suitable educational background and professional profile
English skills
Benefits
ePassi wellbeing benefit
extensive occupational health-care
physical and cultural free-time activities
FinVector
FinVector is a fast-growing and internationally renowned biopharmaceutical company that develops and manufactures viral-based gene therapy products. As a pioneer in its operational field, FinVector has extensive experience of nearly 30 years in cGMP manufacturing. The company’s operations are centered in Kuopio, Finland, and it employs around 330 professionals from over 30 different countries. FinVector works on cutting-edge biopharmaceuticals and has invested in building state-of-the-art development and GMP facilities for Viral Vector and Cell Therapy platforms including vaccines. FinVector is owned by Ferring Ventures, a subsidiary of Ferring Foundation B.V.
The Euro-BioImaging Scientific Ambassadors program aims to raise awareness about the services and opportunities provided by Euro-BioImaging. Our Scientific Ambassadors act as catalysts, connecting with like-minded individuals who share a common goal to impact in their communities. By effectively communicating the services offered by Euro-BioImaging, our Scientific Ambassadors play a crucial role in expanding the reach of Euro-BioImaging. Through their advocacy and engagement, Scientific Ambassadors help foster a greater understanding of Euro-BioImaging services, making imaging technologies more accessible for researchers and creating opportunities for collaboration, scientific advancement, and innovation in bioimaging.
You should become a Scientific Ambassador if you believe in the Euro-BioImaging mission of providing open access to imaging expertise and want to help spread the word about this fabulous opportunity to other researchers. But being a Scientific Ambassador can also contribute to your personal and career development. As a Euro-BioImaging Scientific Ambassador, you can expect a range of valuable offerings and support throughout your journey:
Welcome pack: Upon joining the program, you will receive a special welcome pack containing branded items such as a t-shirt, stickers, bag, pen, notebook, etc. These items not only serve as a token of appreciation but also allow you to represent Euro-BioImaging proudly.
Training by Euro-BioImaging staff: Euro-BioImaging is committed to equipping its Scientific Ambassadors with the necessary knowledge and skills to excel in their roles. You will receive training directly from the experienced staff at Euro-BioImaging, ensuring you understand the organisation, its mission, and the scientific principles it operates on.
Presentation and teaching materials: To support your advocacy efforts, Euro-BioImaging will provide you with materials that you can use for presentations, teaching, or workshops. These resources will help you effectively communicate the benefits and opportunities offered by Euro-BioImaging to your community and beyond.
Recognition on the Euro-BioImaging website: Your role as a Scientific Ambassador will be acknowledged and highlighted on the Euro-BioImaging website and social media. Your activities and achievements will be showcased, demonstrating your impact and serving as an inspiration for others.
Networking opportunities: As a Euro-BioImaging Scientific Ambassador, you will have the chance to network with professionals from Euro-BioImaging and other ambassadors. This networking provides a platform for collaboration, knowledge sharing, and building meaningful connections within the scientific community.
Travel grants: With support from the EVOLVE project, you’ll have the chance to pitch for potential travel funding opportunities to attend events in which you can present Euro-BioImaging. The maximum limit is 1,500 Euros per person.
Personalised support and guidance: The Euro-BioImaging team will provide personalised support and guidance throughout your ambassadorial journey. Whether you have questions, need assistance organising events, or require advice on engaging your community, the Euro-BioImaging team will help you every step of the way.
Growth opportunities: Euro-BioImaging is committed to supporting your personal and professional growth. If you have a particular area of interest within bioimaging, the organisation will provide resources, connections, and opportunities to develop your expertise further and expand your knowledge.
Increased visibility: As a Euro-BioImaging Scientific Ambassador, you will gain increased visibility for yourself and your community. Your active involvement and contributions to the program will be recognised and celebrated. Euro-BioImaging will actively promote and highlight your activities through various communication channels, including social media platforms and newsletters. This visibility showcases the impactful work you do as an ambassador, inspiring others to engage with Euro-BioImaging and its services.
How it works
The Euro-BioImaging Scientific Ambassadors program follows a structured process consisting of three distinct phases that unroll over one year in close collaboration with Euro-BioImaging Hub team staff.
Onboarding phase
During the onboarding phase, which lasts approximately one month, you will be introduced to Euro-BioImaging along with other selected Euro-BioImaging Scientific Ambassadors. This phase aims to foster a sense of community and provides you with a comprehensive understanding of Euro-BioImaging’s mission, services, and opportunities. You will have the chance to explore different aspects of Euro-BioImaging and identify which areas are most interesting to you and where you would like to develop your knowledge further.
Running phase
Once the onboarding phase is complete, the running phase begins, spanning a period of one year. This phase allows you to choose your preferred activities from a diverse portfolio of options Euro-BioImaging offers or propose your own innovative ideas. The aim is to provide you with a range of impactful activities that align with your interests and strengths.
Offboarding
Lastly, the offboarding phase marks the conclusion of your journey. As a token of appreciation for your dedication and efforts, we will award you with a digital badge recognising your contribution as a Euro-BioImaging Scientific Ambassador. This ensures that your valuable work continues to benefit others beyond the program. We will collect your feedback and impressions on the process of being a Euro-BioImaging Scientific Ambassador so you can shape the continued development of this program. And your profile will stay on our website!
