Processingenjör - Lediga jobb

Processingenjör till spännande projekt inom processindustrin

Vill du arbeta i en tekniskt avancerad miljö där du får bidra till utvecklingen av framtidens processindustri?

Vi söker nu en erfaren och engagerad processingenjör till vår kund – ett etablerat ingenjörsbolag som arbetar med projekt inom flera olika processindustrier.

I denna roll får du möjlighet att arbeta i spännande projekt från tidiga förstudier till driftsättning, tillsammans med kompetenta kollegor i multidisciplinära team.

Arbetet kan utgå från kontor i Stockholm, Göteborg, Uppsala eller Malmö, samt delvis på distans eller ute hos kund.

Om rollen

Som processingenjör kommer du att spela en viktig roll i tekniska projekt inom processindustrin. Du kommer att arbeta både självständigt och i team med att utveckla och optimera processlösningar.

Dina arbetsuppgifter kan bland annat inkludera:

Delta i kunduppdrag, förstudier och projektleveranser

Utveckla och designa processlösningar

Ta fram P&ID, processbeskrivningar och komponentlistor

Arbeta med 2D-layouter i AutoCAD

Ta fram och tolka kravspecifikationer och förfrågningsunderlag

Vara teknisk kontaktperson mot leverantörer och entreprenörer

Delta i riskanalyser såsom HAZOP och projektriskanalyser

Samverka med andra discipliner såsom instrument, automation, el och rörkonstruktion

Vi söker dig som

Har minst 5 års erfarenhet inom processindustrin

Har en högskole- eller civilingenjörsexamen

Har erfarenhet från exempelvis energi, kemisk industri, livsmedel eller läkemedel

Har erfarenhet av AutoCAD och framtagning av P&ID

Har god förståelse för multidisciplinära projekt

Har erfarenhet av riskanalyser som HAZOP

Talar och skriver flytande svenska och engelska

Har B-körkort

Om vår kund

Vår kund är ett etablerat ingenjörsbolag som arbetar med projekt och konsulttjänster inom processindustrin. Bolaget levererar både specialistkompetens och kompletta projektlösningar till kunder inom bland annat energi, kemi, livsmedel och läkemedel.

Med lång erfarenhet i branschen arbetar företaget nära sina kunder genom hela projektcykeln – från idé och design till implementation och driftsättning. Fokus ligger på teknisk kvalitet, innovation och långsiktiga kundrelationer.

I skärningspunkten mellan teknik, process och verklig påverkan formas framtidens Life Science. Hos AFRY kliver du in i ett växande segment där fokus ligger på att förstå, utveckla och förbättra processer inom Life Science-branschen, där varje förbättring kan göra skillnad på riktigt. Här arbetar du nära både kundernas verksamhet och interna utvecklingsprojekt, i en roll som rör sig fritt mellan analys, problemlösning och praktiskt förbättringsarbete. Det är en miljö där processingenjören inte bara följer flöden, utan formar dem. Vi ser fram emot din ansökan!

Om tjänsten

AFRY är ett ledande ingenjörs- och designbolag med verksamhet inom energi, industri och infrastruktur. InomLife Science-segmentet arbetar teamet idag uteslutande mot kunder inom läkemedel, bioteknik och medicinteknik, med fokus på att utveckla säkra, effektiva och hållbara processer. I detta segment samlas experter inom hela livscykeln för industriella processer, från tidiga studier och processdesign till produktion, kvalitet och förbättring av befintliga anläggningar. AFRY arbetar nära sina kunder för att optimera produktivitet, säkerställa hög produktkvalitet och bidra till mer resurseffektiva och hållbara lösningar inom Life Science-industrin. Med ett dedikerat team av Life Science-ingenjörer stöttar AFRY kunder genom hela produktionskedjan inom läkemedel, bioteknik och medicinteknik. Fokus ligger på att kombinera teknisk expertis med förståelse för högt ställda krav på kvalitet, spårbarhet och regulatorisk efterlevnad.

I Uppsala växer teamet och fler processingenjörer rekryteras till en konsultverksamhet där uppdragen varierar i både längd, komplexitet och tekniskt fokus. Rollen innebär att du rör dig mellan olika miljöer inom Life Science-industrin, där du snabbt blir en del av kundens organisation och arbetar nära både produktion, kvalitet och teknik. Gemensamt för uppdragen är närheten till verkliga processer, där analys, problemlösning och förbättringsarbete sker direkt i verksamheten, snarare än på distans. Arbetet är ofta tvärfunktionellt och innebär ett nära samarbete med flera delar av organisationen. Du kan ena dagen arbeta med att analysera och förstå avvikelser i en process, och nästa dag delta i förbättringsarbete kopplat till flöden, utrustning eller arbetssätt. Rollen kräver en förmåga att snabbt sätta sig in i nya system, miljöer och arbetssätt, samtidigt som du bidrar med struktur, teknisk förståelse och ett analytiskt förhållningssätt. Konsultrollen innebär också en hög grad av variation, där du successivt bygger erfarenhet från olika typer av verksamheter inom Life Science.

Parallellt med kunduppdragen finns även interna AFRY-projekt, där processer och lösningar utvecklas för att senare implementeras hos kund. Här arbetar du mer konceptuellt och utvecklingsdrivet, ofta i team, med fokus på att förbättra och effektivisera framtida processlösningar.

