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 [email protected] 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.

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. Key responsibilities 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. Skills and Competencies 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. About Bohus Biotech 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 For more information about this position, please contact: Krishan Johansson Haque, PhD Sr Recruitment Consultant, QRIOS Life Science & Engineering T: +46 (0)72-070 16 53 E: [email protected]

Därför är detta jobb för dig Här blir du en del av regionens främsta Life Science-konsulter och ett bolag med lång erfarenhet inom branschen. Vi bidrar tillsammans med våra kunder till att förbättra människans liv och livskvalitet genom att bland annat utveckla produktion, kvalitet och projektverksamhet. Här sätts du och din utveckling i fokus, du kommer ha en kontinuerlig dialog med din närmsta ledare om dina utvecklingsmöjligheter framåt för att forma en plan som passar dig och dina ambitioner. Därtill blir du en del av ett team med kunniga kollegor som både har roligt tillsammans och hjälper varandra i uppdrag och projekt. Kontorets placering i Uppsala Business Park ger oss även närhet till intressanta dialoger och föredrag med andra kunder samt tillgång till flertalet aktiviteter som anordnas. Du blir en del av vårt affärsområde inom Compliance & Management där vi stöttar en effektiv omställning till digitala, hållbara och säkra lösningar genom expertkunskap inom exempelvis kvalitet, säkerhet, hållbarhet och projektstyrning. Arbetsuppgifter Hos oss finns möjligheter till varierande och utvecklande uppdrag hos våra kunder inom Life Science. Vår bredd av kunder gör att vi utifrån dina erfarenheter, egenskaper och ambitioner hittar ett uppdrag där du trivs och din expertis kommer tillrätta. Du kommer exempelvis arbeta inom något av följande områden: validering/kvalificering QA QA IT/datoriserade system projektledning processteknik produktionsutveckling Kvalifikationer Vi söker dig som har en förmåga att arbeta förbättringsorienterat och som är lösningsfokuserad. Du trivs också med att dela erfarenheter och kunskap med kollegor. Utöver dina personliga egenskaper vill vi att du har: Dokumenterad erfarenhet av arbete inom läkemedelsindustrin eller den medicintekniska branschen inom ex. validering, processteknik eller QA Vana av att jobba enligt GMP utbildning inom exempelvis bioteknik, kemiteknik, maskinteknik, medicinteknik eller motsvarande Du har flytande kunskaper i svenska och engelska, i tal och skrift En spännande resa med Knightec Group Knightec Group är idag en av Norra Europas ledande strategiska partners inom produkt- och digital tjänsteutveckling – hur häftigt är inte det? Genom att förena ingenjörskompetens, digital expertis och affärsförståelse hjälper vi våra kunder att omvandla ny teknik till verkliga lösningar som skapar värde. Vi arbetar i skärningspunkten mellan affärsstrategi och teknikutveckling och stöttar våra kunder genom hela resan – från de första idéerna till utveckling, implementering och vidare utveckling. På Knightec Group samlas människor med olika perspektiv, erfarenheter och specialistområden. Tillsammans skapar vi innovation som gör verklig skillnad – för företag, människor och samhället i stort. För våra medarbetare innebär det stora möjligheter att vara med och forma framtidens lösningar genom meningsfulla projekt i teknikens absoluta framkant. Här får du inte bara utvecklas och växa i din roll – du blir också en del av ett team där nyfikenhet, samarbete och modet att utmana driver oss framåt. Låter det som platsen för dig? Häng med på vår fortsatta resa! Praktisk information Detta är en tillsvidareanställning med en provanställning på sex månader, placerad på vårt kontor på Dragarbrunnsgaten 45 i Uppsala. Resor i tjänsten kan förekomma till våra kunder. Startdatum är enligt överenskommelse. Skicka in din ansökan så snart som möjligt, men senast 2026-08-23. Om du har några frågor om tjänsten är du välkommen att kontakta Kicki Björ, Talent Acquisition Specialist. Vi hanterar alla ansökningar via vår karriärsida för att säkerställa en trygg och säker hantering av dina personuppgifter i enlighet med GDPR. Vi ser fram emot att höra från dig!

