3.8.2026 | Avoimet työpaikat
https://duunitori.fi/tyopaikat/tyo/target-discovery-lead-cancer-genomics-scsom-19902349?utm_source=loimu&utm_medium=site
Job description
We are seeking an accomplished Target Discovery Lead to join our client’s Cancer Genomics Research Team. The Target Discovery Lead drives innovation in cancer genomics by identifying and validating novel therapeutic targets. This role combines strategic thinking, scientific leadership, and cross-functional collaboration to advance high-impact ideas through the discovery pipeline. The ideal candidate will have a strong track record in target identification and validation, preferably within the small molecule space.
Key Responsibilities
Scientific Strategy & Innovation
- Monitor emerging trends and breakthroughs in cancer genomics to inspire new target concepts.
- Lead ideation sessions and foster a culture of creativity and scientific rigor in target discovery.
Target Identification & Prioritisation
- Design and implement strategies for identifying high-potential therapeutic targets in collaboration with bioinformatics and translational research teams.
- Evaluate and prioritise target ideas based on biological relevance, feasibility, and clinical impact.
Validation & Advancement
- Oversee experimental validation of selected targets, ensuring robust scientific evidence. Develop and conduct complex assays. Analyse and interpret experimental data, synthesise insights, and communicate results effectively in internal reviews and external presentations.
- Define clear advancement criteria and decision-making frameworks to progress targets through the pipeline.
Leadership & Accountability
- Act as the primary owner for target ideation goals, ensuring timely delivery and alignment with organisational strategy.
- Collaborate cross-functionally internally and externally to integrate insights from genomics, bioinformatics, and clinical research.
- Initiate and manage strategic collaborations with CROs, academic institutions, and industry partners to accelerate target discovery and validation.
- You will work closely with a multidisciplinary team to discover and validate novel cancer targets and help develop first- or best-in-class targets from concept to clinical candidate. This is a unique opportunity to contribute to cutting-edge cancer therapies that can make a real difference for patients.
What We Offer
- A chance to work with experienced scientists in a dynamic R&D environment.
- A supportive workplace with opportunities for growth.
- The opportunity to contribute to innovative therapies that improve patients’ lives.
- A culture of friendliness, respect, mutual appreciation, and diversity, creating a safe environment to strive for excellence.
- Career paths and development opportunities that support innovation and impact on quality of life.
Key Qualifications
- Ph.D. in Molecular Biology, Cancer Genomics, Genetics, or related field.
- Postdoctoral industry experience in oncology research, target discovery, or drug development.
- Proven track record in target identification and validation within cancer biology.
- Strong understanding of genomics, bioinformatics, and translational research.
- Demonstrated ability to lead teams and drive projects to completion.
- Excellent communication and strategic thinking skills.
- Experience with CRISPR-based functional genomics and gene-editing technologies.
- Proficiency in multi-omics data analysis (genomics, transcriptomics, proteomics), with experience in flow cytometry, advanced microscopy techniques.
Preferred Skills
- Familiarity with computational biology tools and pipelines for target discovery.
- Knowledge of tumor biology and resistance mechanisms.
- Strong ability to interpret large-scale datasets and integrate insights into experimental design.
- Prior experience in pharma or biotech environments with drug discovery exposure.
TSP Talent Solutions and our customers are affirmative action/equal opportunity employers (Minorities/Females/Veterans/Disabled)
3.8.2026 | Avoimet työpaikat
https://duunitori.fi/tyopaikat/tyo/qa-manager-development-scsom-20455198?utm_source=loimu&utm_medium=site
Apply latest by 30.8.2026
Job description
Are you looking for an exciting professional challenge?
We are one of the leading European contract manufacturers in the pharmaceutical, biotech and healthcare sectors, with some 2,300 employees in Germany, France, Finland, UK and Norway. For us, the next step is always the one that matters most. Our fast pace drives us forward, fills our working environment with life and spurs our growth. Our winning formula for shared success: room for passion. Because we know that passion is the best medicine when it comes to excellent service around the world. Welcome to NextPharma.
