Civilingenjör, bioteknik

Sök bland 12 lediga jobb som Civilingenjör, bioteknik och börja ditt nya yrkesliv idag!

Director Manufacturing Operations/Avdelningschef Produktion till Valneva

Brinner du för utveckling och produktion av läkemedel och att leda människor i en läkemedelstillverkningsorganisation? Vill du arbeta på ett framåtdrivet vaccinföretag med att säkerställa tillverkning av produkter som når en global marknad och gör skillnad i människors liv? Valneva söker nu en Avdelningschef Produktion (Director Manufacturing Operations) till företaget. I denna roll ansvarar du för hela produktionskedjan av företagets vaccinprodukter och leder ett team av gruppchefer inom Drug Substance, Drug Product och Final Product. Arbetet innebär ett helhetsansvar inom personalledning, arbetsmiljö, budget, kvalitet, GMP-tillverkning av vaccinprodukter och en målsättning att kontinuerligt bidra till ytterligare produktivitetsförbättringar. Vi letar efter dig som har erfarenhet av att leda människor inom GMP-produktion och med fördel inom steril-/vaccintillverkning. Du är van att arbeta tvärfunktionellt för att uppnå gemensamma mål och att lösa problem. Du erbjuds en viktig och utvecklande roll med både strategiska och operativa inslag där du leder och utvecklar ditt team i en organisation där beslutsvägarna är korta och möjligheten att påverka är hög. Du ingår i företagets ledningsgrupp och är med och utvecklar vår verksamhet. På Valneva har vi en god gemenskap och du samarbetar dagligen med duktiga och engagerade kollegor och tillsammans har vi en spännande resa framför oss! Tjänsten är en tillsvidareanställning hos Valneva med placering i Solna och start enligt överenskommelse med rätt kandidat. Urval och intervjuer sker löpande så vi välkomnar din ansökan Om tjänsten Som Director Manufacturing Operations har du huvudansvaret för att leda, organisera och utveckla produktionsverksamheten på Valneva. Du rapporterar till företagets VD och ingår i ledningsgruppen på företaget. Huvudsakliga ansvarsområden/arbetsuppgifter innefattar: - Leda funktionen Manufacturing Operations på Valneva med ansvar för tillverkning av Drug Substance, Drug Product och Final Product. - Säkerställa produktion av koleravaccin och nya vaccinprodukter enligt utsatt plan, kvalitet och affärsmål - Personal- och budgetansvar samt kompetensutveckling av personal inom produktion - Ansvar för miljö, hållbarhet och säkerhet - Driva förbättrings- och effektiviseringsarbete för produktionsverksamheten - Utveckling av produktionsplaner och strategier för att nå verksamhetsmål - Utveckling av produktionsorganisation för att dynamiskt kunna stödja Valnevas affärsmål. - Ingå i viktiga tvärfunktionella samarbeten inom Valneva Solna och övriga sites - Ledningsgruppsansvar inom Manufacturing Operations Solna Vem är du? Vi söker dig som har: - Akademisk examen inom bioteknik, kemiteknik eller motsvarande - Mångårig erfarenhet från GMP-tillverkning av biologiska läkemedel exempelvis steril/vaccintillverkning - Goda ledaregenskaper med mångårig erfarenhet av personalledning och utveckling av medarbetare och team inom läkemedelstillverkning - Erfarenhet av strategi-/ledningsgruppsansvar och att leda chefer med operativt ansvar inom GMP-produktion är starkt meriterande - God produktionsteknisk förståelse och erfarenhet från arbete i tekniska projekt, kvalificering och validering samt erfarenhet från att lösa komplexa utmaningar relaterade till GMP-tillverkning - Goda kunskaper i svenska och engelska, i både tal och skrift. Vi söker dig som vill leda och utveckla engagerade och kompetenta medarbetare inom läkemedelstillverkning. Som person är du strukturerad, lösningsorienterad och du kan hantera komplicerade frågor med detaljfokus och starkt beslutsfattande. Du är en kommunikativ, förtroendeskapande och lyhörd ledare med förmågan att skapa delaktighet, motivera och inspirera ditt team. Rollen fordrar att du kan skaffa dig en bra överblick, samarbeta effektivt, följa upp aktiviteter inom verksamheten samt ha en god beredskap för att säkerställa verksamhetens mål nås enligt utsatt tid, budget och kvalitet. Du stimuleras av både strategiskt och operativt arbete, av att driva effektiviserings- och förbättringsinitiativ och har god förmåga att byta perspektiv mellan det långsiktiga strategiska arbetet och de dagliga frågorna. Du kommer in ett spännande skede där dina kompetenser och idéer kommer göra betydande skillnad för oss och där du är med och bidrar till Valnevas fortsatta framgång. Om verksamheten Valnevas vision är att bidra till en värld där ingen dör eller lider av en sjukdom som kan förebyggas av vaccination. Valneva har flera vacciner under utveckling, inklusive världens första vaccin mot chikungunyavirus, den enda borreliavaccinkandidaten där vi samarbetar med Pfizer, liksom vaccinkandidater mot zikavirus och andra globala hälsofaror. Valnevas portfölj innehåller två kommersiella vaccin för resenärer: ett för förebyggande av japansk encefalit och ett för förebyggande av kolera. Valneva har verksamhet i Österrike, Sverige, Storbritannien, Frankrike, Kanada och USA med runt 800 anställda. Valneva Sweden AB är den svenska delen av Valneva och har en lång historia. Bolaget bildades 1993 när dåvarande SBL, Statens Bakteriologiska Laboratorium, delades in i en myndighetsdel, Smittskyddsinstitutet (i dag en del av Folkhälsomyndigheten) och en bolagsdel, SBL Vaccin AB. Våren 2015 såldes vaccinbolaget av sin dåvarande ägare Crucell Sweden AB i Solna till det österrikisk-franska vaccinbolaget Valneva SE.” Mer information hittar du på www.valneva.com.