At Nouryon, our global team takes positive action every day, to reach higher collectively and individually. We create innovative and sustainable solutions for our customers to answer society’s needs – today and in the future. We are looking for a Process Analytics Engineer who combines chemical process expertise with a passion for data and digital tools to drive operational excellence at our manufacturing sites. Does that sound like you? Join the Digital Manufacturing team dedicated to making Nouryon’s manufacturing sites smarter, safer, and more efficient. As our new Process Analytics Engineer, you will work at the intersection of process engineering and data analytics – using digital tools to uncover improvement opportunities, optimize process control, and build lasting capabilities across our sites. You will collaborate closely with site engineers, science & technology teams, and other regional functions to turn data into real operational impact. In your future role as Process Analytics Engineer you will Conduct digital data mining to collect, interpret, and report process-related improvement opportunities at our manufacturing sites Review and optimize the process control layer using available digital tools, combined with your practical and theoretical process knowledge Connect and collaborate with focus sites and other Digital Manufacturing teams within Nouryon to drive the Digital Manufacturing roadmap Share knowledge and build digital, analytical, and process control capabilities – both within the regional team and at site level Contribute as a domain expert in cross-functional improvement projects, including stakeholder management We believe you bring A degree at academic level in Chemical Engineering or a related field Experience from the process industry – experience in process control or plant optimization is a strong plus Strong computer and analytical skills, with a data-savvy mindset and comfort using modern digital and AI-supported tools Excellent communication skills in English, both verbal and written A proven ability to collaborate across functions and manage stakeholders at different levels of the organization Great if you have: Hands-on experience with process data systems, DCS/SCADA, or advanced process control tools Experience leading or participating in process improvement or digitalization projects Familiarity with data analysis tools or programming languages (e.g. Python), and experience working with AI tools such as Claude or Claude Code We believe you are... Someone who takes a helicopter view of complex manufacturing environments and uses data and facts to identify where the biggest improvements can be made. You have a natural ability to communicate and to bring people along with you – whether you are presenting an idea to site management or collaborating with hands-on process engineers. You are curious, self-driven, and embrace change. You thrive in a cross-functional environment where no two days look the same. We offer you At Nouryon, we provide a great job and friendly coworkers, plus benefits in addition to salary. Our collective agreement is with IKEM. Plus, we offer unilateral perks, such as bonus, reduced hours, health care allowance, lunch allowance, and more. You will be part of a dynamic Digital Manufacturing team working with some of the most exciting digital transformation challenges in the specialty chemicals industry. This is a role where you can genuinely see the impact of your work – at site level every day, and at company level over time. Have we got your interest? This is a permanent position on a full-time basis, reporting to the Manager Process Analytics, and based at one of our ISC manufacturing sites in Sweden. Please apply via our online recruitment system. We will not accept applications via e-mail. Once it’s with us we will review to see if we have a match between your skills and the role! For more information about our hiring process, visit: nouryon.com/careers/how-we-hire/ As an applicant, you may be subject to a background check before employment, depending on the requirements of the role. You will receive more information about this later in the recruitment process. We work actively and systematically with HSE matters to ensure a safe and sustainable working environment for our employees. As an employee, you may therefore be required to undergo drug testing on a random basis. This is part of our commitment to safeguarding the safety and well-being of our staff. We look forward to receiving your application! We kindly ask our internal candidates to apply with your Nouryon email via Success Factors. About Nouryon Explore careers and life at Nouryon If you’re looking for your next career move, apply today and join Nouryon’s worldwide team in providing essential solutions that our customers use to manufacture everyday products such as personal care, cleaning, paints and coatings, agriculture and food, pharmaceuticals, and building products. Our employees are driven by the wish to make an impact and actively drive positive change. If that describes you, we will gladly make way for your ambitions. From day one we support you with your personal growth, through challenging positions and comprehensive learning and development opportunities, in a dynamic, international, diverse, and proactive working environment. Visit our website and follow us on LinkedIn. Contact If you have any questions about the recruitment process or your application or need assistance, please contact: [email protected] For union-related inquiries: Akademikerklubben: Katarina Risö – [email protected] Unionen: Helene Rosenlund –[email protected] Ledarna: Sanna Backman – [email protected] #WeAreNouryon #GrowWithUs We have already chosen our sourcing channels for this recruitment and kindly ask not to be contacted by any advertisement agents, recruitment agencies or staffing companies.