What are the requirements?
To become a Euro-BioImaging Scientific Ambassador, there are certain requirements that we look for in potential candidates:
Must have:
We seek individuals who are passionate about imaging and are eager to make a positive impact. Scientific Ambassadors should be enthusiastic advocates for Euro-BioImaging’s services and opportunities.
It is important that the Scientific Ambassadors align with Euro-BioImaging’s values and mission:
To provide open access, services and training to state-of-the-art imaging technologies for all life scientists in Europe and beyond.
To foster the liaison and cooperation of all its stakeholders (including scientists, industry, and national and European authorities).
Experience in the imaging field: This experience can range from academic research to practical applications in the imaging field or related.
Euro-BioImaging member state and/or European residency.
Nice to have:
Strong communication skills, both written and verbal, are essential for effectively conveying the message and values of Euro-BioImaging.
Familiarity with Euro-BioImaging Services: It is a plus if applicants have previously utilised Euro-BioImaging services. This firsthand experience allows Scientific Ambassadors to effectively communicate the benefits and value of these services to others.
Early Career Researchers, students and young researchers are specifically encouraged to apply.
Who cannot apply:
As this program focuses on extending the reach of Euro-BioImaging to new communities, Node staff and members of Euro-BioImaging governing bodies are not eligible to apply.
What can you expect from the program?
Time Commitment
Flexible: The Euro-BioImaging Scientific Ambassadors program offers flexibility in terms of time commitment. You can choose activities that align with your interests and fit your schedule.
Ambassadorship calls: We will organise monthly networking sessions for ambassadors to connect with their peers and Euro-BioImaging staff. We strive to make these calls accessible and considerate of different time zones.
Expected dedication: We anticipate ambassadors to spend at least 2 sessions of 2 hours in online meetings during the onboarding phase. During the running phase, we expect Scientific Ambassadors to complete at least one activity. It is entirely up to Scientific Ambassadors to make the most of the program.
How to apply?
Applying to become a Euro-BioImaging Scientific Ambassador is a straightforward process. Follow this link to submit your application. The form will require you to provide relevant information about yourself, including your background, experience, and motivation for becoming a Euro-BioImaging Scientific Ambassador.
Are you ready to take your career in Medical Affairs to the next level? Thermo Fisher Scientific Inc. is seeking a highly motivated and experienced Medical Scientific Reviewer to join our outstanding team.
We are dedicated to enabling our customers to make the world healthier, cleaner, and safer. As one of the global leaders in the industry, we strive for flawless execution and world-class innovation. This is the perfect opportunity for a proven professional to showcase their expertise and make a significant impact in the field of medical research.
The job involves assisting the Medical and Scientific Affairs Team with review processes and activities in the Clinical Sequencing business. We are working towards enabling Precision Medicine globally by providing effective sequencing solutions for clinical and translational research. Our goal is to expand our clinical reach through supporting studies and generating evidence in the molecular diagnostics field.
Key Responsibilities:
Conduct detailed reviews of scientific, medical, and promotional documents to ensure consistency, scientific validity, and compliance with regulations and guidelines.
Collaborate with regulatory and legal teams to ensure compliance with applicable requirements and international standards for diagnostics, including oncology.
Apply medical or related field expertise to evaluate clinical data, research findings, and diagnostic information, ensuring scientific accuracy and relevance in oncology and pathology.
Contract Management: Supervise the management of contracts, including reviewing, negotiating, and ensuring compliance with requirements.
Quality Assurance: Participate in quality assurance activities, including reviewing protocols, clinical study reports, scientific papers, and contracts for accuracy and adherence to regulatory guidelines.
Cross-Functional Teamwork: Collaborate with all internal partners to ensure scientific, regulatory, and contractual alignment.
Process Improvement: Identify areas for improvement in the review and contracting process, developing and implementing strategies to increase efficiency while maintaining quality standards.
Minimum Requirements/Qualifications:
Bachelor’s or advanced degree in a health-related field such as Oncology, Molecular Biology, Biochemistry, or a closely related field.
Minimum of 3 years of experience in medical/scientific review, regulatory compliance, and contract management within the diagnostics or pharmaceutical industry.
In-depth knowledge of oncology diagnostics and related scientific principles.
Familiarity with global regulatory requirements (FDA, EMA, etc.).
Experience in contract review and management within a scientific or medical setting.
Proficiency in medical writing and document management systems is a plus.
Familiarity with software tools for document submission and review, as well as contract management software.
Excellent attention to detail and ability to handle complex scientific data.
Ability to work collaboratively in a fast-paced, multidisciplinary environment.
Join our team and be part of a company that values diverse experiences, backgrounds, and perspectives. Thermo Fisher Scientific is an equal opportunity employer and offers reasonable accommodations for individuals with disabilities during the application process.