1 mars 2024
Sista ansökan:
31 mars 2024
Valideringsledare Life Science

Därför är detta jobbet för dig Därför att du vet att validering är så mycket mer än bara dokumentation. Du vet att det handlar om att vara drivande i att få alla att jobba mot ett gemensamt mål - en säker produkt och förbättrad livskvalitet för användaren. Vi har ett teamorienterat arbetssätt vilket gör det möjligt för dig att ta dig an och leda uppdrag och projekt utanför dina tidigare erfarenheter då du arbetar tillsammans med den samlade kompetensen och expertisen inom hela Knightec. Detta gör det även möjligt att för dig som valideringsledare att ingå i team med juniora kollegor inom kompetensområdet och hjälpa dem utvecklas och ta del av dig kunskap. Kärnan är validering och kvalificering av datoriserade system, processer och utrustning inom Life Science- industrin. Men det är inte allt. Du kommer kunna ta stort ansvar i dina projekt kring valideringsaktiviteter, men även ha möjlighet att vara involverad i design, inköp och commissioning vilket gör att du på riktigt kan påverka resultat och utfall. Den gemensamma grunden är samarbete, kvalitetsmedvetenhet och kunskapsdelning. Vägen framåt ligger i dina händer. Du är den som har kunskap och kompetens inom området och vet hur den ska användas för att nå bästa resultat. Vi vill lyssna på dig och nyttja din expertis för att tillsammans utvecklas och ta nästa steg Skapa en karriär att vara stolt över Vart du än ser dig själv i framtiden så är vi här för att stötta dig. Oavsett om du vill ta dig an en ny roll, utvecklas vidare inom din specialitet, eller utveckla din ledarskapsförmåga så kommer vi hjälpa dig hitta vägen framåt. Din vilja och ambition visar vägen, vi förser dig med de verktyg och förutsättningar som krävs för att du ska nå dina mål. För att stimulera din utveckling kommer du vara del av vårt kompetensområde Validation Management, en kompetensgrupp som finns för att främja kunskapsdelning och samarbete. Genom aktiviteter som workshops, mentorskapsprogram och diskussionsforum ger det dig förutsättningar för att utveckla dig själv och dela din kunskap till andra kollegor, vilket ger dig förutsättningarna för att ta nästa steg i din karriär. Och när du gör det kommer du alltid ha dina kollegor bakom dig, redo att stötta när det behövs. Dina erfarenheter Du har ett kvalitetsorienterat angreppssätt, men viktigast av allt, en vilja att utveckla dig själv och dina kollegor, lära dig nya saker och dela din kunskap. Du har även: - En ingenjörsexamen inom bioteknik, medicinsk teknik, kemiteknik, datateknik eller liknande - Självständigt drivit arbetet med validering inom Life Science där du varit ansvarig för DQ/IQ/OQ/PQ-faserna - Självständigt drivit arbete med krav- och avvikelsehantering - God kunskap inom GxP-regelverk. Specifik kunskap inom GAMP5, 21 CFR part 11 och Eudralex Annex 11 är det meriterande - God kommunikationsförmåga - Erfarenhet av att leda valideringsarbetet och ansvara för tidsplanering/resursplanering Du kommunicerar obehindrat på svenska och engelska. Knightec Knightec drivs av övertygelsen att team som präglas av mångfald i erfarenhet, kompetens och bakgrund är nyckeln till framgång. Vi arbetar aktivt för att upplevas som det tjänsteföretag som bäst kan stödja våra kunders transformation. Vår industriella erfarenhet kombinerad med digital expertis och ett mänskligt angreppssätt ger våra 800 medarbetare goda möjligheter att lyckas.

