Biomedicinsk analytiker - Lediga jobb

We call ourselves a 60-year-old startup. Decades of scientific heritage, paired with the speed, ambition and hands-on energy of a company being built from the ground up. Right now, we're scaling manufacturing fast, and that means the way we assure sterility needs to scale with it. We're looking for a Sterility Assurance Lead who wants to own that agenda from day one, not just maintain a system, but shape how sterility assurance grows alongside the site.

You will own and drive the site’s sterility assurance strategy. This role ensures compliance with global regulatory requirements and serves as the SME for contamination control, aseptic processing, and sterilization validation.

Key Responsibilities

• Lead the Sterility Assurance Program (SAP) and Contamination Control Strategy (CCS) in line with EU GMP Annex 1 and global standards.

• Oversee environmental monitoring, cleanroom qualification, and aseptic practices.

• Review sterilization validations and lead media fill programs.

• Drive contamination risk assessments, investigations, and CAPAs.

• Act as SME during audits and inspections.

• Provide training and mentorship in sterility assurance best practices.

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

You are a highly motivated sterility assurance professional with a strong quality mindset and a passion for patient safety. You combine deep technical expertise with leadership capabilities and are comfortable acting as a site Subject Matter Expert. You're energized rather than unsettled by a fast-scaling environment, you bring a proactive, solution-oriented approach that lets you spot risks early, drive improvements, and push operational excellence forward even as priorities shift.

You thrive in a collaborative, cross-functional environment and can communicate complex technical topics clearly to both technical and non-technical stakeholders. You're confident leading investigations, mentoring colleagues, and driving initiatives that strengthen contamination control and aseptic manufacturing performance, and you see this growth phase as a chance to grow your own scope right along with it.

Requirements

• Bachelor's or Master's degree in Microbiology, Biotechnology, Pharmacy, or another relevant life science discipline.

• 8–12 years of experience in sterile manufacturing, microbiology, or sterility assurance within the pharmaceutical, biologics, or medical device industry.

• Proven experience working in GMP-regulated environments and supporting regulatory inspections and audits.

• Hands-on experience with contamination control strategies, environmental monitoring programs, and aseptic manufacturing operations.

Skills

• Deep technical expertise in aseptic processing, sterilization technologies (moist heat, dry heat, filtration), and microbial contamination control.

• Strong knowledge of cleanroom operations, HVAC qualification, isolators/RABS, and environmental monitoring systems.

• Solid understanding of EU GMP Annex 1 requirements and familiarity with global regulatory expectations (FDA, EMA, PIC/S).

• Experience performing risk assessments using tools such as FMEA, HACCP, or similar methodologies.

• Strong analytical mindset with the ability to interpret data trends and drive continuous improvement initiatives.

• Excellent documentation skills and a structured approach to problem-solving and investigations.

• Strong communication and collaboration skills with the ability to influence cross-functional teams.

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. Because we understand that the skin, we are in shapes our lives, we are advancing dermatology for every skin story.

We aim to empower each employee and promote their personal growth while ensuring business needs are met now and into the future. Across our company, we embrace diversity and respect the dignity, privacy, and personal rights of every employee.

We call ourselves a 60-year-old startup. Decades of scientific heritage, paired with the speed, ambition and hands-on energy of a company being built from the ground up. Right now, we're scaling manufacturing fast, and that means the way we assure sterility needs to scale with it. We're looking for a Sterility Assurance Lead who wants to own that agenda from day one, not just maintain a system, but shape how sterility assurance grows alongside the site.

You will own and drive the site’s sterility assurance strategy. This role ensures compliance with global regulatory requirements and serves as the SME for contamination control, aseptic processing, and sterilization validation.

Key Responsibilities

• Lead the Sterility Assurance Program (SAP) and Contamination Control Strategy (CCS) in line with EU GMP Annex 1 and global standards.

• Oversee environmental monitoring, cleanroom qualification, and aseptic practices.

• Review sterilization validations and lead media fill programs.

• Drive contamination risk assessments, investigations, and CAPAs.

• Act as SME during audits and inspections.

• Provide training and mentorship in sterility assurance best practices.

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

You are a highly motivated sterility assurance professional with a strong quality mindset and a passion for patient safety. You combine deep technical expertise with leadership capabilities and are comfortable acting as a site Subject Matter Expert. You're energized rather than unsettled by a fast-scaling environment, you bring a proactive, solution-oriented approach that lets you spot risks early, drive improvements, and push operational excellence forward even as priorities shift.