Camurus is an international, science-led biopharmaceutical company committed to developing and commercializing innovative, long-acting medicines for improving the lives of patients with severe and chronic diseases. New drug products with best-in-class potential are conceived based on the company’s proprietary FluidCrystal® technology and its extensive R&D expertise. The R&D pipeline includes products for the treatment of dependence, pain, cancer, and endocrine diseases. Camurus has operations across Europe, the US, and Australia, with headquarters in Lund Sweden. The company’s shares are listed on Nasdaq Stockholm under the ticker CAMX. For more information, visit www.camurus.com and LinkedIn. In this role, you will get the opportunity to work with committed colleagues in a collaborative team, close to both commercialised products and development projects. Camurus is a rapidly growing and innovative company, and you will have a strong impact on the outsourced manufacturing processes throughout the product lifecycle. We are looking for an experienced Senior Process Engineer to join our Manufacturing Operations team. In this role, you will be responsible for leading technology transfer activities for manufacturing processes for injectable pharmaceutical products, from development into manufacturing environments at Contract Manufacturing Organizations (CMOs). You will support products from clinical development through to commercial supply. As Senior Process Engineer, you will act as a subject matter expert in pharmaceutical manufacturing processes, working closely with internal stakeholders and external partners to ensure robust, scalable, and GMP-compliant manufacturing operations. You will report to the Director Manufacturing Operations. Main responsibility Among others, your responsibilities will include: · Lead technology transfers of injectable pharmaceutical products from development into commercial manufacturing at CMOs. · Partner with R&D to ensure that formulation and process development activities support successful scale-up, manufacturability, and long-term process robustness. · Provide technical support for process development, scale-up, validation, and commercial manufacturing activities at CMOs. · Act as technical lead for investigations and troubleshooting of process deviations, OOS results, manufacturing failures, and other complex technical challenges. · Contribute to CMC documentation in support of global regulatory submissions and product lifecycle management. · Ensure that manufacturing processes are executed in accordance with applicable GMP requirements and regulatory expectations. Candidate profile We are looking for a professional with at least 7 years of experience from pharmaceutical manufacturing operations. You hold a Master’s degree in Engineering, Life Sciences, or a related scientific discipline. You have hands-on experience from manufacturing process development, technology transfer, and GMP-regulated pharmaceutical manufacturing, preferably within sterile or injectable products. Experience from fill-finish operations and combination products development is considered a strong merit. As a person, you are collaborative, responsible, and driven by solving problems. You enjoy getting to the bottom of complex technical challenges and you are a pragmatic team player who takes ownership and follows through on commitments. At the same time, you are humble and low-prestige, always willing to support colleagues and contribute wherever needed. You thrive in a dynamic environment where technical expertise, collaboration, and problem-solving go hand in hand. Fluency in spoken and written English is required. Camurus offers This a great opportunity to join a highly dynamic company during a very exciting phase of growth. Camurus has been very successful in bringing pharmaceutical products to the market – and the ambitions are not to be lowered. With a diversified project portfolio in different stages, the commercial potential is considerable. The position offers an international work environment and corporate culture, with the possibility for individual development and growth. You will have great opportunities to influence, and you will work together with highly competent colleagues, caring for each other. Camurus has almost 300 employees with the head office located in Lund. The corporate culture is driven by our core values of innovation, collaboration, ownership, quality, and passion for realizing our patient-centric commitment. Information and application For more information about this job-opening, please contact recruitment consultant Tobias Lorentzon at TOBLOR Consulting, phone: +46 735 11 10 60. You apply for this position through TOBLOR’s career site, https://career.toblor.se/, by uploading your CV and personal letter. For more information about Camurus, please visit: https://www.camurus.com/. We are looking forward to seeing your application!