5 februari 2024
Sista ansökan:
7 april 2024
Development Engineer - Focus

Who we are Olink Proteomics is a rapidly growing life science company committed to advancing the understanding of human diseases through proteomics. We are dedicated to innovation, quality, rigor and transparency, providing outstanding solutions and support for human protein biomarker discovery. The vital role of proteins in understanding human biology has been recognized for many decades, but technological limitations severely restricted the comprehensive investigation of the huge number of proteins that could be important in different biological processes and diseases. With Olink, scientists can now simultaneously measure thousands of human proteins using just a few µL of blood sample, with highly specific, thoroughly validated assays that cover a very wide dynamic range (fg/mL to µg/mL). In a few years, Olink has grown rapidly from a small, Sweden-based company offering assays for a few hundred proteins, to a NASDAQ-listed (https://eur01.safelinks.protection.outlook.com/?url=https%3A%2F%2Finvestors.olink.com%2Finvestor-relations&data=05%7C01%7Cthomas.bennett%40olink.com%7C44d00a4e60cc45da8f8b08da2d189513%7C0bc012cfb3e946bd95a6cecc37315bb1%7C1%7C0%7C637871880838157918%7CUnknown%7CTWFpbGZsb3d8eyJWIjoiMC4wLjAwMDAiLCJQIjoiV2luMzIiLCJBTiI6Ik1haWwiLCJXVCI6Mn0%3D%7C3000%7C%7C%7C&sdata=%2F1avRLTDgaZQT7%2FHLQVoC2z6iY%2FlV6p088C3xz0TkuI%3D&reserved=0) organization with a strong global presence, a broad portfolio (https://eur01.safelinks.protection.outlook.com/?url=https%3A%2F%2Fwww.olink.com%2Fproducts-services%2F&data=05%7C01%7Cthomas.bennett%40olink.com%7C44d00a4e60cc45da8f8b08da2d189513%7C0bc012cfb3e946bd95a6cecc37315bb1%7C1%7C0%7C637871880838157918%7CUnknown%7CTWFpbGZsb3d8eyJWIjoiMC4wLjAwMDAiLCJQIjoiV2luMzIiLCJBTiI6Ik1haWwiLCJXVCI6Mn0%3D%7C3000%7C%7C%7C&sdata=67Dhfg2OK3oTJU4HR9ipLduzEFYVrwrcHRERFZ%2BShm8%3D&reserved=0) of flexible protein biomarker solutions and library of high quality, thoroughly validated assays that covers ~5400 proteins. For more information about Olink, please visit www.olink.com Position Description We are seeking a highly motivated and driven Development Engineer to join our R&D team responsible for development of our customized product - Olink Focus. In this role, you will lead your own projects and the work is carried out in close contact with the customer, with high demands on good communication, high quality work, and deliveries within set timeframes. You will have the opportunity to work on new and exciting customer projects and contribute to the development of future innovative products. Primary Responsibilities - Project planning and follow-up on set timelines - Ordering of reagents, planning and executing of laboratory experiments - Evaluation and analysis of experimental results - Compiling and reporting of results, internally and externally to customers - Participation in customer meetings during the development process of the projects - Take an active part in the team´s continuous improvement work Qualifications/skills - University degree in life sciences (e.g., Biochemistry, Molecular Biology, Immunology) or corresponding education - Minimum of 5 years of experience in development work within the field - Documented skills and experience in laboratory work (e.g., DNA sequencing techniques such as PCR, qPCR and NGS) - Experience of project management - Strong analytical and problem-solving skills - Excellent teamwork and communication skills - Flexible, customer oriented and pragmatic - Familiarity with relevant software and data analysis tools If you are driven and customer focused with a passion for developing innovative protein assays and want to be part of a team at the forefront of biotechnology, we encourage you to apply. Please submit your resume and a cover letter detailing your relevant experience and why you are the ideal candidate for this position. The last day of application is on the 25th of February.

2 februari 2024
Sista ansökan:
21 juli 2024
Pharmacovigilance Consultant

Job description We are now looking for experts within the field of pharmacovigilance (PV). Do you have experience from the PV field and want to broaden your wings as a consultant, where you get the opportunity to help our costumers on different assignments? Don't hesitate to apply today! We see that you have a miniumum of 1 year experience in PV and knowledge of one or several of the following: Global AE reporting ICSR quality review Safety surveillance Risk Management activities Periodic and ad hoc safety reports Periodic Adverse Drug Experience Reports (PADERs) Periodic Safety Update Reports (PSURs) / Periodic Benefit-Risk Evaluation Reports (PBRERs) Development Safety Update Reports (DSURs) Responsibilities Lead pharmacovigilance related tasks. Qualifications ·  Degree in Life Science or Health Care ·  At least 1 years of experience in the pharmaceutical industry working in pharmacovigilance ·  Strong knowledge of pharmacovigilance regulatory requirements ·  Strong skills in English ·  Good understanding of safety reporting and pharmacovigilance compliance About the company Randstad At Randstad, we see the possible in people. With business all over Sweden and in all areas of expertise, we help people find work that feels good, where they get the opportunity to develop and realize their true potential. With close to 600 000 employees in 38 countries, Randstad is the global leader in the HR services industry. Our mission is to become the world’s most valued working life partner. By combining our passion for people with the power of today’s technology, we support people and organizations in realizing their true potential. We call it Human Forward.