Sektionen präglas av stark sammanhållning och en prestigelös kultur där kompetens delas generöst. Trots att konsulterna ofta sitter ute hos kund finns en tydlig gemenskap, med regelbundna träffar, AWs och ett klimat där det alltid finns kollegor att bolla tekniska frågeställningar och utmaningar med.

Det här är ett konsultuppdrag vilket innebär att du kommer vara anställd av Academic Work och arbeta som konsult hos AFRY. Uppdraget kommer att vara på heltid och är långsiktigt. Målet med samarbetet är att du på sikt ska bli överrekryterad direkt till AFRY, förutsatt att alla parter är nöjda med samarbetet.

Du erbjuds

• En roll i ett nytt och växande Life Science-segment inom AFRY
• Variation mellan kunduppdrag och interna utvecklingsprojekt
• Närhet till tekniska processer i läkemedel, bioteknik och medicinteknik
• En stark teamkänsla med hög grad av samarbete och kunskapsdelning
• Kontinuerlig kompetensutveckling genom utbildningar och tekniska nätverk

Arbetsuppgifter

Som processingenjör arbetar du brett med att förstå, analysera och förbättra processer inom Life Science-industrin. Rollen är varierad och du kan både arbeta nära kundens verksamhet och i interna AFRY-projekt som utvecklas vidare till framtida kundlösningar. Du kommer bland annat att:

• Analysera och optimera processer för att förbättra kvalitet, effektivitet och robusthet
• Arbeta med avvikelseutredningar, felsökning och rotorsaksanalys
• Bidra i förbättringsarbete kopplat till processer, flöden och arbetssätt
• Kravställa och utvärdera utrustning och tekniska lösningar
• Delta i utveckling och dokumentation av processer och arbetsmetoder
• Arbeta tvärfunktionellt med produktion, kvalitet och teknik
• Delta i både kunduppdrag och interna utvecklingsinitiativ inom AFRY

Vi söker dig som

• Har en universitetsutbildning inom exempelvis maskinteknik, kemi, bioteknik, medicinteknik eller liknande
• Har erfarenhet från Life Science, exempelvis produktion, laborativ miljö, kvalitet eller liknande tekniska roller
• Har ett starkt tekniskt intresse och trivs i miljöer där du får förstå hur processer fungerar i praktiken
• Har god systemvana och förståelse för tekniska flöden
• Talar och skriver obehindrat på svenska och engelska då det krävs för att utföra arbetet

Det är meriterande, men inget krav, om du har

• Erfarenhet av processutveckling, förbättringsarbete eller Lean
• Arbetat i GMP-reglerad verksamhet

I rollen som konsult är det särskilt viktigt att du har förmågan att snabbt sätta dig in i nya miljöer och skapa förtroende i olika organisationer. Du är nyfiken, ansvarstagande och trivs i en vardag där du växlar mellan analys och mer praktiskt, verksamhetsnära arbete. Vidare är du strukturerad och kvalitetsmedveten, med en god förmåga att självständigt driva ditt arbete framåt även i nya sammanhang. Du har lätt för att samarbeta med olika typer av människor och funktioner, och trivs i rollen som en flexibel och lösningsorienterad lagspelare i olika team och konstellationer.

Övrig information

• Start: Efter sommaren
• Omfattning: Heltid, kontorstider
• Placering: Uppsala

Vår rekryteringsprocess

Denna rekryteringsprocess hanteras av Academic Work och vår kunds önskemål är att alla frågor rörande tjänsten skickas till Academic Work.

Vi tillämpar löpande urval och kommer plocka ner annonsen när tillräckligt många kandidater har nått slutskedet i rekryteringsprocessen. Vid ansökan efterfrågas ett CV. Personligt brev använder vi inte som urvalsmetod och behöver därför inte bifogas. Rekryteringsprocessen innehåller två urvalstest: ett personlighetstest och ett test i kognitiv

Bohus Biotech is an innovative company focused on the development and manufacture of high-quality products containing hyaluronic acid (HA). We are now in an expansive phase, investing in the products and processes of the future. We are looking for a driven Process Engineer who wants to become part of Bohus’s future and contribute to the continued development of hyaluronic acid and its products.

As our Process Engineer, you will be responsible for developing, optimizing, validating, and maintaining manufacturing processes to ensure product quality, process robustness, regulatory compliance, and operational efficiency. The role supports both existing production processes and the introduction of new products and technologies. You will be working closely with dedicated and highly competent colleagues within Production, Quality Assurance, Regulatory Affairs, Supply Chain, and R&D. You will get the exciting opportunity to build, shape and optimize our processes and apply your experience and expertise to ensure the highest manufacturing standards. If this sounds interesting to you - Come join us!

This is a full-time position and based in our company location in Strömstad, Sweden. On-site in Strömstad preferred, but hybrid solutions are possible for the right candidate. We will interview candidates continuously and welcome your application today.

The Process Engineer is responsible for ensuring that manufacturing processes are robust, efficient, validated, and compliant throughout the product lifecycle. You will bridge day-to-day manufacturing support with longer-term process development and operational excellence initiatives. The position reports to the COO.