Sr Product Specialist Human Predictive Genomics (HPG)
Thermo Fisher Scientific Inc. (NYSE: TMO) is the world leader in serving science, with annual revenue over $40 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, increasing efficiency in their laboratories, improving patient health through diagnostics or the development and manufacture of life-changing therapies, we are here to support them. Our distributed team of more than 100,000 colleagues delivers an unrivaled combination of innovative technologies, purchasing convenience and pharmaceutical services through our industry-leading brands, including Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services and Patheon. Please visit www.thermofisher.com.
The Life Sciences Group of Thermo Fisher Scientific currently has a vacancy for a Sr Product Specialist in our TSS Vertical Division in Nordic & Baltics region.
Deliver compelling presentations that highlight our capabilities and value proposition with validated communication and presentation skills.
Collaborate closely with cross-functional teams, including Marketing, Sales, and other business units, to optimize customer value creation.
Ability to identify prospective opportunities in PG and PGx areas. Proven experience in conducting business in local terms and via channel partners. Driving compliance in accordance with company procedures, business needs and all applicable local and international regulations.
Research and identify new market opportunities to drive business expansion and settle competitive positioning.
Ability to work in a matrix and very disperse region: extensive travel, effectively network inside and outside Company’s organization, influencing skills, ability to align regional and business strategies, effectively conflict management
Teamwork with others, look for alliances across businesses, encourage team spirit across organization, deal with complex logistics, adapt and act quickly.
Coordinate key projects and ensure compliance with all applicable local and international regulations.
Qualifications
Masters or equivalent experience in Life Sciences; PhD or equivalent experience preferred.
Solid background in Genetics.
Microarray Business Understanding , workflow and applications.
Minimum 5 years of sales experience in life sciences, with proven success in handling complex deals and projects.
Ability to travel 50%-75% of the time, depending on business need.
Outstanding grasp of success metrics and territory planning.
Cultural awareness and ability to work in a matrix organization.
Join our passionate team, where your contributions will help us succeed and flourish in the marketplace.
Field Application Scientist, Flow Cytometry (Nordics Region)
For Sony Biotechnology Europe
Location: Denmark, Sweden, Norway, Finland (Home Office)
Are you ready to take your scientific expertise to the next level and help craft the future of biotechnology?
Sony Biotechnology is a global leader in cell-based research analytical systems, offering innovative solutions such as flow cytometers, spectral analyzers, software, and reagents. With a strong commitment to innovation and customer satisfaction, we empower researchers worldwide with high-performance tools that advance their scientific discovery.
We’re looking for a passionate Field Application Scientist to join our team in the Nordics region. In this dynamic role, you’ll bridge science and technology, supporting researchers with pre- and post-sales expertise. By combining your technical knowledge and customer-focused attitude, you’ll enable our clients to unlock the full potential of their research.
You Will
Technical Support And Customer Engagement
Schedule and perform pre-sale demonstrations and customer training on assigned instrumentation.
Engage with customers, providing post-installation support and troubleshooting assistance.
Ensure all information is logged via demo forms (pre-demo), demo reports, ServiceMax (post-sale), and Salesforce (pre-sale).
Continuous Improvement:
Master the team’s core technologies and tools.
Give ideas for improving technical workflows and processes.
Account Management
Handle assigned accounts, ensuring high levels of customer satisfaction.
Identify leads for post-instrument sales, upgrades, and accessories.
Collaboration And Teamwork
Work closely with territory sales personnel and other support teams.
Participate in team meetings and training sessions
You will bring
Minimum of 2 years in field support or operating flow cytometers.
Bachelor’s degree in Biological Sciences or related field.
Solid understanding of flow cytometry or related fields.
Problem-solving skills paired with a customer-centric approach.
Outstanding communication and interpersonal abilities.
Self-motivation and a team-oriented attitude.
Willingness to travel frequently (approximately 80%).
Full driving license
What We Offer
A chance to drive innovation and leave a lasting impact in flow cytometry.
The opportunity to represent Sony Biotechnology as a key player in the Nordics research community.
A collaborative, forward-thinking environment where your contributions matter.
Join us at Sony Europe and help shape the future of biotechnology!
Life at Sony
We ensure competitive salaries and benefits by using established benchmarking. We encourage healthy work-life balance supported by hybrid and flexible working policies. We are a positive community who dream big together, respect each other, and enjoy a collaborative culture.
We like to celebrate our colleagues who make a real difference using our recognition platform. We also provide access to numerous services and platforms for all aspects of wellbeing. We listen to our people through conversations and surveys, respect their suggestions, then act on them. We also provide allowances for volunteering days so that our staff can support the causes they are most passionate about.
You can build your career around you with our fantastic range of learning & personal development programs to enhance your skills. We also encourage our staff to try exciting new roles, in a wide range of countries, with a supportive mobility team to support you if you take that leap!
Bring your uniqueness to Sony
We are passionate about creating a culture that promotes equity and cultivates inclusion, diversity, and belonging. We want employees with diverse backgrounds and perspectives that will stimulate innovation and have a direct impact on our creation of social value to fulfil Sony’s purpose – ‘to fill the world with emotion, through the power of creativity and technology’. We want you to bring your unique self to work and help shape our culture.
We are Sony Europe.
Our people collaborate in an environment of respect, integrity, and open-mindedness. Diverse teams from all over Europe are the driving force for our business, and we embrace the differences that make each of us original and unique.
