Now, there is a great opportunity for a , full-time position at our clinic in Västerås. Are you our new colleague and embryologist at Västerås IVF. A great opportunity This is an exciting and rare opportunity. We are a rapidly expanding clinic, which gives you a unique position for personal development. And you will work closely with highly skilled embryologist. Your role We are looking for a dedicated embryologist with a strong commitment to quality and safety.You are a highly motivated embryologist, with a passion for improving the success rates for our couples. The post is ideally suited for you with at least 3 years of hands on clinical experience. You need to be up-to-date with the latest advances in clinical embryology, and aim for the highest level of quality in every task you undertake. A desire for constant improvement is a must. You should ideally be in Europe and/or have European citizenship. You must have excellent interpersonal skills, be a team player and be able to work independently. A brand new lab Last year we built a brand new state-of-the art lab built by specialist in IVF lab construction. We have equipped the lab with a dedicated ventilation system including the innovative Life Aire technology ror the removal of VOCs to make sure the air is as clean as possible. Our lab are highly equipped and run using the latest technology. You will be working alongside our highly competent embryologist, and also enjoy the benefits of colleagues focused on quality management. This position requires collaborating with physicians and other medical providers by providing expert care and service for fertility treatments. Key Responsibilities: - Perform all clinical embryology and andrology duties following appropriate training and competency assessment. - Participate in laboratory maintenance tasks and assist in validation within the laboratory. - Assist in the management and maintenance of laboratory equipment. - Oversee the procurement of laboratory products and services. - Adhere to all standard operation procedures. - Inform patients of treatment options, and treatment outcomes and discuss the implications. - Meet laboratory key Performance Indexes for all critical laboratory tasks. - Assist in the implementation of decisions regarding the embryology area. Qualifications and experiences - Life sciences degree - PhD or Masters in reproductive science is preferred. - At least 3 years of hands-on clinical embryology experience - A willingness to learn Swedish -relevant language skills are considered positive (e.g. understanding Scandinavian language). Salary: based on experience. Preferably full time. To learn more about our company and culture, visit here : www.vasterasivf.se Interested applicants should submit a CV, cover letter and lab performance indicators.

vid Institutionen för miljövetenskap. Sista ansökningsdag: 2024-06-03. Institutionen för miljövetenskap är en av de större institutionerna inom Naturvetenskapliga fakulteten. Institutionen består av fyra enheter med drygt 190 anställda forskare, lärare, doktorander och teknisk/administrativ personal från mer än 30 olika länder. Forskning och undervisning bedrivs inom miljökemi, atmosfärsvetenskap, biogeokemi och ekotoxikologi. Som medarbetare på Institutionen för miljövetenskap blir du en del av en dynamisk miljö med stark internationell prägel. Forskningen på Enheten för Miljöföroreningarnas Kemi är inriktad mot förekomsten av föroreningar i miljön och teknosfären. Områden med särkilt fokus är upptäckten av nya miljöföroreningar, att förstå de fysiska, kemiska och biologiska spridningsvägar som miljöföroreningar följer samt utvecklingen av nya verktyg och tekniker för provtagning och analys. Vi strävar efter att bygga upp vår vetenskapliga förståelse om källor, transport, transformation, bioackumulering och farmakokinetik för miljöföroreningar i matematiska modeller som inspirerar till nya vetenskapliga hypoteser och ta fram vetenskapligt underlag till beslutsfattare inom miljöområdet. Ämne Miljökemi av organiska föroreningar med inriktning mot datavetenskapliga verktyg. Ämnesbeskrivning Miljökemi av organiska föroreningar med inriktning mot datavetenskapliga verktyg innefattar studier av förekomst och processer av organiska föroreningar i miljön eller teknosfären och kombinerar teori med toppmodern analytisk kemi och dataanalysmetoder. Arbetsuppgifter Forskning samt viss undervisning och handledning.   Behörighetskrav Behörig att anställas som biträdande lektor är den som har avlagt doktorsexamen eller har utländsk examen som bedöms motsvara doktorsexamen. Främst bör den komma ifråga som avlagt sådan examen högst fem år före ansökningstidens utgång. Även den som har avlagt sådan examen tidigare kan dock komma i fråga om det finns särskilda skäl. Samtliga läraranställningar vid Stockholms universitet förutsätter att den sökande har förmåga att samarbeta och lämplighet i övrigt för att fullgöra arbetsuppgifterna. Bedömningsgrunder Särskild vikt fästs vid vetenskaplig skicklighet. Viss vikt fästs även vid pedagogisk skicklighet. Den vetenskapliga skickligheten kommer i första hand att bedömas inom ämnesområdet för anställningen. Anställningsvillkor Anställningsformen biträdande lektor ingår i universitetets karriärväg (”tenure track”) och regleras i Högskoleförordningen (SFS 2017:844). För denna anställning gäller att den biträdande lektorn anställs tills vidare, dock längst sex år. Anställningen kan förlängas till maximalt åtta år om särskilda skäl finns. Särskilda skäl kan t.ex. vara sjukfrånvaro eller föräldraledighet. Efter ansökan och prövning