Processingenjör - Lediga jobb

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.

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.

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.

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.

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.

Vi söker en engagerad och nyfiken processingenjör för ett konsultuppdrag via Lernia i Uppsala. Tjänsten passar dig som vill arbeta med processutveckling, förbättringsarbete och teknisk support i produktions- och utvecklingsmiljöer samt trivs i en miljö där både självständigt arbete och tvärfunktionellt samarbete är centralt.

Tjänsten är ett konsultuppdrag via Lernia. Uppdraget är på heltid med möjlighet till förlängning för rätt person.

Om tjänsten

Som processingenjör kommer du att arbeta med utveckling, optimering och dokumentation av produktionsprocesser. Du deltar i projekt som syftar till att förbättra kapacitet, kvalitet och kostnadseffektivitet samt minska variation och slöseri. Du samarbetar nära produktion, kvalitet, underhåll och produktutveckling för att säkerställa robusta och skalbara processlösningar.

Dina huvudsakliga arbetsuppgifter inkluderar:

• Analys och förbättring av befintliga processer med hjälp av metodik som Lean och Six Sigma

• Utveckling av arbetsinstruktioner, processflöden och styrdokument

• Genomförande av provkörningar, valideringar och processförändringar i pilot- och produktionsmiljö

• Planering och uppföljning av processtester samt analys av mätdata för att identifiera förbättringspotential

• Samarbete med leverantörer och interna team för att säkerställa komponentval och tillverkningsmetoder

• Stöd vid felsökning och avvikelsehantering samt initiering av korrigerande åtgärder

• Delta i projektplanering, riskbedömningar och kontinuerligt förbättringsarbete

Om dig

Formell kompetens

• Teknisk högskoleutbildning eller motsvarande erfarenhet inom relevant område (t.ex. maskinteknik, processteknik, mekatronik eller industriell ekonomi)

• Flera års erfarenhet av processutveckling, produktionsteknik eller liknande roller

• God vana vid att arbeta med processteg, mätmetoder och statistisk analys

• Erfarenhet av att ta fram och uppdatera arbetsinstruktioner, processdokumentation och valideringsunderlag

• God kommunikativ förmåga i svenska och engelska i tal och skrift

Meriterande

Det är meriterande om du har erfarenhet av:

• Arbete med Lean, Six Sigma eller liknande förbättringsmetodik

• Projektarbete i produktionsnära utvecklingsprojekt eller industrimiljö

• Arbete med automation, styrsystem eller inbyggda system

• Erfarenhet av kvalitetsstandarder och regelverk inom relevant bransch

• PAS-X

Som person är du strukturerad, analytisk och problemlösningsorienterad. Du arbetar proaktivt, trivs i team och kan kommunicera teknisk information tydligt med både tekniska och icke-tekniska intressenter. Du har en praktisk inställning och driv att driva förbättringsprojekt från idé till implementering.

Anställningsvillkor

• Anställningsform: Uppdrag via Lernia, start enligt överenskommelse

• Omfattning: Heltid

• Arbetstid: Dagtid

• Placeringsort: Uppsala

• Lön: Enligt överenskommelse

Om Lernia

Lernia är ett av Sveriges ledande bemannings- och rekryteringsföretag. Vi arbetar nära våra kunder för att hitta rätt kompetens och erbjuder våra konsulter marknadsmässig lön, semester, pensionsavsättning, försäkringar och tillgång till företagshälsovård. Som konsult hos oss får du en konsultchef som stöttar din utveckling och arbetsmiljö under uppdraget.

Hur du söker tjänsten

För att söka tjänsten, scrolla ner till ansökningsformuläret nedan och skicka in din ansökan. Urval och intervjuer sker löpande, så skicka in din ansökan redan idag. Vid frågor om tjänsten, hör av dig till bemanning.uppsala@lernia.se

Bakgrundskontroll

I vissa uppdrag ingår bakgrundskontroll som en del av rekryteringsprocessen. Om du går vidare i processen kommer du behöva verifiera din identitet via BankID innan kontrollen genomförs.

Som en av oss

Som anställd bemanningskonsult hos oss får du alltid en marknadsmässig lön, semester, pensionsavsättning, försäkringar och anslutning till vårt kollektivavtal. Vi vill att du ska må bra hos oss så självklart erbjuder vi våra konsulter friskvårdsbidrag och företagshälsovård. Under din anställning har du en konsultchef som är ansvarig för ditt uppdrag, stöttar dig och bidrar till din utveckling i yrkesrollen.