Mpya Sci & Tech was created by and for people who love technology and science. We’re not here to do what everyone else is doing. We believe that real talent lies in individuals who dare to keep growing throughout their entire lives. With extensive experience and deep industry knowledge, we’ve built a forward-leaning and cutting-edge company—our way. At Mpya Sci & Tech, we believe in a sustainable working life where we build a culture together based on genuine involvement, eager curiosity, and the freedom to be yourself. Learn more at: www.mpyascitech.com . Har du erfarenhet från läkemedels- eller medicinteknisk industri och funderar på konsultrollen? Eller är du redan konsult och vill jobba på ett bolag med stark kultur som värdesätter sina konsulter? Mpya Sci & Tech är specialiserade inom Life Science och erbjuder konsultuppdrag hos etablerade bolag i Mälardalen. Vi är ett tajt bolag där du aldrig är ett nummer – hos oss känner alla varandra och vi hjälps åt. Om rollen Som konsult hos oss arbetar du ute hos våra kunder i uppdrag där kvalitet och regelefterlevnad är centrala. Du blir en del av vårt konsultteam samtidigt som du är en del av kundens verksamhet – och vi finns alltid med som ett stöd genom hela uppdraget. Utifrån din erfarenhet och ditt intresse matchas du mot uppdrag inom till exempel: Validering och kvalificering – process, utrustning och datoriserade system (IQ/OQ/PQ, CSV) samt Cleaning Validation Processutveckling – som processingenjör med fokus på processoptimering, processteknisk expertis, processvalidering, avvikelseutredning, Change Control och förändringsarbete Analytisk utveckling – metodutveckling, metodvalidering, CMC, tech transfer samt arbete med avancerande instrumenttekniker, såsom kromatografi och/eller bioanalys QA – kvalitetssäkring, avvikelsehantering, kvalitetsdokumentation enligt relevanta regelverk, samt deltagande i QA projekt. Du behöver inte ha erfarenhet inom alla områden – vi matchar dig mot uppdrag som passar din profil, och arbetar samtidigt aktivt för att du ska få utvecklas inom det som driver dig. Vem är du? Vi söker dig som har en utbildning inom kemi, bioteknik, life science eller motsvarande, samt erfarenhet från läkemedels- eller medicinteknisk industri i ett eller flera av ovanstående områden. Erfarenhet av att arbeta i en GMP-reglerad miljö är en förutsättning för rollen. Du bör även ha god kommunikativ förmåga i både svenska och engelska. Erfarenhet av att ha jobbat i projektledande och koordinerande roller inom ovanstående områden är meriterande. Du trivs i miljöer där struktur och kvalitet är viktiga, men där det också krävs flexibilitet, samarbete och förmåga att hitta lösningar framåt. Du är van vid att arbeta i reglerade verksamheter och känner dig trygg i att ta ansvar, driva ditt arbete och snabbt sätta dig in i nya sammanhang. Samtidigt är du kommunikativ och bygger förtroende genom ett professionellt och prestigelöst arbetssätt. Om Mpya Sci & Tech På Mpya Sci & Tech kombinerar vi specialistkompetens med ett mänskligt och långsiktigt konsultliv. Här får du möjlighet att arbeta i varierande uppdrag ute i industrin – utan att tappa tillhörigheten till ett team som förstår din vardag. Vi tror på frihet under ansvar, nära ledarskap och att rätt människor gör störst skillnad när de får rätt förutsättningar. Därför lägger vi stor vikt vid att matcha uppdrag utifrån både kompetens och motivation. Hos oss blir du en del av ett nätverk där erfarenhetsutbyte, samarbete och utveckling hör till vardagen. Nyfiken på nästa steg? Detta är en proaktiv annons för kommande uppdrag till hösten. Vi går igenom ansökningar löpande och tar gärna en dialog om vad du söker och hur vi kan matcha det. Är du nyfiken på rollen eller konsultlivet hos oss? Skicka in din ansökan så hör vi av oss. På grund av sommarledighet kan återkopplingen dröja lite extra. Vi ser fram emot att lära känna dig! 💜

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.