NextPharma Tampere has several decades of extensive experience in pharmaceutical development, commercial manufacturing and packaging of ophthalmic products BFS (Blow Fill Seal), MD (Multi dose) and PFMD (preservative free multi dose ophthalmic products). The products we manufacture are globally exported.
Interested in shaping Quality Excellence in Pharmaceutical Development?
We are seeking an experienced and highly motivated QA Manager – Development to join our Quality organization in Tampere. In this critical leadership role, you will provide QA oversight for late-stage pharmaceutical development activities, process validation, technology transfer and commercial readiness. You will ensure that development programs progress in compliance with GMP requirements while supporting the successful transition from development to commercial manufacturing. You and your team (3-4 Specialists) work closely together especially with the site Product Development Team and Production.
This is an exciting opportunity for a quality professional who combines People skills, strong GMP expertise, scientific understanding and a collaborative mindset to support innovative pharmaceutical products through pivotal development stages.
Key Responsibilities:
Leadership
- Coach and develop QA professionals within the Development Quality function.
- Serve as a trusted business partner to cross-functional development teams.
- Influence quality decisions while maintaining independent quality oversight.
Quality Oversight of Development Activities
- Provide QA support for late-stage development programs, including Phase III and registration-enabling activities.
- Ensure compliance with applicable GMP, ICH, FDA, EMA, and other regulatory requirements.
- Review and approve development documentation, protocols, reports, and other quality-related documents.
Process Validation & Commercial Readiness
- Lead QA oversight of process validation activities, including:
- Process validation
- Cleaning Validation
- Hold Time Studies
- Analytical Method Validation and Transfer
- Review and approve validation master plans, protocols, and final reports.
- Ensure validation strategies are scientifically sound and compliant with regulatory expectations.
- Support process characterization and risk management activities.
Technology Transfer
- Act as QA representative for technology transfer projects.
- Partner with Manufacturing, Product Development, Engineering, Validation, and Supply Chain teams.
- Ensure readiness for commercial manufacturing and regulatory inspections.
Quality Systems & Compliance
- Manage investigations, deviations, CAPAs, change controls, and risk assessments related to development and validation activities.
- Monitor quality metrics and identify opportunities for continuous improvement.
- Support internal audits, supplier audits, and regulatory inspections.
- Promote a culture of quality excellence and compliance throughout the organization.
What we hope you bring:
- Bachelor’s or Master’s degree in Pharmacy, Chemistry, Biotechnology, Life Sciences, Engineering or a related scientific discipline.
- Minimum of 3 years of experience in the pharmaceutical or other highly regulated industry.
- Strong expertise in GMP regulations and pharmaceutical quality systems.
- Leadership Experience / Potential, Excellent communication and stakeholder management skills.
- Hands-on experience with process validation and late-stage product development.
- Experience supporting technology transfer and commercialization activities.
- Fluency in Finnish and English.
We Appreciate:
- Experience interacting with health authorities and supporting regulatory inspections.
What We Offer:
- Opportunity to contribute to innovative therapies that improve patients’ lives.
- A pivotal role within a growing and dynamic organization.
- Collaborative international environment with strong cross-functional exposure.
- Competitive compensation and benefits like flexible working hours, lunch and well-being benefit, leisure insurance and company events.
- Professional development and career growth opportunities.
It is a permanent senior white-collar position and you would report to Head of Quality Tampere. We hope you could start working in September-October 2026.
Say yes to what’s next: Would you like to know more about the position? Please contact: Head of Quality Stefan Weber Stefan.weber@nextpharma.com / +358 44 430 4739. The best time to reach him is 4th or 11th Aug between 2 p.m. and 5 p.m. We look forward to receiving your application preferably on our website nextpharma.com/careers before 31st of Aug 2026. Please also include your earliest possible start date. NextPharma Oy Niittyhaankatu 20, Tampere.
