Lediga job som Biolog

Rarity Bioscience develops ultrasensitive molecular diagnostics based on our proprietary superRCA® technology, enabling detection of rare mutations that standard methods miss. As our portfolio of pharma and clinical collaborations grows, so does our Scientific Services team - and we are now looking for a Senior Scientist to help lead that work.

You will lead and contribute to scientific collaboration projects in molecular diagnostics and cancer genomics, from initial dialogue to final report. In this role, you combine scientific leadership with involvement across assay development, performance evaluation, sample testing, data interpretation, and customer dialogue. You bring enough scientific depth to be a trusted discussion partner in cancer genetics, while also being practical enough to plan experiments, assess results, provide guidance to junior colleagues, and help move projects from first dialogue to final report or publication. In addition, the role can be expected to include some hands-on lab work to build familiarity with our assays, workflows, and daily operations, with the level of involvement varying depending on project needs.

• Coordinate and execute service projects involving internal laboratory teams, academic researchers, clinical collaborators, and pharmaceutical partners.

• Plan, perform, analyze, and report laboratory work across oncology, precision medicine, and mutation detection projects.

• Analyze, interpret, and report experimental and genomic data in relation to clinical data, somatic mutation profiles, and biomarker analyses.

• Present results to customers and collaborators, and represent Rarity at scientific conferences and meetings.

• Act as a scientific and technical subject matter expert in assay development, cancer genomics, and molecular diagnostics.

• Supervise and mentor junior team members in daily operations and project work.

• Contribute to scientific publications, technical reports, and conference abstracts.

• Maintain technical documentation in line with Rarity's QMS and applicable regulatory requirements.

You will be part of a small, cross-functional team where the distance between a question and a decision is short. The role is based at our office, soon located at Uppsala Business Park, where all functions will be under one roof. Around 30 people today, growing steadily - the kind of place where you know everyone, and where what you do is visible.

You have deep knowledge of cancer genetics, built through years of working with cancer cohorts, patient data, and somatic mutation profiles. You know what variant assessment means in practice, and you can have a real scientific conversation with a pharma R&D team or a clinical researcher without losing the thread.

You can lead a project and bring people along with you. You are structured, logical, and not easily derailed but you can change course when the data tells you to. You want to work on something that matters, in a team where no one is afraid of getting their hands dirty and everyone pulls in the same direction.

• PhD in Molecular Biology, Cancer Biology, Genetics, Genomics, or a related discipline, with approximately five years of relevant experience in academia, a clinical setting, or industry. Strong MSc candidates with equivalent depth will be considered.

• Solid expertise in cancer genetics and molecular oncology, including experience working with cancer cohorts and interpreting patient and clinical data.

• Experience with variant calling, variant assessment, and interpretation of NGS data.

• Hands-on experience with molecular biology techniques such as qPCR, digital PCR, RCA, NGS-based applications, and/or flow cytometry.

• Experience in assay development, optimization, and validation.

• Strong data analysis skills — R or equivalent is an advantage.

• Excellent written and verbal communication in English.

• Experience presenting scientific results to customers, collaborators, or at conferences.

• Experience collaborating with pharmaceutical companies or translational research groups is an advantage.

Yes, it is a long list. But then again, we are not just any company - we are a team pushing the boundaries of what mutation detection can do, and we are looking for someone who is genuinely excited about that.

If this sounds like the right next step for you, submit your application no later than mid-October. We review applications on a rolling basis, so do not wait too long.

Questions about the role or the process? Reach out to Sandra Bydell Sveder, Senior Recruitment Consultant at SallyQ (sandra.sveder@sallyq.se, 0763 19 96 88).

Rarity Bioscience develops ultrasensitive molecular diagnostics based on our proprietary superRCA® technology, enabling detection of rare mutations that standard methods miss. As our portfolio of pharma and clinical collaborations grows, so does our Scientific Services team - and we are now looking for a Senior Scientist to help lead that work.

You will lead and contribute to scientific collaboration projects in molecular diagnostics and cancer genomics, from initial dialogue to final report. In this role, you combine scientific leadership with involvement across assay development, performance evaluation, sample testing, data interpretation, and customer dialogue. You bring enough scientific depth to be a trusted discussion partner in cancer genetics, while also being practical enough to plan experiments, assess results, provide guidance to junior colleagues, and help move projects from first dialogue to final report or publication. In addition, the role can be expected to include some hands-on lab work to build familiarity with our assays, workflows, and daily operations, with the level of involvement varying depending on project needs.

• Coordinate and execute service projects involving internal laboratory teams, academic researchers, clinical collaborators, and pharmaceutical partners.

• Plan, perform, analyze, and report laboratory work across oncology, precision medicine, and mutation detection projects.

• Analyze, interpret, and report experimental and genomic data in relation to clinical data, somatic mutation profiles, and biomarker analyses.