Job Scope Why does the role exist? High level purpose of function. The Senior Process Engineer plays a key role in defining, stabilising, and optimising manufacturing processes within a battery cell production environment. This role is responsible for ensuring robust, repeatable, and high-performing processes across the full production lifecycle, from industrialisation through ramp-up to full-scale manufacturing. Acting as a Subject Matter Expert (SME), the Senior Process Engineer is responsible for the methodology, process flow, and parameter definition (recipe) of their assigned area. They define and control how the process performs, ensuring it consistently meets product quality, capability, and cost targets. This role combines hands-on shop floor engineering, deep technical expertise, and structured problem-solving to drive process capability, reduce variation, and sustain high-performing operations. The Senior Process Engineer works cross-functionally with Manufacturing Engineering, Quality Engineering, and Operations to deliver stable and scalable production processes. Key Responsibilities Overall areas of responsibilities and activities Key responsibilities include (but are not limited to) Own end-to-end process performance (Ppk), including defining targets, monitoring stability, and driving sustained improvements to ensure processes consistently meet quality and capability requirements. Define, implement, and maintain process recipes (setpoints, parameter windows, and sequencing), ensuring consistent, repeatable, and controlled production. Design, implement, and sustain the process control strategy, including SPC application, control limits, and structured response to process variation. Analyse process behaviour to identify variation drivers, performance gaps, and yield losses, and translate findings into robust and sustainable improvements. Own the development and maintenance of Bill of Process (BoP) and Standard Operating Procedures (SOPs) to ensure consistent and standardised process execution. Establish and maintain robust process windows to support industrialisation, production ramp-up, and sustained process performance. Lead Process Failure Mode and Effects Analysis (PFMEA), ensuring process risks are identified, prioritised, and effectively mitigated. Lead structured Root Cause Analysis (RCA) for complex process deviations, quality issues, and performance losses, ensuring resolution of underlying causes. Define and maintain process-specific reaction plans to ensure rapid and effective containment and recovery from process deviations. Act as a technical leader and escalation point for complex or high-impact process issues, driving resolution across cross-functional teams. Drive process improvements focused on variation reduction, capability improvement, and production stability, ensuring solutions are scalable across lines and future expansions. Work closely with Manufacturing Engineering and Quality Engineering to ensure alignment between process capability, equipment capability, and product specifications. Maintain strong presence on the shop floor, supporting trials, troubleshooting, and real-time process optimisation in production environments. Requirements Educational background and previous experience required for the role Qualifications and Experience Master’s degree in Chemical Engineering, Materials Science, Mechanical Engineering, or a related field. Minimum of 7 years of relevant work experience in process engineering within a manufacturing environment. Proven track record of developing, stabilising, and optimising manufacturing processes in high-volume production environments using structured and data-driven methodologies. Demonstrated experience in owning process performance (Ppk) and delivering sustained improvements in process stability, capability, and yield. Extensive experience in industrialisation, process qualification, and production ramp-up, including establishing robust process windows and control strategies. Experience working in fast-paced, high-growth environments, ideally within battery, semiconductor, chemical, electrochemical, or similar industries. Strong experience in Statistical Process Control (SPC), process capability analysis, and variation reduction techniques. Demonstrated ownership and leadership of Process Failure Mode and Effects Analysis (PFMEA) and implementation of effective risk mitigation strategies. Proven experience in defining and managing process recipes, parameter control strategies, and process standards. Experience working to industry standards and certification requirements such as ISO, IATF, and VDA. Specific skills & Knowledge Strong analytical mindset with the ability to interpret complex process data and translate insights into sustainable improvements. Deep technical curiosity and the ability to operate as a Subject Matter Expert across process domains, with strong understanding of process behaviour, variation, and control. Strong knowledge of process control methodologies, including SPC, control limits, and reaction planning. Excellent structured problem-solving skills, including Root Cause Analysis (RCA), A3, and Six Sigma methodologies. Ability to clearly document and communicate complex technical challenges and solutions. Proven ability to mentor, coach, and develop engineers and technicians, contributing to overall team capability growth. Highly autonomous with a proactive, ownership-driven mindset. Strong collaboration and communication skills, with the ability to work effectively across multiple engineering and operational functions. Excellent English skills, both written and oral, are essential. Basic Swedish and other language skills are a plus. Ability to work within varying environments including clean-rooms and dry-rooms, while wearing appropriate PPE. Comfortable operating in high-profile, international, and high-pressure production environments. A genuine technical interest and passion for working within manufacturing and process engineering is highly valued. Öppen för alla Vi fokuserar på din kompetens, inte dina övriga förutsättningar. Vi är öppna för att anpassa rollen eller arbetsplatsen efter dina behov.