25.4.2026 | Avoimet työpaikat
https://duunitori.fi/tyopaikat/tyo/assay-development-scientist-lateral-flow-assays-biohit-oyj-sesil-20211463
Apply latest by 7.5.2026
Job description
Are you a self-reliant and solution-oriented person? Would you like to be part of a fast-growing company and work on impactful diagnostics development?
Our customer Biohit Oyj is looking for an Assay Development Scientist to join a team focused on Lateral Flow Assay (LFA) product development. The position is full-time and permanent, and the employment contract is formed directly with Biohit Oyj. The workplace is located along good transport links in Roihupelto in Helsinki. The work is mainly done at the office, but partial remote work is possible. We hope that you could start in the position as soon as possible.
About the role
In this role, you will work hands-on in the laboratory to develop and optimize lateral flow immunoassays. You will translate assay needs into clear experimental plans (”design inputs”), generate and document evidence-based assay performance (”design outputs”), and support verification activities by defining test approaches, acceptance criteria, and performance summaries. You will collaborate with relevant internal stakeholders (e.g., development, quality interfaces, manufacturing interfaces as needed) to ensure assay development deliverables are clear, complete, and ready for next-stage work.
Main responsibilities
- Hands-on laboratory development and optimization of lateral flow assays, including iterative troubleshooting and robustness improvements
- Define assay development objectives and requirements (design inputs) and convert them into clear experimental plans, protocols, and study outlines
- Execute experiments with strong attention to detail, maintain structured lab records, and produce clear, concise development reports
- Analyze and summarize assay performance using appropriate data handling and basic statistics; communicate conclusions and recommendations clearly
- Produce assay development deliverables (design outputs), such as optimized assay conditions, preliminary specifications/targets, and documented rationale for key design choices
- Support verification/performance evaluation from the assay-development perspective by helping define test methods, sample/data needs, and acceptance criteria, and by summarizing results in a structured format
- Contribute to feasibility studies and investigations, including collaboration with external partners when needed, and participate in continuous improvement of development ways of working
What we require
- Degree in biochemistry, biotechnology, biomedical/chemical engineering, analytical chemistry, or a related field (or equivalent relevant competence)
- Strong biochemistry laboratory techniques and good laboratory practices
- Strong theoretical background in biochemistry/biotechnology relevant to immunoassays
- Proven capability in experimental design with clear, detailed, and concise planning and reporting
- Basic biomedical data analysis and statistics skills applicable to assay development
- Excellent documentation skills in English
- Strong problem-solving skills and high attention to detail
- Hands-on experience with immunoassays; lateral flow assay experience is strongly preferred
Languages
- Fluent professional English (written and spoken)
- Fluency in Finnish is considered a plus
You will succeed in this position if you are
- Self-reliant, organized, and comfortable driving hands-on lab work forward
- Curious and practical, with a structured approach to troubleshooting and iteration
- Clear and consistent in documentation and communication across a multidisciplinary team
Biohit Oyj offers you
An interesting and challenging position with versatile assignments. You get to work in a dynamic work environment with amazing and professional colleagues. You will have a great opportunity to work on exciting projects and become part of a fast-growing company. Biohit Oyj supports you to learn and develop your personal skills and gives you the opportunity to grow within the company. Biohit Oyj offers many benefits such as lunch benefit and sport benefit. Biohit Oyj also provides occupational healthcare services. The monthly salary range for this role is 3600-4400 €, depending on experience.
For further information about the position and the recruitment process, please contact Eilakaisla’s HR Consultant, Hanna Kekkonen, by email at firstname.lastname@eilakaisla.fi or by phone at +358 50 431 4017. Hanna is happy to answer questions by phone on 29.4. between 10-11 and on 6.5. between 15-16.
