Bioanalytiikan laboratoriossa kehitetään ja validoidaan analyyttisiä menetelmiä (esim. LC-MS/MS) pienien molekyylien kvantitointiin asiakkaiden tarpeiden mukaisesti. Bioanalytiikan avulla saadaan lisätietoa altistumisesta prekliinisissä tai kliinisissä farmakokineettisissä tutkimuksissa, mutta lisäksi kehitetään menetelmiä biomarkkeri- ja ympäristötutkimuksiin. Laboratorio on GLP-sertifioitu. Bioanalyytikan laboratorio sijaitsee Aurumissa, jossa on opetukseen ja laboratoriotyöskentelyyn täysin uudet ja nykyaikaiset puitteet.
Työtehtävät
Projektitutkijan tehtäviin kuuluu kvantitatiiviset näyteanalyysit. Lisäksi hän osallistuu innovatiivisten LC-MS/MS –menetelmien kehittämiseen moninaisille näytematriiseille. Hän osallistuu käytännön töihin laboratoriossa sekä osallistuu tutkimussuunnitelmien ja tutkimusraporttien kirjoittamiseen. Tehtävä voi soveltua tieteellisen jatkotutkinnon aloittamiseen Turun yliopistossa.
Edellytykset
Soveltuva ylempi korkeakoulututkinto (esimerkiksi kemian, biokemian tai elintarvikekemian alalta)
Bioanalyyttinen tutkimuskokemus ja -taidot, erityisesti nestekromatografisista ja massaspektrometrisista menetelmistä
Microsoft Office -ohjelmien hallinta
Oma-aloitteellisuus, hyvät sosiaaliset taidot ja aktiivisuus
Organisointikyky ja sopeutumisvalmius muuttuviin/vaihtuviin työtilanteisiin
Sujuva suomen- ja englanninkielen taito
Tehtävään voidaan valita myös maisteriopintojen loppuvaiheessa oleva henkilö. Tällöin tehtävänimike on tutkimusavustaja.
Eduksi katsotaan
GLP-kokemus tai valmius kouluttautua GLP-ympäristöön
Kokemus LC-MS/MS-laitteiden huollosta ja ylläpidosta
Kokemus erilaisista näytteenkäsittelytekniikoista
Palkka
Projektitutkijan tehtäväkohtainen palkkaus määräytyy yliopistojen palkkausjärjestelmän opetus- ja tutkimushenkilöstön vaativuustasojen 2-4 mukaisesti (2078,27– 2591,28 €/kk). Tehtäväkohtaisen palkanosan lisäksi maksetaan henkilökohtaiseen suoriutumiseen perustuvaa palkanosaa, joka on 6 – 50 % tehtäväkohtaisesta palkanosasta. Tutkimusavustajan tehtävässä vaativuustaso on 1, jolloin tehtäväkohtainen palkanosa on 1889,69 €/kk.
Tehtävässä on kuuden (6) kuukauden koeaika.
Hakeminen
Hakemukset tulee jättää viimeistään torstaina 20.1.2022 (klo 23:59) yliopiston sähköisellä hakulomakkeella. Linkki hakulomakkeeseen löytyy osoitteessa www.utu.fi/tyopaikat kyseisen tehtävän tiedoista hakemuksen yläosasta kohdasta ”Täytä hakemus”.
Hakemukseen tulee liittää motivaatiokirje, cv ja tutkintotodistukset. Suosittelijoita, jotka ovat antaneet luvan, että käytät heitä suosittelijoina, pyydetään nimeämään kaksi (2).
Hakuprosessista lisätietoja antaa henkilöstöasiantuntija Kristiina Nuutila (kristiina.nuutila@utu.fi), +358 503135224 tai henkilöstösihteeri Päivi Aalto, paivi.aalto@utu.fi
We keep growing and we are now looking for Downstream Specialists to reinforce our Manufacturing team.
Downstream is one of the four Manufacturing Streams. Downstream team focuses on the purification of the drug substance. We use chromatographic and filtration purification methods in our biological manufacturing process. The process itself is run by programmed production equipment.