• Present results to customers and collaborators, and represent Rarity at scientific conferences and meetings.

• Act as a scientific and technical subject matter expert in assay development, cancer genomics, and molecular diagnostics.

• Supervise and mentor junior team members in daily operations and project work.

• Contribute to scientific publications, technical reports, and conference abstracts.

• Maintain technical documentation in line with Rarity's QMS and applicable regulatory requirements.

You will be part of a small, cross-functional team where the distance between a question and a decision is short. The role is based at our office, soon located at Uppsala Business Park, where all functions will be under one roof. Around 30 people today, growing steadily - the kind of place where you know everyone, and where what you do is visible.

You have deep knowledge of cancer genetics, built through years of working with cancer cohorts, patient data, and somatic mutation profiles. You know what variant assessment means in practice, and you can have a real scientific conversation with a pharma R&D team or a clinical researcher without losing the thread.

You can lead a project and bring people along with you. You are structured, logical, and not easily derailed but you can change course when the data tells you to. You want to work on something that matters, in a team where no one is afraid of getting their hands dirty and everyone pulls in the same direction.

• PhD in Molecular Biology, Cancer Biology, Genetics, Genomics, or a related discipline, with approximately five years of relevant experience in academia, a clinical setting, or industry. Strong MSc candidates with equivalent depth will be considered.

• Solid expertise in cancer genetics and molecular oncology, including experience working with cancer cohorts and interpreting patient and clinical data.

• Experience with variant calling, variant assessment, and interpretation of NGS data.

• Hands-on experience with molecular biology techniques such as qPCR, digital PCR, RCA, NGS-based applications, and/or flow cytometry.

• Experience in assay development, optimization, and validation.

• Strong data analysis skills — R or equivalent is an advantage.

• Excellent written and verbal communication in English.

• Experience presenting scientific results to customers, collaborators, or at conferences.

• Experience collaborating with pharmaceutical companies or translational research groups is an advantage.

Yes, it is a long list. But then again, we are not just any company - we are a team pushing the boundaries of what mutation detection can do, and we are looking for someone who is genuinely excited about that.

If this sounds like the right next step for you, submit your application no later than mid-October. We review applications on a rolling basis, so do not wait too long.

Questions about the role or the process? Reach out to Sandra Bydell Sveder, Senior Recruitment Consultant at SallyQ (sandra.sveder@sallyq.se, 0763 19 96 88).

Rarity Bioscience develops ultrasensitive molecular diagnostics based on our proprietary superRCA® technology, enabling detection of rare mutations that standard methods miss. As our portfolio of pharma and clinical collaborations grows, so does our Scientific Services team - and we are now looking for a Senior Scientist to help lead that work.

You will lead and contribute to scientific collaboration projects in molecular diagnostics and cancer genomics, from initial dialogue to final report. In this role, you combine scientific leadership with involvement across assay development, performance evaluation, sample testing, data interpretation, and customer dialogue. You bring enough scientific depth to be a trusted discussion partner in cancer genetics, while also being practical enough to plan experiments, assess results, provide guidance to junior colleagues, and help move projects from first dialogue to final report or publication. In addition, the role can be expected to include some hands-on lab work to build familiarity with our assays, workflows, and daily operations, with the level of involvement varying depending on project needs.

• Coordinate and execute service projects involving internal laboratory teams, academic researchers, clinical collaborators, and pharmaceutical partners.

• Plan, perform, analyze, and report laboratory work across oncology, precision medicine, and mutation detection projects.

• Analyze, interpret, and report experimental and genomic data in relation to clinical data, somatic mutation profiles, and biomarker analyses.

• Present results to customers and collaborators, and represent Rarity at scientific conferences and meetings.

• Act as a scientific and technical subject matter expert in assay development, cancer genomics, and molecular diagnostics.

• Supervise and mentor junior team members in daily operations and project work.

• Contribute to scientific publications, technical reports, and conference abstracts.

• Maintain technical documentation in line with Rarity's QMS and applicable regulatory requirements.

You will be part of a small, cross-functional team where the distance between a question and a decision is short. The role is based at our office, soon located at Uppsala Business Park, where all functions will be under one roof. Around 30 people today, growing steadily - the kind of place where you know everyone, and where what you do is visible.

You have deep knowledge of cancer genetics, built through years of working with cancer cohorts, patient data, and somatic mutation profiles. You know what variant assessment means in practice, and you can have a real scientific conversation with a pharma R&D team or a clinical researcher without losing the thread.

You can lead a project and bring people along with you. You are structured, logical, and not easily derailed but you can change course when the data tells you to. You want to work on something that matters, in a team where no one is afraid of getting their hands dirty and everyone pulls in the same direction.

• PhD in Molecular Biology, Cancer Biology, Genetics, Genomics, or a related discipline, with approximately five years of relevant experience in academia, a clinical setting, or industry. Strong MSc candidates with equivalent depth will be considered.