Duties and responsibilities include:

• Develop, implement, and continuously improve manufacturing processes to enhance quality, yield, and efficiency.

• Lead root cause investigations and implement corrective and preventive actions (CAPA).

• Plan, execute, and document validation activities, including Process Validation, Equipment Qualification (IQ/OQ/PQ), Cleaning Validation, and Test Method Validation/Verification.

• Provide technical support to production, investigating process deviations, non-conformities, and out-of-specification results.

• Lead continuous improvement initiatives using structured problem-solving methods such as Root Cause Analysis, FMEA, and 5 Why.

• Ensure processes comply with ISO 13485, EU MDR 2017/745, ISO 14971, and GMP principles.

• Support audits and inspections by customers, regulatory authorities, and Notified Bodies.

• Support technology transfers from R&D to production and participate in cross-functional development projects.

• Approve process validation documentation according to delegated authority and escalate process risks impacting product quality, compliance, or supply.

The suitable candidate has the following qualifications:

• Formal academic degree level (BSc. or MSc.) in chemical engineering, biotechnology, pharmaceutical science or related.

• Strong background in process engineering preferably combined with validation engineering experience.

• Experience working in a manufacturing environment within a regulated industry (e.g. Medical Devices, Pharmaceuticals, Biotechnology, or other regulated industries).

• Experience with process optimization, process validation and problem solving.

• Experience with sterile processes, equipment qualification (IQ, OQ, PQ), process validation, troubleshooting, and continuous improvement would be highly valuable.

• Experience working with Quality Management Systems.

• Knowledge of statistical analysis and process capability concepts.

• Excellent communication and documentation skills in English are required

The successful candidate for this position will be someone who:

• Has a strong technical and analytical mindset.

• Enjoys solving complex manufacturing and process-related challenges.

• Is structured and detail-oriented.

• Takes ownership and drives improvements independently.

• Communicates effectively across departments and organizational levels.

• Combines hands-on problem solving with a systematic approach.

• Thrives in a fast-paced environment where quality, compliance, and operational performance are equally important.

We offer a dynamic working environment with significant opportunity to make an impact — contributing to Bohus’s success as well as your own growth and development.

Founded in 1993, BOHUS has been at the forefront of Hyaluronic Acid (HA) development and manufacturing for over three decades. Our journey began with a vision to revolutionize the HA industry through innovation and commitment to excellence.

With more than 30 years of expertise, the company has established a strong international presence with products distributed to hospitals, clinics, and physicians in over 60 countries worldwide.

Bohus Biotech focuses exclusively on high quality hyaluronic acid technologies across three therapeutic areas:

• Ophthalmology – OVD solutions supporting tissue protection during cataract surgery

• Aesthetics – Dermal fillers based on the proprietary SHAPE™ technology platform

• Orthopaedics – Injectable treatments for osteoarthritis

All research, development, and manufacturing are located in Strömstad, Sweden, ensuring full control over product quality and innovation. For more information, visit the company's web sites at: www.bohusbiotech.com

Krishan Johansson Haque, PhD

Sr Recruitment Consultant, QRIOS Life Science & Engineering

T: +46 (0)72-070 16 53

E: krishan.johansson-haque@qrios.se

Bohus Biotech is an innovative company focused on the development and manufacture of high-quality products containing hyaluronic acid (HA). We are now in an expansive phase, investing in the products and processes of the future. We are looking for a driven Process Engineer who wants to become part of Bohus’s future and contribute to the continued development of hyaluronic acid and its products.

As our Process Engineer, you will be responsible for developing, optimizing, validating, and maintaining manufacturing processes to ensure product quality, process robustness, regulatory compliance, and operational efficiency. The role supports both existing production processes and the introduction of new products and technologies. You will be working closely with dedicated and highly competent colleagues within Production, Quality Assurance, Regulatory Affairs, Supply Chain, and R&D. You will get the exciting opportunity to build, shape and optimize our processes and apply your experience and expertise to ensure the highest manufacturing standards. If this sounds interesting to you - Come join us!

This is a full-time position and based in our company location in Strömstad, Sweden. On-site in Strömstad preferred, but hybrid solutions are possible for the right candidate. We will interview candidates continuously and welcome your application today.

The Process Engineer is responsible for ensuring that manufacturing processes are robust, efficient, validated, and compliant throughout the product lifecycle. You will bridge day-to-day manufacturing support with longer-term process development and operational excellence initiatives. The position reports to the COO.

Duties and responsibilities include:

• Develop, implement, and continuously improve manufacturing processes to enhance quality, yield, and efficiency.

• Lead root cause investigations and implement corrective and preventive actions (CAPA).

• Plan, execute, and document validation activities, including Process Validation, Equipment Qualification (IQ/OQ/PQ), Cleaning Validation, and Test Method Validation/Verification.

• Provide technical support to production, investigating process deviations, non-conformities, and out-of-specification results.

• Lead continuous improvement initiatives using structured problem-solving methods such as Root Cause Analysis, FMEA, and 5 Why.

• Ensure processes comply with ISO 13485, EU MDR 2017/745, ISO 14971, and GMP principles.

• Support audits and inspections by customers, regulatory authorities, and Notified Bodies.

• Support technology transfers from R&D to production and participate in cross-functional development projects.