Your primary responsibilities as Specialist include documentation of GMP operations and performing manufacturing operations hands-on in cleanroom environment according current GMP guidelines. The focus of documentation is on SOPs, deviations, change controls and CAPAs. You will also be the first support contact for the manufacturing operators.
It is an advantage if you already have some experience in GMP-work and/or you have knowledge on quality systems.
You could be the person if..
You enjoy the combination of hands-on work and documentation.
You produce clear, easily understandable and accurate documentation in English.
Your working style is precise and you achieve objectives set to you in a timely manner.
You pay attention to details but you also easily manage entities.
You want to develop yourself and become an expert in your own field.
In order to succeed, you would need a degree in the field of biotechnology, engineering, biochemistry, chemistry or any other related field of study.
As a person, we would like you to be open-minded towards new challenges and spread good team spirit. You also need to communicate fluently both in written and spoken English.
Our Manufacturing team is working in shifts.
Your employment is permanent and we would like you to start preferably in February. We offer you active and lively work community with highly skilled and experienced personnel in gene therapy manufacturing. Working with us, you are entitled to good employment benefits, such as extensive occupational health-care and we support your physical and cultural free-time activities. We provide you wide initial training and a warm welcome. FinVector is located in vibrant Kuopio, which offers a safe living environment, friendly atmosphere and clean nature.
Apply by 24th January!
For more information, please contact Team Lead Johanna Hiltunen tel. 044 430 4674 or Vesa Huusko tel. 040 736 4399 on Wednesday to Friday during 11:00-15:00.
Haemme lääketieteen laitokselle yliopisto-opettajaa. Työ sijoittuu Kuopion kampukselle ja alkaa 01.06.2022. Lue lisää alta, ja hae viimeistään 31.01.2022. (Hakuajan jatkaminen)
Tehtävä ja palkkaus
Biolääketieteen yliopisto-opettajan tehtävässä työskentelet lääketieteen laitoksen biolääketieteen yksikössä, Kuopion kampuksella. Laitos kuuluu terveystieteiden tiedekuntaan. Lisätietoja yksikkömme toiminnasta löydät verkkosivuiltamme https://www.uef.fi/fi/yksikko/biolaaketieteen-yksikko
Yliopisto-opettajan (biolääketiede) tehtäviin kuuluu
opetustehtävät biolääketieteen kandidaatti- ja maisterivaiheen koulutuksessa sekä ihmisen biologian opintojaksoilla (kampuksella ja verkkoympäristössä),
biolääketieteen yksikön oppimisympäristön kehittäminen ja toteuttaminen yhteistyössä opettajayhteisön kanssa,
tutkinto-opiskelijoiden opinto-ohjaus,
opinnäytetöiden ohjaaminen ja tarkastaminen,
tutkimustyö biolääketieteen yksikössä sekä
hallinnolliset tehtävät yksikkö- ja laitostasolla
Tehtävä täytetään määräajalle 01.06.2022 – 31.05.2026. Määräaikaisuuden perusteena on 2021 toteutunut määräaikainen koulutuslaajennus sekä opetustyön uudelleen organisointi yksikössä. Uuden työntekijän tullessa tehtävään käytetään koeaikaa.
Tehtävän palkkaus määräytyy yliopistojen opetus- ja tutkimushenkilöstön palkkausjärjestelmän mukaisesti. Palkka koostuu tehtäväkohtaisesta palkanosasta ja henkilökohtaiseen suoriutumiseen perustuvasta palkanosasta. Tässä tehtävässä tehtäväkohtainen palkanosa on vaativuustasoluokittelussa tasoilla 4 – 5 (2591,28 – 3000,49 €). Lisäksi maksetaan henkilökohtaiseen suoriutumiseen perustuvaa palkanosaa, joka on 6 – 50 % tehtäväkohtaisesta palkanosasta. Henkilökohtaisesta palkanosasta riippuen palkka työsuhteen alkaessa on noin 2850,40 – 3660,60 €/kk.
Mitä edellytämme ja toivomme sinulta?