With offices in 28 European countries, Sony Europe caters to consumer, professional, semiconductor and healthcare markets with innovative electronics products and solutions. Our European laboratories research and develop new technologies and capabilities that contributes to the Sony Group and important issues on a planetary scale.
Bring your passion, creativity and ambitions to Sony Europe. Apply now, and let’s create the future together.
Equal Opportunity
Sony Europe is an Equal Opportunity Employer. All qualified applicants will receive equal consideration for employment regardless of race, colour, religion, gender, citizenship, ancestry, age, physical or mental disability, sexual orientation, gender identity, medical condition, or any other protected characteristics.
Disability Accommodation for Applicants to Sony Europe
Sony Europe will provide reasonable accommodation for any qualified individuals with disabilities in the application process. For reasonable accommodation requests, please contact us by email at AccommodationRequest@eu.sony.com or by mail to: Sony Europe B.V, Human Resources Department, The Heights, Brooklands, Surrey, KT13 0XW, UK. When contacting us please indicate the position you are applying for, and the accommodation required.
This is a really exciting opportunity for a Preclinical Imaging Scientist to join a well-established CRO located in Kuopio, Finland. This is a brand-new role to join a team of 5 (Nuclear Imaging Scientist, MRI Imaging Scientist, Electrophysiologist and 2 Data Analysts) as the lab expands their capability in oncology/neuro science.
The ideal candidate will have expertise in multimodal in vivo imaging techniques for rodents (PET, SPECT, MRI, ultrasound, optical), with a focus on nuclear imaging and MRI. Experience with oncology models is preferred. Day-to-day you will report to the Group Leader as part of a multi-disciplinary preclinical research team.
Roles And Responsibilities
Lead and manage client-sponsored preclinical imaging studies as Study Director/Lead Scientist, providing scientific guidance in a global, cross-functional setting.
Develop new services and serve as a scientific authority for both the local site and the broader company business unit.
Collaborate with internal commercial teams to enhance client communication and create scientific marketing content.
Demonstrate a commitment to ongoing learning and career growth in the field.
Qualifications
Doctoral degree (Ph.D.) is advantageous. Master’s degree (M.Sc.) or equivalent degree in biological science, life science, biomedical physics, or related discipline.
Three years of experience with in vivo imaging and studies in small animals in a publicly traded company, in academia, or a in government-funded research agency. Experience from pharmaceutical or biotech industry in a scientific role is advantageous.
Knowledge and practical experience in oncology models is essential. Experience in conducting preclinical drug efficacy studies in is advantageous. Experience in pre-clinical central nervous system disease models is advantageous.
Skills/Competencies
Excellent planning, problem-solving and organizational skills. Ability to work flexibly across projects and adapt to new priorities in a fast-paced environment.
Collaborative team player comfortable working and communicating in a cross-functional and international environment. Track record in people and project management and ability to mentor and train staff will be an asset.
Excellent verbal and written skills in English, scientific writing skills, good presentation skills with ability to professionally communicate with internal and external stakeholders.
Knowledge on humanized oncology models and immune oncology is advantageous.
Right to design procedures and projects involving laboratory animals in Finland through a FELASA-accredited course is advantageous.
Logistics
This is a hybrid role, the candidate will be based in Kuopio, Finland and expected to be on-site 2-3 days a week.
Language requirements: English
VISA and relocation package support are available for this role
At PrecisionPhage, we are on a mission to transform healthcare with bacteriophage-based solutions that address the escalating threat of antibiotic resistance. As a cutting-edge startup at the intersection of biotechnology and data science, we are developing advanced bioinformatics software to analyse key information from genomic data. We are now looking for an experienced Quality Manager to be our first dedicated quality professional, playing a crucial role in setting up and maintaining quality systems for our innovative solutions.
Why join us?
Join a team dedicated to tackling one of the world’s most pressing healthcare challenges – antibiotic resistance. You will be a core part of a growing team and shape the future of our company’s quality management and get to work alongside industry experts and scientists pushing the boundaries of biotech.
Role overview:
As our Quality Manager, you will be involved in building and implementing quality processes from the ground up and ensuring compliance with an initial focus on our bioinformatics software. The ideal candidate will have a strong background in pharmaceutical and medical device regulation, CE certification process, software quality management, relevant standards and certifications (including audits) with understanding of bioinformatics or a related field. This position will give you a unique opportunity to build and lead quality efforts and help us in our mission of combating antibiotic resistance.
The position is partly remote, partly on-site meetings and work in Jyväskylä OR Turku. Therefore, we particularly focus on applications from people residing in Jyväskylä OR Turku regions.
Key responsibilities:
With our executive team, develop, refine, execute & update a comprehensive quality strategy.
With our company executives, design and establish a quality management system (QMS) tailored to required quality requirements.
Help to create, maintain and update quality protocols, testing methodologies, and validation processes for a bioinformatics software analysing genome data.
Develop risk management,SOPs, guidelines, and other quality documentation for software maintenance, development and updates, ensuring traceability and compliance.
Oversee software testing efforts.
Lay the groundwork for future audits and ensure readiness by establishing clear documentation practices and staying current with relevant regulations and certifications.