You thrive in a collaborative, cross-functional environment and can communicate complex technical topics clearly to both technical and non-technical stakeholders. You're confident leading investigations, mentoring colleagues, and driving initiatives that strengthen contamination control and aseptic manufacturing performance, and you see this growth phase as a chance to grow your own scope right along with it.

Requirements

• Bachelor's or Master's degree in Microbiology, Biotechnology, Pharmacy, or another relevant life science discipline.

• 8–12 years of experience in sterile manufacturing, microbiology, or sterility assurance within the pharmaceutical, biologics, or medical device industry.

• Proven experience working in GMP-regulated environments and supporting regulatory inspections and audits.

• Hands-on experience with contamination control strategies, environmental monitoring programs, and aseptic manufacturing operations.

Skills

• Deep technical expertise in aseptic processing, sterilization technologies (moist heat, dry heat, filtration), and microbial contamination control.

• Strong knowledge of cleanroom operations, HVAC qualification, isolators/RABS, and environmental monitoring systems.

• Solid understanding of EU GMP Annex 1 requirements and familiarity with global regulatory expectations (FDA, EMA, PIC/S).

• Experience performing risk assessments using tools such as FMEA, HACCP, or similar methodologies.

• Strong analytical mindset with the ability to interpret data trends and drive continuous improvement initiatives.

• Excellent documentation skills and a structured approach to problem-solving and investigations.

• Strong communication and collaboration skills with the ability to influence cross-functional teams.

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. Because we understand that the skin, we are in shapes our lives, we are advancing dermatology for every skin story.

We aim to empower each employee and promote their personal growth while ensuring business needs are met now and into the future. Across our company, we embrace diversity and respect the dignity, privacy, and personal rights of every employee.

We call ourselves a 60-year-old startup. Decades of scientific heritage, paired with the speed, ambition and hands-on energy of a company being built from the ground up. Right now, we're scaling manufacturing fast, and that means the way we assure sterility needs to scale with it. We're looking for a Sterility Assurance Lead who wants to own that agenda from day one, not just maintain a system, but shape how sterility assurance grows alongside the site.

You will own and drive the site’s sterility assurance strategy. This role ensures compliance with global regulatory requirements and serves as the SME for contamination control, aseptic processing, and sterilization validation.

Key Responsibilities

• Lead the Sterility Assurance Program (SAP) and Contamination Control Strategy (CCS) in line with EU GMP Annex 1 and global standards.

• Oversee environmental monitoring, cleanroom qualification, and aseptic practices.

• Review sterilization validations and lead media fill programs.

• Drive contamination risk assessments, investigations, and CAPAs.

• Act as SME during audits and inspections.

• Provide training and mentorship in sterility assurance best practices.

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

You are a highly motivated sterility assurance professional with a strong quality mindset and a passion for patient safety. You combine deep technical expertise with leadership capabilities and are comfortable acting as a site Subject Matter Expert. You're energized rather than unsettled by a fast-scaling environment, you bring a proactive, solution-oriented approach that lets you spot risks early, drive improvements, and push operational excellence forward even as priorities shift.

You thrive in a collaborative, cross-functional environment and can communicate complex technical topics clearly to both technical and non-technical stakeholders. You're confident leading investigations, mentoring colleagues, and driving initiatives that strengthen contamination control and aseptic manufacturing performance, and you see this growth phase as a chance to grow your own scope right along with it.

Requirements

• Bachelor's or Master's degree in Microbiology, Biotechnology, Pharmacy, or another relevant life science discipline.

• 8–12 years of experience in sterile manufacturing, microbiology, or sterility assurance within the pharmaceutical, biologics, or medical device industry.

• Proven experience working in GMP-regulated environments and supporting regulatory inspections and audits.

• Hands-on experience with contamination control strategies, environmental monitoring programs, and aseptic manufacturing operations.

Skills

• Deep technical expertise in aseptic processing, sterilization technologies (moist heat, dry heat, filtration), and microbial contamination control.

• Strong knowledge of cleanroom operations, HVAC qualification, isolators/RABS, and environmental monitoring systems.

• Solid understanding of EU GMP Annex 1 requirements and familiarity with global regulatory expectations (FDA, EMA, PIC/S).

• Experience performing risk assessments using tools such as FMEA, HACCP, or similar methodologies.

• Strong analytical mindset with the ability to interpret data trends and drive continuous improvement initiatives.

