Forskare med inriktning mot metabolomik - Lediga jobb

We're looking for a passionate and driven Senior Manufacturing Scientist – Aseptic Processing to join our Manufacturing Science & Technology (MS&T) team in Uppsala and play a critical role in ensuring the robustness, compliance, and continuous improvement of our aseptic manufacturing processes. At Galderma, we're not just offering a job, we're inviting you to be part of something bigger.

You serve as the site's subject matter expert for aseptic manufacturing and contamination control, providing scientific and technical leadership across critical aseptic operations. You work cross-functionally to support routine operations, troubleshoot complex process challenges, lead investigations, and drive continuous improvement. A key part of the role is leading the site's media fill program and contamination control strategy, and ensuring compliance with evolving regulatory expectations, including EU GMP Annex 1 and global health authority requirements.

Key Responsibilities

• Provide scientific oversight and technical expertise across aseptic manufacturing operations, including compounding, filtration, and filling processes.

• Lead the site's media fill / Aseptic Process Simulation (APS) program: design, execution, evaluation, reporting, and timely CAPA implementation to strengthen sterility assurance.

• Lead and support the Contamination Control Strategy (CCS) through scientific risk assessments spanning facility design, HVAC, environmental monitoring, cleaning and disinfection, and aseptic practices.

• Lead complex deviation investigations, root cause analyses, and CAPA activities related to aseptic processes.

• Design and evaluate smoke studies to verify airflow performance and first-air protection.

• Act as a trusted SME in audits, inspections, technology transfers, process improvements, and the implementation of new manufacturing technologies.

The role is based at Galderma's production site in Uppsala and requires on-site presence up to four days per week.

You're a curious, proactive, and scientifically minded professional who enjoys solving complex challenges and driving improvement in highly regulated manufacturing environments. You take ownership naturally, influence stakeholders with confidence, and navigate complexity while keeping compliance and continuous improvement front of mind.

Qualifications

• Bachelor's, Master's, or PhD in Chemistry, Biochemistry, Chemical Engineering, Pharmaceutical Sciences, or a related discipline, with several years of experience in a biopharmaceutical or other highly regulated manufacturing environment.

• Strong expertise in aseptic processing, contamination control, media fills, and sterility assurance principles within GMP-regulated operations.

• Experience with EU GMP, Annex 1 requirements, and regulatory expectations for sterile manufacturing.

• Proven track record leading deviation investigations, root cause analyses, and CAPA implementation.

• Excellent analytical, problem-solving, and technical writing skills.

• Strong stakeholder management and collaboration across multiple functions.

• Ability to independently manage complex projects and drive continuous improvement initiatives.

If you believe this can be a right career change for you, please send in an application as soon as possible. We are evaluating the application continuously so please do not wait to send in your application.

Galderma is the emerging pure-play dermatology category leader, present in approximately 90 countries. We deliver an innovative, science-based portfolio of premium flagship brands and services that span the full spectrum of the fast-growing dermatology market through Injectable Aesthetics, Dermatological Skincare, and Therapeutic Dermatology. Since our foundation in 1981, we have dedicated our focus and passion to the human body's largest organ, the skin, meeting individual consumer and patient needs with superior outcomes in partnership with healthcare professionals.

Our site in Uppsala is Galderma's Global Center of Excellence for Aesthetics, home to over 800 professionals working across R&D, manufacturing, clinical development, and commercial functions. Here, cutting-edge science meets world-class manufacturing, creating an environment where innovation moves rapidly from concept to patient impact. As a Senior Manufacturing Scientist – Aseptic Processing, you'll influence critical manufacturing processes, contribute to regulatory excellence, and play a direct role in delivering high-quality products to patients around the world, joining a collaborative and highly skilled team where your expertise is valued and your ideas are heard.

We're looking for a passionate and driven Senior Manufacturing Scientist – Aseptic Processing to join our Manufacturing Science & Technology (MS&T) team in Uppsala and play a critical role in ensuring the robustness, compliance, and continuous improvement of our aseptic manufacturing processes. At Galderma, we're not just offering a job, we're inviting you to be part of something bigger.

