GENEVIA TECHNOLOGIES’ Production Team is recruiting!
This job position is available for fully remote or locally at Tampere, Finland!
We are looking for a seasoned bioinformatics scientist with a passion for providing bioinformatics services to research groups in the academic and industry sectors. As a Project Manager, your most important responsibilities include:
planning the required bioinformatics workflow with our clients, then
dissecting that workflow into more specific analysis tasks to both our production bioinformatics team and to yourself, and
analyzing the data, integrating, interpreting and reporting analysis results back to the client’s team.
OUR CLIENTS are researchers who are using a wide variety of omics technologies from standard mRNA sequencing, DNA sequencing and epigenetics to completely novel experimental platforms. You are already familiar with standard computational methods for omics data analysis, such as how to ascertain the quality of an experiment, statistical testing, as well as the specialised computational tools of the trade, such as genome alignment, genome assembly and annotation, SNP calling, peak calling, pathway analysis, and are excited to learn new tools for new technologies. The biological applications our clients are working with range from microbiology, to plants and animals, to biomedical applications, such as immunology or cancer. We don’t expect that you are an expert in all areas, but you will have enough base understanding to be able to quickly grasp the essence of our clients’ research questions.
SUCCEEDING IN THE POSITION REQUIRES
understanding a wide variety of omics data types,
understanding typical analysis workflows for most omics data types,
ability to implement analysis tasks, and interpret the validity of the results
experience in publishing omics-heavy applied research papers
enthusiasm to learn new biology and technology, and
a knack for science outreach and communication (in written text, data visualisations and conversation/presentations).
If you have practical experience in publishing biological research papers with a bioinformatics component, and/or have worked in a bioinformatics core laboratory, for example, you are already quite familiar with our projects. The position would be ideal for an academic bioinformatician who wants to work in management, but also to remain firmly within the research realm of life sciences and bioinformatics. We wish you could start early 2022 (between January and March 2022).
CHECK OUT WHAT YOUR FUTURE COLLEAGUES HAVE TO SAY about being a Project Manager at Genevia Technologies. Read more about Project manager’s role at Genevia here: https://geneviatechnologies.com/bioinformatics-company/bioinformatics-jobs/project-manager-career/
If you feel like you might be just the person we are looking for, please take 5 min to answer these few warmup guestions and upload your CV. Please note that the application form requires log in to your google account before it opens. Link to the warmup guestions is here: https://forms.gle/fiPDXLTaJ1LNvSg3A
Please complete the warmup form by December 13th 2021.
QUESTIONS AND ADDITIONAL INFORMATION regarding the position is available from Klaus Breitholtz (+358 40 747 7672 / klaus.breitholtz@geneviatechnologies.com)
Partner, Business Development Director at Genevia Technologies. Executive Director at Future Board association. PHD researcher focused on board of directors’ motivation & rewarding Job Poster Location
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.
Sales Application Specialist Finland
JOB ID: EMEA02316
LOCATION: Finland/Remote
DEPARTMENT: EMEA02316
EMPLOYMENT TYPE: Regular Full-Time
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
Support the sales process both pre and post sales by providing technical details, product-, application-, and workflow expertise.
Carry out product and instrument demos, support customers throughout the product lifecycle and provide customer product trainings as needed for the QIAGEN products from the set-up of an instrument to trouble shooting.
Support on-site LDT implementation or conversion from existing workflows to new
Support the whole QIAGEN solution set-up including instrument connectivity and LIMS integrations.
Meet/Exceed sales targets. Increase sales by actively selling to end users. Support other specialists and representatives and develop tactical plans to maximize revenues.
Drive and initiate development of new business opportunities and references for QIAGEN products and reagents. Upselling, including additional menu and cross selling.
Maintain and develop a good relationship with key customers and references. Aim to further increase customer satisfaction.
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.
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
Minimum 3 years sales experience.
Knowledge of relevant markets.
Fluent in Finnish and excellent verbal and written English skills.
Valid driver’s license.
Personal Requirements
Excellent communication, presentation and interpersonal skills.
Open communication style to ensure efficient and fruitful team-work
Strong desire to win business and establish long-term customer relationships.
Stress resistant and flexible with working hours.
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.
