Haemme osaavaan ja aikaansaavaan mikrobiologiseen tiimiimme Tampereen tehtaalle ylempää toimihenkilöä toistaiseksi voimassa olevaan työsuhteeseen.
Mitkä ovat tähän toimeen kuuluvat tehtävät?
vastata lääkevalmisteiden, raaka-aineiden ja vesinäytteiden mikrobiologisesta testauksesta
vastata poikkeamien selvittämisestä sekä raporttien ja riskiarviointien laatimisesta
valvoa ja johtaa laboratoriotyötä paikan päällä
osallistua puhdastilojen mikrobiologiseen olosuhdevalvontaan
osallistua menetelmänsiirto- ja kehitysprojekteihin, olla vastuussa mikrobiologisten menetelmien kehittämisestä ja validoinnista
osallistua asiakas- ja viranomaistarkastuksiin
Mitä odotamme hakijalta?
ylempi korkeakoulututkinto, mikrobiologia tai vastaava
hyvää suomen ja englannin kielen osaamista
hyviä vuorovaikutustaitoja, organisointikykyä ja asiakaslähtöisyyttä
kykyä itsenäiseen työskentelyyn ja päätöksentekoon
joustavuutta ja positiivista asennetta
Lisäksi arvostamme:
kokemusta lääketeollisuudesta ja GMP:n tuntemusta tai kokemusta laboratoriotyöstä SFS-EN ISO/IEC 17025 mukaisesti
kokemusta esihenkilötehtävistä
Kiinnostuitko?
Say yes to what’s next: Lisätietoja antaa Head of QC Päivi Waris paivi.waris@nextpharma.com / +358 40 838 9070. Lähetä hakemuksesi nettisivujemme https://careers.nextpharma.com/ kautta viimeistään 13.1.2023. Ilmoitathan hakemuksessasi palkkatoiveesi sekä ajankohdan, jolloin voisit aloittaa työt. Niittyhaankatu 20, Tampere.
Olemme yksi johtavista lääketeollisuuden, biotekniikan ja terveydenhuollon sopimusvalmistajista Euroopassa, ja meillä on noin 2000 työntekijää Saksassa, Ranskassa ja Suomessa. Meille seuraava askel on aina se tärkein. Nopea tempomme vie meitä eteenpäin, tuo työympäristöömme elämää ja kannustaa kasvuun. Avaimemme menestykseen on innostus ja haluamme tarjota erinomaista palvelua asiakkaillemme ympäri maailman. Tervetuloa NextPharmaan.
Tehtaamme Suomessa sijaitsee Tampereella ja on erikoistunut aseptiseen silmälääkkeiden tuotantoon, josta meillä on pitkä kokemus. Tampereen tehtaalla valmistamme ja pakkaamme nestemäisiä silmälääkkeitä BFS (Blow Fill Seal), MD (Multi dose) three piece (korkki, tiputin, pullo) ja PFMD (preservative free multi dose) tuotteina. Tuotantomme tuotteet ovat globaaleja ja ne ovat markkinoilla useissa maissa.
The University of Eastern Finland is inviting applications for a Postdoctoral Researcher/Project Researcher/ Doctoral Researcher (Translational Immunology) position in Kuopio. The position will be filled for 1 March 2023 to 31 August 2024 (or as agreed). Please find more information below and submit your application no later than 16 January 2023.
Role and salary
As our new Postdoctoral, Project or Doctoral Researcher in Translational Immunology, you will be working in the School of Medicine in the Faculty of Health Sciences, Kuopio Campus.
Our research focuses on the immunological disturbances in autoimmune diseases, with a special emphasis on CD4+ T cells. We utilize a state-of-the-art single-cell methodology to study clinical samples from children with type 1 diabetes and juvenile idiopathic arthritis. More details on the research group and research interests can be found at https://uefconnect.uef.fi/en/group/translational-immunology-group/.
The successful candidate will work on a project funded by the Academy of Finland aiming to analyse CD4+ T cell phenotypic alterations related to autoimmunity in type 1 diabetes. The candidate may also participate in projects studying immune responses in patients with juvenile idiopathic arthritis and in patients undergoing immune checkpoint inhibitor therapy for cancers.