Työsuhteen tyyppi: permanent, full-time
18.1.2026 | Avoimet työpaikat
https://duunitori.fi/tyopaikat/tyo/patent-counsel-sosri-19892107?utm_source=loimu&utm_medium=site
Apply latest by 28.1.2026
Job description
We are seeking a Patent Counsel to help build and manage robust patent portfolios for Orion Corporation’s expanding pipeline in the pharmaceuticals industry. The ideal candidate brings deep knowledge of chemistry or biotechnology and experience in (bio)pharmaceutical R&D. You combine outstanding professional competence with agility and you thrive both as an individual contributor and as a collaborative team player.
Your key responsibilities
- Identify and draft patent applications on pharmaceutical inventions in close interaction with inventors
- Prosecute and defend patents in opposition proceedings in all major jurisdictions.
- Manage patent portfolios in a time- and cost-efficient manner
- Conduct freedom-to-operate (FTO) risk assessments and landscape evaluations for both innovative portfolio as well as our generic portfolio development purposes and monitor patent filing activities of competitors
- Advise R&D and broader in house stakeholders on patenting strategy, FTO and risk mitigation
- Provide expert patent opinions and evaluations to stakeholders and senior leadership, particularly in the context of external asset evaluations and strategic decision-making
- Contribute to the further development of the IPR processes in the Company
You will work closely with R&D and business teams and coordinate with external IP partners to execute our tasks according to the strategy. Your expertise will play an important role in shaping and implementing decisions that support Orion’s innovation pipeline and business goals. The responsibily area of the role will be defined in alignment with your skills and capabilities.
This is a full-time and permanent position located in Espoo, and we also support hybrid working model. This position reports to Director Intellectual Property Rights.
What we offer
At Orion, your work creates true impact and well-being for our customers, patients and society at large. Our culture of friendliness, respect, mutual appreciation and diversity creates a safe working environment where you can strive for excellence. We offer a wealth of career paths and development opportunities that support the development of innovative solutions and improving the quality of life.
Please visit our website to find further information about our values and Orion as an employer https://www.orion.fi/en/careers/orion-as-an-employer/.
Our expectations
- Diploma or Master’s degree in Chemistry, Biochemistry, Biotechnology, Pharma, or (Molecular) Biology
- Hands on experience with biopharmaceutical technologies and/or drug discovery and development
- European Patent Attorney qualification (part/full) is considered as an advantage
- Several years’ proven experience in pharmaceutical patenting (at least in EU and US), gained in-house or private practice
- Strong analytical mindset and attention to details. You have proven ability to plan, organize, and prioritize multiple tasks efficiently
- Highly motivated, collaborative working style with excellent communication skills (English being the main working language)
- Ability to simplify complex scientific and legal concepts and provide clear, pragmatic advice in a commercial context
How to apply and additional information
Please submit your resume and application letter detailing your relevant experience and why you are the best candidate to become our new colleague by January 28th, 2026.
If you have any questions related to the position, please contact Heidi Adler, Director, Intellectual Property Rights, on January 23rd, 2026, at 9.00-11.00 EET and January 26th, 2026, at 9.30-11.00, tel. +358 50 966 2640.
We typically review applications already during the application period and may start interviewing candidates before the application deadline. Therefore, we invite you to send your application as soon as possible.
#LI-ORION
Approved medical examination which also includes drug testing is required prior to the employment. We will also carry out a security clearance prior to the employment for the selected person.
Unit description
Corporate Functions contributes to the achievement of Orion’s business objectives by providing expert services and specialized knowledge. We serve Orion in several ways: as providers of expertise and services needed for the business, most prominent experts in our fields of expertise, contributors to the development of processes and operations, and organizers of certain mandatory corporate functions. Our organization includes Compliance, Corporate Responsibility, Intellectual Property Rights, Legal Affairs, and Public Affairs.