• Solid expertise in cancer genetics and molecular oncology, including experience working with cancer cohorts and interpreting patient and clinical data.

• Experience with variant calling, variant assessment, and interpretation of NGS data.

• Hands-on experience with molecular biology techniques such as qPCR, digital PCR, RCA, NGS-based applications, and/or flow cytometry.

• Experience in assay development, optimization, and validation.

• Strong data analysis skills — R or equivalent is an advantage.

• Excellent written and verbal communication in English.

• Experience presenting scientific results to customers, collaborators, or at conferences.

• Experience collaborating with pharmaceutical companies or translational research groups is an advantage.

Yes, it is a long list. But then again, we are not just any company - we are a team pushing the boundaries of what mutation detection can do, and we are looking for someone who is genuinely excited about that.

If this sounds like the right next step for you, submit your application no later than mid-October. We review applications on a rolling basis, so do not wait too long.

Questions about the role or the process? Reach out to Sandra Bydell Sveder, Senior Recruitment Consultant at SallyQ (sandra.sveder@sallyq.se, 0763 19 96 88).

Rarity Bioscience develops ultrasensitive molecular diagnostics based on our proprietary superRCA® technology, enabling detection of rare mutations that standard methods miss. As our portfolio of pharma and clinical collaborations grows, so does our Scientific Services team - and we are now looking for a Senior Scientist to help lead that work.

You will lead and contribute to scientific collaboration projects in molecular diagnostics and cancer genomics, from initial dialogue to final report. In this role, you combine scientific leadership with involvement across assay development, performance evaluation, sample testing, data interpretation, and customer dialogue. You bring enough scientific depth to be a trusted discussion partner in cancer genetics, while also being practical enough to plan experiments, assess results, provide guidance to junior colleagues, and help move projects from first dialogue to final report or publication. In addition, the role can be expected to include some hands-on lab work to build familiarity with our assays, workflows, and daily operations, with the level of involvement varying depending on project needs.

• Coordinate and execute service projects involving internal laboratory teams, academic researchers, clinical collaborators, and pharmaceutical partners.

• Plan, perform, analyze, and report laboratory work across oncology, precision medicine, and mutation detection projects.

• Analyze, interpret, and report experimental and genomic data in relation to clinical data, somatic mutation profiles, and biomarker analyses.

• Present results to customers and collaborators, and represent Rarity at scientific conferences and meetings.

• Act as a scientific and technical subject matter expert in assay development, cancer genomics, and molecular diagnostics.

• Supervise and mentor junior team members in daily operations and project work.

• Contribute to scientific publications, technical reports, and conference abstracts.

• Maintain technical documentation in line with Rarity's QMS and applicable regulatory requirements.

You will be part of a small, cross-functional team where the distance between a question and a decision is short. The role is based at our office, soon located at Uppsala Business Park, where all functions will be under one roof. Around 30 people today, growing steadily - the kind of place where you know everyone, and where what you do is visible.

You have deep knowledge of cancer genetics, built through years of working with cancer cohorts, patient data, and somatic mutation profiles. You know what variant assessment means in practice, and you can have a real scientific conversation with a pharma R&D team or a clinical researcher without losing the thread.

You can lead a project and bring people along with you. You are structured, logical, and not easily derailed but you can change course when the data tells you to. You want to work on something that matters, in a team where no one is afraid of getting their hands dirty and everyone pulls in the same direction.

• PhD in Molecular Biology, Cancer Biology, Genetics, Genomics, or a related discipline, with approximately five years of relevant experience in academia, a clinical setting, or industry. Strong MSc candidates with equivalent depth will be considered.

• Solid expertise in cancer genetics and molecular oncology, including experience working with cancer cohorts and interpreting patient and clinical data.

• Experience with variant calling, variant assessment, and interpretation of NGS data.

• Hands-on experience with molecular biology techniques such as qPCR, digital PCR, RCA, NGS-based applications, and/or flow cytometry.

• Experience in assay development, optimization, and validation.

• Strong data analysis skills — R or equivalent is an advantage.

• Excellent written and verbal communication in English.

• Experience presenting scientific results to customers, collaborators, or at conferences.

• Experience collaborating with pharmaceutical companies or translational research groups is an advantage.

Yes, it is a long list. But then again, we are not just any company - we are a team pushing the boundaries of what mutation detection can do, and we are looking for someone who is genuinely excited about that.

If this sounds like the right next step for you, submit your application no later than mid-October. We review applications on a rolling basis, so do not wait too long.

Questions about the role or the process? Reach out to Sandra Bydell Sveder, Senior Recruitment Consultant at SallyQ (sandra.sveder@sallyq.se, 0763 19 96 88).