A person to be appointed to the Postdoctoral Researcher or Project Researcher position is required to hold a suitable doctoral degree. If you have been awarded your doctoral degree less than five years ago, the post will be one of a Postdoctoral Researcher. If the doctoral degree has been awarded more than five years ago, the post will be one of a Project Researcher. In this context, five years is the net period of time, which does not include maternity leave, parental leave, military service, etc. The position of postdoctoral researcher and project researcher shall always be filled for a fixed term (UEF University Regulations, Section 31).
A person appointed to the Doctoral Researcher position shall be qualified to pursue postgraduate studies, i.e., they are required to have completed a suitable higher university degree or an equivalent education abroad that would qualify the person for similar academic studies. The positions of doctoral researcher shall always be filled for a fixed term (UEF University Regulations, Section 31).
The position will be filled for 1.3.2023-31.8.2024 (or as agreed). The position will be filled for a fixed term due to it pertaining to a specific project. A probationary period is applied to all new members of the staff.
The salary of the position is determined in accordance with the salary system of the Finnish universities. The salary comprises two components: a job requirement component and a personal performance component. For a Postdoctoral Researcher/Project Researcher, the job requirement component is 3,044,00 euros/month, based on level 5 of the job requirement chart for teaching and research staff. For a Doctoral Researcher, the job requirement component is 2,108,40 -2,628,85 euros/month, based on levels 2-4 of the job requirement chart for teaching and research staff. The personal performance component can be a minimum of 6 % and a maximum of 50 % of the above-mentioned sum. At the beginning the salary will be between 3,348-3,866 € (as post-doctoral/project researcher) or 2,319-3,339 € (as doctoral researcher).
Our requirements and expectations
A PhD in immunology or a related discipline (Postdoctoral/Project Researcher) or an MSc in biosciences or a related discipline (Doctoral Researcher)
Good knowledge of written and spoken English
Able to work independently and supervise students
Be willing to contribute to writing peer-reviewed publications and applications for research funding
Previous experience in some of the following techniques is considered highly advantageous:
High-parameter flow cytometry with experience in panel design and analysis
You will have an opportunity to work in an interesting role as part of our international, creative, participatory and inclusive academic community.
Enjoy your life in Finland! Known for its cleanliness, welfare know-how, modern technology and superb education system, Finland is an exotic and safe country to work in. Please visit the Life in Finland section on our website to learn more.
How to apply?
Submit your application by using our electronic application form no later than 16 January 2023 (by 24.00 hours Finnish time).
Please note that you must include the following appendices in your application:
For further information on the position, please contact: Professor Tuure Kinnunen, +358 29 4454980, tuure.kinnunen@uef.fi.
For further information on the application procedure, please contact HR-secretary Sanna Partanen, +358 29 4454634, sanna.partanen@uef.fi.
University of Eastern Finland and the Faculty of Health Sciences in brief
The University of Eastern Finland, UEF, is one of the most multidisciplinary universities in Finland. We have a staff of 3,200 members, and our academic community comprises around 16,000 degree students. Our campuses are located in Joensuu and in Kuopio. Our research is ranked among the best in the world in several fields. We generate research-based knowledge and make it openly accessible for the benefit of all. To learn more about our university please visit our website at www.uef.fi/en. On our website, you’ll also find information about the university as a work community and as an employer (https://www.uef.fi/en/article/one-university-a-thousand-stories), as well as our employees’ career stories (https://www.uef.fi/en/career-stories).
The Faculty of Health Sciences operates at the Kuopio Campus of the University of Eastern Finland. The Faculty is research-intensive, and its internationally recognised research activities are closely linked to the strategic research areas of the University. There are approximately 3 090 degree students and about 580 PhD students in the Faculty. The faculty has 800 staff members. http://www.uef.fi/en/ttdk/etusivu
Are you looking to join a dynamic, innovation-driven, international company, building a better future for us all? UPM leads the forest based bioindustry into a sustainable, innovation-driven, and exciting future. The competence, integrity and drive of our people make us unique. We live by our values – trust and be trusted, achieve together, renew with courage.
We are now looking for a Quality Manager to join our Biomedicals team in Helsinki or Lappeenranta, Finland.