• Approve process validation documentation according to delegated authority and escalate process risks impacting product quality, compliance, or supply.

The suitable candidate has the following qualifications:

• Formal academic degree level (BSc. or MSc.) in chemical engineering, biotechnology, pharmaceutical science or related.

• Strong background in process engineering preferably combined with validation engineering experience.

• Experience working in a manufacturing environment within a regulated industry (e.g. Medical Devices, Pharmaceuticals, Biotechnology, or other regulated industries).

• Experience with process optimization, process validation and problem solving.

• Experience with sterile processes, equipment qualification (IQ, OQ, PQ), process validation, troubleshooting, and continuous improvement would be highly valuable.

• Experience working with Quality Management Systems.

• Knowledge of statistical analysis and process capability concepts.

• Excellent communication and documentation skills in English are required

The successful candidate for this position will be someone who:

• Has a strong technical and analytical mindset.

• Enjoys solving complex manufacturing and process-related challenges.

• Is structured and detail-oriented.

• Takes ownership and drives improvements independently.

• Communicates effectively across departments and organizational levels.

• Combines hands-on problem solving with a systematic approach.

• Thrives in a fast-paced environment where quality, compliance, and operational performance are equally important.

We offer a dynamic working environment with significant opportunity to make an impact — contributing to Bohus’s success as well as your own growth and development.

Founded in 1993, BOHUS has been at the forefront of Hyaluronic Acid (HA) development and manufacturing for over three decades. Our journey began with a vision to revolutionize the HA industry through innovation and commitment to excellence.

With more than 30 years of expertise, the company has established a strong international presence with products distributed to hospitals, clinics, and physicians in over 60 countries worldwide.

Bohus Biotech focuses exclusively on high quality hyaluronic acid technologies across three therapeutic areas:

• Ophthalmology – OVD solutions supporting tissue protection during cataract surgery

• Aesthetics – Dermal fillers based on the proprietary SHAPE™ technology platform

• Orthopaedics – Injectable treatments for osteoarthritis

All research, development, and manufacturing are located in Strömstad, Sweden, ensuring full control over product quality and innovation. For more information, visit the company's web sites at: www.bohusbiotech.com

Krishan Johansson Haque, PhD

Sr Recruitment Consultant, QRIOS Life Science & Engineering

T: +46 (0)72-070 16 53

E: krishan.johansson-haque@qrios.se

Bohus Biotech is an innovative company focused on the development and manufacture of high-quality products containing hyaluronic acid (HA). We are now in an expansive phase, investing in the products and processes of the future. We are looking for a driven Process Engineer who wants to become part of Bohus’s future and contribute to the continued development of hyaluronic acid and its products.

As our Process Engineer, you will be responsible for developing, optimizing, validating, and maintaining manufacturing processes to ensure product quality, process robustness, regulatory compliance, and operational efficiency. The role supports both existing production processes and the introduction of new products and technologies. You will be working closely with dedicated and highly competent colleagues within Production, Quality Assurance, Regulatory Affairs, Supply Chain, and R&D. You will get the exciting opportunity to build, shape and optimize our processes and apply your experience and expertise to ensure the highest manufacturing standards. If this sounds interesting to you - Come join us!

This is a full-time position and based in our company location in Strömstad, Sweden. On-site in Strömstad preferred, but hybrid solutions are possible for the right candidate. We will interview candidates continuously and welcome your application today.

The Process Engineer is responsible for ensuring that manufacturing processes are robust, efficient, validated, and compliant throughout the product lifecycle. You will bridge day-to-day manufacturing support with longer-term process development and operational excellence initiatives. The position reports to the COO.

Duties and responsibilities include:

• Develop, implement, and continuously improve manufacturing processes to enhance quality, yield, and efficiency.

• Lead root cause investigations and implement corrective and preventive actions (CAPA).

• Plan, execute, and document validation activities, including Process Validation, Equipment Qualification (IQ/OQ/PQ), Cleaning Validation, and Test Method Validation/Verification.

• Provide technical support to production, investigating process deviations, non-conformities, and out-of-specification results.

• Lead continuous improvement initiatives using structured problem-solving methods such as Root Cause Analysis, FMEA, and 5 Why.

• Ensure processes comply with ISO 13485, EU MDR 2017/745, ISO 14971, and GMP principles.

• Support audits and inspections by customers, regulatory authorities, and Notified Bodies.

• Support technology transfers from R&D to production and participate in cross-functional development projects.

• Approve process validation documentation according to delegated authority and escalate process risks impacting product quality, compliance, or supply.

The suitable candidate has the following qualifications:

• Formal academic degree level (BSc. or MSc.) in chemical engineering, biotechnology, pharmaceutical science or related.

• Strong background in process engineering preferably combined with validation engineering experience.

• Experience working in a manufacturing environment within a regulated industry (e.g. Medical Devices, Pharmaceuticals, Biotechnology, or other regulated industries).

• Experience with process optimization, process validation and problem solving.

• Experience with sterile processes, equipment qualification (IQ, OQ, PQ), process validation, troubleshooting, and continuous improvement would be highly valuable.

• Experience working with Quality Management Systems.

• Knowledge of statistical analysis and process capability concepts.

• Excellent communication and documentation skills in English are required

The successful candidate for this position will be someone who:

• Has a strong technical and analytical mindset.