Rarity Bioscience develops ultrasensitive molecular diagnostics based on our proprietary superRCA® technology, enabling detection of rare mutations that standard methods miss. As our portfolio of pharma and clinical collaborations grows, so does our Scientific Services team - and we are now looking for a Senior Scientist to help lead that work.

You will lead and contribute to scientific collaboration projects in molecular diagnostics and cancer genomics, from initial dialogue to final report. In this role, you combine scientific leadership with involvement across assay development, performance evaluation, sample testing, data interpretation, and customer dialogue. You bring enough scientific depth to be a trusted discussion partner in cancer genetics, while also being practical enough to plan experiments, assess results, provide guidance to junior colleagues, and help move projects from first dialogue to final report or publication. In addition, the role can be expected to include some hands-on lab work to build familiarity with our assays, workflows, and daily operations, with the level of involvement varying depending on project needs.

• Coordinate and execute service projects involving internal laboratory teams, academic researchers, clinical collaborators, and pharmaceutical partners.

• Plan, perform, analyze, and report laboratory work across oncology, precision medicine, and mutation detection projects.

• Analyze, interpret, and report experimental and genomic data in relation to clinical data, somatic mutation profiles, and biomarker analyses.

• Present results to customers and collaborators, and represent Rarity at scientific conferences and meetings.

• Act as a scientific and technical subject matter expert in assay development, cancer genomics, and molecular diagnostics.

• Supervise and mentor junior team members in daily operations and project work.

• Contribute to scientific publications, technical reports, and conference abstracts.

• Maintain technical documentation in line with Rarity's QMS and applicable regulatory requirements.

You will be part of a small, cross-functional team where the distance between a question and a decision is short. The role is based at our office, soon located at Uppsala Business Park, where all functions will be under one roof. Around 30 people today, growing steadily - the kind of place where you know everyone, and where what you do is visible.

You have deep knowledge of cancer genetics, built through years of working with cancer cohorts, patient data, and somatic mutation profiles. You know what variant assessment means in practice, and you can have a real scientific conversation with a pharma R&D team or a clinical researcher without losing the thread.

You can lead a project and bring people along with you. You are structured, logical, and not easily derailed but you can change course when the data tells you to. You want to work on something that matters, in a team where no one is afraid of getting their hands dirty and everyone pulls in the same direction.

• PhD in Molecular Biology, Cancer Biology, Genetics, Genomics, or a related discipline, with approximately five years of relevant experience in academia, a clinical setting, or industry. Strong MSc candidates with equivalent depth will be considered.

• Solid expertise in cancer genetics and molecular oncology, including experience working with cancer cohorts and interpreting patient and clinical data.

• Experience with variant calling, variant assessment, and interpretation of NGS data.

• Hands-on experience with molecular biology techniques such as qPCR, digital PCR, RCA, NGS-based applications, and/or flow cytometry.

• Experience in assay development, optimization, and validation.

• Strong data analysis skills — R or equivalent is an advantage.

• Excellent written and verbal communication in English.

• Experience presenting scientific results to customers, collaborators, or at conferences.

• Experience collaborating with pharmaceutical companies or translational research groups is an advantage.

Yes, it is a long list. But then again, we are not just any company - we are a team pushing the boundaries of what mutation detection can do, and we are looking for someone who is genuinely excited about that.

If this sounds like the right next step for you, submit your application no later than mid-October. We review applications on a rolling basis, so do not wait too long.

Questions about the role or the process? Reach out to Sandra Bydell Sveder, Senior Recruitment Consultant at SallyQ (sandra.sveder@sallyq.se, 0763 19 96 88).

Rarity Bioscience develops ultrasensitive molecular diagnostics based on our proprietary superRCA® technology, enabling detection of rare mutations that standard methods miss. As our portfolio of pharma and clinical collaborations grows, so does our Scientific Services team - and we are now looking for a Senior Scientist to help lead that work.

You will lead and contribute to scientific collaboration projects in molecular diagnostics and cancer genomics, from initial dialogue to final report. In this role, you combine scientific leadership with involvement across assay development, performance evaluation, sample testing, data interpretation, and customer dialogue. You bring enough scientific depth to be a trusted discussion partner in cancer genetics, while also being practical enough to plan experiments, assess results, provide guidance to junior colleagues, and help move projects from first dialogue to final report or publication. In addition, the role can be expected to include some hands-on lab work to build familiarity with our assays, workflows, and daily operations, with the level of involvement varying depending on project needs.

• Coordinate and execute service projects involving internal laboratory teams, academic researchers, clinical collaborators, and pharmaceutical partners.

• Plan, perform, analyze, and report laboratory work across oncology, precision medicine, and mutation detection projects.

• Analyze, interpret, and report experimental and genomic data in relation to clinical data, somatic mutation profiles, and biomarker analyses.

• Present results to customers and collaborators, and represent Rarity at scientific conferences and meetings.