Edellytämme sinulta
työtehtävään soveltuvaa ylempää korkeakoulututkintoa sekä hyvää opetustaitoa,
hyvää suomen- ja englanninkielen suullista ja kirjallista taitoa,
kokemusta alan yliopisto-opetuksesta,
hyviä yhteistyö- ja kommunikointitaitoja,
kiinnostusta akateemista uraa kohtaan
Katsomme eduksi
pedagogisen koulutuksen,
tutkimusansiot,
kiinnostuksen osallistua tutkimustyöhön biolääketieteen yksikössä toimivassa tutkimusryhmässä
Tarjoamme sinulle
mielenkiintoisen ja monipuolisen työtehtävän osana kansainvälistä, luovaa, osallistuvaa ja osallistavaa yliopistoyhteisöä,
mahdollisuuden joustavaan monipaikkatyöhön sekä
Itä-Suomen yliopiston henkilöstöedut, joihin kuuluvat muun muassa kattava työterveyshuolto, laaja henkilöstökoulutustarjonta, edulliset kampusravintolalounaat ja Sykettä-liikuntapalvelut
Hae näin
Jätä hakemus viimeistään 31.01.2022 sähköisellä hakulomakkeella.
Cepheid is a molecular diagnostic company dedicated to improving healthcare by developing, manufacturing and marketing accurate yet easy-to-use molecular systems and tests. By automating highly complex and time-consuming manual procedures, the company’s solutions deliver a better way for institutions of any size to perform sophisticated genetic testing for organisms and genetic-based diseases. Through its strong molecular biology capabilities, Cepheid is focusing on applications where accurate, rapid and actionable test results are needed most, such as managing infectious diseases and cancer.
Make a difference in healthcare and join us on this mission!
What You Will Be Doing
The Technical Support Biologist is responsible for providing advanced product support to customers requiring assistance with our GeneXpert product line. As a member of the Tier 2 Technical Support Team, you provide product support to internal and external customers via phone, email and web serving as the technical expert in Cepheid’s Customer Care experience.
For this position is mandatory to speak Finnish at a mother tongue level.
You will be responsible for
Engage customers to collect and compile detailed information about customer complaints
Conduct advanced data analysis and troubleshooting, understanding customer sample collection, processing and laboratory practices
Investigate and resolve advanced customer complaints
Document complaints and resulting investigations in the complaint management system
Interface with Service and Global Product Support to escalate and resolve more complex cases
Adhere to Quality Management System procedures
Maintain product knowledge and support continuous improvement efforts
Contribute to quality compliance through accurate and concise case documentation
Represent Technical Support on projects and operational teams, communicating findings back to Technical Support
Complete all assigned and required training satisfactorily and on time
Performs additional tasks as assigned by the Technical Support Manager or Supervisor
What Skills & Experience You’ll Bring To Us
Bachelor’s degree in Clinical Laboratory Science (or equivalent) with minimum 2 years of relevant experience as a Virology/Microbiological Laboratory Technician
In alternative experience as Clinical Laboratory Scientist for Virology/Microbiology in a hospital OR commercial clinical laboratory OR in a Technical Support position
Fluent Finnish and English (written and oral) is required (additional languages would be an advantage – Swedish, Norwegian, Danish, Russian)
Customer oriented – understands customer expectations and can empathize with customer & patient needs
Knowledge and use of commercial computer application packages (MS Office)
Familiarity with SalesForce.com (or similar CRM System) is a plus
Laboratory or Technical Support Experience in one or more of the following preferred:
PCR and Microbiology, Molecular Biology Oncology or Virology
Patient sample collection practices and workflow
Sample preparation practices and methodologies
Laboratory analytical diagnostic equipment, medical devices and software
Able to follow complex procedures and processes
Excellent written and verbal communication skills
Curious & self-motivated with ability to learn a complex technology platform quickly
Works independently in a structured manner with the ability to prioritize critical tasks
Builds collaborative work relationships with different teams, including Field Service Sales, Marketing and Quality
Thrives in a dynamic and fast-paced environment
Cepheid is part of Danaher Corporation, a global science & technology innovator committed to helping our customers solve complex challenges and improve quality of life worldwide.