kan den biträdande lektorn befordras till anställning tills vidare som universitetslektor. Specifika kriterier för befordran från biträdande lektor till universitetslektor är fastställda av Områdesnämnden för naturvetenskap. Ansökan om befordran till universitetslektor ska inlämnas till fakulteten senast nio månader innan förordnandet som biträdande lektor löper ut. Övriga upplysningar Stockholms universitet strävar efter att vara en arbetsplats som är fri från diskriminering och ger lika möjligheter för alla. Fakulteten välkomnar ansökningar från kvinnor då flertalet lärare inom forskningsmiljön vid institutionen är män. Kontakt Upplysningar om anställningen lämnas av prefekten, professor Anna Sobek, [email protected], tfn 08-674 7230 eller professor Jonathan Benskin, [email protected], tfn  08-674 70 99. Frågor om anställningsförfarandet kan ställas till handläggaren Carina Nymark, [email protected]. Fackliga företrädare Ingrid Lander (Saco-S), tfn 0708-16 26 64, [email protected], Alejandra Pizarro Carrasco (Fackförbundet ST/OFR), tfn 08-16 34 89, [email protected], samt [email protected] (SEKO). Ansökan Du söker anställningen via Stockholms universitets rekryteringssystem. Du som sökande ansvarar för att ansökan är komplett i enlighet med annonsen och att den är universitetet tillhanda senast sista ansökningsdag. Vi ser gärna att din ansökan skrivs på engelska, då den kommer att granskas av internationella sakkunniga varvid engelska är arbetsspråket. Universitetets anställningsordning och anvisningar för sökande finns på webbsidan: att söka en anställning. Välkommen med din ansökan! Stockholms universitet bidrar till det hållbara demokratiska samhällets utveckling genom kunskap, upplysning och sanningssökande.

Camurus is a Swedish research-based pharmaceutical company committed to developing and commercializing innovative and long-acting medicines for the treatment of severe and chronic conditions, including opioid dependence, pain, cancer and endocrine disorders. New drug products are based on our proprietary FluidCrystal ® drug delivery technologies with the purpose to deliver improved quality of life, treatment outcomes and resource utilization. The company’s share is listed on Nasdaq Stockholm under the ticker “CAMX”. For more information, visit camurus.com. At Camurus you will get the opportunity to work with committed colleagues in a fantastic team, where the colleagues support and care for each other. Camurus is an innovative company that is currently expanding and establishing in new markets. Camurus is strengthening their global Patient Safety department with a new position - Patient Safety Associate. As Patient Safety Associate you will be a part of the global Patient Safety and Medical Affairs department at the headquarter in Lund, and you will report to the Director of Patient Safety. The position is based in Lund, and you will work in a dedicated team of 8 colleagues. As Patient Safety Associate you will belong to the global case processing team, with the responsibilities of monitoring mailboxes and co-ordination of case processing activities, with the aim to ensure that safety data is managed with high quality, efficiently and in compliance with worldwide pharmacovigilance regulations. Role and responsibilities Being the Patient Safety Associate, you are committed to ensure patients’ safety and product quality across the Camurus products. You will first and foremost ensure a compliant Pharmacovigilance System for Camurus products. Your responsibility includes, but is not limited to: - Management of individual case safety reports (ICSRs) and serious adverse events (SAEs) e.g. monitoring of safety mailboxes, perform ICSR download from health authorities including initial assessment, triage and logging of ICSRs and distribution of follow-up questions. - Processing of ICSRs in the Safety database - Support and perform reconciliations - Support and perform entries in XEVMPD - Support in co-ordination of activities in relation to safety in clinical trials - Support in SOP writing by preparing and reviewing Safety/PV SOPs and other related procedural documents This role involves daily cooperation with several departments internally, and it is a true coordination and spider-in-the-web type of role. Candidate profile We are looking for a candidate with a minimum of 2 years’ experience within drug/patient safety/pharmacovigilance or medical information, from the pharmaceutical/medical device industry. You probably have a background as a pharmacist, nurse or an education within pharmacology or pharmaceutical science. You have experience from managing ICSRs and SAEs, you are used to work with safety databases (e.g. ARISg/LSSMV or Argus). You have an analytical, but open mindset, you are comfortable in raising objections and enjoy solving problems and mediating issues that may arise and the ability to propose new and more efficient ways of work. To be successful in this job, you need a structural sense and attention to details. Furthermore, you enjoy working in a dynamic and changing environment. This position requires an ability to work with autonomy and independence, as well as cross-functional collaboration. You are able to prioritise effectively and meet multiple deadlines successfully. Enjoying a dynamic and multitasking business environment. A good level of spoken and written English is required. Camurus offers This is a great opportunity to join a highly innovative and 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 in a research-driven company, with the possibility make a real difference for Patient Safety. You will have the opportunity to make a career in a growing company, and you will work together with committed and knowledgeable colleagues. Camurus has approximately 200 employees with the head office located in Lund. The corporate culture is driven by innovation, strong collaboration internally and externally, ownership, quality, and passion about realizing ideas to achieve a patient-centric vision. 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: camurus.com. (https://www.camurus.com/) We are looking forward to seeing your application!