Greetings from your future colleagues
“We are looking for a diligent professional with a solid experience in ISO 13485 to maintain our QMS and also to help leading the implementation of FDA and GMP compliance.” – Johana Kuncová-Kallio, Director, Biomedicals
“UPM proprietary nanocellulose technologies open a wide range of business opportunities in the biomedical field. Together with our professional and enthusiastic team, you will play a key role in securing the product quality and regulatory compliance and also have a possibility to participate in new business development.” – Kari Luukko, Director, QA Biomedicals
What You’ll Do
You share the vision for our products and for your part are responsible for its high-quality execution, the strategy implementation, and the roadmap development
You maintain and develop our ISO 13485 quality management system (QMS) in accordance with applicable regulations
You manage and develop QMS processes such as annual planning, non-conformities (NC) treatment, CAPA, change control and supplier management
You manage the process of legislation and standards monitoring
You maintain and develop UPM Biomedicals’ QMS database
You support and steer the team members in daily quality operations such as quality control, document management, NC and CAPA processes, design and development
You plan and co-ordinate management reviews, personnel trainings, as well as internal and external audits
You are the main contact for our notified body
You will be responsible for regulatory compliance on general level and support our teams in product-specific compliances. You will also participate in risk management processes of our products
You manage the regulatory strategy process of our products’ global market expansions and collaborate with our business developers and product managers
Who You Are
You have a university science degree and minimum if 5 years in a managerial role within quality management systems and regulatory affairs with focus to medical devices, ideally biomaterials rather than diagnostics or software
You have a deep understanding and working knowledge of ISO 13485, QC, GMP, MDR and FDA practices and document management. Your documentation practices are exact and persistent
You have proven business acumen and working knowledge of the industry and supplier base
You have excellent communication and problem solving skills
You are positive thinking, solution oriented, multitasking, persistent and proactive team player
You are fluent in written and spoken English. Finnish is seen as a benefit
Seen as a benefit:
You have previous experience of medical device or in vitro medical device product development for the Clinical market
You have previous experience in management of clinical trials
You know medical device registration processes in different territories
This Is What We Offer For You
Meaningful job: We are proud of what we do. Our work highlights the expertise of our personnel, the high quality of our products and the company’s values.
Inspired and motivated teams: We have highly skilled workforce. We are a multifaceted, international organisation that works as a team to achieve our shared objectives.
Development opportunities: With us you can build up your expertise. We provide opportunities to support your development throughout every stage of your career.
Responsibility for people and environment: Our ethical principles embrace people as well as the environment. We are always striving to build a more sustainable future.
Additional Information
At the beginning (first 2 years), the job requires intensive presence in Finland (Lappeenranta or Helsinki) to adapt Biomedicals operations, later the location is negotiable in UPM sites in Europe.The recruitment will be done in cooperation with our recruitment partner George James Ltd.For more information, please contact Kari Luukko, Director, QA Biomedicals on +358400259866 at the following times:
December 15th 2022 9-11 a.m. EET
January 5th 2023 from 9-11 a.m. EET
January 12th 2023 from 9-11 a.m. EET
Please send your application via link latest by 15.01.2023. We will start going through the applications already during application period so please submit your application as soon as possible.For support with submitting your application, please contact the HR Service Center at careers@upm.com or tel. +358204146600.A security background check may be performed for those selected to UPM positions, in accordance with the company recruitment guidelines and the Security Clearance Act 726/2014.UPM is a non-smoking workplace in Finland.
UPM Biomedicals is the forerunner in producing high quality nanofibrillar cellulose for medical and life science applications. More than 300 patents protect the existing and future products that rely on the Finnish birch pulp. We actively collaborate with universities, research centres and key industrial partners on innovations and products in the field of high throughput drug screening, personalized medicine, advanced cell therapies, 3D bioprinting, tissue engineering and wound care. www.upmbiomedicals.com
When you’re part of Thermo Fisher Scientific, you’ll do challenging work, and join a team that values performance, quality and innovation. As part of a successful, growing global organization you will be encouraged to perform at your best. With revenues of more than $40 billion and the largest investment in R&D in the industry, we give our people the resources and chances to create significant contributions to the world.