• Excellent documentation skills and a structured approach to problem-solving and investigations.

• Strong communication and collaboration skills with the ability to influence cross-functional teams.

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. Because we understand that the skin, we are in shapes our lives, we are advancing dermatology for every skin story.

We aim to empower each employee and promote their personal growth while ensuring business needs are met now and into the future. Across our company, we embrace diversity and respect the dignity, privacy, and personal rights of every employee.

We call ourselves a 60-year-old startup. Decades of scientific heritage, paired with the speed, ambition and hands-on energy of a company being built from the ground up. Right now, we're scaling manufacturing fast, and that means the way we assure sterility needs to scale with it. We're looking for a Sterility Assurance Lead who wants to own that agenda from day one, not just maintain a system, but shape how sterility assurance grows alongside the site.

You will own and drive the site’s sterility assurance strategy. This role ensures compliance with global regulatory requirements and serves as the SME for contamination control, aseptic processing, and sterilization validation.

Key Responsibilities

• Lead the Sterility Assurance Program (SAP) and Contamination Control Strategy (CCS) in line with EU GMP Annex 1 and global standards.

• Oversee environmental monitoring, cleanroom qualification, and aseptic practices.

• Review sterilization validations and lead media fill programs.

• Drive contamination risk assessments, investigations, and CAPAs.

• Act as SME during audits and inspections.

• Provide training and mentorship in sterility assurance best practices.

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

You are a highly motivated sterility assurance professional with a strong quality mindset and a passion for patient safety. You combine deep technical expertise with leadership capabilities and are comfortable acting as a site Subject Matter Expert. You're energized rather than unsettled by a fast-scaling environment, you bring a proactive, solution-oriented approach that lets you spot risks early, drive improvements, and push operational excellence forward even as priorities shift.

You thrive in a collaborative, cross-functional environment and can communicate complex technical topics clearly to both technical and non-technical stakeholders. You're confident leading investigations, mentoring colleagues, and driving initiatives that strengthen contamination control and aseptic manufacturing performance, and you see this growth phase as a chance to grow your own scope right along with it.

Requirements

• Bachelor's or Master's degree in Microbiology, Biotechnology, Pharmacy, or another relevant life science discipline.

• 8–12 years of experience in sterile manufacturing, microbiology, or sterility assurance within the pharmaceutical, biologics, or medical device industry.

• Proven experience working in GMP-regulated environments and supporting regulatory inspections and audits.

• Hands-on experience with contamination control strategies, environmental monitoring programs, and aseptic manufacturing operations.

Skills

• Deep technical expertise in aseptic processing, sterilization technologies (moist heat, dry heat, filtration), and microbial contamination control.

• Strong knowledge of cleanroom operations, HVAC qualification, isolators/RABS, and environmental monitoring systems.

• Solid understanding of EU GMP Annex 1 requirements and familiarity with global regulatory expectations (FDA, EMA, PIC/S).

• Experience performing risk assessments using tools such as FMEA, HACCP, or similar methodologies.

• Strong analytical mindset with the ability to interpret data trends and drive continuous improvement initiatives.

• Excellent documentation skills and a structured approach to problem-solving and investigations.

• Strong communication and collaboration skills with the ability to influence cross-functional teams.

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. Because we understand that the skin, we are in shapes our lives, we are advancing dermatology for every skin story.

We aim to empower each employee and promote their personal growth while ensuring business needs are met now and into the future. Across our company, we embrace diversity and respect the dignity, privacy, and personal rights of every employee.

We call ourselves a 60-year-old startup. Decades of scientific heritage, paired with the speed, ambition and hands-on energy of a company being built from the ground up. Right now, we're scaling manufacturing fast, and that means the way we assure sterility needs to scale with it. We're looking for a Sterility Assurance Lead who wants to own that agenda from day one, not just maintain a system, but shape how sterility assurance grows alongside the site.

You will own and drive the site’s sterility assurance strategy. This role ensures compliance with global regulatory requirements and serves as the SME for contamination control, aseptic processing, and sterilization validation.

Key Responsibilities

• Lead the Sterility Assurance Program (SAP) and Contamination Control Strategy (CCS) in line with EU GMP Annex 1 and global standards.

• Oversee environmental monitoring, cleanroom qualification, and aseptic practices.

• Review sterilization validations and lead media fill programs.

• Drive contamination risk assessments, investigations, and CAPAs.

• Act as SME during audits and inspections.