Charles Riverin työntekijät ovat työskennelleet jo 70 vuoden ajan auttaakseen uusien lääkehoitojen löytämisessä, kehittämisessä ja turvallisessa valmistuksessa. Kun olet liittynyt perheeseemme, sinulla on mahdollisuus vaikuttaa merkittävästi ihmisten terveyteen ja hyvinvointiin eri puolilla maailmaa. Olipa taustasi biolääketieteessä, rahoituksessa, tietotekniikassa, myynnissä tai muualla, taidoilla on tärkeä rooli suorittamassamme työssä. Vastineeksi auttamme sinua rakentamaan uran, josta voit olla ylpeä.
TÄRKEÄÄ: Jotta tulisi harkituksi tähän tehtävään, täytyy ansioluettelo/CV olla liitettynä hakemukseen järjestelmässä. Ole ystävällinen ja tarkista, että työhistoria ja koulutus on lisätty oikein.
osallistuu solulaboratoriotöiden sekä muiden mittausten valmisteluun, datan keräämiseen, dokumentointiin ja syöttöön kokeen tarpeen mukaisesti
valmistaa koekansioita ja –lomakkeita
oma-aloitteinen osallistuminen yksikön laadunvalvonnan kehittämiseen, perehdyttää uusia laborantteja sekä työssä että laitteiden käytössä
laboratoriolaitteiden toiminnan seuranta ja ennaltaehkäisevän huollon suunnitteluun osallistuminen
yksikön muut tukitoiminnot ja muissa tehtävissä avustaminen tarvittaessa
Pätevyysvaatimukset
soveltuva pätevyys ammattikoulutuksen kautta hankittuna, tehtävään sopiva koulutus voi olla esimerkiksi laborantti, bioanalyytikko, FM soveltuvalta alalta
pitkäaikainen käytännön laboratoriokokemus hiiren ja rotan primäärineuroneiden viljelystä alkioista ja vasta-syntyneistä poikasista
pitkäaikainen käytännön laboratoriokokemus soluviljelmien altistamisesta kemiallisille aineille ja erilaisista mittauksista (esim. LDH-mittaus)
pitkäaikainen käytännön laboratoriokokemus solujen värjäyksestä vasta-aineilla
monipuolinen kokemus linjasolujen viljelystä
hyvä atk-tuntemus, vähintään Microsoft Office- ohjelmiston käyttö
hyvä suullinen ja kirjallinen englanninkielentaito katsotaan eduksi
kykenevä itsenäiseen työskentelyyn
tehokas tiimityöskentely ja aktiivinen kommunikointi välttämätöntä
Tietoa Discovery-liiketoimintayksiköstä
Charles River Discovery on todistetusti ollut mukana kehittämässä uusia onnistuneita hoitomuotoja. Viimeisten 17 vuoden aikana asiakkaamme ovat saaneet yli 320 patenttia ja 74 prekliinistä lääkekandidaattia. Meillä on yli 650 tutkijaa, jotka hyödyntävät uusinta teknologiaa ja uusimpia ohjelmistoja. Näin kattava, yhtenäinen tuotevalikoimamme tarjoaa kemian, biologian ja farmakologian palveluita, jotka tukevat asiakkaitamme ensimmäisestä löydöksestä uuteen tutkimuslääkkeeseen asti. Asiakaslähtöisen, yhteistyöhön perustuvan lähestymistapamme avulla luomme todellisen kumppanuuden, jossa ennakoidaan haasteet, selvitään esteistä ja kuljetaan yhdessä koko matka tuotaessa uusia lääkkeitä markkinoille.
Tietoa Charles Riveristä
Charles River on varhaisen vaiheen sopimustutkimusyritys (CRO). Toimintamme perustana on koe-eläintiede ja -lääketiede. Sille pohjalle olemme rakentaneet monipuolisen tuotevalikoiman Discovery- ja lääketurvallisuusarviointipalveluita, niin hyvän laboratoriokäytännön (GLP) mukaisia kuin sen ulkopuolisia (non-GLP), tukeaksemme asiakkaita alkaen kohteen tunnistamisesta aina prekliiniseen lääkekehitykseen asti. Charles River tarjoaa myös valikoiman tuotteita ja palveluita, joiden avulla tuemme asiakkaidemme kliinisiä laboratoriotestaustarpeita ja tuotantotoimintaa. Tätä laajaa tuote- ja palveluvalikoimaa hyödyntämällä asiakkaamme voivat luoda joustavamman lääkekehitysmallin, mikä vähentää heidän kustannuksiaan sekä parantaa tuottavuutta ja tehokkuutta ja siten nopeuttaa tuotteen pääsyä markkinoille.