Qualifications:
Education: A suitable degree. Suitable certifications are a plus.
Experience: Experience in regulatory / quality work in a biotech / life sciences setting and quality management for software products. Basic understanding of bioinformatics a strong plus.
Skills:
Expertise in quality management and testing methodologies.
Expertise in pharmaceutical and medical device regulation.
Expertise in CE certification process.
Knowledge of regulatory requirements and industry standards in bioinformatics and healthcare software (e.g., GxP).
Strong analytical skills with attention to detail.
Excellent documentation skills and a systematic approach to process design and implementation.
Skills in bioinformatics a strong plus.
Up for the challenge? · Please send your CV and motivation letter to careers@precisionphage.com with a title “Quality Manager / [Your name]” ·In the motivation letter, include the timing you would be able to start. ·Send application by March 31, 2025. ·We appreciate every application. Should we proceed with your application, we will get back to you.
Työnimike: Laatujohtaja Sijainti: Hybridi, Suomi, Jyväskylä OR Turku / Etätyö Yritys: PrecisionPhage Oy
Tietoa meistä: PrecisionPhage Oy on omistautunut kehittämään bakteriofageihin perustuvia ratkaisuja, jotka vastaavat antibioottiresistenssin kasvavaan uhkaan. Edustamme bioteknologian ja datatieteen innovatiivista kärkeä ja kehitämme edistynyttä bioinformatiikkaohjelmistoa genomidatan analysointiin. Etsimme nyt kokenutta laatujohtajaa ensimmäiseksi laadunhallinnan ammattilaiseksemme. Tulet olemaan keskeisessä roolissa laatujärjestelmien kehittämisessä ja ylläpidossa innovatiivisten ratkaisujemme laadun takaamiseksi.
Miksi liittyä tiimiimme? Liity tiimiin, joka on omistautunut vastaamaan yhteen maailman kiireellisimmistä terveydenhuollon haasteista – antibioottiresistenssiin. Sinusta tulee kasvavan tiimimme keskeinen jäsen, ja saat muokata yrityksemme laadunhallinnan tulevaisuutta sekä työskennellä alan huippuasiantuntijoiden ja tutkijoiden kanssa, haastaen bioteknologian rajoja.
Tehtävänkuvaus: Laatujohtajana olet mukana rakentamassa ja toteuttamassa laatuprosesseja alusta alkaen, varmistamalla vaatimustenmukaisuuden, aluksi bioinformatiikkaohjelmistomme osalta. Ihanteellisella hakijalla on vahva tausta lääke- ja lääkinnällisten laitteiden regulaatiosta, CE-sertiointiprosessista, ohjelmistojen laadunhallinnassa, liittyvistä standardeista ja sertifikaateista (mukaan lukien auditoinnit) sekä ymmärrystä bioinformatiikasta tai vastaavalta alalta. Tässä roolissa sinusta tulee operatiivisen tiimimme keskeinen asiantuntija ja saat ainutlaatuisen mahdollisuuden rakentaa ja johtaa laadunhallintaa sekä auttaa meitä missiossamme antibioottiresistenssin torjunnassa.
Keskeiset vastuualueet:
Kehitä, hienosäädä, toteuta ja päivitä kattava laatustrategia johtoryhmämme kanssa.
Kehitä ja pystytä johtoryhmän kanssa laatujärjestelmä (QMS), joka täyttää tarvittavat laatuvaatimukset.
Auta kehittämään ja toteuttamaan laatuprotokollia, testausmetodologioita ja validointiprosesseja genomidatan analysointiin tarkoitetulle ohjelmistolle.
Kehitä riskien hallintaa, SOP:ia, ohjeistuksia ja muuta laadunhallintadokumentaatiota ohjelmiston ylläpidolle, kehitykselle ja päivityksille.
Valvo ohjelmiston testausprosesseja.
Varmista auditointivalmius luomalla selkeät dokumentointikäytännöt ja pysymällä ajan tasalla vaadituista ja hyödyllisistä säädöksistä ja sertifioinneista.
Pätevyydet:
Koulutus: Soveltuva korkeakoulututkinto. Sertifikaatit laadunhallinnasta ovat etu.
Kokemus: Kokemusta regulaatiotyöstä / laadunhallinnasta bioteknologia- tai terveysalalta sekä laadunhallinnasta ohjelmistotuotteille. Ymmärrys bioinformatiikasta suuri etu.
Taidot:
Vankka asiantuntemus laadunhallintasta ja testausmenetelmistä.
Tuntemusta lääke- ja lääkinnällisten laitteiden sääntelystä.
Asiantuntemus CE-sertifiointiprosessista.
Tietoa bioinformatiikan ja terveydenhuollon ohjelmistojen säädöksistä ja standardeista (esim. GxP).
Vahvat analyyttiset taidot ja huomiokyky yksityiskohtiin.
Erinomainen dokumentointiosaaminen ja järjestelmällinen lähestymistapa prosessien suunnitteluun ja toteutukseen.