• Provide training and mentorship in sterility assurance best practices.

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

You are a highly motivated sterility assurance professional with a strong quality mindset and a passion for patient safety. You combine deep technical expertise with leadership capabilities and are comfortable acting as a site Subject Matter Expert. You're energized rather than unsettled by a fast-scaling environment, you bring a proactive, solution-oriented approach that lets you spot risks early, drive improvements, and push operational excellence forward even as priorities shift.

You thrive in a collaborative, cross-functional environment and can communicate complex technical topics clearly to both technical and non-technical stakeholders. You're confident leading investigations, mentoring colleagues, and driving initiatives that strengthen contamination control and aseptic manufacturing performance, and you see this growth phase as a chance to grow your own scope right along with it.

Requirements

• Bachelor's or Master's degree in Microbiology, Biotechnology, Pharmacy, or another relevant life science discipline.

• 8–12 years of experience in sterile manufacturing, microbiology, or sterility assurance within the pharmaceutical, biologics, or medical device industry.

• Proven experience working in GMP-regulated environments and supporting regulatory inspections and audits.

• Hands-on experience with contamination control strategies, environmental monitoring programs, and aseptic manufacturing operations.

Skills

• Deep technical expertise in aseptic processing, sterilization technologies (moist heat, dry heat, filtration), and microbial contamination control.

• Strong knowledge of cleanroom operations, HVAC qualification, isolators/RABS, and environmental monitoring systems.

• Solid understanding of EU GMP Annex 1 requirements and familiarity with global regulatory expectations (FDA, EMA, PIC/S).

• Experience performing risk assessments using tools such as FMEA, HACCP, or similar methodologies.

• Strong analytical mindset with the ability to interpret data trends and drive continuous improvement initiatives.

• Excellent documentation skills and a structured approach to problem-solving and investigations.

• Strong communication and collaboration skills with the ability to influence cross-functional teams.

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. Because we understand that the skin, we are in shapes our lives, we are advancing dermatology for every skin story.

We aim to empower each employee and promote their personal growth while ensuring business needs are met now and into the future. Across our company, we embrace diversity and respect the dignity, privacy, and personal rights of every employee.

We call ourselves a 60-year-old startup. Decades of scientific heritage, paired with the speed, ambition and hands-on energy of a company being built from the ground up. Right now, we're scaling manufacturing fast, and that means the way we assure sterility needs to scale with it. We're looking for a Sterility Assurance Lead who wants to own that agenda from day one, not just maintain a system, but shape how sterility assurance grows alongside the site.

You will own and drive the site’s sterility assurance strategy. This role ensures compliance with global regulatory requirements and serves as the SME for contamination control, aseptic processing, and sterilization validation.

Key Responsibilities

• Lead the Sterility Assurance Program (SAP) and Contamination Control Strategy (CCS) in line with EU GMP Annex 1 and global standards.

• Oversee environmental monitoring, cleanroom qualification, and aseptic practices.

• Review sterilization validations and lead media fill programs.

• Drive contamination risk assessments, investigations, and CAPAs.

• Act as SME during audits and inspections.

• Provide training and mentorship in sterility assurance best practices.

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

You are a highly motivated sterility assurance professional with a strong quality mindset and a passion for patient safety. You combine deep technical expertise with leadership capabilities and are comfortable acting as a site Subject Matter Expert. You're energized rather than unsettled by a fast-scaling environment, you bring a proactive, solution-oriented approach that lets you spot risks early, drive improvements, and push operational excellence forward even as priorities shift.

You thrive in a collaborative, cross-functional environment and can communicate complex technical topics clearly to both technical and non-technical stakeholders. You're confident leading investigations, mentoring colleagues, and driving initiatives that strengthen contamination control and aseptic manufacturing performance, and you see this growth phase as a chance to grow your own scope right along with it.

Requirements

• Bachelor's or Master's degree in Microbiology, Biotechnology, Pharmacy, or another relevant life science discipline.

• 8–12 years of experience in sterile manufacturing, microbiology, or sterility assurance within the pharmaceutical, biologics, or medical device industry.

• Proven experience working in GMP-regulated environments and supporting regulatory inspections and audits.

• Hands-on experience with contamination control strategies, environmental monitoring programs, and aseptic manufacturing operations.

Skills

• Deep technical expertise in aseptic processing, sterilization technologies (moist heat, dry heat, filtration), and microbial contamination control.

• Strong knowledge of cleanroom operations, HVAC qualification, isolators/RABS, and environmental monitoring systems.