Meillä on yli 18 000 työntekijää 100 laitoksessa 24 maassa ympäri maailmaa. Näin pystymme strategisesti koordinoimaan resursseja maailmanlaajuisesti ja soveltamaan monialaisia näkökulmia ratkaistessamme asiakkaidemme ainutlaatuisia haasteita. Asiakaskuntaamme kuuluu globaaleja lääkeyhtiöitä, biotekniikan yrityksiä, valtion virastoja ja sairaaloita sekä korkeakouluja ympäri maailmaa.
Me Charles Riverillä suhtaudumme intohimoisesti rooliimme ihmisten elämänlaadun parantamisessa. Missiomme, tapamme tehdä tiedettä erinomaisesti ja vahva tarkoituksen tunne opastavat meitä kaikessa, mitä teemme. Aloitamme jokaisen päivän tietäen, että työmme auttaa parantamaan monien ihmisten terveyttä ja hyvinvointia ympäri maailmaa. Vuonna 2019 olemme olleet mukana kehittämässä noin 85:ttä prosenttia FDA:n hyväksymistä lääkkeistä.
We are now looking for a professional with thorough understanding of the overall drug development process and with excellent working knowledge of document authoring to work in an exciting and challenging global role based in Clinical Development & Operations team in Finland in Espoo as
SUBMISSION MEDICAL WRITER
Your Tasks And Responsibilities
Independently author study level clinical documents and clinical submission documents, reviews and is responsible for their consistency.
Implement the submission authoring strategy under the leadership of the MW Strategist.
Supports the MW Strategist to manage the activity, resource and time planning for the clinical part of submissions.
Drives the design of clinical submission documents in support of the Clinical Development Plan, validates individual study protocol design, key messages of the clinical study report and other clinical submission documents, for assigned projects.
Maintains current knowledge on all regulatory agency medical review guidelines and drug approval requirements for assigned projects.
Implement the content strategy for all clinical documents as assigned.
Accountable for the format, content and adherence to global and electronic publishing standards of the individual clinical documents that he/she is the author of.
Mentors Associate Submission Medical Writers and Senior Scientific Medical Writers (internal and insourced) in developing expertise.
Active communication and collaboration with study teams.
Support other medical writing processes as applicable.
Who You Are
This position requires a Bachelor’s degree and a minimum of 10 years experience in the pharmaceutical industry or a Master degree and a minimum of 8 years experience in the pharmaceutical industry or a PhD and a minimum of 6 years experience in the pharmaceutical industry. In all cases, the candidate should have at least 6 years experience in regulatory medical writing, 4 of which should be in writing the submission documents (Safety Summaries, Efficacy Summaries, Clinical Overviews, etc.).
PhD in natural sciences or equivalent degree is highly preferred.
The incumbent must possess strong planning and project management skills and experiences. Project management certification is highly preferred.
The incumbent must have experience in developing clinical documents in support of regulatory submissions globally (i.e., multiple regions).
The incumbent must have an in depth understanding of all regulatory guidance, standards and requirements pertaining to regulatory medical writing worldwide (eg ICH, FDA, EMEA).
The incumbent must have a thorough understanding of the overall drug development process. Specific knowledge of the clinical study report development process, regulatory and drug safety requirements, and clinical data management and statistical processes/functions is required.
Experience in supporting diverse indications is preferred.
The incumbent must have experience in leading teams and mentoring medical writers for at least 2 years.
The incumbent must also have an excellent working knowledge of current electronic authoring, document management and electronic regulatory submissions.
The incumbent must demonstrate strong communication skills, both written and verbal required to articulate concepts and ideas.
The incumbent must be diplomatic, persuasive and be able to establish rapport with all key functional leaders and experts in the Pharma Research & Development organization.
We offer a competitive compensation, independent and challenging role in an international environment with a chance to develop your skills and experience further. To be considered for this exciting opportunity, please submit your application by 15 Dec, 2021. Candidates will be reviewed on continuous basis and the position will be filled after the suitable candidate has been found.
If you feel this unique role is just what you are looking for, we are keen to hear from you! For further information, please contact Päivi Norja, Head of Authoring II, 8 Dec 2021 at 13.00-14.00 (EET) and 9 Dec 2021 at 15.00-15.30 phone +358 40 0423633.