Job Title: Marketing Manager Location: Hybrid: Finland, Jyväskylä OR Turku / Remote Company: PrecisionPhage Oy
About Us: At PrecisionPhage, we are pioneering innovative solutions in the fight against antibiotic-resistant infections through bacteriophage- based solutions. We are a team of experts with academic and entrepreneurial backgrounds, and we are looking for an enthusiastic Marketing Manager to join us as our first dedicated marketing professional.
Why Join Us?
Join a team dedicated to tackling one of the world’s most pressing healthcare challenges – antibiotic resistance. You will be a core part of a growing team and shape the future of our company’s marketing and get to work alongside industry experts and scientists pushing the boundaries of biotech.
Role Overview: As our Marketing Manager, you will be at the forefront of shaping and executing our marketing strategy, brand, and messaging from the ground up. This role is ideal for a hands-on, creative, and data-driven professional who is excited about the challenge of building a brand in a revolutionary deep-tech field. You will have the unique opportunity to build and lead marketing efforts that communicate our mission and position PrecisionPhage as an integral part of the emerging bacteriophage technology ecosystem.
The position is primarily remote, with occasional on-site meetings and work in Jyväskylä OR Turku. Therefore, we particularly focus on applications from people residing in Jyväskylä OR Turku regions.
Salary negotiable.
Key Responsibilities:
Develop, refine, execute & update marketing strategy: With our executive team, you will play an integral part in creating a comprehensive marketing strategy to meet company goals.
Take role in brand development, ensuring clear and compelling messaging that aligns with and promotes company mission and vision.
Develop, execute, and oversee content and brand asset creation and publication across various channels.
With our executive team, create a comprehensive tracking system enabling data-driven marketing efforts. Report key data to company executives.
Plan and execute various digital campaigns.
Take part in company meetings sharing ideas and reporting progress.
Take part in national and international conferences (optional).
Qualifications:
Education: Suitable degree in marketing, communications, or another related field. A background in science or healthcare communications is a bonus.
Experience: Experience in marketing, strategy work, and content creation. Basic understanding of bacteriophages, bioinformatics, biotechnology industry and start-up sectors are strong pluses.
Skills:
Proven expertise in digital marketing.
Excellent English writing skills.
Content and brand asset creation with relevant tools such as Adobe Illustrator /Photoshop, Figma, Canva.
Tasteful and restrained utilisation of various AI tools.
Strong analytical skills with experience using marketing analytics tools.
Ability to work in a fast-paced, dynamic startup environment. Comfortable taking initiative and handling multiple responsibilities.
Basic level of Microsoft Office tools
Up For the Challenge?
Please send your CV, motivation letter, and any relevant portfolio work to careers@precisionphage.comwith a title “Marketing Manager / [Your name]”
In the motivation letter, include the timing you would be able to start.
Send application by January 6, 2025.
We appreciate every application. Should we proceed with your application, we will get back to you.
Työnimike: Markkinointipäällikkö Sijainti: Hybridi: Suomi, Jyväskylä TAI Turku / Etätyö Yritys: PrecisionPhage Oy
Tietoa meistä: PrecisionPhage Oy kehittää innovatiivisia ratkaisuja antibioottiresistenttien infektioiden torjuntaan bakteriofageihin perustuvien ratkaisujen avulla. Tiimimme koostuu asiantuntijoista, joilla on akateemista ja yritystaustaa, ja etsimme nyt innostunutta markkinointipäällikköä ensimmäiseksi markkinoinnin ammattilaiseksi tiimiimme.
Miksi liittyä tiimiimme?
Liity tiimiin, joka on sitoutunut vastaamaan yhteen maailman suurimmista terveydenhuollon haasteista – antibioottiresistenssiin. Sinusta tulee kasvavan tiimimme ydinosa ja pääset muokkaamaan yrityksemme markkinoinnin tulevaisuutta sekä työskentelemään bioteknologian rajoja haastavien asiantuntijoiden ja tutkijoiden kanssa.
Tehtävänkuvaus: Markkinointipäällikkönä olet avainasemassa markkinointistrategiamme, brändimme ja viestintämme suunnittelussa ja toteutuksessa alusta alkaen. Tämä rooli sopii käytännönläheiselle, luovalle ja dataohjautuvalle ammattilaiselle, joka on innostunut rakentamaan brändiä kasvavalla syväteknologian kentällä. Sinulla on ainutlaatuinen mahdollisuus rakentaa ja johtaa markkinointitoimia, jotka välittävät missiotamme ja asemoivat PrecisionPhagen olennaiseksi osaksi kehittyvää bakteriofagiteknologian ekosysteemiä.
Tehtävä on pääasiassa etätyötä, mutta satunnaisia tapaamisia ja työskentelyä paikan päällä Jyväskylässä TAI Turussa. Siksi keskitymme erityisesti hakijoihin, jotka asuvat Jyväskylän TAI Turun alueella.
Palkka neuvoteltavissa.
Keskeiset vastuualueet:
Kehitä, muokkaa, toteuta ja päivitä markkinointistrategiaa: Yhdessä johtoryhmän kanssa luot kattavan markkinointistrategian yrityksen tavoitteiden saavuttamisen edistämiseksi.
Ota vastuuta brändin kehittämisestä varmistaen, että viestintämme on selkeää ja vakuuttavaa ja tukee yrityksen missiota ja visiota.