• Act as a scientific and technical subject matter expert in assay development, cancer genomics, and molecular diagnostics.

• Supervise and mentor junior team members in daily operations and project work.

• Contribute to scientific publications, technical reports, and conference abstracts.

• Maintain technical documentation in line with Rarity's QMS and applicable regulatory requirements.

You will be part of a small, cross-functional team where the distance between a question and a decision is short. The role is based at our office, soon located at Uppsala Business Park, where all functions will be under one roof. Around 30 people today, growing steadily - the kind of place where you know everyone, and where what you do is visible.

You have deep knowledge of cancer genetics, built through years of working with cancer cohorts, patient data, and somatic mutation profiles. You know what variant assessment means in practice, and you can have a real scientific conversation with a pharma R&D team or a clinical researcher without losing the thread.

You can lead a project and bring people along with you. You are structured, logical, and not easily derailed but you can change course when the data tells you to. You want to work on something that matters, in a team where no one is afraid of getting their hands dirty and everyone pulls in the same direction.

• PhD in Molecular Biology, Cancer Biology, Genetics, Genomics, or a related discipline, with approximately five years of relevant experience in academia, a clinical setting, or industry. Strong MSc candidates with equivalent depth will be considered.

• Solid expertise in cancer genetics and molecular oncology, including experience working with cancer cohorts and interpreting patient and clinical data.

• Experience with variant calling, variant assessment, and interpretation of NGS data.

• Hands-on experience with molecular biology techniques such as qPCR, digital PCR, RCA, NGS-based applications, and/or flow cytometry.

• Experience in assay development, optimization, and validation.

• Strong data analysis skills — R or equivalent is an advantage.

• Excellent written and verbal communication in English.

• Experience presenting scientific results to customers, collaborators, or at conferences.

• Experience collaborating with pharmaceutical companies or translational research groups is an advantage.

Yes, it is a long list. But then again, we are not just any company - we are a team pushing the boundaries of what mutation detection can do, and we are looking for someone who is genuinely excited about that.

If this sounds like the right next step for you, submit your application no later than mid-October. We review applications on a rolling basis, so do not wait too long.

Questions about the role or the process? Reach out to Sandra Bydell Sveder, Senior Recruitment Consultant at SallyQ (sandra.sveder@sallyq.se, 0763 19 96 88).

Rarity Bioscience develops ultrasensitive molecular diagnostics based on our proprietary superRCA® technology, enabling detection of rare mutations that standard methods miss. As our portfolio of pharma and clinical collaborations grows, so does our Scientific Services team - and we are now looking for a Senior Scientist to help lead that work.

You will lead and contribute to scientific collaboration projects in molecular diagnostics and cancer genomics, from initial dialogue to final report. In this role, you combine scientific leadership with involvement across assay development, performance evaluation, sample testing, data interpretation, and customer dialogue. You bring enough scientific depth to be a trusted discussion partner in cancer genetics, while also being practical enough to plan experiments, assess results, provide guidance to junior colleagues, and help move projects from first dialogue to final report or publication. In addition, the role can be expected to include some hands-on lab work to build familiarity with our assays, workflows, and daily operations, with the level of involvement varying depending on project needs.

• Coordinate and execute service projects involving internal laboratory teams, academic researchers, clinical collaborators, and pharmaceutical partners.

• Plan, perform, analyze, and report laboratory work across oncology, precision medicine, and mutation detection projects.

• Analyze, interpret, and report experimental and genomic data in relation to clinical data, somatic mutation profiles, and biomarker analyses.

• Present results to customers and collaborators, and represent Rarity at scientific conferences and meetings.

• Act as a scientific and technical subject matter expert in assay development, cancer genomics, and molecular diagnostics.

• Supervise and mentor junior team members in daily operations and project work.

• Contribute to scientific publications, technical reports, and conference abstracts.

• Maintain technical documentation in line with Rarity's QMS and applicable regulatory requirements.

You will be part of a small, cross-functional team where the distance between a question and a decision is short. The role is based at our office, soon located at Uppsala Business Park, where all functions will be under one roof. Around 30 people today, growing steadily - the kind of place where you know everyone, and where what you do is visible.

You have deep knowledge of cancer genetics, built through years of working with cancer cohorts, patient data, and somatic mutation profiles. You know what variant assessment means in practice, and you can have a real scientific conversation with a pharma R&D team or a clinical researcher without losing the thread.

You can lead a project and bring people along with you. You are structured, logical, and not easily derailed but you can change course when the data tells you to. You want to work on something that matters, in a team where no one is afraid of getting their hands dirty and everyone pulls in the same direction.

• PhD in Molecular Biology, Cancer Biology, Genetics, Genomics, or a related discipline, with approximately five years of relevant experience in academia, a clinical setting, or industry. Strong MSc candidates with equivalent depth will be considered.

• Solid expertise in cancer genetics and molecular oncology, including experience working with cancer cohorts and interpreting patient and clinical data.