Camurus is a Swedish research-based pharmaceutical company committed to developing and commercializing innovative and long-acting medicines for the treatment of severe and chronic conditions, including opioid dependence, pain, cancer and endocrine disorders. New drug products are based on our proprietary FluidCrystal ® drug delivery technologies with the purpose to deliver improved quality of life, treatment outcomes and resource utilization. The company’s share is listed on Nasdaq Stockholm under the ticker “CAMX”. For more information, visit camurus.com. At Camurus you will get the opportunity to work with committed colleagues in a fantastic team, where the colleagues support and care for each other. Camurus is an innovative company that is currently expanding and establishing in new markets. Camurus is strengthening their global Patient Safety department with a new position -Patient Safety Manager. As Patient Safety Manager you will be a part of the global Patient Safety and Medical Affairs department and work in a dedicated team of 8 colleagues. The position is based at the headquarter in Lund and you will report to the Director of Patient Safety. You will be a part of the global case processing and surveillance, with the aim to deliver efficiency, quality, and compliance with worldwide pharmacovigilance regulations. As Patient Safety Manager you will overview cases and conduct safety surveillance by monitoring the benefit-risk balance of the products on the market and in clinical studies. Roles & Responsibilities: Being the Patient Safety Manager, you are committed to ensure patients’ safety and product quality across the Camurus products. You will first and foremost ensure a compliant Pharmacovigilance System for safety surveillance for Camurus products. You will also support the digital surveillance by using data driven methods and approaches. Your responsibility includes, but is not limited to: This role involves daily cooperation with several departments internally, and it is a true coordination and problem-solving type of role. - Have the overview of the medicinal product safety profiles and benefit-risk evaluations during its lifecycle, including monthly overview of individual case safety report (ICSR)/serious adverse event (SAE), perform signal detection and author aggregate reports. - Act as product specialist and have a good knowledge of Camurus products and ensure that information is captured and presented accurately in the safety database. - Act as subject matter expert in relation to benefit-risk evaluations. - Conduct and drive the digitalisation, automatization, and surveillance activities of safety system and database in accordance with applicable legislation. - Ensure compliance of all activities under Camurus responsibility within surveillance for Camurus products and with partners with whom Camurus hold a Safety Data Exchange Agreement (SDEA). - Conduct review and quality control of ICSRs/SAE. - Ensure timely submission and exchange of ICSRs/SAEs. - Support in the review and compilation of ICSR submission and ICSR exchange compliance. - Develop the quality system in the area of expertise, as per GVP requirement. - Support the QPPV to enable the QPPV to maintain oversight of the PV system, in particular for benefit-risk evaluations activities. Candidate profile We are looking for a candidate with a minimum of 5 years’ experience within drug/patient safety/pharmacovigilance from the pharmaceutical/medical device industry. You probably have a background as a pharmacist, nurse or have an education within pharmacology or pharmaceutical science. You have experience from ICSR/SAE processing, risk management plan writing, signal detection, aggregate report compilation, and have worked with clinical trials. Previous experience from working with case processing in safety databases is required and if you have IT experience it is a merit. Head office/Headquarters level experience is a merit. You have an analytical mindset, and you enjoy solving problems This position requires an ability to work with autonomy and independence, as well as cross-functional collaboration. You are able to prioritise effectively and meet multiple deadlines successfully. Enjoying a dynamic and multitasking business environment. A good level of spoken and written English is required. Camurus offers This is a great opportunity to join a highly innovative and 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 in a research-driven company, with the possibility make a real difference for Patient Safety. You will have the opportunity to build something from scratch, and you will work together with committed and knowledgeable colleagues. Camurus has approximately 200 employees with the head office located in Lund. The corporate culture is driven by innovation, strong collaboration internally and externally, ownership, quality, and passion about realizing ideas to achieve a patient-centric vision. Camurus offers 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!