Kehitä, toteuta ja hallinnoi sisällön ja brändiaineistojen luomista ja julkaisua eri kanavissa.
Luo yhdessä johtoryhmän kanssa kattava seuranta- ja raportointijärjestelmä, joka mahdollistaa dataohjautuvan markkinoinnin. Raportoi keskeiset tulokset yrityksen johdolle.
Suunnittele ja toteuta erilaisia digitaalisia kampanjoita.
Osallistu yrityksen sisäisiin kokouksiin tuoden uusia ideoita ja raportoi edistymisestä.
Osallistu kansallisiin ja kansainvälisiin konferensseihin (ei pakollinen).
Pätevyydet:
Koulutus: Soveltuva tutkinto markkinoinnin, viestinnän tai muun vastaavan alan opinnoista. Tausta tieteen tai terveysalan viestinnässä on etu.
Kokemus: Kokemusta markkinoinnista, strategiatyöstä ja sisällöntuotannosta. Perustiedot bakteriofageista, bioinformatiikasta, bioteknologiateollisuudesta ja startup-sektorista ovat vahvoja plussia.
Are you interested in shaping the future of food by producing new sustainable food ingredients with cutting edge technology and with superb colleagues who are top experts in their field? Onego Bio might be just the place for you.
Onego Bio is a Finnish leading food-biotech company producing animal-free egg protein with precision fermentation. The company’s award-winning technology has placed them at the forefront of the industry, having cracked the code to producing bioidentical egg proteins that provide the same taste, functionality, and nutrition but without the poor efficiency and harmful impacts of animal agriculture. Onego Bio is launching its first product Bioalbumen® as an ingredient for the food industry and transforming the food system to meet the urgent sustainability requirements of the world. The company is focused on scaling precision fermentation to industrial scale with the superior Trichoderma reesei production platform.
Founded by alternative protein pioneer Maija Itkonen (CEO) and precision fermentation trailblazer Christopher Landowski (CTO), Onego Bio is a spin-off that salutes the remarkable work done by VTT Technical Research Centre of Finland for the next level cellular agriculture products and applications. In April 2024 Onego raised a $40M Series A funding round (one of the largest in the Nordics) for fueling scale up and go-to-market in the US. Similarly, in July 2024 Onego secured €14M / $15.2M new funding from the European Innovation Council (EIC) Accelerator Program and additional Series A investors. In 2024 Onego Bio has successfully raised altogether €50.5M / $55M, bringing the company’s total funding to € 65M / $70.8M. Since launching, the company has received massive international recognition, including being selected as a winner of Fast Company’s 2023 World Changing Ideas Awards. Onego Bio is a founding member of Food Fermentation Europe and Precision Fermentation Alliance US. Get to know us better by exploring our webpage www.onego.bio/about-us
We are now looking for an experienced Protein Scientist to join our R&D team in Helsinki, Finland
In this position, you will play an essential role in supporting and leading development projects within R&D and contribute towards our greater goal of providing animal-free egg protein ingredients to the world. We aim to play a significant role in building the sustainable food system with the help of our partners throughout the world. Towards this goal our team utilizes microbial production systems for expressing egg white proteins using filamentous fungi.
Your responsibilities as Protein Scientist:
Conducting scientific projects in the fields of molecular biology and protein production.
Using your expertise in molecular biology and protein engineering to address challenges in egg white protein production.
Developing protein screening technologies and workflows for novel egg white protein production.
Further developing our protein expression platforms with the newest innovations.
Comprehensive and timely documentation of activities in electronic lab notebooks and relevant databases.
Who we are looking for:
Candidate should have a Master’s degree in biotechnology, molecular biology, protein chemistry, or related field.
Proven, excellent laboratory skills and experience in molecular biology and protein science techniques, including DNA cloning and mutagenesis, protein expression, protein purification using chromatography techniques, protein analysis, assay development, and protein functional characterization.
Preference will be given to candidates with experience working in yeast or filamentous fungi.
Industrial experience working in a biotechnology company would be a big plus.
Good scientific reporting skills.
Good written and spoken English skills.
Proven ability to effectively execute and manage scientific activities: both on the bench and beyond.
As a person, we hope that you:
Independently plan your work and execute experiments skillfully and precisely.
Are self-motivated and willing to take the initiative to get things accomplished.
Eagerly want to continuously develop methods and ways of working.
Have effective communication skills.
Work well with other team members and contribute to a good working environment.
Can tolerate pressure and maintain a good work-life balance.
Are flexible to take on a variety of tasks anticipated in a start-up company.
With Onego Bio, you’ll enjoy:
Molecular biology with an impact. Onego Bio works on creating cutting-edge microbial protein production systems. Microbial production technology to produce egg white protein shows potential to significantly mitigate environmental impacts up to 90% according to recent study published in Nature Food. The positive impact of our technology does not only contribute positively on the environment but also supply chain stability, global health, food security and animal welfare. Egg is one of the world’s most popular proteins and our team stands to meet the demand in a way that preserves the future of our planet.