Location/Division Specific Information
Location: – Remote / Field within EuropeDivision: Genetic Sciences Division – Human Identification (HID)
Discover Impactful Work:
Join us as a Field Applications Specialist (FAS) and assist us in our mission to become the world leader in serving science. This multifaceted position involves providing scientific training, guidance, application support and troubleshooting for our customers in Russian-speaking countries.
A day in the Life:
Deliver on-site and remote scientific application support & training support to our customers on our HID products.
Supporting our customers with the implementation of new products, applications or workflows.
Diagnose & resolve product performance problems and customer queries/complaints by phone, email or onsite.
Work with sales representatives on sales calls to customer laboratories to provide technical and applications assistance in response to customer inquiries.
Assist the regional sales team in the development of accounts by giving technical seminars and presentations that promote the use of our products.
Providing pre-sales support activities like product demonstrations, user meetings or seminars.
Visit and represent our company on scientific or commercial meetings, conferences, trade shows, congresses, etc.
Establish contacts to key opinion leaders in the field and develop local references.
Maintain up-to-date technical expertise and in-depth knowledge of our product portfolio and scientific developments in the forensic DNA-identification workflow.
Become a strong internal Voice of Customer by providing customer feedback on our products to local and European Sales & Marketing.
Build trust with our customers and excel in customer service.
Keys to Success:
Education
Degree in Biology, Biotechnology, Biomedical Sciences, Genetics, Molecular Biology, Biochemistry or similar (Masters or PhD preferred)
Experience
Extensive technical hands-on experience (+5 years) in a forensics lab environment such as data analysis and/or research & development.
Previous experience in a support / training-related position or hands-on experience with Thermo Fisher Scientific HID technology is appreciated.
Knowledge, Skills, Abilities
High degree of technical competence & confidence.
Able to connect with and support people optimally with varying levels of technical knowledge and expertise.
Customer-centricity with the emotional intelligence to understand customer concerns and aware of markets, trends and competitors.
Good computer (especially MS Office) and/or IT skills and have an interest for groundbreaking innovation and technology.
Excellent communication & presentation skills.
Fluent Russian and English language skills – oral and written.
Willingness to travel internationally (mainly Russian-speaking countries / CIS with the exception of Russia and Belarus; and within Europe).
Valid driver’s license.
We are offering an employment with an innovative, growing organisation with outstanding career and development prospects and an exciting company culture which stands for integrity, intensity and innovation. The role comes with a competitive salary plan, company pension scheme, bonus plan, company car and further employee benefits.
Interested? Please apply in English language.
Our Mission is to enable our customers to make the world healthier, cleaner and safer. Watch as our colleagues explain 5 reasons to work with us. As one team of 100,000+ colleagues, we share a common set of values – Integrity, Intensity, Innovation and Involvement – working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need. #StartYourStory at Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued.Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
Are you a recent graduate and do you have less than 6 months clinical experience? Did you study in the life sciences/data sciences/data analytics/clinical/nursing area?
The Accelerated Program of Education, Exposure, and Experience for CRAs (APEX CRA) provides foundational clinical research training – including project and system experience – to new CRA hires who are recent college graduates and have less than a year of monitoring experience.
Through this program, you’ll transform into a credible and experienced CRA I. As you progress, APEX CRAs perform billable project tasks to support the CRAs and Clinical Operations Leads (COLs) with a focus in three developmental areas: Project Support, Initiation CRA support, and Site Facing support. You’ll be required to complete the ACRP Entry Level Knowledge Assessment and are enrolled in a 1-year membership to the ACRP.
You’ll also work closely with CRAs to gain exposure to and experience with the CRA role and its responsibilities across a period of three to six months. During this experience, you’ll have the opportunity to practically apply in-class concepts with day-to-day application by working with clinical systems including Clinical Trial Management Systems (CTMS), Electronic Data Capture, Safety Information Systems, and TMF platforms, and benefit from both instructor-led trainings and ongoing coaching and support of Line Managers and COLs.
Finally, APEX CRAs accompany CRAs for observational and co-monitoring support on-site or during remote visits which combines learning for the APEX CRAs and workload aid for their CRA colleagues. Upon completion of the program, you’re well-positioned to independently function within the CRA role and to immediately begin successful monitoring!