• Enjoys solving complex manufacturing and process-related challenges.

• Is structured and detail-oriented.

• Takes ownership and drives improvements independently.

• Communicates effectively across departments and organizational levels.

• Combines hands-on problem solving with a systematic approach.

• Thrives in a fast-paced environment where quality, compliance, and operational performance are equally important.

We offer a dynamic working environment with significant opportunity to make an impact — contributing to Bohus’s success as well as your own growth and development.

Founded in 1993, BOHUS has been at the forefront of Hyaluronic Acid (HA) development and manufacturing for over three decades. Our journey began with a vision to revolutionize the HA industry through innovation and commitment to excellence.

With more than 30 years of expertise, the company has established a strong international presence with products distributed to hospitals, clinics, and physicians in over 60 countries worldwide.

Bohus Biotech focuses exclusively on high quality hyaluronic acid technologies across three therapeutic areas:

• Ophthalmology – OVD solutions supporting tissue protection during cataract surgery

• Aesthetics – Dermal fillers based on the proprietary SHAPE™ technology platform

• Orthopaedics – Injectable treatments for osteoarthritis

All research, development, and manufacturing are located in Strömstad, Sweden, ensuring full control over product quality and innovation. For more information, visit the company's web sites at: www.bohusbiotech.com

Krishan Johansson Haque, PhD

Sr Recruitment Consultant, QRIOS Life Science & Engineering

T: +46 (0)72-070 16 53

E: krishan.johansson-haque@qrios.se

Bohus Biotech is an innovative company focused on the development and manufacture of high-quality products containing hyaluronic acid (HA). We are now in an expansive phase, investing in the products and processes of the future. We are looking for a driven Process Engineer who wants to become part of Bohus’s future and contribute to the continued development of hyaluronic acid and its products.

As our Process Engineer, you will be responsible for developing, optimizing, validating, and maintaining manufacturing processes to ensure product quality, process robustness, regulatory compliance, and operational efficiency. The role supports both existing production processes and the introduction of new products and technologies. You will be working closely with dedicated and highly competent colleagues within Production, Quality Assurance, Regulatory Affairs, Supply Chain, and R&D. You will get the exciting opportunity to build, shape and optimize our processes and apply your experience and expertise to ensure the highest manufacturing standards. If this sounds interesting to you - Come join us!

This is a full-time position and based in our company location in Strömstad, Sweden. On-site in Strömstad preferred, but hybrid solutions are possible for the right candidate. We will interview candidates continuously and welcome your application today.

The Process Engineer is responsible for ensuring that manufacturing processes are robust, efficient, validated, and compliant throughout the product lifecycle. You will bridge day-to-day manufacturing support with longer-term process development and operational excellence initiatives. The position reports to the COO.

Duties and responsibilities include:

• Develop, implement, and continuously improve manufacturing processes to enhance quality, yield, and efficiency.

• Lead root cause investigations and implement corrective and preventive actions (CAPA).

• Plan, execute, and document validation activities, including Process Validation, Equipment Qualification (IQ/OQ/PQ), Cleaning Validation, and Test Method Validation/Verification.

• Provide technical support to production, investigating process deviations, non-conformities, and out-of-specification results.

• Lead continuous improvement initiatives using structured problem-solving methods such as Root Cause Analysis, FMEA, and 5 Why.

• Ensure processes comply with ISO 13485, EU MDR 2017/745, ISO 14971, and GMP principles.

• Support audits and inspections by customers, regulatory authorities, and Notified Bodies.

• Support technology transfers from R&D to production and participate in cross-functional development projects.

• Approve process validation documentation according to delegated authority and escalate process risks impacting product quality, compliance, or supply.

The suitable candidate has the following qualifications:

• Formal academic degree level (BSc. or MSc.) in chemical engineering, biotechnology, pharmaceutical science or related.

• Strong background in process engineering preferably combined with validation engineering experience.

• Experience working in a manufacturing environment within a regulated industry (e.g. Medical Devices, Pharmaceuticals, Biotechnology, or other regulated industries).

• Experience with process optimization, process validation and problem solving.

• Experience with sterile processes, equipment qualification (IQ, OQ, PQ), process validation, troubleshooting, and continuous improvement would be highly valuable.

• Experience working with Quality Management Systems.

• Knowledge of statistical analysis and process capability concepts.

• Excellent communication and documentation skills in English are required

The successful candidate for this position will be someone who:

• Has a strong technical and analytical mindset.

• Enjoys solving complex manufacturing and process-related challenges.

• Is structured and detail-oriented.

• Takes ownership and drives improvements independently.

• Communicates effectively across departments and organizational levels.

• Combines hands-on problem solving with a systematic approach.

• Thrives in a fast-paced environment where quality, compliance, and operational performance are equally important.

We offer a dynamic working environment with significant opportunity to make an impact — contributing to Bohus’s success as well as your own growth and development.

Founded in 1993, BOHUS has been at the forefront of Hyaluronic Acid (HA) development and manufacturing for over three decades. Our journey began with a vision to revolutionize the HA industry through innovation and commitment to excellence.

With more than 30 years of expertise, the company has established a strong international presence with products distributed to hospitals, clinics, and physicians in over 60 countries worldwide.