• Experience with variant calling, variant assessment, and interpretation of NGS data.

• Hands-on experience with molecular biology techniques such as qPCR, digital PCR, RCA, NGS-based applications, and/or flow cytometry.

• Experience in assay development, optimization, and validation.

• Strong data analysis skills — R or equivalent is an advantage.

• Excellent written and verbal communication in English.

• Experience presenting scientific results to customers, collaborators, or at conferences.

• Experience collaborating with pharmaceutical companies or translational research groups is an advantage.

Yes, it is a long list. But then again, we are not just any company - we are a team pushing the boundaries of what mutation detection can do, and we are looking for someone who is genuinely excited about that.

If this sounds like the right next step for you, submit your application no later than mid-October. We review applications on a rolling basis, so do not wait too long.

Questions about the role or the process? Reach out to Sandra Bydell Sveder, Senior Recruitment Consultant at SallyQ (sandra.sveder@sallyq.se, 0763 19 96 88).

Klinisk patologi och genetik ingår i Verksamhetsområde laboratoriemedicin. Inom enheten jobbar cirka 70 personer och vi utför diagnostik på vävnads- och cellprover åt beställare inom huvudsakligen Örebro län inklusive den högspecialiserade sjukvården. Vi ansvarar också för kallelsesystemet och rutiner för den gynekologiska hälsokontrollen.

Du kommer att arbeta på laboratoriet för molekylär klinisk patologi och genetik där det utförs många olika typer av molekylärgenetiska analyser. Du kommer att arbeta med molekylärgenetiska metoder såsom DNA-extraktion, qPCR och sekvensering, framför allt Next Generation Sequencing för diagnostik av både ärftliga och förvärvade tillstånd.

Vi erbjuder ett omväxlande arbete med goda utvecklingsmöjligheter på en klinik som ligger långt fram både gällande analyser samt instrumentering.

Vår enhet är forskningstät och verksamhetsutveckling är en naturlig del av arbetet. Hos oss får du arbeta i ett positivt gäng där vi tillsammans tar oss an utmaningar och förändringar. Vi är en del av det nationella initiativet Genomic Medicine Sweden (GMS) samt en nod inom Clinical Genomics i SciLifeLab.

Vi söker disputerad molekylärbiolog med erfarenhet av laboration samt analys av molekylärgenetiska metoder. Svenska språknivå C1, alternativt norska eller danska.

Vi fäster stor vikt vid personliga egenskaper som ett gott bemötande av kollegor och kunder, ansvarskänsla samt god samarbetsförmåga och kvalitetsmedvetenhet.

Intervjuer sker fortlöpande.

Ansökan ska innehålla CV och personligt brev. Intyg, betyg, examensbevis med mera ska lämnas vid en eventuell intervju.

Om du är eller tidigare varit anställd i Region Örebro län kommer vi ta interna referenser från din nuvarande eller tidigare chef, om du blir aktuell för anställning.

Kontroll av registerutdrag från Polismyndigheten kan komma att ske enligt aktuell lagstiftning.

Som anställd i Region Örebro län omfattas du av trygga kollektivavtal. Läs mer om villkor och förmåner.

Vi sätter löner individuellt och differentierat. Läs mer om lön och lönestatistik.

Vi krigsplacerar våra tillsvidareanställda och i vissa fall även visstidsanställda. Läs mer om vad det innebär.

Verksamhetsområde laboratoriemedicin har ett samlat ansvar för den laboratoriemedicinska service som bedrivs vid laboratorierna inom Universitetssjukhuset Örebro, Karlskoga lasarett och Lindesbergs lasarett. Vi driver en bred verksamhet inom områdena klinisk kemi, bakteriologi, virologi, immunologi, transfusionsmedicin inklusive terapeutisk plasmaferesbehandling, patologi, cytologi och molekylärgenetik. Inom verksamhetsområdet ryms även Sterilteknik. Här arbetar närmare 300 personer med rutindiagnostik, forskning och utveckling samt utbildning.

På Universitetssjukhuset Örebro, ett av landets sju universitetssjukhus, arbetar vi för att ge alla patienter en god, säker och jämlik vård. Vi tillhandahåller allt från bassjukvård till nationell högspecialiserad och tekniskt avancerad vård. Vården finns till för såväl länets egna invånare som för vissa patientgrupper från andra delar av landet när det gäller viss specialiserad vård. Inom området bedrivs även universitetssjukvård med klinisk patientnära forskning och verksamhetsförlagd utbildning inom flertalet vårdprofessioner. Som en av länets största arbetsplatser ger vi dig som medarbetare goda möjligheter till utveckling och karriär samtidigt som du får vara med och göra skillnad för människor varje dag. Tillsammans utvecklar vi framtidens hälso- och sjukvård!

