excellent oral and written communication skills in Swedish

Instructions for your application
The application must contain a personal letter describing how you fulfill the desired qualifications, a CV and diploma.

Other
The university applies individual salary setting. Please indicate your salary claim in your application.

Type of employment Permanent position
Contract type Full time
First day of employment January 1, 2022, or according to agreement
Salary Monthly salary
Number of positions 1
Full-time equivalent 100
City Lund
County Skåne län
Country Sweden
Reference number PA2021/3792
Contact
  • Markus Heidenblad, recruiting manager, 046-2220000
  • Emelie Falck, HR coordinator, 046-2220000
Published 25.Nov.2021
Last application date 12.Dec.2021 11:59 PM CET

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