Bohus Biotech focuses exclusively on high quality hyaluronic acid technologies across three therapeutic areas:

• Ophthalmology – OVD solutions supporting tissue protection during cataract surgery

• Aesthetics – Dermal fillers based on the proprietary SHAPE™ technology platform

• Orthopaedics – Injectable treatments for osteoarthritis

All research, development, and manufacturing are located in Strömstad, Sweden, ensuring full control over product quality and innovation. For more information, visit the company's web sites at: www.bohusbiotech.com

Krishan Johansson Haque, PhD

Sr Recruitment Consultant, QRIOS Life Science & Engineering

T: +46 (0)72-070 16 53

E: krishan.johansson-haque@qrios.se

Bohus Biotech is an innovative company focused on the development and manufacture of high-quality products containing hyaluronic acid (HA). We are now in an expansive phase, investing in the products and processes of the future. We are looking for a driven Process Engineer who wants to become part of Bohus’s future and contribute to the continued development of hyaluronic acid and its products.

As our Process Engineer, you will be responsible for developing, optimizing, validating, and maintaining manufacturing processes to ensure product quality, process robustness, regulatory compliance, and operational efficiency. The role supports both existing production processes and the introduction of new products and technologies. You will be working closely with dedicated and highly competent colleagues within Production, Quality Assurance, Regulatory Affairs, Supply Chain, and R&D. You will get the exciting opportunity to build, shape and optimize our processes and apply your experience and expertise to ensure the highest manufacturing standards. If this sounds interesting to you - Come join us!

This is a full-time position and based in our company location in Strömstad, Sweden. On-site in Strömstad preferred, but hybrid solutions are possible for the right candidate. We will interview candidates continuously and welcome your application today.

The Process Engineer is responsible for ensuring that manufacturing processes are robust, efficient, validated, and compliant throughout the product lifecycle. You will bridge day-to-day manufacturing support with longer-term process development and operational excellence initiatives. The position reports to the COO.

Duties and responsibilities include:

• Develop, implement, and continuously improve manufacturing processes to enhance quality, yield, and efficiency.

• Lead root cause investigations and implement corrective and preventive actions (CAPA).

• Plan, execute, and document validation activities, including Process Validation, Equipment Qualification (IQ/OQ/PQ), Cleaning Validation, and Test Method Validation/Verification.

• Provide technical support to production, investigating process deviations, non-conformities, and out-of-specification results.

• Lead continuous improvement initiatives using structured problem-solving methods such as Root Cause Analysis, FMEA, and 5 Why.

• Ensure processes comply with ISO 13485, EU MDR 2017/745, ISO 14971, and GMP principles.

• Support audits and inspections by customers, regulatory authorities, and Notified Bodies.

• Support technology transfers from R&D to production and participate in cross-functional development projects.

• Approve process validation documentation according to delegated authority and escalate process risks impacting product quality, compliance, or supply.

The suitable candidate has the following qualifications:

• Formal academic degree level (BSc. or MSc.) in chemical engineering, biotechnology, pharmaceutical science or related.

• Strong background in process engineering preferably combined with validation engineering experience.

• Experience working in a manufacturing environment within a regulated industry (e.g. Medical Devices, Pharmaceuticals, Biotechnology, or other regulated industries).

• Experience with process optimization, process validation and problem solving.

• Experience with sterile processes, equipment qualification (IQ, OQ, PQ), process validation, troubleshooting, and continuous improvement would be highly valuable.

• Experience working with Quality Management Systems.

• Knowledge of statistical analysis and process capability concepts.

• Excellent communication and documentation skills in English are required

The successful candidate for this position will be someone who:

• Has a strong technical and analytical mindset.

• Enjoys solving complex manufacturing and process-related challenges.

• Is structured and detail-oriented.

• Takes ownership and drives improvements independently.

• Communicates effectively across departments and organizational levels.

• Combines hands-on problem solving with a systematic approach.

• Thrives in a fast-paced environment where quality, compliance, and operational performance are equally important.

We offer a dynamic working environment with significant opportunity to make an impact — contributing to Bohus’s success as well as your own growth and development.

Founded in 1993, BOHUS has been at the forefront of Hyaluronic Acid (HA) development and manufacturing for over three decades. Our journey began with a vision to revolutionize the HA industry through innovation and commitment to excellence.

With more than 30 years of expertise, the company has established a strong international presence with products distributed to hospitals, clinics, and physicians in over 60 countries worldwide.

Bohus Biotech focuses exclusively on high quality hyaluronic acid technologies across three therapeutic areas:

• Ophthalmology – OVD solutions supporting tissue protection during cataract surgery

• Aesthetics – Dermal fillers based on the proprietary SHAPE™ technology platform

• Orthopaedics – Injectable treatments for osteoarthritis

All research, development, and manufacturing are located in Strömstad, Sweden, ensuring full control over product quality and innovation. For more information, visit the company's web sites at: www.bohusbiotech.com

Krishan Johansson Haque, PhD

Sr Recruitment Consultant, QRIOS Life Science & Engineering

T: +46 (0)72-070 16 53

E: krishan.johansson-haque@qrios.se

Bohus Biotech is an innovative company focused on the development and manufacture of high-quality products containing hyaluronic acid (HA). We are now in an expansive phase, investing in the products and processes of the future. We are looking for a driven Process Engineer who wants to become part of Bohus’s future and contribute to the continued development of hyaluronic acid and its products.