At the Vitrolife Group, we work every day to unlock the full potential of science and technology to reduce the barriers towards building a family. Together we help our customers and their patients to fulfill the dream of having a baby. About the role We are now looking for a Process Engineer. This team will consist of different competencies, such as biomedicine, biotechnique, validation, automation and mechatronic. You will be responsible for automation/mechatronic knowledge within the department. You will also be responsible for one of our manufacturing processes and drive the work with continues improvements. Whenever there is a question regarding automation/mechatronic from your colleagues you will be asked to help. This is a team with a lot of cross-functional collaborations and responsibilities with both internal and external stakeholders from a variety of countries. Key Responsibilities Developing and implementing new production processes Driving continuous improvements on existing processes in close collaboration with all production departments Ensuring that existing production is compliant for all our in-house production within the business area Process engineering will also work with our outsourced products and the assessment and approval of our suppliers’ processes in close collaboration with our Quality Assurance, Supply Chain and Product Development department. This is a permanent, full-time position based at our office in Gothenburg. Travel and work from other Vitrolife sites and contract manufacturers might be part of the position. Your Profile Bachelor or master’s degree in biomedicine, chemistry, biology, mechanic, automation or equivalent Experiences from working with quality standards and processes (ISO-13485, GMP) 5 years’ experience of automation/mechatronic work Fluent in Swedish and good knowledge in English both oral and written You are thorough, structured, can see the whole picture and are able to prioritize and meet deadlines. You are also service-oriented, solution-focused and communicative and you enjoy working in a changing and dynamic environment. Applications will be reviewed on an ongoing basis, so please submit your application as soon as possible. Vitrolife Group is a global provider of medical devices and genetic services. Based on science and advanced research capabilities, we develop services and products for personalized genetic information and medical device products. We support our customers by improving their clinical practice for the patient's outcome of fertility treatment. We are currently approximately 1 100 colleagues worldwide, with headquarters in Gothenburg, Sweden. Vitrolife Group's products and services are available in more than 110 countries through our own presence in 30 countries and a network of distributors. Vitrolife Group is a sustainable market leader and aims to be the preferred partner for IVF-clinics by providing superior products and services with the vision of fulfilling the dream of having a baby. The Vitrolife share is listed on Nasdaq Stockholm.

Silex Microsystems is the world’s leading pure-play MEMS foundry, customizing solutions for prominent global clients in industries such as pharmaceuticals, consumer electronics, and automotive. We’re now growing more than ever, and are expanding our Manufacturing organization with new Process Engineer positions in several areas. Read more about Silex here. The Area The area consists of a team of both engineers and service technicians where collaboration is critical to ensure good process stability, tool up-time and continuous improvement. All Process Engineers report to the Area Manager in their area. Wet A fast-paced, varied and unique area where the processes differ a lot: wet-etching, deposition and vapor techniques are used to both remove and build material on our chips. The team consists of five Service Technicians and ten Process Engineers. The role Your overall responsibility is to ensure manufacturing goals are met, together with operators and service technicians. Your days will be a mix of meetings with Product Managers and developing new processes that meet customers' specifications. You will also participate in creating work routines for operators and solving problems that occur in the area, driving improvement projects to enhance our workflow and processes in the area. In this role, you will: Develop, maintain and improve processes. Handle stopped production batches and development material together with process integration engineers (PIs). Be a part of creating/improving the infrastructure for operator training and make sure current routine is available and up to date. Participate in process qualification of new equipment/materials and release to them production. Participate in the startup of new products, review specifications and process flows. Grow into taking responsibility for area equipment, improving the tool uptime, maintain and develop new standardized process modules. Drive improvement projects independently. We are looking for someone who has A master's degree in engineering, specializing in Applied Physics, Chemical Engineering, Material Science, or a related field. At least one year of experience in an engineering role, preferably in production/development environments. The ability to see opportunities for improvement and manage projects to follow through with those improvements in a proactive way. Strong problem-solving skills and the ability to work effectively in a team environment. Strong skills in documentation and quality management. Excellent communication skills in English; proficiency in Swedish is considered a merit. What we offer you An opportunity to work closely with talented and inspiring colleagues in a collaborative environment. A chance to be part of a world-leading company, driving the future of MEMS technology. The ability to engage with cutting-edge innovations that shape global industries and everyday life. The satisfaction of contributing directly to transformative technologies at the industry’s most advanced pure-play MEMS foundry. About Silex Sweden’s Silex Microsystems manufactures mechanical and electrical systems in micro scale, in the form of MEMS chips. MEMS technology makes it possible to produce pressure sensors that are small enough to be injected into the human bloodstream. Silex was founded in 2000, and now has an annual turnover of approximately SEK 1 billion and 350 employees. With around 80 active customers globally, Silex is one of the world’s leading independent MEMS manufacturers. The recruitment process We review applications on a rolling basis, so we encourage you to apply as soon as possible. To apply, please attach your CV or LinkedIn-profile, and answer a few questions. You don't need to write a cover letter. Our recruitment process is designed to ensure a fair and objective assessment. If you progress through the full process, you will start with a digital interview with a Talent Acquisition Partner, followed by a personality and logical ability test. Next, you will meet with the Area Manager for an in-person Hiring Manager interview, and finally with our VP of Manufacturing for a concluding interview. Before an offer, we also conduct reference checks, a background check, and a drug test. Randomized alcohol- and drug testing is conducted for all of our employees during employment.