12 januari 2024
Sista ansökan:
29 mars 2024
Scientist Oligo Design

Who we are Olink Proteomics is a rapidly growing life science company committed to advancing the understanding of human diseases through proteomics. We are dedicated to innovation, quality, rigor and transparency, providing outstanding solutions and support for human protein biomarker discovery. The vital role of proteins in understanding human biology has been recognized for many decades, but technological limitations severely restricted the comprehensive investigation of the huge number of proteins that could be important in different biological processes and diseases. With Olink, scientists can now simultaneously measure thousands of human proteins using just a few µL of blood sample, with highly specific, thoroughly validated assays that cover a very wide dynamic range (fg/mL to µg/mL). In a few years, Olink has grown rapidly from a small, Sweden-based company offering assays for a few hundred proteins, to a NASDAQ-listed (https://eur01.safelinks.protection.outlook.com/?url=https%3A%2F%2Finvestors.olink.com%2Finvestor-relations&data=05%7C01%7Cthomas.bennett%40olink.com%7C44d00a4e60cc45da8f8b08da2d189513%7C0bc012cfb3e946bd95a6cecc37315bb1%7C1%7C0%7C637871880838157918%7CUnknown%7CTWFpbGZsb3d8eyJWIjoiMC4wLjAwMDAiLCJQIjoiV2luMzIiLCJBTiI6Ik1haWwiLCJXVCI6Mn0%3D%7C3000%7C%7C%7C&sdata=%2F1avRLTDgaZQT7%2FHLQVoC2z6iY%2FlV6p088C3xz0TkuI%3D&reserved=0) organization with a strong global presence, a broad portfolio (https://eur01.safelinks.protection.outlook.com/?url=https%3A%2F%2Fwww.olink.com%2Fproducts-services%2F&data=05%7C01%7Cthomas.bennett%40olink.com%7C44d00a4e60cc45da8f8b08da2d189513%7C0bc012cfb3e946bd95a6cecc37315bb1%7C1%7C0%7C637871880838157918%7CUnknown%7CTWFpbGZsb3d8eyJWIjoiMC4wLjAwMDAiLCJQIjoiV2luMzIiLCJBTiI6Ik1haWwiLCJXVCI6Mn0%3D%7C3000%7C%7C%7C&sdata=67Dhfg2OK3oTJU4HR9ipLduzEFYVrwrcHRERFZ%2BShm8%3D&reserved=0) of flexible protein biomarker solutions and library of high quality, thoroughly validated assays that covers ~5400 proteins. For more information about Olink, please visit www.olink.com Position Description Scientist - Technical Projects Olink Proteomics continues to grow, and we are now seeking a Scientist to join our R&D team with a focus on oligo design and technical development for our highplex products. Technical Projects works with developing technical solutions for new products as well as improving existing products. The work is performed in projects where one or several projects are run in parallel. The role is based in our Uppsala headquarters. Primary responsibilities - Design oligos for highplex products. - Analyze large data sets and draw conclusions. - Design and evaluate molecular methods. - Plan and perform laboratory experiments to validate and optimize protocols and technical solutions. - Documenting results in technical reports. Qualifications/skills - Ph.D. from the Life Science area. - A deep knowledge in molecular biology and nucleic acid structure prediction. - Documented experience with bioinformatics tools. - Proficiency in Python and/or Perl. - Experience of tackling complex analytical workflows. - Experience from method development especially experience with multiplex assay development is highly desirable. - Experience from molecular techniques such as NGS, qPCR and PCR. - Well documented experience from lab work. - Experience of working in projects. To succeed in this role, we believe that you are committed, driven and solution oriented. You are a team player that can work with many personalities and you are thorough and have strong problem-solving skills. It is also important that you are positive and can adjust to changed circumstances. Please submit your resume and a cover letter detailing your relevant experience and why you are the ideal candidate for this position. The last day for applying is on the 28th of January 2024 but please submit your application as soon as possible.