About the role Join our dynamic team at Altris, a leading Sodium Ion Cathode Material manufacturer and battery developer, as a Life Cycle Assessment (LCA) Specialist. In this pivotal role, you will spearhead the development of LCAs across our portfolio of products, driving sustainability and innovation within our organization. Your responsibilities will include crafting LCA strategies, collaborating with internal teams and external partners, and guiding the implementation of decarbonization and recycled content roadmaps. With your expertise, you will play a crucial role in shaping our sustainability initiatives, contributing to strategic decision-making, and ensuring our company remains at the forefront of environmental responsibility. If you're passionate about making a difference and thrive in a fast-paced, cutting-edge environment, we invite you to join us in revolutionizing the future of battery technology. What you will do - Lead entire Life Cycle Assessments across Altris’ portfolio of products within both cathode and cell development - Develop sustainability and LCA strategies and approaches - Work with internal teams to roll out Altris’ sustainability strategy - Train the suppliers in performing LCA’s and manage suppliers specific needs with regards to LCA and sustainability topics - Conduct adhoc LCA’s to support strategic decision making within the company - Work with external collaborators (including Universities) to strengthen the data and evaluation of LCAs - Lead the development of decarbonization roadmaps and recycled content roadmaps - Prepare regular updates and present these updates cross company to inform on the status of our LCA, targets and approach to achieve the targets - Keep up to date with the latest developments in the field of LCA including competitor analysis and regulations - Contribute to the development of related policy frameworks and regulations globally Qualifications - Bachelors or Master’s Degree in a Relevant Field (i.e. Sustainability, Chemical Engineering, Environmental Engineering, Mechanical Engineering) - 3+ years post graduation working experience working within Life Cycle Assessments Specific skills: - Understanding of life cycle assessments and demonstrated ability to conduct life cycle assessments - Experience with conducting LCA’s according to European Standards - A strong interest in supply chain sustainability and demonstrated ability to work with suppliers internationally to assess their life cycle assessment and sustainability targets - Experience championing sustainability across an organizations - An analytical mindset and ability to tackle complex issues in a structured and logical way - Ability to work effectively in a team environment and cross functionally, as well as independently - Excellent communicator in English, both written and oral skills Personal success factors: - Creativity and GRIT with a can-do attitude - Accountability and responsibility - Organizational skills - Openness for people’s ideas

SPÄNNANDE TJÄNST HOS OSS Som BMA hos oss blir du en viktig del av den digitala och fysiska vården, där du genomför hälsoundersökningar på plats hos våra kunder. Din arbetsplats varierar mellan kundbesök runt Stockholm men även runt om i landet och Norden. I korthet kommer du att: - Genomföra hälsoundersökningar för våra kunders medarbetare. Här (https://onelab.se/halsotester) kan du läsa mer om vilka prover vi tar! - Samarbeta med kollegor för att planera och genomföra våra hälsoinsatser. - Förutom teamet med sjuksköterskor kommer du att arbeta nära kollegor inom andra kompetensområden som Customer Success, Tech och Sales! VÅRT ERBJUDANDE TILL DIG - Positivt arbetsklimat med fantastiska kollegor som stöttar och hjälper varandra. - Utvecklingsmöjligheter med regelbundna