Ajankohtaista

Tuotespesialisti – Triolab Oy, Turku

12.2.2023 | Avoimet työpaikat

https://duunitori.fi/tyopaikat/tyo/triolab-tuotespesialisti-sdsuu-16297558?utm_source=loimu&utm_medium=email

Työpaikkakuvaus

Triolab Oy hakee tuotespesialistia

Pääasiallisena työtehtävänäsi on nesteenkäsittelyautomaatiotuotteiden ja muiden laboratorioratkaisujen myynti- ja tuotetukitehtävissä toimiminen koko Suomen alueella. Asiakkaina ovat mm. sairaalalaboratoriot, tutkimusyksiköt sekä teollisuuden toimijat.

Tehtävä tarjoaa mielenkiintoisia haasteita henkilölle, joka on kiinnostunut luonnontieteellisistä laboratoriomenetelmistä ja moderneista teknologioista. Etsimme uteliasta, rohkeaa ja itsenäistä henkilöä, jolla on intoa kohdata asiakkaita ja mielenkiintoa pohtia sopivia ratkaisuja heidän prosessiensa kehittämiseksi ja tehostamiseksi.

Odotamme työtehtäviin soveltuvaa teknillisen tai luonnontieteellisen alan koulutusta, matkustusvalmiutta sekä erityisesti halukkuutta asiakaslähtöiseen kenttämyyntityöhön. Edellytyksenä on hyvä suomen ja englannin kielen taito, ruotsin kielen taito on plussaa. Ajokortti pitää olla. Eduksi katsotaan kokemus laboratorioautomatiikasta sekä tutkimus- ja teollisuusaloista.

Tarjoamme sinulle paikan reilussa ja iloisessa, töitä tosissaan tekevässä työporukassa sekä kilpailukykyisen palkkauksen ja työsuhde-edut. Tehtävä on toistaiseksi voimassa oleva. Meiltä saat monipuolisen koulutuksen myyntityöhön sekä tarvittavan perehdytyksen tuotteisiin. Asiantuntevat kollegat ovat myös aina tukenasi.

Tuo kokemuksesi ja kiinnostuksesi esille vapaamuotoisella hakemuksella, niin voimme yhdessä miettiä tarkempaa työnkuvaasi. Lähetä hakemuksesi osoitteeseen rekry@triolab.fi. Liitä mukaan myös CV:si ja palkkatoiveesi. Hae paikkaa viimeistään 28.2.2023.

Lisätietoja antaa Triolab Oy:n myyntijohtaja Maria Berlin, p. 040 776 2358 – tavoitettavissa varmimmin ti 14.2. ja ti 21.2. aikaväleillä 8.30-10 ja 16-17.

Triolab Oy on vuonna 1986 perustettu korkealaatuisten diagnostiikka- ja tutkimustuotteiden myyntiin, tuotetukeen ja huoltoon erikoistunut asiantuntijayritys. Meillä työskentelee lähes 50 alan ammattilaista. Triolabin pääkonttori ja varasto sijaitsevat Turussa. Sen lisäksi meillä on aluetoimistot Espoossa ja Tampereella. Yrityksemme kuuluu pörssinoteerattuun AddLife-konserniin.

Hae työpaikkaa

Doctoral and Postdoctoral researcher or Senior Research Fellow, Research Unit of Health Sciences and Technology – Faculty of Medicine University of Oulu

12.2.2023 | Avoimet työpaikat

https://www.linkedin.com/jobs/view/3479519340

About the job

The University of Oulu is one of the biggest and most multidisciplinary universities in Finland. We create new knowledge and innovations that help to solve global challenges. We offer you an international and inspiring working environment where you are given responsibility and can use your skills, develop yourself and do work that matters. Our flexible and family-friendly workplace makes it easy for you to balance work and leisure. The University of Oulu is ranked in the top 3% of the world´s universities.

We are seeking talented scientists for

Doctoral and Postdoctoral researcher or Senior Research Fellow

positions in the research group of Professor Ali Mobasheri in the Research Unit of Health Sciences and Technology, Faculty of Medicine. Positions are available in Academy of Finland funded activities:

  • FIBROBESITY programme – as part of this university wide program we aim to better understand development of osteoarthritis with underlying obesity and metabolic dysfunctions.
  • Academy of Finland, Research project – we are seeking novel therapies for intervertebral disk degeneration with emphasis on the biology of the cartilage end-plate.

The short description of the research group and the Doctoral and Postdoctoral researcher or Senior research fellow positions

Applications are invited for doctoral and postdoctoral researcher or senior research fellow positions in the new research group led by Ali Mobasheri. The new team is funded by the Academy of Finland and the FIBROBESITY programme at the University of Oulu. The successful candidate will work on a project focused on understanding pathogenic mechanisms in osteoarthritis and intervertebral disc degeneration with emphasis on identifying biomarkers and developing next generation biological therapeutics for these diseases.