5 januari 2024
Sista ansökan:
23 juni 2024
Innovation Scientist

Who we are Olink Proteomics is a rapidly growing life science company committed to advancing the understanding of human diseases through proteomics. We are dedicated to innovation, quality, rigor, and transparency, providing outstanding solutions and support for human protein biomarker discovery. The vital role of proteins in understanding human biology has been recognized for many decades, but technological limitations severely restricted the comprehensive investigation of the huge number of proteins that could be important in different biological processes and diseases. With Olink, scientists can now simultaneously measure thousands of human proteins using just a few µL of blood sample, with highly specific, thoroughly validated assays that cover a very wide dynamic range (fg/mL to µg/mL). In a few years, Olink has grown rapidly from a small, Sweden-based company offering assays for a few hundred proteins, to a NASDAQ-listed (https://eur01.safelinks.protection.outlook.com/?url=https%3A%2F%2Finvestors.olink.com%2Finvestor-relations&data=05%7C01%7Cthomas.bennett%40olink.com%7C44d00a4e60cc45da8f8b08da2d189513%7C0bc012cfb3e946bd95a6cecc37315bb1%7C1%7C0%7C637871880838157918%7CUnknown%7CTWFpbGZsb3d8eyJWIjoiMC4wLjAwMDAiLCJQIjoiV2luMzIiLCJBTiI6Ik1haWwiLCJXVCI6Mn0%3D%7C3000%7C%7C%7C&sdata=%2F1avRLTDgaZQT7%2FHLQVoC2z6iY%2FlV6p088C3xz0TkuI%3D&reserved=0) organization with a strong global presence, a broad portfolio (https://eur01.safelinks.protection.outlook.com/?url=https%3A%2F%2Fwww.olink.com%2Fproducts-services%2F&data=05%7C01%7Cthomas.bennett%40olink.com%7C44d00a4e60cc45da8f8b08da2d189513%7C0bc012cfb3e946bd95a6cecc37315bb1%7C1%7C0%7C637871880838157918%7CUnknown%7CTWFpbGZsb3d8eyJWIjoiMC4wLjAwMDAiLCJQIjoiV2luMzIiLCJBTiI6Ik1haWwiLCJXVCI6Mn0%3D%7C3000%7C%7C%7C&sdata=67Dhfg2OK3oTJU4HR9ipLduzEFYVrwrcHRERFZ%2BShm8%3D&reserved=0) of flexible protein biomarker solutions and library of high quality, thoroughly validated assays for more than 5,000 proteins. For more information about Olink, please visit www.olink.com Position Description Do you want to be part of creating the next generation of world-leading products in large-scale proteomics? Are you creative and innovative and have a great knowledge of molecular biology and an analytical mind? Then maybe you are the one we are looking for at Olink's Innovation Center! The Innovation Center works to promote innovation and to drive a strategic and long-term development agenda, which includes new technology, new methods, and a continuous development of our patent portfolio - All in line with Olink's vision: "Enable understanding of real-time human biology". The Innovation Center is led by the Chief Innovation Officer (CIO). The team currently consists of 8 Scientists as well as our Chief Technology Officer (CTO) who reports to the CIO. During the year, we want to expand the team with another Innovation Scientist. Primary Responsibilities - Invent, develop and evaluate technical solutions based on strategic goals. - Plan, set up and carry out laboratory experiments. - Conduct literature searches and reviews of new techniques. - Analyze, compile and present ideas, plans and results. - Actively participate in the development of the team. Qualifications/Skills - Degree in Molecular Biology/Chemistry or related field. A PhD within Life Science and prior research experience is a plus. - Deep knowledge in and experience of working with different methods in molecular biology. - A few years of working experience from a similar role within the Life Science industry is highly beneficial. - A strong interest in technology, problem solving and innovation. - Good skills in data analysis (experience with R and handling large data sets is advantageous). - Knowledge in proteomics and/or immunology is also beneficial, as well as experience in different methods in protein chemistry. - You are fluent in spoken and written English and are a good communicator. As a person, you are creative and innovative, but at the same time efficient and driven. You work with foresight and take clear ownership of your tasks. You are a quick learner and can easily absorb and use new knowledge and concepts. Furthermore, you are a team player who is good at communicating clearly and effectively. As we are a rapidly growing company and constantly adapt to the needs of the customer and the market, it is also important that you have a positive attitude and that you can adapt to changing circumstances. In short, you choose to look for solutions instead of seeing problems. The last application day for this role is 2024.01.15. Please, be aware that the position might be filled before the last application date. If this sounds interesting to you, please send us your application, and come join Olink!

22 december 2023
Sista ansökan:
9 juni 2024
Development Engineer QC -Design transfer