Minimum Bachelor’s degree in life sciences/data sciences/pharmacy/nursing or other related discipline
1 year or less of monitoring/clinical experience
Complete Finnish language proficiency
Strong interpersonal, written, and verbal communication skills within a matrixed team
Experience working in a self-driven capacity, with a sense of urgency and limited oversight
A client-focused approach to work and flexible attitude with respect to assignments/new learning
The ability to manage multiple tasks, evaluate unpredictable scenarios and achieve project timelines while applying your understanding of study protocol(s)An honest and ethical work approach to promote the development of life changing treatments for patients
Strong computer skills and aptitude to learn quickly
Aurealis Therapeutics is a Swiss-Finnish private biopharmaceutical company focusing on the development of a 4-in-1 synthetic biology, cell and gene therapy platform to address unmet medical needs in three therapy areas: chronic wounds, oncology, and inflammation.
We at Aurealis Therapeutics are looking for aMedical Monitor for a permanent-term contract in Kuopio or potentially other location in Finland, the Netherlands, Germany, or Switzerland. The start date of the job is negotiable, but we wish you could start during the first quarter of 2023. You will be working full-time.
We are looking for a team player for the medical monitoring and drug safety management of the company. As a Medical Monitor, you are responsible for medical and safety aspects of clinical development, advising and consulting on safety event evaluation, providing physician-level opinions on multiple trials and sites, consulting on protocol design, patient safety concerns, deciding if a specific adverse event requires un-blinding, mediating between sponsor, CRO and trial sites, reviewing whether concomitant medications and adverse events are coded and reported properly, examining the protocols of a clinical study, planning and initiating a trial, dealing with the data (analysis, interpretation, exploration). You are also responsible for pharmacovigilance/drug safety (Drug Safety Officer).
Your previous work experience and knowledge defines your position and responsibilities, so you have the opportunity to affect your role. Successful candidate for this role must be able to communicate efficiently in English.
We hope that you have at least +2 years of experience in similar roles and in depth, hands-on experience and understanding of clinical trial execution and follow-up. You have a degree in Medicine (MD). Working experience in chronic wound indications is an advantage, but not a must. You would be reporting to our Chief Medical Officer, and working closely with the clinical and regulatory teams and with external service providers (CROs). You are collaborative, highly organized and enjoy working with different systems. If so, you might be our new colleague!
Experience and skills required:
Overall knowledge and experience of the drug development process, clinical trial conduct, data management, drug safety, and biostatistics
Deep knowledge of relevant regulations e.g., ICH/GCP/GVP, EMA, and FDA guidelines
Excellent organizational, decision making and project management skills
Experience in working with software programs (EDC, eTMF, etc.)
We will offer you a position in an international and dynamic working environment where you have the opportunity to develop your career path. Join our team!
If you are interested in the position, please fill-in the application at https://aurealistherapeutics.com/medical-monitor/. We will be interviewing during the application time.
If you have any questions regarding the position, please contact Maija Rusi, our Financial and Administrative Director, by email at maija@aurealistherapeutics.com
Biovian on vahvasti kasvava turkulainen bioteknologiayritys. Tarjoamme sopimusvalmistusta, -analysointia ja prosessikehitystä biotekniikkayrityksille, jotka kehittävät innovatiivisia geeniterapioita tai biofarmaseuttisia tuotteita. Saatamme asiakasprojekteja laboratoriosta kliiniseen potilaskäyttöön asti taidolla, innolla ja sydämellä – tämä on meillä Manufacturing Happiness.
Haemme Analytical Scientistiä HPLC-tiimiimme
Yhtiön kasvaessa haemme vahvistusta laadunvalvontalaboratoriomme. Analytical scientist tehtävässä päävastuusi on HPLC analyysien suunnittelu, validointi, tarkastaminen, tulosten raportointi ja työn ohjaus. Lisäksi osallistut analyysimenetelmien kehittämiseen, laboratorion yleistoimintoihin ja toimit asiantuntijana asiakaspalavereissa. Analysoitavat tuotteet ovat pääasiassa proteiineja, joten aikaisempi työskentely vastaavien tuotteiden parissa on eduksi.