You serve as the site's subject matter expert for aseptic manufacturing and contamination control, providing scientific and technical leadership across critical aseptic operations. You work cross-functionally to support routine operations, troubleshoot complex process challenges, lead investigations, and drive continuous improvement. A key part of the role is leading the site's media fill program and contamination control strategy, and ensuring compliance with evolving regulatory expectations, including EU GMP Annex 1 and global health authority requirements.

Key Responsibilities

• Provide scientific oversight and technical expertise across aseptic manufacturing operations, including compounding, filtration, and filling processes.

• Lead the site's media fill / Aseptic Process Simulation (APS) program: design, execution, evaluation, reporting, and timely CAPA implementation to strengthen sterility assurance.

• Lead and support the Contamination Control Strategy (CCS) through scientific risk assessments spanning facility design, HVAC, environmental monitoring, cleaning and disinfection, and aseptic practices.

• Lead complex deviation investigations, root cause analyses, and CAPA activities related to aseptic processes.

• Design and evaluate smoke studies to verify airflow performance and first-air protection.

• Act as a trusted SME in audits, inspections, technology transfers, process improvements, and the implementation of new manufacturing technologies.

The role is based at Galderma's production site in Uppsala and requires on-site presence up to four days per week.

You're a curious, proactive, and scientifically minded professional who enjoys solving complex challenges and driving improvement in highly regulated manufacturing environments. You take ownership naturally, influence stakeholders with confidence, and navigate complexity while keeping compliance and continuous improvement front of mind.

Qualifications

• Bachelor's, Master's, or PhD in Chemistry, Biochemistry, Chemical Engineering, Pharmaceutical Sciences, or a related discipline, with several years of experience in a biopharmaceutical or other highly regulated manufacturing environment.

• Strong expertise in aseptic processing, contamination control, media fills, and sterility assurance principles within GMP-regulated operations.

• Experience with EU GMP, Annex 1 requirements, and regulatory expectations for sterile manufacturing.

• Proven track record leading deviation investigations, root cause analyses, and CAPA implementation.

• Excellent analytical, problem-solving, and technical writing skills.

• Strong stakeholder management and collaboration across multiple functions.

• Ability to independently manage complex projects and drive continuous improvement initiatives.

If you believe this can be a right career change for you, please send in an application as soon as possible. We are evaluating the application continuously so please do not wait to send in your application.

Galderma is the emerging pure-play dermatology category leader, present in approximately 90 countries. We deliver an innovative, science-based portfolio of premium flagship brands and services that span the full spectrum of the fast-growing dermatology market through Injectable Aesthetics, Dermatological Skincare, and Therapeutic Dermatology. Since our foundation in 1981, we have dedicated our focus and passion to the human body's largest organ, the skin, meeting individual consumer and patient needs with superior outcomes in partnership with healthcare professionals.

Our site in Uppsala is Galderma's Global Center of Excellence for Aesthetics, home to over 800 professionals working across R&D, manufacturing, clinical development, and commercial functions. Here, cutting-edge science meets world-class manufacturing, creating an environment where innovation moves rapidly from concept to patient impact. As a Senior Manufacturing Scientist – Aseptic Processing, you'll influence critical manufacturing processes, contribute to regulatory excellence, and play a direct role in delivering high-quality products to patients around the world, joining a collaborative and highly skilled team where your expertise is valued and your ideas are heard.

We're looking for a passionate and driven Senior Manufacturing Scientist – Aseptic Processing to join our Manufacturing Science & Technology (MS&T) team in Uppsala and play a critical role in ensuring the robustness, compliance, and continuous improvement of our aseptic manufacturing processes. At Galderma, we're not just offering a job, we're inviting you to be part of something bigger.