Superb colleagues. We offer working in a passionate environment within a fun and diverse team who want to make an impact in the world. With Onego Bio, you will join a dedicated group of top experts in their respective fields who foster a culture of trust, openness, and sharing ideas.
Competitive salary. We want to attract the best people, so we will provide competitive salaries.
Nordic work–life balance. Working in Finland, the happiest country in the world, enables a high quality of life. At Onego Bio, we make our people’s well-being a priority. We offer 6 weeks paid vacation a year, among other benefits including extended occupational healthcare, and exercise and culture benefits.
Employment type: Full-time, Permanent
Location: Helsinki Finland (on site)
Apply now and join our community of brilliant minds!
Please send your CV, application letter and salary request as a combined file as soon as possible but at the latest by 30th November 2024. 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: Senior Scientist, Dr. Sudeep Karki, email: sudeep.karki@onego.bio
Orion Animal Health is seeking to hire a Regulatory Affairs Officer to join our team of regulatory professionals!
Description of Position
The purpose of this role is to contribute to the management and support of regulatory activities for veterinary medicinal products, ensuring they meet global standards. As a Regulatory Affairs Officer you will have the opportunity to develop expertise in regulatory procedures, particularly for new marketing authorisation applications in the EU and US. You’ll also gain a deeper understanding of regulatory guidelines and processes while collaborating with internal teams, and global partners. Additionally, the position involves ensuring compliance with Good Manufacturing Practices (GMP) and regulatory procedures, playing a key part in supporting the company’s broader regulatory strategy.
As a Regulatory Affairs Officer, you will play a key role in the entire lifecycle of veterinary medicinal products – from the development of new medicinal products to initial global marketing authorisation applications, market launches as well as maintaining current authorisations.
You will collaborate closely with the Orion Animal Health regulatory team located in Finland, Belgium and France, as well as with other organisations and stakeholders internally and externally.
Your main responsibilities as a Regulatory Affairs Officer will include:
preparing administrative documentation for global regulatory submissions (e.g. Clinical Trial Authorisations, Marketing Authorisation Applications, variations) in EU, USA and elsewere
engaging with Competent Health Authorities before and during regulatory proceedings
preparing and updating product information materials (Summary of Product Characteristics, label, package leaflet)
serving as a regulatory affairs expert in cross-functional teams and/or in projects
documenting outcome of regulatory procedures in our IT-systems and request change controls
review and approval of artwork
coordinate regulatory procedures internally, with service providers and global partners
follow GxP practices, regulatory procedures, and processes
You have the opportunity to develop yourself as a regulatory affairs expert and to contribute to global regulatory strategies. This is a permanent position based in Turku, Finland.
Description of Unit
This position is located in the Regulatory Affairs & Pharmaceutical Development team, which belongs to the Animal Health R&D organisation within the Orion Animal Health Business Unit. In this dynamic cross-functional team we have experts from different areas of expertise working across different countries: Finland, France and Belgium.
Orion Corporation’s business division Animal Health (AH) comprises more than 350 employees in 11 countries. We produce and distribute over 300 veterinary medicines and are present in over 100 markets around the world servicing the needs of our customers in both the companion animal and livestock sectors. Our manufacturing and supply chain operations are located in Finland, France and Belgium.
Orion Corporation is a pharmaceutical company listed on the Helsinki, Finland stock exchange. Read more about Orion as an employer from the website https://www.orion.fi/en/careers/orion-as-an-employer/
We Offer
We offer you versatile, interesting and challenging responsibilities in a multi-professional and international environment. You will be part of a great team with skilled and highly motivated colleagues. Appreciation of colleagues and continuous development are part of our core values. You will have the chance to grow your skills, learn new things, and improve your strengths. We offer a supportive working environment and development opportunities.
Requirements
The ideal candidate would have the following qualifications and competencies:
A relevant educational background, such as Bachelor’s or Master’s degree in, e.g. Pharmacy, Life sciences or Languages
Good co-operation and team working skills, but also capability to work independently
Strong attention to detail and precision
Willing to stick to deadlines
A desire to learn and grow
Readiness to take responsibility and willingness to develop processes further
Proactiveness and solution-orientated mindset
Fluent communication and negotiation skills in English. Skills in other languages is an adventage
Good skills in MS Office
Hands-on experience of regulatory affairs or other expert work in the pharmaceutical industry is considered an advantage.
Additional Information
If you think this position is made for you, please send your CV and your application no later than 17th November 2024.
Inquiries can be done by telephone: Kristina Bergström, Senior Regulatory Affairs Manager, tel. +358 50966 7618 on 4th Nov 9:00-11:30, 7th Nov 11:00-12:00 and 14th Nov 12:00-14:30.
We will carry out a security clearance prior to the employment for the selected person.
Orion Corporation operates in more than 30 countries, where we Orionees, 3600 in total, work in all kinds of positions. Among us there are Research Scientists, Laboratory Technicians, Engineers and IT Specialists as well as people working in Production, just to mention some examples. We offer diverse and responsible jobs to our personnel in a truly multi-disciplinary work environment. We encourage people to develop their competences and offer opportunities to affect the job description and creating their own career path at Orion. We are searching for top talents who are ready to share our passion for the work that we do.