4.11.2025 | Avoimet työpaikat
Apply latest by 15.11.
https://duunitori.fi/tyopaikat/tyo/image-analysis-specialistengineercoordinator-helsinki-bioimaging-shsel-19664630
Job description
We are seeking a highly motivated and goal-oriented Image Analysis Specialist/Engineer/Coordinator to develop and apply cutting-edge light microscopy image analysis workflows. The salary range is 3 140 – 4 440 € / month. Title and salary will be based on your experience, skills and merits. The position is initially available from 1.1.2026 to 31.12.2028.
The position
This role offers a unique opportunity to apply and integrate advanced image processing techniques to progress the fields of biomedical and life sciences. Working within a team of biologists, physicists and engineers, the specialist will help build robust and reproducible protocols to extract meaningful quantitative information from both simple and complex microscopy datasets and present it effectively.
This is a joint position between Biomedicum Imaging Unit BIU at the Meilahti campus and Light Microscopy Unit LMU at the Viikki campus, which are open access core facilities offering a wide variety of basic and advanced light microscopy techniques to several hundred local, national and international users annually.
Specific tasks
• Develop and apply different image analysis approaches to, for example, segment, track, and characterize cellular structures and dynamics in biological systems, including 3D and timelapse light microscopy data, and embed these approaches into the general service portfolio of BIU/LMU.
• Maintain custom scripts and software tools for microscopy image analysis and data processing, implement image analysis according to FAIR principles.
• Create a well organised, version controlled (including software version packaging) space for sharing image analysis workflows.
• Communicate concepts of image analysis and their relevance for biological questions to experts and non-experts.
• Take part in the planning stage of users’ imaging projects.
• Organise monthly Helsinki Bioimaging Call4Help sessions for users.
Qualifications
• PhD in computer science, biological science (e.g. cell biology, biophysics, bioengineering), physical science, or related science or engineering field; or equivalent combination of degree and experience required.
• Extensive experience with image analysis principles and algorithms.
• Proficiency with command line prompting and at least one programming language.
• Familiarity with software engineering practices such as version management, build management, and testing.
• Ability to work both independently and as part of a group.
In addition, one or more of the following would be advantageous:
• Knowledge of light microscopy imaging modalities, and image artifacts.
• Experience with 3D image data analysis and 3D image visualization.
• Experience with machine learning or deep learning-based segmentation algorithms.
• Experience with statistical analysis to interpret quantitative image data and generate biological insights.
• Experience in working in a multi-disciplinary environment in academic or industrial settings.
Contract & salary
The position is initially available from 1.1.2026 to 31.12.2028.
The salary is based on the salary system of Finnish universities for technical and support staff. In addition, the appointee will be paid a salary component based on personal performance. The salary range is 3 140 – 4 440 € / month. Title and salary will be based on your experience, skills and merits.
How to apply
Applications are to be sent by November 15th, 2025, using the UH recruitment system via the button ”Apply now”. The application should include a short cover letter (max 1 page) describing your expertise and motivation for the position, a CV (max 2 pages), and the names and contact information for at least two references.
Contact details
Further inquiries regarding the project scope or position details, please contact: maria.vartiainen@helsinki.fi
Maria Vartiainen, Research director
E-mail: maria.vartiainen@helsinki.fi
HiLIFE/Institute of Biotechnology, University of Helsinki, Finland
University of Helsinki (UH) is one of the world’s leading universities for multidisciplinary research. Helsinki Institute of Life Science HiLIFE is an independent research institute at UH that supports high-quality life science research across campuses and faculties. Coordination of open access life science research infrastructures is one of the key roles of HiLIFE, and these facilities are grouped into 17 thematic platforms. One such platform is Helsinki Bioimaging (https://www.helsinki.fi/en/infrastructures/bioimaging), which provides expertise and state-of-the-art equipment for modern light and electron microscopic bioimaging applications.