As our Process Engineer, you will be responsible for developing, optimizing, validating, and maintaining manufacturing processes to ensure product quality, process robustness, regulatory compliance, and operational efficiency. The role supports both existing production processes and the introduction of new products and technologies. You will be working closely with dedicated and highly competent colleagues within Production, Quality Assurance, Regulatory Affairs, Supply Chain, and R&D. You will get the exciting opportunity to build, shape and optimize our processes and apply your experience and expertise to ensure the highest manufacturing standards. If this sounds interesting to you - Come join us!

This is a full-time position and based in our company location in Strömstad, Sweden. On-site in Strömstad preferred, but hybrid solutions are possible for the right candidate. We will interview candidates continuously and welcome your application today.

The Process Engineer is responsible for ensuring that manufacturing processes are robust, efficient, validated, and compliant throughout the product lifecycle. You will bridge day-to-day manufacturing support with longer-term process development and operational excellence initiatives. The position reports to the COO.

Duties and responsibilities include:

• Develop, implement, and continuously improve manufacturing processes to enhance quality, yield, and efficiency.

• Lead root cause investigations and implement corrective and preventive actions (CAPA).

• Plan, execute, and document validation activities, including Process Validation, Equipment Qualification (IQ/OQ/PQ), Cleaning Validation, and Test Method Validation/Verification.

• Provide technical support to production, investigating process deviations, non-conformities, and out-of-specification results.

• Lead continuous improvement initiatives using structured problem-solving methods such as Root Cause Analysis, FMEA, and 5 Why.

• Ensure processes comply with ISO 13485, EU MDR 2017/745, ISO 14971, and GMP principles.

• Support audits and inspections by customers, regulatory authorities, and Notified Bodies.

• Support technology transfers from R&D to production and participate in cross-functional development projects.

• Approve process validation documentation according to delegated authority and escalate process risks impacting product quality, compliance, or supply.

The suitable candidate has the following qualifications:

• Formal academic degree level (BSc. or MSc.) in chemical engineering, biotechnology, pharmaceutical science or related.

• Strong background in process engineering preferably combined with validation engineering experience.

• Experience working in a manufacturing environment within a regulated industry (e.g. Medical Devices, Pharmaceuticals, Biotechnology, or other regulated industries).

• Experience with process optimization, process validation and problem solving.

• Experience with sterile processes, equipment qualification (IQ, OQ, PQ), process validation, troubleshooting, and continuous improvement would be highly valuable.

• Experience working with Quality Management Systems.

• Knowledge of statistical analysis and process capability concepts.

• Excellent communication and documentation skills in English are required

The successful candidate for this position will be someone who:

• Has a strong technical and analytical mindset.

• Enjoys solving complex manufacturing and process-related challenges.

• Is structured and detail-oriented.

• Takes ownership and drives improvements independently.

• Communicates effectively across departments and organizational levels.

• Combines hands-on problem solving with a systematic approach.

• Thrives in a fast-paced environment where quality, compliance, and operational performance are equally important.

We offer a dynamic working environment with significant opportunity to make an impact — contributing to Bohus’s success as well as your own growth and development.

Founded in 1993, BOHUS has been at the forefront of Hyaluronic Acid (HA) development and manufacturing for over three decades. Our journey began with a vision to revolutionize the HA industry through innovation and commitment to excellence.

With more than 30 years of expertise, the company has established a strong international presence with products distributed to hospitals, clinics, and physicians in over 60 countries worldwide.

Bohus Biotech focuses exclusively on high quality hyaluronic acid technologies across three therapeutic areas:

• Ophthalmology – OVD solutions supporting tissue protection during cataract surgery

• Aesthetics – Dermal fillers based on the proprietary SHAPE™ technology platform

• Orthopaedics – Injectable treatments for osteoarthritis

All research, development, and manufacturing are located in Strömstad, Sweden, ensuring full control over product quality and innovation. For more information, visit the company's web sites at: www.bohusbiotech.com

Krishan Johansson Haque, PhD

Sr Recruitment Consultant, QRIOS Life Science & Engineering

T: +46 (0)72-070 16 53

E: krishan.johansson-haque@qrios.se

Bohus Biotech is an innovative company focused on the development and manufacture of high-quality products containing hyaluronic acid (HA). We are now in an expansive phase, investing in the products and processes of the future. We are looking for a driven Process Engineer who wants to become part of Bohus’s future and contribute to the continued development of hyaluronic acid and its products.

As our Process Engineer, you will be responsible for developing, optimizing, validating, and maintaining manufacturing processes to ensure product quality, process robustness, regulatory compliance, and operational efficiency. The role supports both existing production processes and the introduction of new products and technologies. You will be working closely with dedicated and highly competent colleagues within Production, Quality Assurance, Regulatory Affairs, Supply Chain, and R&D. You will get the exciting opportunity to build, shape and optimize our processes and apply your experience and expertise to ensure the highest manufacturing standards. If this sounds interesting to you - Come join us!

This is a full-time position and based in our company location in Strömstad, Sweden. On-site in Strömstad preferred, but hybrid solutions are possible for the right candidate. We will interview candidates continuously and welcome your application today.