utbildningar och workshops. - Delta i en spännande resa med ett passionerat företag som förändrar företagshälsovård och hälsa i Sverige. VI SÖKER DIG SOM Förutom ett brinnande intresse för hälsa, söker vi dig som har erfarenhet av följande: - Minst 2 års erfarenhet av kliniskt arbete med provtagning inklusive blodtrycksmätning. - Erfarenhet av att arbeta inom service. - Körkort B och möjlighet att resa i tjänsten. - Goda kunskaper i svenska och engelska. MAGISKT VORE DET SÅKLART OM DU HAR - Erfarenhet av rådgivande samtal över telefon/video, särskilt inom psykisk ohälsa. - Språkkunskaper i danska, norska eller finska. - Intresse/utbildning inom hälsocoachning, hälsopedagogik eller kostrådgivning. För att lyckas i rollen ser vi att du har ett genuint intresse för att hjälpa människor och förstår vikten av bemötande och god service, eftersom det är företag och dess medarbetare vi jobbar med. Det är viktigt att du är en teamspelare och tar ansvar för att driva både ditt eget och teamets arbete framåt. I utbyte har du stor möjlighet att påverka och utveckla vårt gemensamma arbete. Vi har en vision om att skapa hållbar hälsa för alla medarbetare och våra BMAs är nyckelpersoner i arbetet att förverkliga OneLabs mission! Med rätt hälsoinsatser i rätt tid skapa förutsättningar för en hållbar framtid - för människan, företagen och samhället! ÖVRIG INFORMATION Start: Omgående enligt överenskommelse. Plats: Utgångspunkt i Stockholm, resor till annan ort förekommer. Omfattning: Tillsvidare, 80-100% efter önskemål. Ansökan: Skicka in Linkedin-profil eller CV och svara på frågorna när du klickar dig vidare på ‘’Skicka ansökan’’. Ersättning: Lön enligt överenskommelse. Arbetstider: Varierande mellan måndag - fredag 08.00-17.00 (övernattningar på annan ort förekommer) Låter detta intressant? Klicka på "Skicka ansökan" och ansök nu! Urval sker löpande, så skicka din ansökan så snart som möjligt.

BioGaia Production AB är ett produktionsbolag tillhörande BioGaia AB som i sin tur är ett innovativt svenskt hälsoföretag som utvecklar, marknadsför och säljer probiotiska produkter med dokumenterade, positiva hälsoeffekter. Produkterna säljs genom distributörer, varav flertalet är läkemedelsföretag i ett stort antal länder globalt. BioGaia har ett stort antal anställda i Sverige (Lund, Eslöv och Stockholm), USA, Japan och Singapore. Nu behöver produktionsbolaget i Eslöv stärka Quality Control teamet med en duktig laborant, som kan ta sig an följande uppgifter: - genomföra interna- och beställa externa analyser samt sammanställa och rapportera resultat - Sköta dagliga rutiner såsom beställning av varor, kontroll samt underhåll av utrustning. - Bidra till löpande förbättringsarbete kopplade till dagliga rutiner samt uppdatering av instruktioner. - Utföra kvalificeringar av utrustningar på laboratoriet. Den vi söker: - har relevant akademisk utbildning, t e x biomedicinsk analytiker eller naturvetenskaplig utbildning eller motsvarande arbetslivserfarenhet inom relevant område. - har ett genuint intresse för att arbeta laborativt med mikrobiologiska analyser som du har god praktisk erfarenhet av. - Du är noggrann, initiativrik, driven och prestigelös samt har ett sinne för "ordning och reda". - Du har utmärkt samarbetsförmåga och har ett lösningsorienterat angreppssätt på problem. - Du har goda kunskaper i Office - främst Word och Excel. Kunskaper i ERP-systemet Pyramid är meriterande liksom tidigare erfarenhet att arbeta i GMP miljö. - Goda kunskaper i svenska (tal och skrift) samt i engelska är en förutsättning för tjänsten. Tjänsten är en tillsvidareanställning hos BioGaia Production AB och ansökningar kommer att behandlas löpande. Vi behöver dig snarast så hör gärna av dig så snart som möjligt så berättar vi mer! Varmt välkommen med din ansökan!