Region Örebro län är en av länets största arbetsgivare. Tillsammans med 11 000 kollegor kan du skapa ett bättre liv för de vi finns till för. Hos oss finns meningsfulla och samhällsviktiga jobb där du kan göra skillnad i invånarnas vardag, hälsa och livskvalitet. Dygnet runt, året om, ansvarar vi för hälso- och sjukvård, tandvård och länets kollektivtrafik. Vi har också det regionala utvecklingsansvaret i länet och ett uppdrag att bidra till kulturlivet.

Välkommen med din ansökan!

Vi har gjort vårt medieval för denna rekrytering och undanber oss därför erbjudanden om annonserings- och rekryteringshjälp i samband med denna annonsering.

Klinisk patologi och genetik ingår i Verksamhetsområde laboratoriemedicin. Inom enheten jobbar cirka 70 personer och vi utför diagnostik på vävnads- och cellprover åt beställare inom huvudsakligen Örebro län inklusive den högspecialiserade sjukvården. Vi ansvarar också för kallelsesystemet och rutiner för den gynekologiska hälsokontrollen.

Du kommer att arbeta på laboratoriet för molekylär klinisk patologi och genetik där det utförs många olika typer av molekylärgenetiska analyser. Du kommer att arbeta med molekylärgenetiska metoder såsom DNA-extraktion, qPCR och sekvensering, framför allt Next Generation Sequencing för diagnostik av både ärftliga och förvärvade tillstånd.

Vi erbjuder ett omväxlande arbete med goda utvecklingsmöjligheter på en klinik som ligger långt fram både gällande analyser samt instrumentering.

Vår enhet är forskningstät och verksamhetsutveckling är en naturlig del av arbetet. Hos oss får du arbeta i ett positivt gäng där vi tillsammans tar oss an utmaningar och förändringar. Vi är en del av det nationella initiativet Genomic Medicine Sweden (GMS) samt en nod inom Clinical Genomics i SciLifeLab.

Vi söker disputerad molekylärbiolog med erfarenhet av laboration samt analys av molekylärgenetiska metoder. Svenska språknivå C1, alternativt norska eller danska.

Vi fäster stor vikt vid personliga egenskaper som ett gott bemötande av kollegor och kunder, ansvarskänsla samt god samarbetsförmåga och kvalitetsmedvetenhet.

Intervjuer sker fortlöpande.

Ansökan ska innehålla CV och personligt brev. Intyg, betyg, examensbevis med mera ska lämnas vid en eventuell intervju.

Om du är eller tidigare varit anställd i Region Örebro län kommer vi ta interna referenser från din nuvarande eller tidigare chef, om du blir aktuell för anställning.

Kontroll av registerutdrag från Polismyndigheten kan komma att ske enligt aktuell lagstiftning.

Som anställd i Region Örebro län omfattas du av trygga kollektivavtal. Läs mer om villkor och förmåner.

Vi sätter löner individuellt och differentierat. Läs mer om lön och lönestatistik.

Vi krigsplacerar våra tillsvidareanställda och i vissa fall även visstidsanställda. Läs mer om vad det innebär.

Verksamhetsområde laboratoriemedicin har ett samlat ansvar för den laboratoriemedicinska service som bedrivs vid laboratorierna inom Universitetssjukhuset Örebro, Karlskoga lasarett och Lindesbergs lasarett. Vi driver en bred verksamhet inom områdena klinisk kemi, bakteriologi, virologi, immunologi, transfusionsmedicin inklusive terapeutisk plasmaferesbehandling, patologi, cytologi och molekylärgenetik. Inom verksamhetsområdet ryms även Sterilteknik. Här arbetar närmare 300 personer med rutindiagnostik, forskning och utveckling samt utbildning.

På Universitetssjukhuset Örebro, ett av landets sju universitetssjukhus, arbetar vi för att ge alla patienter en god, säker och jämlik vård. Vi tillhandahåller allt från bassjukvård till nationell högspecialiserad och tekniskt avancerad vård. Vården finns till för såväl länets egna invånare som för vissa patientgrupper från andra delar av landet när det gäller viss specialiserad vård. Inom området bedrivs även universitetssjukvård med klinisk patientnära forskning och verksamhetsförlagd utbildning inom flertalet vårdprofessioner. Som en av länets största arbetsplatser ger vi dig som medarbetare goda möjligheter till utveckling och karriär samtidigt som du får vara med och göra skillnad för människor varje dag. Tillsammans utvecklar vi framtidens hälso- och sjukvård!

Region Örebro län är en av länets största arbetsgivare. Tillsammans med 11 000 kollegor kan du skapa ett bättre liv för de vi finns till för. Hos oss finns meningsfulla och samhällsviktiga jobb där du kan göra skillnad i invånarnas vardag, hälsa och livskvalitet. Dygnet runt, året om, ansvarar vi för hälso- och sjukvård, tandvård och länets kollektivtrafik. Vi har också det regionala utvecklingsansvaret i länet och ett uppdrag att bidra till kulturlivet.