Functional area: Clinical Development & Operations
During the summer you will gain valuable experience from your own field of study. We offer versatile and responsible tasks in an international company that builds for a more sustainable tomorrow? We are inspired by the limitless opportunities offered by the bioeconomy, and we lead the way towards a future beyond fossils. Join us on this exciting path!
We are now looking for Summer Trainee to UPM Biomedicals’ cell culture laboratory, at Biomedicum in Helsinki.
Greetings from future team
“You will have the opportunity to implement familiar things from your studies in practice and you will learn more about 3D cell culture modelling. Working in our team is fun, diverse, and rewarding. We are looking forward to welcoming you to our team!” – Product Development team
What You’ll Do
Participate in and provide help for customers technical support
Work with and get to know more about GrowDex product family
Working with cell models in 3D culture condition
Carry out assays and report the results to Product Development team
Maintenance of cell laboratory operations
Who You Are
We are looking student who have already advanced a bit in their studies. We appreciate a positive and energetic attitude, as well as taking initiative and responsibility. You will need excellent English skills. Other language skills are considered as an asset. Other attributes are:
BSc/MSc student in Cell Biology, Biotechnology, or a related discipline
Cell Biology experience is essential
Experience of aseptic working in cell culture laboratory, including hands on experience of cell culturing, and basic analysis methods such as live/dead staining of cells, robust luminescence, and fluorescence assays
What We Offer To 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. You will become a part of our motivated and supporting work community.
Development opportunities: With us you can build up your expertise. We provide opportunities to support your development throughout every stage of your summer traineeship. We offer you a chance to develop in an innovative work environment. Many of our summer trainees continue with UPM as Thesis Workers or return to us later in their 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.
Are you ready?
Read more about summer recruitment process, applying, timeline, all available positions and more information on www.upm.com/summer or www.upm.com/kesa in Finnish. Application period ends 14 February 2022. Notice that new positions can still be opened during application period.
We will start processing the applications already during the application period. Please add your resume and CV at the same stage of application.
For support with submitting your application please contact HR Service Center at summer@upm.com or +358204146600.
We are committed to being a responsible employer and participate in Responsible Summer Job -campaign.
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.
Etsimmme luovan kirjoittamisen ammattilaista, joka osaa tehdä vaikeista lääketieteellisistä aiheista mielenkiintoisia ja ymmärrettäviä tarinoita. Työskentelykieli meillä on suomi, mutta osaat myös hyvin englanti ja ruotsia.
Professor Akseli Hemminki at the University of Helsinki, Cancer Gene Therapy Group (CGTG) invites applications for the position of
DOCTORAL STUDENT in Cancer Gene Therapy
The appointment will be for a year starting upon agreement but 1.2.2022 is preferable. Trial period of 6 months will be applied.
CGTG is located in Haartman Institute on the Helsinki Academic Medical Campus in Meilahti, Helsinki, Finland. Our research involves cancer immunotherapy with oncolytic viruses, checkpoint inhibitors and adaptive cell therapies such as T-cell therapy, and their interplay. Please see https://www.helsinki.fi/en/researchgroups/cancer-gene-therapy-group for more information.
We offer you:
• an opportunity to work in a highest quality group at the very cutting edge of cancer research, both nationally and internationally
• a chance to be involved in translational and cross-field science utilizing techniques from genetic engineering, immunology, virology, cell biology, molecular biology, clinical medicine and animal work
• a stimulating research environment on the largest biomedical research campus in Finland, with tight collaborations locally and globally
• a chance for completing a PhD and growing into an independent researcher
What is expected of you:
• MSc or equivalent degree in biological, biomedical or medical sciences field or in related Tech/Engineering
• high motivation level and work morale
• capability to work and plan experiments independently and to manage overlapping projects
• some previous experience in immunology, oncology, bioengineering or virology is required
• some skills and/or training in working with model animals (rodents) are required. The project will involve animal work.
• experience in laboratory work with viral vectors, biologicals and/or cell therapies will count in your favor
• experience in cell and molecular biology methodology, e.g. flow cytometry, qPCR, and cell proliferation assays will count in your favor
• knowledge and/or previous experience of statistical analyses and programs (GraphPad Prism, R, or SPSS) will count in your favor
• adequate written and oral skills in the English language
• excellent teamwork skills
• possibility of interviewing at CGTG in person
The appointee should either already have the right to pursue a doctoral degree at the University of Helsinki by the start of the appointment or apply for the right and obtain it within the probationary period of six months of their appointment. If the candidate does not already have the right to pursue a doctoral degree at the University of Helsinki, it must be applied for separately: https://www.helsinki.fi/en/admissions-and-education/apply-doctoral-programmes.