Päätehtäväsi on
– Toimia HPLC-analytiikan asiantuntijana ja kehittää työtä. – Projekteihin liittyvä raportointi, dokumentointi ja työohjeiden kirjoitus. – Vastata työn aikatauluttamisesta ja tarkastaa analyysien tulokset. – Opastaa HPLC-analyysien tekijöitä. – Toimia GMP-ohjeistuksen mukaisesti. – Osallistua asiakaspalavereihin asiantuntijana.
Työssä onnistuaksesi
Odotamme sinulta laajaa työkokemusta HPLC-analytiikasta. Sinulla on soveltuva ylemmän korkeakoulun tutkinto (esim. biolääketieteestä tai biokemiasta) sekä käytännön kokemusta analytiikasta. Olet tottunut dokumentoimaan ja kirjoittamaan raportteja englanniksi.
Toivomme, että sinulla on vahvaa osaamista jollakin alla mainitusta osa-alueesta sekä asiantuntemusta useimmista niistä:
Olet työskentelytyyliltäsi tarkka, järjestelmällinen, reipas ja toimelias henkilö. Sinulla on myös hyvät vuorovaikutus- ja ryhmätyötaidot. Toivomme sinulta myös joustavaa työotetta sekä kykyä työskennellä itsenäisessä tehtävässä.
Työohjeet ja dokumentointi tehdään englanniksi, joten toivomme sinulta hyvän suomen kielen taidon lisäksi myös hyvää englannin kielen taitoa.
Mitä sinä saat meiltä?
– Tarjoamme sinulle merkityksellisiä ja vastuullisia työtehtäviä lääkkeiden ja biologisten prosessien parissa. – Pääset osaksi huipputiimiämme, joka koostuu monialaisista asiantuntijoista. – Saat hyvän perehdytyksen tehtävään ja mahdollisuuden ammatilliseen kehittymiseen monipuolisten tehtävien kautta. – Saat viihtyisän työpaikan, jossa työntekijöitä arvostetaan, sekä hyvät henkilöstöedut – tarjoamme työntekijöillemme esimerkiksi laajan työterveyshuollon, terveysvakuutuksen sekä hyvinvointi- ja liikuntaedun.
Työtehtävä on kokoaikainen ja vakituinen. Työtä tehdään Turussa Kupittaalla, jossa toimipisteemme sijaitsee. Jatkossa sinun on mahdollista työskennellä myös etänä, toivomme kuitenkin, että olet paikan päällä noin neljä päivää viikosta.
Kiinnostuitko?
Lähetä hakemuksesi (suomeksi tai englanniksi) palkkatoiveineen viimeistään maanantaina 16.1.2023.
Lisätietoja tehtävästä antaa QC Manager Anne Rokka, 050 576 3192 9.1.2022 klo 12-13 ja 12.1. klo 9-10.
Käymme hakemuksia läpi hakuaikana ja haastatteluja voidaan aloittaa jo ennen hakuajan umpeutumista.
Tule mukaan työskentelemään kanssamme tulevaisuuden biologisten lääkkeiden parissa ja muuttamaan ideoita tuotteiksi!
WWW-osoite https://biovian.com/ Yhteystiedot Riikka Laine, riikka.laine@biovian.com Työpaikan osoite Tykistökatu 6 A, 20520 TURKU Työ alkaa Sopimuksen mukaan Työaika kokoaikatyö Työn kesto yli 12 kuukautta Haku päättyy 16.01.2023 klo 23:59 Ilmoitus jätetty 29.12.2022 Ilmoitusnumero 11766715
Health Tech Top Expert-RekryKoulutus toteutetaan keväällä 2023 (20.2.-15.6.2023). Koulutus sisältää terveysteknologia-alan erityisosaamiseen liittyvää etäkoulutusta sekä käytännöllisen työssäoppimisjakson alan yrityksessä. Toteutat työssäoppimisen yhteydessä sinulle räätälöidyn kehittämistehtävän, jonka tueksi saat henkilökohtaista sparrausta. Koulutuksessa vahvistat osaamistasi mm. terveysteknologian toimialasta, laadun- ja riskienhallinnasta, kansainvälisestä liiketoiminnasta, myynnistä ja markkinoinnista, projektinhallinnasta sekä tuotekehityksestä. Koulutuksen avulla kehityt huippuosaajaksi terveysteknologian alalle!