At Danaher, you can build a career in a way no other company can duplicate. Our brands allow us to offer dynamic careers across multiple industries. We’re innovative, fast-paced, results-oriented, and we win. We need talented people to keep winning. Here you’ll learn how DBS is used to shape strategy, focus execution, align our people, and create
When you join us, you’ll also be joining Danaher’s global organization, where 69,000 people wake up every day determined to help our customers win. As an associate, you’ll try new things, work hard, and advance your skills with guidance from dedicated leaders, all with the support of powerful Danaher Business System tools and the stability of a tested organization.
At Danaher, we value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes.
If you’ve ever wondered what’s within you, there’s no better time to find out.
Pay range unavailable
Salary information is not available at the moment.
Due to expansion across Europe within our Regulatory function we are looking for Regulatory Professionals in based in UK, Europe, the Nordics or Russia
About Us
IQVIA Biotech is the division of IQVIA which deals with small to medium size biotech companies, most of our employees are involved in clinical research and we are expanding our regulatory affairs team as part of an overall company expansion.
We are looking for candidates at all levels who have experience of regulatory affairs clinical trials submissions for Medical Devices and In-Vitro Diagnostic (IVD) products. We are interested in applicants from the UK, Europe, Nordics, and Russia. The role is home based.
Basic Functions
To provide regulatory and quality support to select clinical research projects involving investigational drugs, medical devices, biologics, or new medical procedures. To provide strategic regulatory guidance and information to projects; to acquire pertinent regulatory information from agencies and organizations; to support regulatory agency interactions, communications, and submissions; and to review project regulatory documentation to ensure compliance with applicable regulatory regulations and guidelines.
Essential Job Functions, Duties And Responsibilities
Assist Associate Director, Regulatory Affairs, in assuming primary or secondary regulatory responsibility for assigned clinical research projects by providing to the project team regulatory information, guidance, training, support and strategic planning based on applicable regulations and guidance’s issued by the applicable regulatory agency(ies).
Identify and interpret regulations, guidelines, and other pertinent information issued by applicable regulatory agencies and other regulatory organizations.
Review protocols, consent forms, reports, scientific documents, publications, and related papers, etc., as appropriate for various clinical research projects to ensure compliance with regulations.
Ensure the compilation and maintenance of pertinent documentation (e.g., files) required for regulatory compliance for assigned clinical research projects.
Serve as a member of groups, teams, or committees related to regulatory affairs, and quality assurance or other designated IQVIA Biotech activities, as appropriate.
Serve as IQVIA Biotech liaison with central IRBs.
Perform other related duties as assigned.
Knowledge Skills And Abilities
Working knowledge of and aptitude for activities related to regulatory affairs and quality assurance, both domestic and ideally also international.
Familiarity with or ability to become familiar with regulatory documents, general contents, organization and the methods of filing and tracking.
Familiarity with or ability to become familiar with principles of Good Clinical Practice, Good Laboratory Practice and Good Manufacturing Practice., ISO standards.
Extensive knowledge of clinical research; knowledge and familiarity with 21CFR11 and EDC systems.
Experience in preparation of audit plans and checklists against applicable standards, execution of audits, and preparation of comprehensive written audit reports.
Good interpersonal skills with the ability to communicate effectively, both orally and in writing, with all levels of staff, and with the public.
Ability to be detail oriented with background adequate to deal with scientific issues related to technical regulations and SOPs.
Ability to read and synthesize technical material and to prepare clear and concise written documents.
Computer literate at a level allowing utilization of event tracking programs, data loading and information processing related to regulatory affairs and quality assurance.
Minimum Requirements
Requires Bachelor’s degree, science degree preferred or equivalent level of education and work experience.
Experience of regulatory affairs submissions for clinical trials in at least one country, multi country experience is desirable but not essential.
Excellent analytical and communication skills, particularly writing skills, are essential.
Demonstrated computer literacy is required.
Please submit your CV’s/application in English.
At IQVIA, we believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. The advanced analytics, technology solutions and contract research services we provide to the life sciences industry are made possible by our 70,000+ employees around the world who apply their insight, curiosity and intellectual courage every step of the way. Learn more at jobs.iqvia.com.