The monthly gross salary will be appr. 2200-2400 € per month depending on the appointee’s qualifications and experience. In addition, University of Helsinki offers comprehensive services to its employees, including occupational health care and opportunities for professional development. Further information at www.helsinki.fi/en/about-us/careers.
Please address your queries to Minna Oksanen, minna.k.oksanen@helsinki.fi, tel. +358 2941 26832.
Please submit your application as a single PDF file containing your CV through the University’s electronic recruitment system by clicking “Apply” link above.
The deadline for applications is December 16, 2021.
The Faculty of Medicine promotes high quality scientific research. It provides research-based undergraduate and postgraduate education in medicine, psychology and logopedics, dentistry,and an international Master’s Programme in Translational Medicine. It also offers psychotherapist education. In addition to its teaching and research activities, the Faculty serves as a significant expert organisation in the healthcare sector and contributes to the discourse on ethics in the field. The Faculty aims to be one of the best medical research faculties in the world, while reinforcing its status as a distinguished institution of medical education.
The Faculty of Medicine at the University of Helsinki constitutes the academic medical centre together with HUS Helsinki University Hospital and the Helsinki Institute of Life Science (HiLIFE). This medical centre has been successful in international comparisons, ranking among the top 10 medical campuses in Europe and the top 50 globally.
Are you interested in working with in areas that have a high impact on society such as biofuels, sustainable food proteins, or animal and human medicine? Would you like to do impactful research in the cutting edge of natural sciences with superb colleagues who are top expert in their field? Do you want to build a science career and work in a versatile role at the interface of academy and industry? VTT might be just the place for you.
VTT is one of the leading applied research organisations in Europe. What unites us are curiosity, a passion for learning and a purpose: to solve the biggest challenges of our time and turn them into sustainable growth and well-being. Our cross-disciplinary community of over 2000 brilliant minds is focused on creating impact through science-based innovation. In recent years, we have created ground-breaking innovations such as the world’s fastest and most accurate radiation detector, a cancer-sniffing sensor device for smartphones, and a headphone set entirely made of microbial materials.
We are now looking for Research Scientists to join our Protein production team.
In these positions, there are several potential roles depending on your level of expertise and skill level such as work in commercial projects where we develop fungal production systems for customers or leading research projects and applying for funding.
Our team, Protein production, works on topics of great important to society such as production of sustainable, animal free food proteins, production of vaccines to reduce antibiotics use in animals, enzyme mixtures for biofuel production, and therapeutic proteins for human medicine. These aims are in line with VTT’s mission to build a sustainable food system and enable bioinspired production for sustainable materials.
Your responsibilities as Research Scientist:
Scientific project work in the fields of protein production systems and fungal biology
Writing scientific reports and presenting research data
Working with customers to help them solve challenges
In some cases, applying for competitive research funding
Working as part of project team and contributing positively to a productive work environment
Who we are looking for:
Excellent laboratory skills and experience in molecular biology techniques, such as DNA cloning, genome engineering, protein analysis, protein purification and possibly in genomic analysis
Completed MSc or PhD in relevant field
One year or more of experience working with yeast or filamentous fungi
Strong spoken and written English skills
Strong academic publication record
Industrial experience working in a biotechnology company
As a person, we hope that you:
are motivated and willing to take initiative in getting projects accomplished
have strong communication skills
can work both independently and as a member of a team
enjoy scientific and technological challenges and have a strong passion for work
are willing to travel to customer and scientific meetings
are an outside-the-box think with ability to learn new things continuously
can tolerate pressure and maintain good work-life balance
With VTT, you’ll enjoy:
Natural sciences with an impact. VTT works on the cutting-edge of natural sciences, and we’ve invested into building state-of-the-art research facilities for natural sciences, such as the Bioruukki pilot infrastructure for bio- and circular economy. Our research agenda is dedicated to solving systemic and technological challenges, such as reaching carbon neutrality and unleashing the power of synthetic biology. That means that at VTT, your expertise in natural sciences will go towards creating real impact. Read more about our strategy – the path of exponential hope.