You serve as the site's subject matter expert for aseptic manufacturing and contamination control, providing scientific and technical leadership across critical aseptic operations. You work cross-functionally to support routine operations, troubleshoot complex process challenges, lead investigations, and drive continuous improvement. A key part of the role is leading the site's media fill program and contamination control strategy, and ensuring compliance with evolving regulatory expectations, including EU GMP Annex 1 and global health authority requirements.

Key Responsibilities

• Provide scientific oversight and technical expertise across aseptic manufacturing operations, including compounding, filtration, and filling processes.

• Lead the site's media fill / Aseptic Process Simulation (APS) program: design, execution, evaluation, reporting, and timely CAPA implementation to strengthen sterility assurance.

• Lead and support the Contamination Control Strategy (CCS) through scientific risk assessments spanning facility design, HVAC, environmental monitoring, cleaning and disinfection, and aseptic practices.

• Lead complex deviation investigations, root cause analyses, and CAPA activities related to aseptic processes.

• Design and evaluate smoke studies to verify airflow performance and first-air protection.

• Act as a trusted SME in audits, inspections, technology transfers, process improvements, and the implementation of new manufacturing technologies.

The role is based at Galderma's production site in Uppsala and requires on-site presence up to four days per week.

You're a curious, proactive, and scientifically minded professional who enjoys solving complex challenges and driving improvement in highly regulated manufacturing environments. You take ownership naturally, influence stakeholders with confidence, and navigate complexity while keeping compliance and continuous improvement front of mind.

Qualifications

• Bachelor's, Master's, or PhD in Chemistry, Biochemistry, Chemical Engineering, Pharmaceutical Sciences, or a related discipline, with several years of experience in a biopharmaceutical or other highly regulated manufacturing environment.

• Strong expertise in aseptic processing, contamination control, media fills, and sterility assurance principles within GMP-regulated operations.

• Experience with EU GMP, Annex 1 requirements, and regulatory expectations for sterile manufacturing.

• Proven track record leading deviation investigations, root cause analyses, and CAPA implementation.

• Excellent analytical, problem-solving, and technical writing skills.

• Strong stakeholder management and collaboration across multiple functions.

• Ability to independently manage complex projects and drive continuous improvement initiatives.

If you believe this can be a right career change for you, please send in an application as soon as possible. We are evaluating the application continuously so please do not wait to send in your application.

Galderma is the emerging pure-play dermatology category leader, present in approximately 90 countries. We deliver an innovative, science-based portfolio of premium flagship brands and services that span the full spectrum of the fast-growing dermatology market through Injectable Aesthetics, Dermatological Skincare, and Therapeutic Dermatology. Since our foundation in 1981, we have dedicated our focus and passion to the human body's largest organ, the skin, meeting individual consumer and patient needs with superior outcomes in partnership with healthcare professionals.

Our site in Uppsala is Galderma's Global Center of Excellence for Aesthetics, home to over 800 professionals working across R&D, manufacturing, clinical development, and commercial functions. Here, cutting-edge science meets world-class manufacturing, creating an environment where innovation moves rapidly from concept to patient impact. As a Senior Manufacturing Scientist – Aseptic Processing, you'll influence critical manufacturing processes, contribute to regulatory excellence, and play a direct role in delivering high-quality products to patients around the world, joining a collaborative and highly skilled team where your expertise is valued and your ideas are heard.

We're looking for a passionate and driven Senior Manufacturing Scientist – Aseptic Processing to join our Manufacturing Science & Technology (MS&T) team in Uppsala and play a critical role in ensuring the robustness, compliance, and continuous improvement of our aseptic manufacturing processes. At Galderma, we're not just offering a job, we're inviting you to be part of something bigger.

You serve as the site's subject matter expert for aseptic manufacturing and contamination control, providing scientific and technical leadership across critical aseptic operations. You work cross-functionally to support routine operations, troubleshoot complex process challenges, lead investigations, and drive continuous improvement. A key part of the role is leading the site's media fill program and contamination control strategy, and ensuring compliance with evolving regulatory expectations, including EU GMP Annex 1 and global health authority requirements.