Who we are Olink Proteomics is a rapidly growing life science company committed to advancing the understanding of human diseases through proteomics. We are dedicated to innovation, quality, rigor and transparency, providing outstanding solutions and support for human protein biomarker discovery. The vital role of proteins in understanding human biology has been recognized for many decades, but technological limitations severely restricted the comprehensive investigation of the huge number of proteins that could be important in different biological processes and diseases. With Olink, scientists can now simultaneously measure thousands of human proteins using just a few µL of blood sample, with highly specific, thoroughly validated assays that cover a very wide dynamic range (fg/mL to µg/mL). In a few years, Olink has grown rapidly from a small, Sweden-based company offering assays for a few hundred proteins, to a NASDAQ-listed organization with a strong global presence, a broad portfolio of flexible protein biomarker solutions and library of high quality, thoroughly validated assays that covers ~5300 proteins. For more information about Olink, please visit www.olink.com Position Description Olink continues to grow, and we are now looking for a Development Engineer Quality Control -Design transfer to join our Quality Control team within Supply Chain. The QC team, which today consists of 10 people, is divided into two sub-teams: One with a focus on checking raw materials, components and finished products and one where the focus is on receiving and implementing new QC methods from RnD/ the Design Transfer process. As the company grows, the need for an additional Development Engineer with a focus on Design transfer activities has increased. The main purpose of the position is to lead the project activities and be responsible for transfer of methods from RnD to Quality Control. The position is based in our Uppsala headquarters and reports to Head of Quality Control. Primary Responsibilities - Lead and coordinate projects and activities within Quality Control. - Actively participate as core team member in Product Development projects (NPI). - Be responsible for driving the QC preparation tasks in the Design transfer process according to internal procedures and routines and act as the Quality Control Preparation Engineer. - Write and review instructions and QC methods. - Manage and drive product care activities within Supply Chain including improvements, non-conformities, CAPAs and Change Control activities. - Actively participate in the business development of the department, i.e. create and improve work processes and routines. Qualifications/skills - MSs within Biotechnology/ Molecular Biology or similar. - At least 2 years’ experience from a role as development engineer or similar within Life Science. - Experience from a similar role as PM/Member/ Production Preparation Engineer of various Product Development Projects. - Experience/ knowledge with ERP systems. - Experience from ISO13485 certified or IVD/MD regulated business is highly beneficial. - Fluent in (speaking/reading/writing) both Swedish and English is mandatory and necessary to be successful in this role. As a person, you should be interested in, and enjoy driving and leading activities and projects. You are a solution oriented team player with integrity who can be pragmatic when needed. You are also open towards changes and is motivated by driving improvements together with others. The selection process is on-going, and the position might get filled before the last day of application so please apply as soon as possible, however no later than 2024.01.14. We accept applications both in English and Swedish.

21 december 2023
Sista ansökan:
8 juni 2024
Scientist - Assay Development

Who we are Olink Proteomics is a rapidly growing life science company committed to advancing the understanding of human diseases through proteomics. We are dedicated to innovation, quality, rigor and transparency, providing outstanding solutions and support for human protein biomarker discovery. The vital role of proteins in understanding human biology has been recognized for many decades, but technological limitations severely restricted the comprehensive investigation of the huge number of proteins that could be important in different biological processes and diseases. With Olink, scientists can now simultaneously measure thousands of human proteins using just a few µL of blood sample, with highly specific, thoroughly validated assays that cover a very wide dynamic range (fg/mL to µg/mL). In a few years, Olink has grown rapidly from a small, Sweden-based company offering assays for a few hundred proteins, to a  NASDAQ-listed (https://eur01.safelinks.protection.outlook.com/?url=https%3A%2F%2Finvestors.olink.com%2Finvestor-relations&data=05%7C01%7Cthomas.bennett%40olink.com%7C44d00a4e60cc45da8f8b08da2d189513%7C0bc012cfb3e946bd95a6cecc37315bb1%7C1%7C0%7C637871880838157918%7CUnknown%7CTWFpbGZsb3d8eyJWIjoiMC4wLjAwMDAiLCJQIjoiV2luMzIiLCJBTiI6Ik1haWwiLCJXVCI6Mn0%3D%7C3000%7C%7C%7C&sdata=%2F1avRLTDgaZQT7%2FHLQVoC2z6iY%2FlV6p088C3xz0TkuI%3D&reserved=0) organization with a strong global presence, a  broad portfolio (https://eur01.safelinks.protection.outlook.com/?url=https%3A%2F%2Fwww.olink.com%2Fproducts-services%2F&data=05%7C01%7Cthomas.bennett%40olink.com%7C44d00a4e60cc45da8f8b08da2d189513%7C0bc012cfb3e946bd95a6cecc37315bb1%7C1%7C0%7C637871880838157918%7CUnknown%7CTWFpbGZsb3d8eyJWIjoiMC4wLjAwMDAiLCJQIjoiV2luMzIiLCJBTiI6Ik1haWwiLCJXVCI6Mn0%3D%7C3000%7C%7C%7C&sdata=67Dhfg2OK3oTJU4HR9ipLduzEFYVrwrcHRERFZ%2BShm8%3D&reserved=0) of flexible protein biomarker solutions and library of high quality, thoroughly validated assays that covers ~5000 proteins. For more information about Olink, please visit www.olink.com Position Description We are now looking for a Scientist to join the Assay Development team within RnD. If you want to work with a world-leading technology that contributes to the development of precision medicine, you might be the person we are looking for. Assay Development has the main responsibility for testing (screening) antibodies and developing immunoassays for Olink's products. Furthermore, Assay Development works with the development and verification of high-plex products. Product development is carried out in projects with members from other departments. Assay Development currently consists of 13 people, but since the company is growing rapidly with very exciting things going on, the group needs to be expanded with additional members. Primary Responsibilities As a Scientist in the group, your duties will vary across project phases. It will consist of both laboratory work, but also data analysis and information handling. The main tasks will be to: - Plan and conduct experiments, mainly using Olinks PEA (Proximity Extension Assay) technology using qPCR and NGS as a readout platform. - Participate in project planning and experimental design to verify product performance. - Analyze data. - Evaluate, report and document results from the laboratory work and contribute to the development of systems/structures for logging results and target information. - Actively participate in the development of the group's and department's activities and participate in improvement projects. - Participate in transfer of information to other groups or functions. - Handle and register data for large amounts of antibodies, antigens and biological samples. Qualifications/skills - Phd within the Life Science area - A few years of working experience from the industry is highly beneficial. - Documented lab experience and extensive scientific and technical knowledge in molecular biology, proteomics/immunology and/or chemistry. - Experience with antibody-based test methods as well as with PCR/qPCR and sequencing is advantageous. - Experience in planning and reporting tests and experiments. - Good skills in data analysis. Experience with R and handling large data sets is a plus. - Fluent in spoken and written English. Swedish skills is a plus. - Good computer skills in general and good knowledge of Excel. - Experience of working in projects is a plus. As a person you are responsible, driven and solution oriented. As we handle large amounts of reagents and data, we value that you are thorough and structured. You are a team player who finds it easy to communicate and interact with others both within the group and with those who work in other departments. It is important that you have a positive attitude and can adapt to changing circumstances, as we have a strong customer focus and are a company in hyper growth. The selection process is on-going, and the position might get filled before the last day of application so please apply as soon as possible, however no later than 2023.11.30.