• Solid understanding of EU GMP Annex 1 requirements and familiarity with global regulatory expectations (FDA, EMA, PIC/S).

• Experience performing risk assessments using tools such as FMEA, HACCP, or similar methodologies.

• Strong analytical mindset with the ability to interpret data trends and drive continuous improvement initiatives.

• Excellent documentation skills and a structured approach to problem-solving and investigations.

• Strong communication and collaboration skills with the ability to influence cross-functional teams.

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. Because we understand that the skin, we are in shapes our lives, we are advancing dermatology for every skin story.

We aim to empower each employee and promote their personal growth while ensuring business needs are met now and into the future. Across our company, we embrace diversity and respect the dignity, privacy, and personal rights of every employee.

We call ourselves a 60-year-old startup. Decades of scientific heritage, paired with the speed, ambition and hands-on energy of a company being built from the ground up. Right now, we're scaling manufacturing fast, and that means the way we assure sterility needs to scale with it. We're looking for a Sterility Assurance Lead who wants to own that agenda from day one, not just maintain a system, but shape how sterility assurance grows alongside the site.

You will own and drive the site’s sterility assurance strategy. This role ensures compliance with global regulatory requirements and serves as the SME for contamination control, aseptic processing, and sterilization validation.

Key Responsibilities

• Lead the Sterility Assurance Program (SAP) and Contamination Control Strategy (CCS) in line with EU GMP Annex 1 and global standards.

• Oversee environmental monitoring, cleanroom qualification, and aseptic practices.

• Review sterilization validations and lead media fill programs.

• Drive contamination risk assessments, investigations, and CAPAs.

• Act as SME during audits and inspections.

• Provide training and mentorship in sterility assurance best practices.

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

You are a highly motivated sterility assurance professional with a strong quality mindset and a passion for patient safety. You combine deep technical expertise with leadership capabilities and are comfortable acting as a site Subject Matter Expert. You're energized rather than unsettled by a fast-scaling environment, you bring a proactive, solution-oriented approach that lets you spot risks early, drive improvements, and push operational excellence forward even as priorities shift.

You thrive in a collaborative, cross-functional environment and can communicate complex technical topics clearly to both technical and non-technical stakeholders. You're confident leading investigations, mentoring colleagues, and driving initiatives that strengthen contamination control and aseptic manufacturing performance, and you see this growth phase as a chance to grow your own scope right along with it.

Requirements

• Bachelor's or Master's degree in Microbiology, Biotechnology, Pharmacy, or another relevant life science discipline.

• 8–12 years of experience in sterile manufacturing, microbiology, or sterility assurance within the pharmaceutical, biologics, or medical device industry.

• Proven experience working in GMP-regulated environments and supporting regulatory inspections and audits.

• Hands-on experience with contamination control strategies, environmental monitoring programs, and aseptic manufacturing operations.

Skills

• Deep technical expertise in aseptic processing, sterilization technologies (moist heat, dry heat, filtration), and microbial contamination control.

• Strong knowledge of cleanroom operations, HVAC qualification, isolators/RABS, and environmental monitoring systems.

• Solid understanding of EU GMP Annex 1 requirements and familiarity with global regulatory expectations (FDA, EMA, PIC/S).

• Experience performing risk assessments using tools such as FMEA, HACCP, or similar methodologies.

• Strong analytical mindset with the ability to interpret data trends and drive continuous improvement initiatives.

• Excellent documentation skills and a structured approach to problem-solving and investigations.

• Strong communication and collaboration skills with the ability to influence cross-functional teams.

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. Because we understand that the skin, we are in shapes our lives, we are advancing dermatology for every skin story.

We aim to empower each employee and promote their personal growth while ensuring business needs are met now and into the future. Across our company, we embrace diversity and respect the dignity, privacy, and personal rights of every employee.

Vill du göra skillnad för patienter – bakom kulisserna?

Varje prov vi hanterar representerar en människa som väntar på svar.

Ett besked. En diagnos. Rätt behandling.

Hos oss på klinisk patologi blir ditt arbete en viktig del av vården – även om patienten kanske aldrig möter dig. Det du gör spelar roll på riktigt!

Nu söker vi fler kollegor som vill arbeta i en verksamhet där kvalitet, precision och samarbete är avgörande för att rädda liv och utveckla framtidens sjukvård.