Key Responsibilities

• Provide scientific oversight and technical expertise across aseptic manufacturing operations, including compounding, filtration, and filling processes.

• Lead the site's media fill / Aseptic Process Simulation (APS) program: design, execution, evaluation, reporting, and timely CAPA implementation to strengthen sterility assurance.

• Lead and support the Contamination Control Strategy (CCS) through scientific risk assessments spanning facility design, HVAC, environmental monitoring, cleaning and disinfection, and aseptic practices.

• Lead complex deviation investigations, root cause analyses, and CAPA activities related to aseptic processes.

• Design and evaluate smoke studies to verify airflow performance and first-air protection.

• Act as a trusted SME in audits, inspections, technology transfers, process improvements, and the implementation of new manufacturing technologies.

The role is based at Galderma's production site in Uppsala and requires on-site presence up to four days per week.

You're a curious, proactive, and scientifically minded professional who enjoys solving complex challenges and driving improvement in highly regulated manufacturing environments. You take ownership naturally, influence stakeholders with confidence, and navigate complexity while keeping compliance and continuous improvement front of mind.

Qualifications

• Bachelor's, Master's, or PhD in Chemistry, Biochemistry, Chemical Engineering, Pharmaceutical Sciences, or a related discipline, with several years of experience in a biopharmaceutical or other highly regulated manufacturing environment.

• Strong expertise in aseptic processing, contamination control, media fills, and sterility assurance principles within GMP-regulated operations.

• Experience with EU GMP, Annex 1 requirements, and regulatory expectations for sterile manufacturing.

• Proven track record leading deviation investigations, root cause analyses, and CAPA implementation.

• Excellent analytical, problem-solving, and technical writing skills.

• Strong stakeholder management and collaboration across multiple functions.

• Ability to independently manage complex projects and drive continuous improvement initiatives.

If you believe this can be a right career change for you, please send in an application as soon as possible. We are evaluating the application continuously so please do not wait to send in your application.

Galderma is the emerging pure-play dermatology category leader, present in approximately 90 countries. We deliver an innovative, science-based portfolio of premium flagship brands and services that span the full spectrum of the fast-growing dermatology market through Injectable Aesthetics, Dermatological Skincare, and Therapeutic Dermatology. Since our foundation in 1981, we have dedicated our focus and passion to the human body's largest organ, the skin, meeting individual consumer and patient needs with superior outcomes in partnership with healthcare professionals.

Our site in Uppsala is Galderma's Global Center of Excellence for Aesthetics, home to over 800 professionals working across R&D, manufacturing, clinical development, and commercial functions. Here, cutting-edge science meets world-class manufacturing, creating an environment where innovation moves rapidly from concept to patient impact. As a Senior Manufacturing Scientist – Aseptic Processing, you'll influence critical manufacturing processes, contribute to regulatory excellence, and play a direct role in delivering high-quality products to patients around the world, joining a collaborative and highly skilled team where your expertise is valued and your ideas are heard.

We're looking for a passionate and driven Senior Manufacturing Scientist – Aseptic Processing to join our Manufacturing Science & Technology (MS&T) team in Uppsala and play a critical role in ensuring the robustness, compliance, and continuous improvement of our aseptic manufacturing processes. At Galderma, we're not just offering a job, we're inviting you to be part of something bigger.

You serve as the site's subject matter expert for aseptic manufacturing and contamination control, providing scientific and technical leadership across critical aseptic operations. You work cross-functionally to support routine operations, troubleshoot complex process challenges, lead investigations, and drive continuous improvement. A key part of the role is leading the site's media fill program and contamination control strategy, and ensuring compliance with evolving regulatory expectations, including EU GMP Annex 1 and global health authority requirements.

Key Responsibilities

• Provide scientific oversight and technical expertise across aseptic manufacturing operations, including compounding, filtration, and filling processes.

• Lead the site's media fill / Aseptic Process Simulation (APS) program: design, execution, evaluation, reporting, and timely CAPA implementation to strengthen sterility assurance.