Avoin paikka: Tekninen asiantuntija
Koulutuksen yrityskumppani, TopCon Healthcare Solutions etsii teknistä asiantuntijaa vastaamaan integraatioista. Topcon Healthcare tarjoaa uusimmat kokonaisvaltaiset ratkaisut silmien terveydenhuoltoon, joihin kuuluvat esim. multimodaaliset kuvantamislaitteet, eri valmistajien laitteisiin sopivat datankäsittelyratkaisut sekä etälääketiedeteknologia.
Teknisenä asiantuntijana vastaat integraatioiden toteuttamisesta ja kehittämisestä. Huolehdit teknisten järjestelmien pystyttämisestä, testaamisesta sekä käyttökoulutuksesta ja palautteeseen pohjautuvasta kehittämisestä. Hakijalta edellytämme soveltuvaa korkeakoulututkintoa sekä ohjelmointiosaamista ja aiempaa kokemusta integraatioiden toteuttamisesta. Työssäsi tarvitset hyviä kommunikointi- ja tiimityötaitoja sekä englannin kielen taitoa, sillä työkielemme on englanti. Tiimimme työskentelee Oulussa. Teemme yhteistyötä myös muualla Suomessa sekä maailmalla kuten New Jerseyssä ja Japanissa työskentelevien kollegoidemme kanssa.
Tavoitteemme on tarjota terveydenhuollon ammattilaisille älykkäitä, arvoa tuottavia ja tehokkaita teknologiaratkaisuja hoidon ja palvelun kehittämiseksi. Tarjoamme sinulle mielenkiintoisen tehtävän kiehtovalla terveysteknologian alalla, huiput työkaverit ja joustavan työympäristön. Jos koet olevasi etsimämme osaaja, hae mukaan ja kerro lisää itsestäsi!
Hakuehdot RekryKoulutukseen
Hakijan tulee olla työtön työnhakija, työttömyysuhan alainen tai osa-aikaisesti työskentelevä. Hakijoilta edellytetään korkeakoulututkintoa (ammattikorkeakoulu tai yliopisto) tai riittävästi muuta työkokemusta esimerkiksi seuraavilta aloilta:
Health Tech Top Expert-RekryKoulutus toteutetaan yhteistyössä Kasve Oy:n, paikallisten TE-palveluiden ja ELY-keskuksen kanssa. Hakuprosessi ja opiskelijoiden rekrytointi tehdään yhteistyössä Pohjois-Pohjanmaan TE-palveluiden kanssa. RekryKoulutus on osallistujalle maksuton.
Health Tech Top Expert-RekryKoulutus toteutetaan keväällä 2023 (20.2.-15.6.2023). Koulutus sisältää terveysteknologia-alan erityisosaamiseen liittyvää etäkoulutusta sekä käytännöllisen työssäoppimisjakson alan yrityksessä. Toteutat työssäoppimisen yhteydessä sinulle räätälöidyn kehittämistehtävän, jonka tueksi saat henkilökohtaista sparrausta. Koulutuksessa vahvistat osaamistasi mm. terveysteknologian toimialasta, laadun- ja riskienhallinnasta, kansainvälisestä liiketoiminnasta, myynnistä ja markkinoinnista, projektinhallinnasta sekä tuotekehityksestä. Koulutuksen avulla kehityt huippuosaajaksi terveysteknologian alalle!
Avoin paikka: Projektipäällikkö Koulutuksen yrityskumppani, M-Solutions hakee projektipäällikköävahvistamaan tiimiään. M-Solutions Oy tuottaa kokonaisvaltaisia ICT- ja tiedonhallintaratkaisuja asiakkailleen teollisuudessa ja pk-sektorilla. Projektipäällikkönä työskentelet tiiviisti asiakkaidemme kanssa ja tuet heitä toiminnan kehittämisessä. Vastaat projektien määrittelytyöstä asiakkaita osallistaen, esität oikeita kysymyksiä, haet ratkaisuja ja huolehdit kokonaisuuden toteutumisesta. Edistät työssäsi myös oman tuotekehityksemme tuloksena syntyneen tiedonhallintajärjestelmämme (M-IDIS) myyntiä. Työhön voi ajoittain kuulua myös matkustamista asiakkaiden luokse eri puolille Suomea tai ulkomaille. Hakijalta edellytämme soveltuvaa korkeakoulututkintoa, teollisuusyritysten prosessien tuntemusta sekä kokemusta tiedolla johtamisesta ja asiakasrajapinnassa työskentelystä. Järjestelmäkehityksen ja ICT-alan ymmärrys on etu. Tehtävässä menestyminen vaatii kykyä hahmottaa kokonaisuuksia ja tunnistaa ongelmia. Toivomme sinulta lisäksi hyvää suomen ja englannin kielen taitoa. Arvostamme lisäksi hyviä vuorovaikutustaitoja, ratkaisukeskeisyyttä ja oma-aloitteisuutta. Vuonna 2016 perustetun yrityksemme päätoimipaikka sijaitsee Pyhäjärvellä, lisäksi tarjoamme mahdollisuuden etätyöhön. Tule mukaan tiimiimme luomaan tulevaisuuden teollisuutta!