Vårt erbjudande

För livet framåt. Region Östergötland har höga ambitioner och ett ansvarsfullt uppdrag. Det handlar om hälsa och vård, om vår regions utveckling och om dem som lever och vistas här. Vi vill fortsätta att vara i framkant, med vård, forskning och utbildning. Det handlar om att våga tänka nytt – och att ha de bästa medarbetarna. Därför erbjuder vi unika möjligheter till vidare lärande och satsar på moderna miljöer med effektiva system och verktyg. Många av oss möter patienter och närstående, andra skapar förutsättningarna för livsviktiga insatser. Hos oss jobbar fantastiska människor mot samma mål – att göra skillnad på riktigt, och för livet framåt.

Det vi ofta hör från våra medarbetare är att kombinationen av mening, utveckling och gemenskap gör jobbet speciellt. Att våra arbetstider är förlagda dagtid samt att vi hjälper patienter och har bra kvalitet är även de återkommande i våra dialoger om vad som är bra hos oss!

Här arbetar du tillsammans med kompetenta och hjälpsamma kollegor i en verksamhet där vi stöttar varandra, delar kunskap och har patienten i fokus.

Vi erbjuder:

• ett arbete som gör verklig skillnad för patienter
• en verksamhet i utveckling där nya metoder och analyser står i fokus
• möjlighet till lärande och kompetensutveckling
• engagerade kollegor och en god arbetsmiljö
• arbetstid dagtid med möjlighet till flex

Läs gärna om dina förmåner hos oss. 

Arbetsbeskrivning

Hos oss blir du en viktig del av den diagnostiska processen, framför allt inom cancersjukvården. Arbetet är varierat och kombinerar praktiskt laboratoriearbete med kvalitet, teknik och utveckling.

Beroende på din erfarenhet och verksamhetens behov kan du bland annat arbeta med:

• hantering och preparering av vävnads- och cellprover
• laborativt arbete inom histologi och cytologi
• manuella och automatiserade analysmetoder
• digitala arbetsflöden och modern utrustning
• utveckling och förbättring av laboratoriets processer och arbetssätt
• kvalitetsuppföljning och metodutveckling
• nära samarbete med kollegor inom flera yrkesgrupper i hela analyskedjan

Vi arbetar i en verksamhet där utvecklingen går snabbt framåt. Nya analysmetoder, digitalisering och modern teknik skapar bättre förutsättningar för snabb och säker diagnostik – och du blir en del av den utvecklingen.

Samtidigt är vår kärnverksamhet beroende av ett stabilt och effektivt flöde varje dag. Ett stort antal prover passerar genom laboratoriet och varje prov representerar en patient som väntar på svar. Därför är det viktigt att vi tillsammans arbetar strukturerat, håller ett bra tempo och tar ansvar för kvaliteten i varje steg av processen.

Hos oss behöver du trivas i en verksamhet där produktion, precision och patientfokus går hand i hand. Vi hjälps åt för att hålla hög kvalitet, möta våra svarstider och säkerställa att varje prov hanteras med noggrannhet och respekt.

Om dig

• du är legitimerad biomedicinsk analytiker, har högskoleexamen inom medicinsk biologi eller annan utbildning som arbetsgivaren bedömer likvärdig
• du har mycket goda kunskaper i svenska i tal och skrift
• du arbetar noggrant/strukturerat och kvalitetsmedvetet
• du trivs både i självständigt arbete och att samarbeta med andra
• du är flexibel och har lätt att växla mellan olika arbetsuppgifter
• du bidrar med positiv energi och ett lösningsfokuserat förhållningssätt

Ansökan och anställning

Tjänsten är en tillsvidareanställning med start enligt överenskommelse.

Arbetstid är vardagar klockan 07.30–16.00 med möjlighet till flex.

Vi kommer börja med intervjuer under vecka 34, efter den 18 augusti. Anställningen kan komma att inledas med sex månaders provanställning.

Inför anställning i ett patientnära arbete inom Region Östergötland kommer du att få fylla i en hälsodeklaration.

Varmt välkommen in med din ansökan! Om du behöver hjälp med att registrera i systemet, kontakta kundtjänst Stöd och service, 010-103 60 00, under kontorstid.

Till bemannings-, förmedlings- och rekryteringsföretag och till dig som är försäljare:

Vi undanber oss vänligen men bestämt direktkontakt med bemannings-, förmedlings- och rekryteringsföretag samt andra externa aktörer och försäljare av ytterligare jobbannonser. Region Östergötland har upphandlade avtal.