• Lead and support the Contamination Control Strategy (CCS) through scientific risk assessments spanning facility design, HVAC, environmental monitoring, cleaning and disinfection, and aseptic practices.

• Lead complex deviation investigations, root cause analyses, and CAPA activities related to aseptic processes.

• Design and evaluate smoke studies to verify airflow performance and first-air protection.

• Act as a trusted SME in audits, inspections, technology transfers, process improvements, and the implementation of new manufacturing technologies.

The role is based at Galderma's production site in Uppsala and requires on-site presence up to four days per week.

You're a curious, proactive, and scientifically minded professional who enjoys solving complex challenges and driving improvement in highly regulated manufacturing environments. You take ownership naturally, influence stakeholders with confidence, and navigate complexity while keeping compliance and continuous improvement front of mind.

Qualifications

• Bachelor's, Master's, or PhD in Chemistry, Biochemistry, Chemical Engineering, Pharmaceutical Sciences, or a related discipline, with several years of experience in a biopharmaceutical or other highly regulated manufacturing environment.

• Strong expertise in aseptic processing, contamination control, media fills, and sterility assurance principles within GMP-regulated operations.

• Experience with EU GMP, Annex 1 requirements, and regulatory expectations for sterile manufacturing.

• Proven track record leading deviation investigations, root cause analyses, and CAPA implementation.

• Excellent analytical, problem-solving, and technical writing skills.

• Strong stakeholder management and collaboration across multiple functions.

• Ability to independently manage complex projects and drive continuous improvement initiatives.

If you believe this can be a right career change for you, please send in an application as soon as possible. We are evaluating the application continuously so please do not wait to send in your application.

Galderma is the emerging pure-play dermatology category leader, present in approximately 90 countries. We deliver an innovative, science-based portfolio of premium flagship brands and services that span the full spectrum of the fast-growing dermatology market through Injectable Aesthetics, Dermatological Skincare, and Therapeutic Dermatology. Since our foundation in 1981, we have dedicated our focus and passion to the human body's largest organ, the skin, meeting individual consumer and patient needs with superior outcomes in partnership with healthcare professionals.

Our site in Uppsala is Galderma's Global Center of Excellence for Aesthetics, home to over 800 professionals working across R&D, manufacturing, clinical development, and commercial functions. Here, cutting-edge science meets world-class manufacturing, creating an environment where innovation moves rapidly from concept to patient impact. As a Senior Manufacturing Scientist – Aseptic Processing, you'll influence critical manufacturing processes, contribute to regulatory excellence, and play a direct role in delivering high-quality products to patients around the world, joining a collaborative and highly skilled team where your expertise is valued and your ideas are heard.

Vid Institutionen för neurovetenskap och fysiologi vid Sahlgrenska akademin bedrivs omfattande forskning och undervisning över stora kunskapsområden - från molekyl till människa. Verksamheten utgörs av fem sektioner; farmakologi, fysiologi, hälsa och rehabilitering, klinisk neurovetenskap samt psykiatri och neurokemi.

Institutionen för neurovetenskap och fysiologi söker nu en forskare med placering vid Sektionen för farmakologi.

Arbetsuppgifter

I anställningen ingår djurexperimentell forskning inom det psykofarmakologiska området, med tonvikt på beteendefarmakologiska studier.

Kvalifikationer

Doktorsavhandling inom preklinisk psykofarmakologi med inriktning på beteendestudier är ett krav. Erfarenhet av forskning om läkemedel mot depression och ångest med användning av relevanta djurmodeller är meriterande. Erfarenhet av in vivo-mikrodialys är också meriterande.

Vi lägger stor vikt vid personlig lämplighet.

Anställning

Anställningen är en tidsbegränsad anställning i 6 månader, 100% av heltid, med placering tills vidare vid Institutionen för neurovetenskap och fysiologi. Tillträde: snarast eller enligt överenskommelse. 