In the Fibrobesity programme we are especially looking for skills related to 3D cell and tissue cultures and subsequent molecular biology techniques and microscopy. In addition, we will value skills related to metabolomics, RNAseq, proteomics and bioinformatics. In the research project related low back pain we are looking for candidates with experience in translational animal models for intervertebral disk degeneration. In this project skills related biomedical imaging and tissue characterization would be considered beneficial.

We offer you:

  • A highly talented research group supported by an excellent network of collaborators in Finland and abroad.
  • A research environment with excellent technological facilities and a motivating and supporting international community at the Faculty of Medicine and Biocenter Oulu, University of Oulu.
  • University’s wide variety of support services, allowing you to focus on your studies and research.
  • Wellness benefit ePassi covering sport, culture and well-being. Read more about other staff benefits here.
  • Work that matters and a workplace that promotes flexibility and work-life balance. Read more about working with us.

Qualification Requirements

You must possess a Master’s or Doctoral degree in the field of molecular biology, biochemistry, physiology, anatomy, pharmacology, biomedical sciences, pathology, medicine, veterinary medicine, biomedical engineering or a topic related to arthritis or intervertebral disc degeneration research. Also candidates completing their Master’s or Doctoral degree in spring 2023 will be considered.

Doctoral researcher will carry out doctoral studies in the Health and Biosciences Doctoral Programme of the University of Oulu Graduate School (or one of the other UniOGS Doctoral Programmes, if appropriate) and you must meet the minimal requirements to receive doctoral study rights as defined in UniOGS.

For Postdoctoral researcher position you must have completed the doctoral degree no more than 10 years ago (excluding career breaks). For Senior research fellow position, you must have a competence of docent (i.e. comprehensive knowledge of your own field, a capacity for independent research work as demonstrated by publications or some other manner and good teaching skills).

You should have strong laboratory skills in cell culture, molecular biology, biochemistry and the use of immunoassays. Experience of working with mammalian cell and tissue culture, animal models and especially synovial joint tissues and the intervertebral disc, as well as skills in bioinformatics would be considered an advantage.

Alternatively, your skill set should include experimental medicine with animal models, tissue processing, histopathology, and biomedical imaging (ultrasound, MRI or CT). Experience in evaluating tissue composition, structure and function would be considered as surplus.

We are looking for candidates with high motivation and ability work independently, as well as in a group. Fluency in both written and spoken English is a pre-requisite. Potential in acquiring supplementary funding and experience in supervision of Bachelor’s, Master’s or Doctoral thesis or other teaching experience will be considered as merits.

Salary

The salary will be based on levels 2-4 for Doctoral researcher, level 5 for Postdoctoral researcher and level 6-7 for Senior research fellow of the demand level chart for teaching and research staff of Finnish universities. In addition, a salary component based on personal work performance will be paid (maximum of 50 % of the job-specific component).

The salary will be, depending on the qualifications, approximately 2 400 – 3 000 € for a Doctoral researcher, 3500-3800 € for a Postdoctoral researcher and 3800-5100 € for Senior research fellow per month (before taxes). For candidates completing their Master’s/Doctoral degree in spring 2023, the salary will be based on the lower demand level chart until finishing the degree.

The doctoral researcher is a 4-years fixed-term position and post-doctoral researcher/senior research fellow is a 3-years fixed-term position. Positions can start earliest in March and latest by September 2023 and will have a trial period of 6 months.

How to apply?

Apply online latest on Tuesday 28.02.2023 at 23:59 (Finnish local time). Please include the following attachments in your application (all in English):

  • A motivation cover letter (max. 2 pages) summarizing the applicant’s educational background, professional experience and describing why the applicant is interested in this position. A summary of the previous projects should also be included.
  • Curriculum vitae following the guidelines of the Finnish Advisory Board on Research Integrity: http://www.tenk.fi/en/template-researchers-curriculum-vitae
  • A complete list of publications, following the guidelines of the Academy of Finland: https://www.aka.fi/en/research-funding/apply-for-funding/how-to-apply-for-funding/az-index-of-application-guidelines2/list-of-publications/. Please mark the five most important ones.

Contact Information

If you have any further questions, please first contact Project Manager Maija Risteli (maija.risteli@oulu.fi).