Hakuehdot RekryKoulutukseen
Hakijan tulee olla työtön työnhakija, työttömyysuhan alainen tai osa-aikaisesti työskentelevä. Hakijoilta edellytetään korkeakoulututkintoa (ammattikorkeakoulu tai yliopisto) tai riittävästi muuta työkokemusta esimerkiksi seuraavilta aloilta:
Health Tech Top Expert-RekryKoulutus toteutetaan yhteistyössä Kasve Oy:n, paikallisten TE-palveluiden ja ELY-keskuksen kanssa. Hakuprosessi ja opiskelijoiden rekrytointi tehdään yhteistyössä Pohjois-Pohjanmaan TE-palveluiden kanssa. RekryKoulutus on osallistujalle maksuton.
Hosting Institute: Afekta in collaboration with University of Eastern Finland
Gross salary: 4,663 euros (+Family allowance if applicable)
Project description:
The PhD project will focus on assessing the impact of lifestyle intervention on blood microsampling metabolite composition when compared to conventional plasma samples. The aim is to find robust biomarker candidates that would readily reflect the metabolic effect of the intervention and the responsiveness of the individual to the lifestyle intervention. The student will work on optimizing the analytics based on the inter-laboratory comparison of the various blood microsampling home-collection devices. The samples to be collected from the lifestyle intervention will be assessed with the chosen collection method and optimized liquid chromatography mass spectrometry conditions. The impact of the lifestyle will be assessed by the non-targeted metabolite profiling approach, as well as compound-centric investigation of target metabolites that have been linked with dietary and exercise response and reflecting also the composition and function of gut microbiota.
We offer an exciting position and a chance to do research in an intersection between industry and academia. Afekta Technologies Ltd. is a science driven company established in 2017. Afekta offers metabolomics analysis services for various research purposes across life sciences. We have specialized in metabolomics analyses related to food, nutrition, and gut microbiota. Afekta has experience in being a beneficiary in several Horizon 2020 projects including a previous Marie-Sklodowska-Curie Doctoral Network action (MSCA-ITN-ETN-action BestTreat). To learn more about Afekta please visit www.afekta.com.
Academic studies related to the position will be done in the University of Eastern Finland (UEF), which will also award the PhD. UEF is a multidisciplinary university with a strong focus on life sciences. UEF has around 16,000 students and 3,000 staff members. Office and laboratory spaces of Afekta Technologies are right next to the UEF campus in Kuopio. Finland, and Kuopio in particular, is a safe, clean and technology-driven place known for its superb education and welfare know-how. To learn more about UEF and the life in Finland visit https://www.uef.fi/en/life-in-finland.
For further information on the position, please contact CEO Dr. Olli Kärkkäinen (olli@afekta.com, +358 44 2432 322).
Key Requirements:
Applicants should have a strong scientific background in the research field of Chemistry, Biochemistry, Biomedicine, Pharmacy, Toxicology, Pharmacology, or a similar field.
The prospective ideal student needs to have hands-on experience in applying liquid chromatography mass spectrometry -based methods for analysis of compounds in biological samples. Experience in mass spectrometry data analysis and in method optimization and/or data analysis are key requirements as well. Interest towards precise laboratory work and experience in metabolomics data analysis are desirable and will be favourably viewed.
The project will involve international and intersectorial secondments/visits to other project partners in the network for the doctoral candidates to learn new skills and foster collaborations.