4.11.2025 | Avoimet työpaikat
Apply latest by 27.11.
https://ats.talentadore.com/apply/tutkijatohtori-ja-vaitoskirjatutkija-kasvitieteeseen-ja-levatutkimukseen/mEovXW?lang=en&UTUID=21078
We are seeking a Postdoctoral researcher and Doctoral researcher (or Research assistant) to join the Photosynthetic Microbes group led by Professor Yagut Allahverdiyeva-Rinne. The positions are part of the AlgaCircle project funded by Business Finland and several Finnish companies. The work will be carried out at the Faculty of Technology, within the Department of Life Technologies, in Turku, Finland. Employment will start on 1 January 2026, or as agreed. The successful candidate will be offered a fixed one-year contract, with the possibility of extension. Doctoral Researcher will be enrolled to the University of Turku Graduate School (UTUGS) and after that the person will be employed for at least 3 years.
About the Photosynthetic Microbes Research Group
We study the regulation of photosynthesis and apply photosynthetic principles to develop sustainable biotechnologies. Our research encompasses several areas, including the elucidation of photosynthetic electron transport pathways, engineering photosynthesis for enhanced bioproduction of solar chemicals, biophotovoltaic (BPV) systems, and large-scale algal cultivation for phytoremediation and the production of green chemicals such as biostimulants and biopesticides
The truly international and large PhotoMicrobes group is involved in several EU, Nordic, and national projects and regularly publishes its research outcomes in highly respected journals. We have established a broad research network with connections to leading international laboratories and industrial partners. Our team members are not only active participants in international conferences but also regularly organize major symposia and meetings in Turku (e.g., the Nordic Photosynthesis Congress, the International Conference on Renewable Resources 2025, and the Nordic Algal Biotechnology Conference).
We are developing the national FIN-BioFoundry research infrastructure roadmap, which provides state-of-the-art equipment and methodologies. In addition, we are actively involved in science policymaking through the SYNERGY pan-European initiative.
To learn more about the Photosynthetic Microbes research group, you can visit our website at www.utu.fi/photo-microbes or follow us on LinkedIN and BlueSky at @PhotoMicrobes.
Job description
The AlgaCircle project aims to utilize effluents from Finnish industries to cultivate microalgae and upgrade the resulting biomass through a multiproduct biorefinery approach. The project is carried out in collaboration with several industrial partners.
Position #1 will focus on testing different algal formulations on crops and will work in close collaboration with researchers operating large photobioreactors. Part of the experiments will be conducted together with the NAPPI plant phenotyping platform.
Position #2 will focus on optimizing the phytoremediation of industrial effluents by adjusting photobioreactor parameters and applying genetic engineering and synthetic biology approaches.
Apply between 16 October 2025 and 27 November 2025 16:00 (Europe/Helsinki)
Who we are looking for
We are looking for highly motivated and enthusiastic applicants. Candidates applying for the postdoctoral researcher position are expected to hold a doctoral degree and have a strong academic background, including first-author publications in the fields of plant science, photosynthesis, agriculture, or biotechnology.
Applicants for the doctoral researcher/project researcher position must hold a Master’s degree (MSc) in biotechnology, plant science, molecular biology, biophysics, or a related field (good academic performance is considered an asset). Students who have not yet completed their degree may also apply and start as research assistants. In such cases, the employment will be temporary until the Master’s degree is completed, after which the title will be updated to project researcher. Once the applicant has received the right to study and has been accepted into the UTUGS doctoral programme, the title will be updated to doctoral researcher.
Eligibility requirements for these positions are defined in the University of Turku’s regulations: https://www.utu.fi/en/university/organisation. A postdoctoral researcher is required to hold a doctoral degree, and a doctoral researcher/project researcher must hold a Master’s degree.
If you are applying for the doctoral researcher position, you must apply for the right to pursue doctoral studies (in the spring/autumn 2026 application round) at the University of Turku. Please familiarize yourself with the student information and application criteria of the University of Turku Graduate School (UTUGS) and its doctoral programmes. Note that you must meet the criteria required for the position. Pay particular attention to the English language proficiency requirements. The position requires fluent written and spoken English skills.