Työsopimuksen voimassaolo: määräaikainen työsopimus | Työsuhteen luonne: kokoaikainen | Paikkojen lukumäärä: 1 | Työllisyysaste: 100 % | Paikkakunta: Oulu | Maakunta: Pohjois-Pohjanmaa | Maa: Finland | Ilmoitusnumero: 2023/103 | Yhteys: Maija Risteli 0000-00-00, | Julkaistu: 2023-02-10 | Haku päättyy: 2023-02-28

Doctoral Researcher, Tissue Engineering – University of Eastern Finland

12.2.2023 | Avoimet työpaikat

https://rekry.saima.fi/certiahome/open_job_view.html?did=5600&jc=16&id=000014509&lang=en

Doctoral Researcher, Tissue Engineering

The University of Eastern Finland is inviting applications for a Doctoral Researcher position in Tissue Engineering at the Department of Technical Physics on the Kuopio campus. The position will be filled for a fixed 2-year term from 1 March 2023 (or starting date as agreed). Please find more information below and submit your application no later than 23 February 2023.

Role and salary

We are seeking for a highly motivated and talented Doctoral Researcher to work full-time on an Academy of Finland funded research project entitled ‘A novel infrared spectroscopic and modelling approach for online monitoring and control of cartilage tissue growth in a bioreactor’.

The project will be conducted at the Biomedical Spectroscopy Laboratory (BSL) and Biophysics of Bone and Cartilage (BBC) research groups, Department of Technical Physics, University of Eastern Finland, under the supervision of Academy Research Fellow Isaac Afara and other senior members of the research team. BSL is a highly multidisciplinary team of more than 15 researchers with background in engineering, physics and mathematics, applying biophotonics principles for tissue characterization and diagnostics. The BBC group is a global leader in the biophysics of bone and cartilage, and consists of more than 50 researchers applying experimental, computational and clinical approaches for understanding and development of innovative techniques for diagnosis of joint diseases.

The primary aim of this project is to combine cutting-edge knowledge on infrared spectroscopy with state-of-the-art paradigm in cartilage tissue engineering (functional tissue engineering) for in situ live monitoring and control of cartilage tissue engineering process. This will be achieved via a multi-disciplinary approach that combines tissue engineering, biophotonics, data science and bioprocess control, and nano-spectroscopic imaging through active national and international collaboration. The project involves active collaboration with the Academy of Finland Center of Excellence in Body-On-Chip Research (Professor Minna Kellomäki and Associate Professor Susanna Miettinen). The primary tasks of the PhD student will include, but not limited to, tissue engineering laboratory experiments involving, but not limited to, creation of cell-hydrogel scaffolds and monitoring of tissue growth using near infrared (NIR) spectroscopy during tissue engineering of articular cartilage. The PhD student will also be actively involved in preparation of personal grant applications, and other tasks assigned by the supervisor.

Candidates who are currently completing or have recently completed a Master’s degree or equivalent are invited to apply. However, a person to be appointed as a Doctoral Researcher shall be qualified to pursue postgraduate studies, i.e. she/he is required to have completed a suitable higher university degree or an equivalent education abroad, which in the country in question would qualify the person for similar academic studies.

A person to be appointed as a Doctoral Researcher shall be qualified to pursue postgraduate studies, i.e. he or she is required to have completed or is currently completing a suitable higher university degree or an equivalent education abroad, which in the country in question would qualify the person for similar academic studies (UEF University Regulations, Section 31).

The position will be filled from 1 March 2023 to 28 February 2025 (or starting date as agreed). The position will be filled for a fixed term due to it pertaining to a specific project. A probationary period is applied to all new members of the staff.

The position of Doctoral Researcher shall always be filled for a fixed term (UEF University Regulations, Section 31).

The salary of the position is determined in accordance with the salary system of the Finnish universities. The salary comprises two components: a job requirement component and a personal performance component. In this position, the job requirement level is based on levels 2–4 on the job requirement chart for teaching and research staff. The personal performance salary element is 6–50% of the job-related salary element. Depending on the personal performance component, the salary will be approximately 2,448.00 – 3,210.00 €/month.

Our requirements and expectations

Requirements

  • the person to be appointed in the position shall hold a suitable higher university degree, e.g. Master’s in biochemistry, biomaterials, tissue engineering, or related biological fields. Candidates who are currently completing or have recently completed a higher university degree are invited to apply.
  • potential candidates should have a good command of the English language.

 Expectations

  • background in biomedical/biological sciences, biochemistry, biomedical engineering with strong biological background or related fields.
  • previous experience in laboratory experiments working with biological samples
  • prior experience in preparation of biological assays
  • basic knowledge of tissue engineering
  • basic knowledge in spectroscopy, especially infrared spectroscopy
  • good publication track record
  • strong experience in statistical analysis and
  • Intermediate programming skills, in Python, C, R, MATLAB etc. (the more the better)

Your benefits 

You will have access to the university’s staff benefits, including:

  • extensive occupational health care
  • staff discount on lunch in our campus restaurants, as well as on a range of other services
  • affordable sports services and tax-free bike benefit

Please read more in the Work at UEF section on our website.