Superb colleagues and community. With VTT, you’ll join a community of over 2000 multidisciplinary experts who foster a culture of trust, openness and sharing knowledge. We work truly across disciplines, and house all the cutting-edge sciences from quantum computing to synthetic biology under one roof. Collaborating with superb colleagues is a source of learning, inspiration, and fun.
Excellent career in research. At VTT, excellence in research is a strategic priority. We offer long-term positions and stable career paths in top-level research. People tend to stay with us over 10 years since there are always new roles and responsibilities to grow into. A combination of cutting-edge academic research and applied customer projects keeps your career path interesting.
Support for your well-being. Our people are our main asset, so we take good care of them. We aim to nurture great team spirit and leadership and offer versatile well-being services to enable a good work–life balance. On top of 6 weeks of paid holidays we offer exercise and culture benefits, hobby clubs, and voluntary well-being services such as meditation programmes and trainings on cognitive ergonomics.
Nordic work–life balance. Working in Finland, the happiest country in the world, enables a great quality of life. At VTT, we make our people’s well-being a strategic priority. We offer 6 weeks paid vacation a year, and our benefits include extended occupational healthcare, and a range well-being services, such as exercise and culture benefits and hobby clubs. Read more here (https://www.vttresearch.com/en/research-jobs-in-finland)
Apply now and join our community of brilliant minds!
Please send your CV and application with a possible salary request via our recruitment system as soon as possible but at the latest by 2nd January 2022. We will process applications as they come in and fill the position as soon as we find the right candidate.
Interested and want to hear more?
For further information, please contact Research Team Leader Chris Landowski, Christopher.Landowski@vtt.fi.
Roche Diagnostics Oy is looking for a Field Product Manager to work in the area of Molecular Diagnostics. You will cover mainly PCR-based solutions – for which you will have the responsibility of product management, supporting and training, while also advancing further sales of our solutions. Our industry-leading systems, broad assay menus, and digital solutions are designed to address real-world needs across the entire healthcare continuum, including infectious disease and blood screening.
As a Field Product Manager, you will have an exciting opportunity to lead the launch of the new product line in Finland. Besides performing hands-on work in the molecular laboratory on one day, you will get the chance to perform sales and product management duties on another. You responsibilities will include contacting and visiting customers to maintain and generate new business and utilizing strong market and sales experience to map customer needs. All in all, this is an excellent opportunity for you with a degree in natural/biomedical sciences to join the world’s leading supplier in In-Vitro Diagnostics!
To be successful as a Field Product Manager for Molecular Diagnostics, you should be a person who truly enjoys working in a changing environment in which you see opportunities rather than threats. You are open to co-create new solutions with our customers and Roche colleagues by listening and reflecting skillfully. In addition of utilizing traditional customer touchpoints, you are able to navigate and make use of different type of digital tools.
REQUIREMENTS:
-You are comfortable working both inside and outside laboratory setting with key opinion leaders when contributing to better patient care with our high-medical-value molecular diagnostics solutions.
-You have a customer oriented mindset and candidates with experience from the sales and/or marketing process are preferred (1-3 years), as part of your job is to introduce and sell our solutions to the customers.
-You already have a strong hands-on experience using molecular diagnostics methods (PCR experience is a must) in a research or routine laboratory.
-You have a Master’s degree in natural/biomedical sciences, while a PhD from a relevant field could also work in your advantage.
– Good project management skills will help you be successful in your work.
– You are able to work in a regulated business environment, stay calm under pressure and are strongly accountable on your actions.
-You are fluent in Finnish and English and willing to travel when required.
As a Product Manager for Roche Molecular Diagnostics, you will work at one of the world’s leading supplier of automated diagnostic systems, helping professionals to recommend treatment solutions that deliver superior patient care. We offer you the opportunity to work with interesting products and solutions, with independent responsibilities combined with the support from our great Finnish team!
At Roche, over 94,000 people across 100 countries are pushing back the frontiers of healthcare. Roche tests are used around the world by laboratories, researchers, doctors, blood banks, and hospitals to support healthcare. Working together, we’ve become one of the world’s leading research-focused healthcare groups. Our success is built on innovation, curiosity and diversity. Roche is an equal opportunity employer.
For further information, please call HR partner Sadaf Baloch +47 939 71 688, on
Friday 12th November between 14:00-14:45 (Norwegian time)
Monday 22nd November between 15:30-16:00 (Norwegian time)
Please apply the open position including your application with salary request and CV in English by 28.11.2021. The position will be filled as soon as suitable candidate is found.