We value collegiality and promote equality, diversity, and inclusivity. We encourage all qualified applicants with different backgrounds to apply for our open positions.
Benefits
We offer you responsible and interesting tasks and the opportunity to develop your professional skills in a versatile operating environment. You get a professional and inspiring team to support your work. We take care of your well-being at work and the functionality of your everyday life, e.g. with the help of flexible working hours and our well-being services.
Please read more about University of Turku as an employee from our Come work with us! pages.
The European Commission has awarded the University of Turku the right to use the HR Excellence in Research quality label. The label is a token of the University’s commitment to continuous development of the position and working conditions of researchers according to the guidelines set forth in the European Charter for Researchers.
The university offers good support and orientation for international hires. Please learn more about the Finnish culture and relocation to Finland:
The University of Turku is among the top of the world’s universities in most rankings and among the best universities in the world in certain fields. Our high-quality basic research, a multidisciplinary research profile and close cooperation in research infrastructures creates the basis for international top research. Read more about University of Turku in international university rankings.
The University of Turku has several high-quality research infrastructures required for cutting-edge research. Learn more about the roadmap of research infrastructures and how the research infrastructure and expert teams offer tailored solutions for businesses and organizations.
Salary and trial period
The salary is determined by the collective agreement system of the Finnish universities. The salaries are determined in accordance with the university salary system for teaching and research personnel. The salary will be commensurate with qualifications and experience based on the University salary system and will at the beginning of the employment be for a postdoctoral researcher approximately 3600-3800 €/month. If a doctoral student is hired for the position, the starting salary will be approximately 2500-2600 €/month and for a research assistant 2280 eur/month.
The position has a trial period of six months.
How to apply
Applicants should enclose with their application:
- motivation letter, including statement of motivation, summarizing scientific work and research interest (max 1 page)
- CV, including education, positions, professional experience, names and contact details of two academic referees (max 2 pages)
- list of publications (please do not attach your thesis or papers)
- degree certificate(s) in English or in Finnish
For further information about the position, please contact: professor Yagut Allahverdiyeva, allahve(at)utu.fi
With questions about the application process, please contact: HR Specialist Paula Luoma paula.luoma(at)utu.fi ( during 3.10.2025 – 7.10.2025 please contact hr-tech(at)utu.fi)
This is an enriching job opportunity in a rapidly evolving field – we warmly welcome you to join our multicultural working community.
14.8.2025 | Avoimet työpaikat
https://careers.roche.com/global/en/job/ROCHGLOBAL202507117378EXTERNALENGLOBAL/Technical-Support-Specialist
The Position
Are you a service engineer with an interest in the healthcare field and doing what patients need next? Roche are looking for a Technical Support Specialist to join our technical expert team. Roche serves their customers in almost all hospitals and other healthcare facilities in Finland in which clinical laboratory analyses are conducted. As a service engineer, you are an extremely important part of our expert services, and your task is to maintain the production of our customer laboratories.
In this role, you will work in Roche’s field service team, responsible for instrument installations, scheduled maintenance, repairs, and instrument modifications. The role requires travel, as work is performed in customers’ laboratories.
Key Responsibilities:
- You install, service, maintain, and troubleshoot diagnostic laboratory systems.
- You collaborate with cross-functional teams internally to deliver comprehensive solutions.
- You foster strong relationships with our international divisions to drive success.
- You engage in customer meetings to understand their needs and provide exceptional service.
Who You Are:
- You have an educational background in laboratory, health technology, biotechnology, automation technology, or mechanical engineering.
- You have basic knowledge of IT, network structures and common operating systems.
- You have a driving license and an interest in traveling.
- You are good at customer management and team work.
- You are fluent in Finnish and English.
Previous experience in a similar role will be considered an advantage, allowing for a smoother transition and quicker contribution to our team.
We will begin interviews immediately, so we encourage you to apply quickly.
Location: Tampere or Turku