The Process Engineer is responsible for ensuring that manufacturing processes are robust, efficient, validated, and compliant throughout the product lifecycle. You will bridge day-to-day manufacturing support with longer-term process development and operational excellence initiatives. The position reports to the COO.

Duties and responsibilities include:

• Develop, implement, and continuously improve manufacturing processes to enhance quality, yield, and efficiency.

• Lead root cause investigations and implement corrective and preventive actions (CAPA).

• Plan, execute, and document validation activities, including Process Validation, Equipment Qualification (IQ/OQ/PQ), Cleaning Validation, and Test Method Validation/Verification.

• Provide technical support to production, investigating process deviations, non-conformities, and out-of-specification results.

• Lead continuous improvement initiatives using structured problem-solving methods such as Root Cause Analysis, FMEA, and 5 Why.

• Ensure processes comply with ISO 13485, EU MDR 2017/745, ISO 14971, and GMP principles.

• Support audits and inspections by customers, regulatory authorities, and Notified Bodies.

• Support technology transfers from R&D to production and participate in cross-functional development projects.

• Approve process validation documentation according to delegated authority and escalate process risks impacting product quality, compliance, or supply.

The suitable candidate has the following qualifications:

• Formal academic degree level (BSc. or MSc.) in chemical engineering, biotechnology, pharmaceutical science or related.

• Strong background in process engineering preferably combined with validation engineering experience.

• Experience working in a manufacturing environment within a regulated industry (e.g. Medical Devices, Pharmaceuticals, Biotechnology, or other regulated industries).

• Experience with process optimization, process validation and problem solving.

• Experience with sterile processes, equipment qualification (IQ, OQ, PQ), process validation, troubleshooting, and continuous improvement would be highly valuable.

• Experience working with Quality Management Systems.

• Knowledge of statistical analysis and process capability concepts.

• Excellent communication and documentation skills in English are required

The successful candidate for this position will be someone who:

• Has a strong technical and analytical mindset.

• Enjoys solving complex manufacturing and process-related challenges.

• Is structured and detail-oriented.

• Takes ownership and drives improvements independently.

• Communicates effectively across departments and organizational levels.

• Combines hands-on problem solving with a systematic approach.

• Thrives in a fast-paced environment where quality, compliance, and operational performance are equally important.

We offer a dynamic working environment with significant opportunity to make an impact — contributing to Bohus’s success as well as your own growth and development.

Founded in 1993, BOHUS has been at the forefront of Hyaluronic Acid (HA) development and manufacturing for over three decades. Our journey began with a vision to revolutionize the HA industry through innovation and commitment to excellence.

With more than 30 years of expertise, the company has established a strong international presence with products distributed to hospitals, clinics, and physicians in over 60 countries worldwide.

Bohus Biotech focuses exclusively on high quality hyaluronic acid technologies across three therapeutic areas:

• Ophthalmology – OVD solutions supporting tissue protection during cataract surgery

• Aesthetics – Dermal fillers based on the proprietary SHAPE™ technology platform

• Orthopaedics – Injectable treatments for osteoarthritis

All research, development, and manufacturing are located in Strömstad, Sweden, ensuring full control over product quality and innovation. For more information, visit the company's web sites at: www.bohusbiotech.com

Krishan Johansson Haque, PhD

Sr Recruitment Consultant, QRIOS Life Science & Engineering

T: +46 (0)72-070 16 53

E: krishan.johansson-haque@qrios.se

Processingenjör med erfarenhet av HAZOP & ATEX – Stockholm/Uppsala

För kunds räkning söker Selectus Bemanning en erfaren Processingenjör till en långsiktig heltidstjänst i Stockholm eller Uppsala.

Vi söker dig som har erfarenhet av processindustri, riskanalyser och säkerhetsarbete kopplat till HAZOP och ATEX.

Om rollen

Som Processingenjör kommer du att arbeta med processutveckling, tekniska utredningar, riskbedömningar och säkerställande av säkra och effektiva processer. Du kommer att samarbeta med projektledare, produktion och tekniska specialister i både pågående projekt och utvecklingsinitiativ.

Vad är HAZOP och ATEX?

HAZOP (Hazard and Operability Study) är en strukturerad metod för att identifiera och hantera risker i processanläggningar.

ATEX omfattar regler och säkerhetskrav för arbete i explosionsfarliga miljöer där gaser, damm eller andra brandfarliga ämnen förekommer.

Vi söker dig som har:

Minst 3–5 års erfarenhet som Processingenjör eller liknande teknisk roll.

Erfarenhet av HAZOP-analyser och/eller ATEX-klassning.

Ingenjörsutbildning från yrkeshögskola, högskola eller universitet inom exempelvis process-, kemi-, maskin- eller energiteknik.

God teknisk förståelse och erfarenhet från industriella processer.

Goda kunskaper i svenska och/eller engelska.

Vi erbjuder

Heltidstjänst.

Långsiktigt uppdrag med goda utvecklingsmöjligheter.

Placering i Stockholm eller Uppsala.

Möjlighet att arbeta i tekniskt avancerade projekt med fokus på säkerhet och kvalitet.

Urval sker löpande, så skicka in din ansökan redan idag.