Välkommen med din ansökan!

Vi har gjort vårt medieval för denna rekrytering och undanber oss därför erbjudanden om annonserings- och rekryteringshjälp i samband med denna annonsering.

Klinisk patologi och genetik ingår i Verksamhetsområde laboratoriemedicin. Inom enheten jobbar cirka 70 personer och vi utför diagnostik på vävnads- och cellprover åt beställare inom huvudsakligen Örebro län inklusive den högspecialiserade sjukvården. Vi ansvarar också för kallelsesystemet och rutiner för den gynekologiska hälsokontrollen.

Du kommer att arbeta på laboratoriet för molekylär klinisk patologi och genetik där det utförs många olika typer av molekylärgenetiska analyser. Du kommer att arbeta med molekylärgenetiska metoder såsom DNA-extraktion, qPCR och sekvensering, framför allt Next Generation Sequencing för diagnostik av både ärftliga och förvärvade tillstånd.

Vi erbjuder ett omväxlande arbete med goda utvecklingsmöjligheter på en klinik som ligger långt fram både gällande analyser samt instrumentering.

Vår enhet är forskningstät och verksamhetsutveckling är en naturlig del av arbetet. Hos oss får du arbeta i ett positivt gäng där vi tillsammans tar oss an utmaningar och förändringar. Vi är en del av det nationella initiativet Genomic Medicine Sweden (GMS) samt en nod inom Clinical Genomics i SciLifeLab.

Vi söker disputerad molekylärbiolog med erfarenhet av laboration samt analys av molekylärgenetiska metoder. Svenska språknivå C1, alternativt norska eller danska.

Vi fäster stor vikt vid personliga egenskaper som ett gott bemötande av kollegor och kunder, ansvarskänsla samt god samarbetsförmåga och kvalitetsmedvetenhet.

Intervjuer sker fortlöpande.

Ansökan ska innehålla CV och personligt brev. Intyg, betyg, examensbevis med mera ska lämnas vid en eventuell intervju.

Om du är eller tidigare varit anställd i Region Örebro län kommer vi ta interna referenser från din nuvarande eller tidigare chef, om du blir aktuell för anställning.

Kontroll av registerutdrag från Polismyndigheten kan komma att ske enligt aktuell lagstiftning.

Som anställd i Region Örebro län omfattas du av trygga kollektivavtal. Läs mer om villkor och förmåner.

Vi sätter löner individuellt och differentierat. Läs mer om lön och lönestatistik.

Vi krigsplacerar våra tillsvidareanställda och i vissa fall även visstidsanställda. Läs mer om vad det innebär.

Verksamhetsområde laboratoriemedicin har ett samlat ansvar för den laboratoriemedicinska service som bedrivs vid laboratorierna inom Universitetssjukhuset Örebro, Karlskoga lasarett och Lindesbergs lasarett. Vi driver en bred verksamhet inom områdena klinisk kemi, bakteriologi, virologi, immunologi, transfusionsmedicin inklusive terapeutisk plasmaferesbehandling, patologi, cytologi och molekylärgenetik. Inom verksamhetsområdet ryms även Sterilteknik. Här arbetar närmare 300 personer med rutindiagnostik, forskning och utveckling samt utbildning.

På Universitetssjukhuset Örebro, ett av landets sju universitetssjukhus, arbetar vi för att ge alla patienter en god, säker och jämlik vård. Vi tillhandahåller allt från bassjukvård till nationell högspecialiserad och tekniskt avancerad vård. Vården finns till för såväl länets egna invånare som för vissa patientgrupper från andra delar av landet när det gäller viss specialiserad vård. Inom området bedrivs även universitetssjukvård med klinisk patientnära forskning och verksamhetsförlagd utbildning inom flertalet vårdprofessioner. Som en av länets största arbetsplatser ger vi dig som medarbetare goda möjligheter till utveckling och karriär samtidigt som du får vara med och göra skillnad för människor varje dag. Tillsammans utvecklar vi framtidens hälso- och sjukvård!

Region Örebro län är en av länets största arbetsgivare. Tillsammans med 11 000 kollegor kan du skapa ett bättre liv för de vi finns till för. Hos oss finns meningsfulla och samhällsviktiga jobb där du kan göra skillnad i invånarnas vardag, hälsa och livskvalitet. Dygnet runt, året om, ansvarar vi för hälso- och sjukvård, tandvård och länets kollektivtrafik. Vi har också det regionala utvecklingsansvaret i länet och ett uppdrag att bidra till kulturlivet.

Välkommen med din ansökan!

Vi har gjort vårt medieval för denna rekrytering och undanber oss därför erbjudanden om annonserings- och rekryteringshjälp i samband med denna annonsering.