Tycker du det vore riktigt fett att driva spännande utvecklingsprojekt av smörjmedel och processer? Är teknisk problemlösning och kemi två av dina favoritintressen? Se hit! Om rollen Hos oss väntar en unik möjlighet för dig att spela en viktig roll i vårt produktutvecklingsarbete och att bibehålla vår höga kundnöjdhet. Med ansvar att planera och driva en rad olika projekt inom nyutveckling och strategi, kommer du bidra till att förbättra existerande produkter och processer, undersöka nya vägar att gå och stärka upp vårt team långsiktigt. Vi tror på att våga misslyckas för att lyckas och kommer ge dig förutsättningarna för att testa dig fram och bidra med dina idéer. Denna roll passar dig som trivs med stor frihet att strukturera upp ditt arbete, men som samtidigt vill vara en del ett dedikerat team och få tillfälle att snacka lite smörja då och då. Som det lilla bolaget i den stora kontexten, erbjuder vi dig flera utvecklingsmöjligheter att växa internt, delta i forskningsprojekt, påverka beslut och ta dig an fler ansvarsområden. Dessutom kommer du samarbeta med och besöka kollegor på våra fabriker i Frankrike, Nederländerna och USA. Om oss Vi har mer än 130 års erfarenhet av smörjfett. Ja, du hörde rätt. Vi är Axel Christiernsson, och vi är världens främsta producent av smörjfett. Från huvudkontoret i Nol, som ligger bara 20 minuter med pendeln från Göteborgs centralstation, når vi ut både inom och utanför Sveriges gränser för att skapa anpassade lösningar utifrån våra kunders behov. Kort och gott är vi det internationella, marknadsledande bolaget med ett starkt varumärke, framgångsrika kunder och en härlig företagskultur. Här kommer du inte bara vara anställd, du kommer även få vara med och utveckla företaget framåt: komma med tankar, idéer och förbättringsmöjligheter. Välkommen till regelbunden massage, flextid, ett välmående bolag och ett gäng glada kollegor. Din profil: Utöver de egenskaper alla söker till sitt företag (kommunikativ, ansvarstagande, driven, lagspelare etc.) så är vi på jakt efter någon som också har: - Mycket goda kemikunskaper (antagligen är du utbildad inom kemi eller har flera års erfarenhet av arbetet inom kemiområdet) - Flerårig erfarenhet av produktutveckling och FoU - Grymma kommunikationskunskaper i både tal och skrift, engelska och svenska - Meriterande med erfarenhet av produktutveckling av smörjmedel, men även polymerer, färg eller andra kolloidala system - Meriterande med erfarenhet från kemisk processindustri och kemiteknik Bli en del av Axel Christiernsson Kan det vara så att just du är vår nya kemiingenjör? Härligt. Då hoppas vi få välkomna dig till vårt kontor på Strandvägen 10. Vi ser fram emot din ansökan! START: Enligt överenskommelse PLATS: Nol OMFATTNING: Heltid LÖN: Fast lön KONTAKT: Talent Manager Fanny Schmidt Fahlén, [email protected] (för frågor om tjänsten, ej ansökningar) Urval sker löpande Som ledande byrå inom employer branding och rekrytering är vi här för att revolutionera vår bransch, matcha talanger med företagskulturer och stärka organisationers arbetsgivarvarumärken. Nyfiken på att veta mer? Välkommen in i  Oddworks värld genom att klicka här (https://oddwork.se/sv/om-oss/) eller hitta fler karriärmöjligheter här. (https://oddwork.se/sv/jobba-hos-oss/)

Camurus is a Swedish research-based pharmaceutical company committed to developing and commercializing innovative and long-acting medicines for the treatment of severe and chronic conditions, including opioid dependence, pain, cancer and endocrine disorders. New drug products are based on our proprietary FluidCrystal ® drug delivery technologies with the purpose to deliver improved quality of life, treatment outcomes and resource utilization. The company’s share is listed on Nasdaq Stockholm under the ticker “CAMX”. For more information, visit camurus.com. At Camurus you will get the opportunity to work with committed colleagues in a team with good atmosphere, where the employees support and care for each other. Camurus is an innovative company that is currently expanding and establishing in new markets. We are looking for a Senior Data Manager to strengthen our Biometrics team within Clinical Development. If you have a passion for data management and enjoy collaboration with dedicated colleagues, Camurus is an excellent company for you. Main responsibility Among others, your responsibilities will include: - Support with oversight of data management activities, for example: - Data cleaning activities - EDC-system and ePRO - Perform UAT - Review/approve relevant biometrics documents - Keep up to date with data management methodology/systems relevant to the pharmaceutical industry and share knowledge - Write or review relevant SOPs - Process improvements The role is based at our HQ in Lund, Sweden. Candidate profile We are looking for a candidate with at least 5 years’ experience within Biometrics in the pharmaceutical industry, or at a clinical CRO, together with a university degree in Engineering, information technology, computer science or related field. You have experience from giving data management support and it is considered a strong merit if you have knowledge in CDISC and SAS programming. Most probably, you are an expert of EDC/ePRO system. Excellent communication skills, both oral/ and written (in English) is required, and you can easily explain complex subjects to non-experts. Even though you like working independently, you are a true team-player, with a flexible mind, able to respond to changing business needs. You are accurate, structured, and organised and you work in a goal-oriented way. Furthermore, you thrive in a dynamic environment, without being micro-managed. Camurus offers This is an excellent opportunity to join a dynamic team supporting the business in our continued 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 close to where decisions are taken. The team consists of three experienced, knowledgeable, and sympathetic colleagues, and you will learn a lot along the way. Camurus has approximately 200 employees with the head office located in Lund, and affiliates in 10 countries. The corporate culture is driven by innovation, strong collaboration internally and externally, ownership, quality, and passion about realizing our ideas to achieve our patient-centric vision. This is an immediate, full-time employment opportunity. 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. We are looking forward to seeing your application!