8 november 2023
Sista ansökan:
26 april 2024
Development Engineer - Assay Development

Who we are Olink Proteomics is a rapidly growing life science company committed to advancing the understanding of human diseases through proteomics. We are dedicated to innovation, quality, rigor and transparency, providing outstanding solutions and support for human protein biomarker discovery. The vital role of proteins in understanding human biology has been recognized for many decades, but technological limitations severely restricted the comprehensive investigation of the huge number of proteins that could be important in different biological processes and diseases. With Olink, scientists can now simultaneously measure thousands of human proteins using just a few µL of blood sample, with highly specific, thoroughly validated assays that cover a very wide dynamic range (fg/mL to µg/mL). In a few years, Olink has grown rapidly from a small, Sweden-based company offering assays for a few hundred proteins, to a  NASDAQ-listed (https://eur01.safelinks.protection.outlook.com/?url=https%3A%2F%2Finvestors.olink.com%2Finvestor-relations&data=05%7C01%7Cthomas.bennett%40olink.com%7C44d00a4e60cc45da8f8b08da2d189513%7C0bc012cfb3e946bd95a6cecc37315bb1%7C1%7C0%7C637871880838157918%7CUnknown%7CTWFpbGZsb3d8eyJWIjoiMC4wLjAwMDAiLCJQIjoiV2luMzIiLCJBTiI6Ik1haWwiLCJXVCI6Mn0%3D%7C3000%7C%7C%7C&sdata=%2F1avRLTDgaZQT7%2FHLQVoC2z6iY%2FlV6p088C3xz0TkuI%3D&reserved=0) organization with a strong global presence, a  broad portfolio (https://eur01.safelinks.protection.outlook.com/?url=https%3A%2F%2Fwww.olink.com%2Fproducts-services%2F&data=05%7C01%7Cthomas.bennett%40olink.com%7C44d00a4e60cc45da8f8b08da2d189513%7C0bc012cfb3e946bd95a6cecc37315bb1%7C1%7C0%7C637871880838157918%7CUnknown%7CTWFpbGZsb3d8eyJWIjoiMC4wLjAwMDAiLCJQIjoiV2luMzIiLCJBTiI6Ik1haWwiLCJXVCI6Mn0%3D%7C3000%7C%7C%7C&sdata=67Dhfg2OK3oTJU4HR9ipLduzEFYVrwrcHRERFZ%2BShm8%3D&reserved=0) of flexible protein biomarker solutions and library of high quality, thoroughly validated assays that covers ~3000 proteins. For more information about Olink, please visit www.olink.com Position Description We are now looking for a Development Engineer to join the Assay Development team within RnD. If you want to work with a world-leading technology that contributes to the development of precision medicine, you might be the person we are looking for. Assay Development has the main responsibility for testing (screening) antibodies and developing immunoassays for Olink's products. Furthermore, Assay Development works with the development and verification of high-plex products. Product development is carried out in projects with members from other departments. Assay Development currently consists of 13 people, but since the company is growing rapidly with very exciting things going on, the group needs to be expanded with additional members. Primary Responsibilities As a Development Engineer in the group, your duties will vary across project phases. It will consist of both laboratory work, but also data analysis and logging of information. The main tasks will be to: - Perform experiments using Olinks PEA (Proximity Extension Assay) technology using qPCR and NGS as a readout platform. - Plan and perform laboratory work in accordance with set project plans and work schedules. - Evaluate, report and document results from the laboratory work. - Actively participate in the development of the group's and department's activities and participate in improvement projects. - Handle and register data for large amounts of antibodies, antigens and biological samples. Qualifications/skills - Master’s degree in life sciences or corresponding education. - Documented lab experience. Experience in pipetting small volumes and of using pipetting robots is advantageous. - A few years of working experience from the industry is highly beneficial. - Experience with antibody-based test methods as well as with PCR/qPCR and sequencing is a plus. - Good computer skills in general and good knowledge of Excel. - Experience of working in projects. - Fluent in spoken and written English is a must. Good Swedish skills is a plus. As a person you are responsible, driven and solution oriented. As we handle large amounts of reagents and data, we value that you are thorough and structured. You are a team player who finds it easy to communicate and interact with others both within the group and with those who work in other departments. It is important that you have a positive attitude and can adapt to changing circumstances, as we have a strong customer focus and are a company in hyper growth. The selection process is on-going, and the position might get filled before the last day of application so please apply as soon as possible, however no later than 2023.11.26.