Kontaktuppgifter för anställningen

Har du frågor om anställningen är du välkommen att kontakta forskare Elias Eriksson, tfn: +46 709 555 055, e-post: mailto:Elias.Eriksson@neuro.gu.se

Ansvarig chef är professor/sektionschef Michael Winder, tfn: +46 31 786 34 77, e-post: mailto:michael.winder@pharm.gu.se

Ansökningshandlingar skickas inte till kontaktpersonerna.

Fackliga organisationer

Fackliga företrädare vid Göteborgs universitet hittar du här: https://www.gu.se/om-universitetet/jobba-hos-oss/hjalp-for-sokande

Ansökan

Du söker anställningen via Göteborgs universitets rekryteringsportal genom att registrera din ansökan elektroniskt via hemsidan: https://www.gu.se/om-universitetet/jobba-hos-oss/lediga-anstallningar

Du som sökande ansvarar för att ansökan är komplett i enlighet med annonsen och att den är universitetet tillhanda senast sista ansökningsdag.

Intyg om doktorsexamen bifogas med ansökan.

Ansökan ska vara inkommen senast: 2026-07-29

Vid Institutionen för neurovetenskap och fysiologi vid Sahlgrenska akademin bedrivs omfattande forskning och undervisning över stora kunskapsområden - från molekyl till människa. Verksamheten utgörs av fem sektioner; farmakologi, fysiologi, hälsa och rehabilitering, klinisk neurovetenskap samt psykiatri och neurokemi.

Institutionen för neurovetenskap och fysiologi söker nu en forskare med placering vid Sektionen för farmakologi.

Arbetsuppgifter

I anställningen ingår djurexperimentell forskning inom det psykofarmakologiska området, med tonvikt på beteendefarmakologiska studier.

Kvalifikationer

Doktorsavhandling inom preklinisk psykofarmakologi med inriktning på beteendestudier är ett krav. Erfarenhet av forskning om läkemedel mot depression och ångest med användning av relevanta djurmodeller är meriterande. Erfarenhet av in vivo-mikrodialys är också meriterande.

Vi lägger stor vikt vid personlig lämplighet.

Anställning

Anställningen är en tidsbegränsad anställning i 6 månader, 100% av heltid, med placering tills vidare vid Institutionen för neurovetenskap och fysiologi. Tillträde: snarast eller enligt överenskommelse. 

Kontaktuppgifter för anställningen

Har du frågor om anställningen är du välkommen att kontakta forskare Elias Eriksson, tfn: +46 709 555 055, e-post: mailto:Elias.Eriksson@neuro.gu.se

Ansvarig chef är professor/sektionschef Michael Winder, tfn: +46 31 786 34 77, e-post: mailto:michael.winder@pharm.gu.se

Ansökningshandlingar skickas inte till kontaktpersonerna.

Fackliga organisationer

Fackliga företrädare vid Göteborgs universitet hittar du här: https://www.gu.se/om-universitetet/jobba-hos-oss/hjalp-for-sokande

Ansökan

Du söker anställningen via Göteborgs universitets rekryteringsportal genom att registrera din ansökan elektroniskt via hemsidan: https://www.gu.se/om-universitetet/jobba-hos-oss/lediga-anstallningar

Du som sökande ansvarar för att ansökan är komplett i enlighet med annonsen och att den är universitetet tillhanda senast sista ansökningsdag.

Intyg om doktorsexamen bifogas med ansökan.

Ansökan ska vara inkommen senast: 2026-07-29

Vid Institutionen för neurovetenskap och fysiologi vid Sahlgrenska akademin bedrivs omfattande forskning och undervisning över stora kunskapsområden - från molekyl till människa. Verksamheten utgörs av fem sektioner; farmakologi, fysiologi, hälsa och rehabilitering, klinisk neurovetenskap samt psykiatri och neurokemi.

Institutionen för neurovetenskap och fysiologi söker nu en forskare med placering vid Sektionen för farmakologi.