At Procella Therapeutics we provide advanced capabilities within stem cell therapy development and have inhouse cGMP manufacturing. We have a globally licensed cardiac stem cell therapy in clinical stages (collaboration with AstraZeneca) and a growing pipeline of stem cell therapies. We are now seeking a Head of Analytical Development to our Analytical Development team. As Head of Analytical Development you will be responsible for providing leadership of the activities related to the analysis, method development, stability and testing of drug substance DS) and drug products (DP) for cell therapy projects. You will provide scientific guidance and technical support and be responsible for building and growing an analytical development group, as well as managing a team of capable analysts. You will be required to work in a leadership capacity, liaising with various other managers from Quality Control (QC), Process Development (PD), Supply Chain (SC), and the MSATs groups. The successful candidate is expected to be an analytical expert with a thorough understanding of cell therapy products and their quality attributes. The incumbent will be empowered to lead the creation and delivery of the analytical strategy to support the development of an analytical platform for cell therapy clinical output. Responsibilities - Support, manage, and tutor a team of analytical scientists in cell therapy analytical technologies, including but not limited to Flow Cytometry, NucleoCounter, ddPCR/PCR, ELISA. - Analytical leader and expert to facilitate the generation of analytical reports required for regulatory submissions and interactions. - Provide strategic insight and leadership required for cell therapy analytical development work in line with the principles of QbD (quality by design). - Responsible for development, qualification and establishment of analytical testing methodologies to control raw materials, intermediates, IPC and final product in compliance with the regulatory guidelines. - The analytical development manager will be required to draft SOPs in line with cGxP for analytical oversight of process development / scale-up and MSATs. - The role will also require limited project management (PM) responsibilities in relation to the analytical development group. - Responsible for coaching, supervising, mentorship, development, support and line leadership of the analytical development group. - Ensure a learning environment and foster a culture of scientific excellence through training, influencing, and leading by example in a fast-paced cell therapy biotech company. - Support the implementation of stability strategies, sampling plans, and work instructions. - Comply with company policies, risk assessments, instructions, and protocols. - Prepare, review, and revise GMP critical documentation; CMC sections related to analytical methods, method validation, specifications, and stability protocols for regulatory submissions. - Provide scientific guidance on investigations related to analytics at Procella, including resolution of out-of-specification (OOS) and out-of-trend (OOT) testing results, change control (CC), and CAPAs. - Participate in and/or lead projects internal and external method transfers. - Ensure team maintenance of good analytical data, laboratory notebooks and results, to ensure data integrity. Required Qualifications & Experience - A minimum of 3 years of experience in leadership in a similar role with proven leadership skills and strategic problem-solving ability. - Cell therapy method expertise, development, qualification, and tech transfer. - A minimum of 5 years of industry experience in analytical development. - Working knowledge of MS Excel, Word, and PowerPoint. - BSc or above in life science or equivalent, a PhD would be preferred. - Experience in cell therapy is desired. - Project Management experience is an asset. - Fluency in English is required. Interested? Submit your application today! We will review applications on an ongoing basis and hope to fill the position as soon as possible. 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 65 employees from more than 20 nationalities.