27 oktober 2023
Sista ansökan:
14 april 2024
Manufacturing Engineer (stem-cell products), Procella Therapeutics AB

At Procella Therapeutics (part of Smartcella Holding AB) we provide advanced capabilities within stem cell therapy development and have inhouse cGMP manufacturing. We have globally licensed cardiac stem cell therapy in clinical stages (in strong collaboration with AstraZeneca) and a growing pipeline of life changing stem cell therapies. We are now seeking motivated Manufacturing Engineers, for permanent positions, to join the growing on-site manufacturing team in Tullinge, Stockholm. Overview You will be responsible for securing GMP compliance and technical readiness of the facility, equipment, process, and product. You will also be required to work within grade D, C, and B cleanroom classified areas applying a high standard of good manufacturing practices (GMP) and good documentation practices (GDP) as outlined by annex 1. Your focus will be to support the GMP (clinical and/or commercial) manufacturing of ATMP, cell products and you will be required to display a continuous improvement mind set. The role includes cross-functional collaboration with other departments such as MSAT, QA, and Supply Chain. The department will ensure compliance with Procella quality management systems, registered files, current regulatory requirements and quality criteria. Responsibilities - Produce clinical and/or commercial stem cells therapies in accordance with regulatory requirements. - Support the daily activities in the GMP, cleanroom facility. - Support cross-functional and external activities related to manufacturing. - Execute GMP processes according to production schedules and instructions (e.g. MBR , eMBR, SOP, PTP, sampling plans, and work instructions). - Take part in media fills / Aseptic process simulations. - Comply with company policies, risk assessments, instructions, and protocols. - Prepare, review, and revise GMP critical documentation. - Participate in projects (e.g., internal, and external tech transfer activities, validations, eMBR construction, etc). - Support periodic calibration, and maintenance and act as a superuser for equipment, instruments, and systems. - Handling CAPA and initiation of deviation and investigations. - Supervise and train team members in cleanroom environments and processes. - Document and monitor quality issues through Procella quality systems. - Initiate, review and approve change cases. - Identifying and implementing areas of improvement. - Ensure GMP compliance by complying with Procellas quality system and relevant guidelines, standards, and regulatory requirements - Ensure GMP compliance within the development of documentation, revision, and training. - Ensure GMP compliance within the validation lifecycle of equipment, systems, utilities, and processes. Required qualifications Practical experience: - At least 2 years of proven experience working in a GMP manufacturing and/or quality control environment, including hands-on laboratory-based cell culturing experiences (preferably experiences growing stem-cells in various conditions). Education: - University degree (eg. BSc, MSc) in life science (biochemistry, chemistry, molecular biology, microbiology or in other relevant area). This is a unique opportunity and you will be part of a great organization within the SmartCella group. Initial focus is to act hands-on to produce life changing products according to critical quality standards and to project plan. As the business grows there will be great opportunities for personal development and to take on new exciting projects/roles. You will receive a competitive compensation package including pension-, health covering- and insurance plans including a competitive monthly salary. Submit your application today! We will review applications on an ongoing basis and hope to fill the position as soon as possible. Reach out to Markus at [email protected] for questions regarding both the position and company. About the company SmartCella is a world-leading biotech & medtech company pioneering the future of targeted therapies by combining first-in-class delivery platforms with cutting-edge cell and gene therapies. The SmartCella group consist of SmartCella Holding AB, ProCella Therapeutics AB, SmartWise AB and SmartCella Solutions AB with a total of 60 employees from more than 20 nationalities. Homepage: https://www.smartcella.com/procella/

17 oktober 2023
Sista ansökan:
4 april 2024