Arbetsuppgifter

I anställningen ingår djurexperimentell forskning inom det psykofarmakologiska området, med tonvikt på beteendefarmakologiska studier.

Kvalifikationer

Doktorsavhandling inom preklinisk psykofarmakologi med inriktning på beteendestudier är ett krav. Erfarenhet av forskning om läkemedel mot depression och ångest med användning av relevanta djurmodeller är meriterande. Erfarenhet av in vivo-mikrodialys är också meriterande.

Vi lägger stor vikt vid personlig lämplighet.

Anställning

Anställningen är en tidsbegränsad anställning i 6 månader, 100% av heltid, med placering tills vidare vid Institutionen för neurovetenskap och fysiologi. Tillträde: snarast eller enligt överenskommelse. 

Kontaktuppgifter för anställningen

Har du frågor om anställningen är du välkommen att kontakta forskare Elias Eriksson, tfn: +46 709 555 055, e-post: mailto:Elias.Eriksson@neuro.gu.se

Ansvarig chef är professor/sektionschef Michael Winder, tfn: +46 31 786 34 77, e-post: mailto:michael.winder@pharm.gu.se

Ansökningshandlingar skickas inte till kontaktpersonerna.

Fackliga organisationer

Fackliga företrädare vid Göteborgs universitet hittar du här: https://www.gu.se/om-universitetet/jobba-hos-oss/hjalp-for-sokande

Ansökan

Du söker anställningen via Göteborgs universitets rekryteringsportal genom att registrera din ansökan elektroniskt via hemsidan: https://www.gu.se/om-universitetet/jobba-hos-oss/lediga-anstallningar

Du som sökande ansvarar för att ansökan är komplett i enlighet med annonsen och att den är universitetet tillhanda senast sista ansökningsdag.

Intyg om doktorsexamen bifogas med ansökan.

Ansökan ska vara inkommen senast: 2026-07-29

Vid Institutionen för neurovetenskap och fysiologi vid Sahlgrenska akademin bedrivs omfattande forskning och undervisning över stora kunskapsområden - från molekyl till människa. Verksamheten utgörs av fem sektioner; farmakologi, fysiologi, hälsa och rehabilitering, klinisk neurovetenskap samt psykiatri och neurokemi.

Institutionen för neurovetenskap och fysiologi söker nu en forskare med placering vid Sektionen för farmakologi.

Arbetsuppgifter

I anställningen ingår djurexperimentell forskning inom det psykofarmakologiska området, med tonvikt på beteendefarmakologiska studier.

Kvalifikationer

Doktorsavhandling inom preklinisk psykofarmakologi med inriktning på beteendestudier är ett krav. Erfarenhet av forskning om läkemedel mot depression och ångest med användning av relevanta djurmodeller är meriterande. Erfarenhet av in vivo-mikrodialys är också meriterande.

Vi lägger stor vikt vid personlig lämplighet.

Anställning

Anställningen är en tidsbegränsad anställning i 6 månader, 100% av heltid, med placering tills vidare vid Institutionen för neurovetenskap och fysiologi. Tillträde: snarast eller enligt överenskommelse. 

Kontaktuppgifter för anställningen

Har du frågor om anställningen är du välkommen att kontakta forskare Elias Eriksson, tfn: +46 709 555 055, e-post: mailto:Elias.Eriksson@neuro.gu.se

Ansvarig chef är professor/sektionschef Michael Winder, tfn: +46 31 786 34 77, e-post: mailto:michael.winder@pharm.gu.se

Ansökningshandlingar skickas inte till kontaktpersonerna.

Fackliga organisationer

Fackliga företrädare vid Göteborgs universitet hittar du här: https://www.gu.se/om-universitetet/jobba-hos-oss/hjalp-for-sokande

Ansökan

Du söker anställningen via Göteborgs universitets rekryteringsportal genom att registrera din ansökan elektroniskt via hemsidan: https://www.gu.se/om-universitetet/jobba-hos-oss/lediga-anstallningar

Du som sökande ansvarar för att ansökan är komplett i enlighet med annonsen och att den är universitetet tillhanda senast sista ansökningsdag.