At the heart of QIAGEN’s business is a vision to make improvements in life possible.
We are on an exciting mission to make a real difference in science and healthcare. We are still the entrepreneurial company we started out as and have today achieved a size where we can bring our full power to many initiatives and to our presence across the globe.
Our most valuable asset are our employees – more than 5000 in over 35 locations around the world. Our ambition is to ensure we have outstanding and passionate people working in the best teams and we are constantly looking for new talent to join us.
There are few players who have shaped the world of modern science and healthcare as much as QIAGEN, and we have only just started.
If you are looking to advance your career, are seeking new challenges and opportunities, enjoy working in dynamic and international, diverse teams and want to make a real impact on people’s lives, then QIAGEN is where you need to be.
Join us. At QIAGEN, you make a difference every day.
JOB ID: EMEA02328
LOCATION: Finland / Remote
DEPARTMENT: Sales / Business Development
EMPLOYMENT TYPE: Full time Limited
Position Description
Do you thrive working with sales, science and people and would you like to become part of a small but dedicated team of clinical sales people serving the hospitals and clinical labs in Finland? We are a team of sales, support and service people who value a high intensity work day and a relaxed and humorous tone and we are looking for a new colleague.
Your tasks will include:
– Responsible for sales of QIAGEN clinical product portfolio in Finland
– Develop and execute designated sales territory strategy to meet/exceed budget.
– Work with QIAGEN specialists to achieve sales targets and offer complete solutions to our customers.
– Drive for customer satisfaction and increase competitive advantage by building trust and relationships..
– Maintain and develop a good relationship with key customers, references and KOLs. Aim to further increase customer satisfaction.
– Drive and initiate development of new business opportunities and references for QIAGEN products and reagents. Upselling, including additional menu and cross selling.
– Use provided CRM tool to log relevant customer, market and competitor information.
– Utilise the CRM database to input and provide information that will increase effectiveness “in front of” the customer and aid sales.
– Provide ongoing feedback and forecast of sales.
Position Requirements
– MSc or PhD Degree in molecular biology or similar discipline, experience with molecular diagnostics or clinical lab work, or equivalent experience.
– Knowledge of DNA/RNA sample preparation, qPCR, NGS and related instrumentation.
– 3+ years sales experience with good track record
– Excellent communication, presentation and interpersonal skills.
– Fluent in Finnish and excellent verbal and written English skills.
– Valid driver’s license.
Personal Requirements
– Temporary position 1.2.2022 – 31.3.2023
– Self-motivated and strong ego-drive.
– Open communication style to ensure efficient and fruitful team-work.
– Stress resistant and flexible with working hours.
– Strong desire to win business and establish long-term customer relationships.
– Home office based, >80% travel required
What we offer
At the heart of QIAGEN are our people who drive our success. We act with passion, always challenging the status quo to drive innovation and continuous improvement. We inspire with our leadership and make an impact with our actions. We create a collaborative, safe and engaging workplace which forms the basis for high performing individuals and teams. We drive accountability and entrepreneurial decision-making and want you to excel your growth and shape the future of QIAGEN.
QIAGEN is committed to creating a diverse environment and is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, sex, age, national origin, religion, sexual orientation, gender identity, status as a veteran, or disability.
As Product Support Specialist, you will have a key role in supporting our Cascadion™ SM Clinical Analyzer and global field based specialist team. You will work with technically advanced instruments in an innovative and international working environment by providing service, training, technical expertise and troubleshooting support. You will also help resolve customer critical issues and provide customer feedback to our product development team.
This is an ideal role for either an experienced Engineer or Technical Specialist who has previously worked with Liquid Chromatography or Mass Spectrometry instruments and applications, OR a Scientist with expertise in LC-MS. If you are in the latter category, we will provide full engineering training.
While the team is primarily based at our Vantaa, Finland site, we are happy to consider to hire this role as remote (working from home), based in Europe in close proximity to a major international airport. Fairly regular international travel (up to 20% per month) may be required when safe to do so.
At Thermo Fisher Scientific we work hard to support our colleagues’ career ambitions, offering great training and development opportunities throughout your career and a chance to work in an international environment. Apply now and achieve your best – both personally and professionally.