Intyg om doktorsexamen bifogas med ansökan.

Ansökan ska vara inkommen senast: 2026-07-29

Forskningsingenjör vid Grimsö forskningsstation

Vi söker en självständig och noggrann person till DNA-laboratoriet på Grimsö forskningsstation. Vi riktar oss till dig som är intresserad av förvaltingen och forskningen av stora rovdjur. Med hjälp av DNA-metoder förser vi olika myndigheter med faktabaserad information som verkar för en hållbar förvaltning av rovdjur i Sverige samt genom forskning öka förståelsen om rovdjurens ekologi. 

Om jobbet

Du kommer att jobba i ett team som analyserar DNA-prov från rovdjur. Det huvudsakliga projektet bygger på att bitså förvaltande myndigheter med DNA-analyser som syftar att inventera och förvalta vargpopulationen i Sverige. Utöver detta bedrivs DNA-analyser på flera andra arter och forskningsprojekt, vilka kan behöva ditt deltagande. 

Arbetsuppgifterna omfattar:

• laborativt och analytiskt arbete, med DNA-extraktion av biologiskt material från djur
• genetisk profilering (genotypbestämning) och hantering av SNP-data för att bland annat identifiera individer och deras släktskap till andra individer i olika populationer
• medverkan i rapportering och framtagning av informationsmaterial
• medverkan i forskningsprojekt och utvecklingen av nya metoder/processer i och utanför DNA-labbet.

Allt arbete kommer ske på Grimsö forskningsstation.

Din bakgrund 

• Akademisk utbildning i biologi, motsvarande minst MSc med flera kurser i genetik och/eller molekylär ekologi. 
• God erfarenhet av att extrahera och analysera DNA-prover och molekylära data.
• Avancerad kunskap av ordbehandlingsprogram, inkluderat Microsoft Word, analysprogram, inkluderat Microsoft Excel och R för programmering. 
• Kunskaper om next-generation sequencing och användandet python- och bash-skript är meriterande.
• B-körkort och tillgång till egen bil.

Det är en förutsättning att du har ett metodiskt arbetssätt, ett kritiskt tänkande, är noggrann och har analytisk förmåga. Andra angelägna personliga egenskaper för arbetet är god samarbetsförmåga, ett flexibelt och självgående arbetssätt samt förmåga att hantera flera parallella arbetsuppgifter samtidigt.

Om oss

Grimsö forskningsstation utgör en unik arbetsmiljö för att studera vilda djur och fåglar. Utöver de ca 40 personer som jobbar på stationen är vi en samlingspunkt som attraherar besökande forskare, myndighetspersoner och studenter. Vi befinner oss i ett forskningsområde på 13 000 hektar som vi använder för forskning och utbildning. Här finns en bred kompetens för att studera vilda djurs ekologi, levnadssätt, livshistoria, utbredning och genetiska variation. Vi bedriver forskning som tillämpas i förvaltningen av stora djur och fåglar i Sverige. Vi har ett stort nätverk av forskare och representanter för myndigheter och civilsamhällesorganisationer. Genom publicering och samarbeten har vi en global spridning av vår unika kunskap om djurs förvaltning och bevarande.  

Mer information om institutionen/avdelningen:https://www.slu.se/om-slu/organisation/institutioner/ekologi/grimso-forskningsstation/om-grimso-forskningsstation/

Läs mer om våra förmåner och hur det är att jobba vid SLU på https://www.slu.se/om-slu/jobba-pa-slu/

Placering:

Grimsö forskningsstation.

Anställningsform:

Tidsbegränsad anställning 12 månader.

Omfattning:

100%.

Tillträde:

Enligt överenskommelse.

Ansökan:

Välkommen med din ansökan via ansökningsknappen nedan senast 2026-07-31.

Fackliga kontaktpersoner:

https://internt.slu.se/min-anstallning/facket/kontaktpersoner/