We look forward to receiving your application, including a CV and cover letter, in English.
What will you do?
Perform installation, repairs, preventive maintenance and troubleshooting of Cascadion™ SM Clinical Analyzers and Assays globally
Active development and delivery of live and remote operator and technical training programs
Accurately document, analyze and report service activities
Timely handling of customer feedback cases and complaint assessment
Continuous improvement of product support documentation and contribution to product change processes
Close collaboration with the global customer care and local research and development organizations
Who we are looking for:
A Degree in Engineering OR in Life Sciences (PhD level preferred)
Hands-on experience of liquid chromatography and mass spectrometry (LC-MS) instrumentation, software and applications (critical)
Some professional experience in servicing analytical or general laboratory instruments (gained either as an Engineer or when working as a Scientist in a lab)
Experience with development of digital training programs, including AR and VR solutions and tools
Ability and mentality to effectively prioritize and resolve technical and analytical problems
Proficiency in written and spoken English; proficiency in other main European languages seen as advantage
Driving license preferred
What’s in it for you:
Annual Incentive Plan performance bonus
Flexible working hours
Onsite nurse and gym
Subsidized lunch
Excellent career progression as part of a global organization
About us:
Thermo Fisher Scientific Inc. is the world leader in serving science, with annual revenue exceeding $35 billion. Our Mission is to enable our customers to make the world healthier, cleaner and safer. Whether our customers are accelerating life sciences research, solving complex analytical challenges, improving patient diagnostics and therapies or increasing productivity in their laboratories, we are here to support them.
is available in the collaborative Academy of Finland -funded CrossBar project at the Universities of Helsinki and Turku, and the National Institute of Health and Welfare (THL). The project PI’s are Associate Professor Tarja Sironen (UH), Adjunct Professor Laura Kakkola (UT) and Research Manager, PhD, Pamela Österlund (THL). The position is offered for a fixed-term position for 3 years (approximately one year in each of the partner institutes).
We seek for a highly motivated and experienced postdoctoral researcher in the field of virology, microbiology, immunology or molecular cell biology to join our international and dynamic consortium. The job description is to plan and execute research on zoonotic viruses with pandemic potential.
The successful candidate:
Has strong organizational skills, is solution-oriented and has the ability to analytical thinking
Has a PhD degree in a relevant field of life sciences and preferably background in virology
Has excellent skills in experimental laboratory work and ability to independently plan and execute the experiments
Has previous experience in working in BSL-3 conditions or is willing to be trained for work in such conditions Is a team player with good collaboration and communications skills
Has good spoken and written English
The degree requirement must be met by the beginning of the employment.The salary is based on the Finnish collective agreement. The position belongs to the category of teaching and research personnel. The salary is in the range of 3100 – 3600 eur/month.The salary level is based on previous qualifications, experience and personal performance in the position according to the hosting institution. The start date is negotiable, and there is a trial period of six months.
The application, together with the required attachments in PDF format (CV, list of publications), must be written in English and submitted through the University of Helsinki electronic recruitment system by clicking on Apply for job. Internal applicants (i.e., current employees of the University of Helsinki) must submit their applications through the SAP HR portal.
A special health examination of the suitability to work in the high containment laboratory is required for the person selected to the position. Also, the selected person, with his or her consent, will be asked for PSC (Personnel Security Clearance) assurance through the National Security Authorities (NSA).
The University of Helsinki welcomes applicants from a variety of genders, linguistic and cultural backgrounds, and minorities.
The deadline for the applications is 15.1.2022.
Further information will be given by email of by phone:
Tarja Sironen, tarja.sironen(at)helsinki.fi, +358-50-4471588
Laura Kakkola, laura.kakkola(at)utu.fi, +358-50-5747101
Huomaathan, että kesän 2022 harjoittelupaikat ovat jo haussa. Muun muassa Orion hakee Turkuun harjoittelijoita. Katsohan paikat osoitteesta: https://www.orion.fi/en/careers/students/ https://www.orion.fi/en/careers/students/apply-for-orions-phase-1-summer-job-program-over-the-period-18-january10-february/