You will have an opportunity to work in an interesting and diverse role as part of our international, creative, participatory and inclusive academic community. 

Enjoy your life in Finland! Known for its cleanliness, welfare know-how, modern technology and superb education system, Finland is an exotic and safe country to work in. Please visit the Life in Finland section on our website to learn more. 

How to apply? 

Submit your application by using our electronic application form no later than 23 January 2023 (by 24 hours Finnish time). 

Please note that you must include the following appendices in your application: 

Questions? 

For further information on the position, please contact Academy Research Fellow Isaac Afara, email: isaac.afara@uef.fi, tel. +358 29 4453305. 

For further information on the application procedure, please contact Executive Assistant Satu Turunen, email: satu.turunen@uef.fi, tel. +358 29 445 3031

University of Eastern Finland and the Faculty of Science, Forestry and Technology in brief 

The University of Eastern Finland, UEF, is one of the most multidisciplinary universities in Finland. We have a staff of 3,200 members, and our academic community comprises around 16,000 degree students. Our campuses are located in Joensuu and in Kuopio. Our research is ranked among the best in the world in several fields. We generate research-based knowledge and make it openly accessible for the benefit of all. To learn more about our university please visit our website at  www.uef.fi/en. On our website, you’ll also find information about the university as a work community and as an employer (https://www.uef.fi/en/article/one-university-a-thousand-stories), as well as our employees’ career stories (https://www.uef.fi/en/career-stories).

The Faculty of Science, Forestry and Technology operates on the Kuopio and Joensuu campuses of the University of Eastern Finland. The mission of the faculty is to carry out internationally recognised scientific research and to offer research-education in the fields of natural sciences and forest sciences. The faculty invests in all of the strategic research areas of the university. The faculty’s environments for research and learning are international, modern and multidisciplinary.  The faculty has approximately 4,400 Bachelor’s and Master’s degree students and some 460 postgraduate students. The number of staff amounts to 630. http://www.uef.fi/en/lumet/etusivu

Global New Product Manager, Innovative Medicines – Orion, Finland

8.2.2023 | Avoimet työpaikat

https://duunitori.fi/tyopaikat/tyo/global-new-product-manager-innovative-medicines-sosri-16275179?utm_source=loimu&utm_medium=email

Työpaikkakuvaus

Are you an experienced Marketing Professional looking to be part of a company that is R&D driven and drives growth through science and innovation? If you are passionate about research and new medicines and want to be part of a journey, where the company is building a whole new portfolio of innovative medicines, you could be the right candidate for our open position in the Global Innovative Medicines division. The location of the role is flexible and there is scope for hybrid working.

Description of position

In the role of Global New Product Manager the main areas of focus are as follows:

  • Responsible for global commercial launch readiness and launch preparations
  • Work with the global commercial strategy, planning, and valuation work of pain / epilepsy products in the pipeline.
  • Assessment of market launch sequence and scenario planning.
  • Assessing market potential of new indications.
  • Plan and facilitate launch readiness reviews, risk mitigation activities and best practices with regions / markets
  • Generate and utilize deep customer insights (patient, phycisian, payer) to create differentiated and winning brand, patient and customer engagement strategies
  • Develop the integrated global brand plan and launch plan together with Global Head of Pain BU and global cross-functional team in Innovative Medicines
  • Responsible for leading the brand marketing cross-functional team incl. agencies
  • Leading the integrated brand plan development in the cross-fucntional team Overseeing the completion of all marketing related milestones, including the creation, training, and roll-out of the marketing campaigns
  • Responsible for directing and monitoring all third-party contractors and vendors related to the product
  • Lead with data. Monitor marketing data dynamics as well as potential competitor/category activities and make recommendations to adjust marketing campaigns and strategies accordingly
  • Coordinate and track progress against launch plan with regions and markets; proactively problem-solve as needed. Develop and report on appropriate metrics (KPIs) to track performance, develop OKRs focusing on outcomes, and provide feedback to brand teams to ensure delivery of integrated marketing plans
  • Work in an agile way and collaborate with all stakeholders (medical affairs, market access, regulatory, marketing, PAG, supply chain, analytics & market research)
  • Act according to Orion values

Description of unit

The Global Innovative Medicines Division is a new division created to strategically lead the business, discovery and development of new medicines at Orion. In Innovative Medicines Business Division, the unmet needs of the patients’ meet innovation that brings the best, new treatments to promote health and well-being in society. One of the core areas we focus on is Pain & Epilepsy and as we work on developing new assets, we are growing and need new colleagues to join the Global team.

We offer

This position offers you a unique opportunity to join the Global Innovative Medicine team contributing to development and launch of novel treatments in pain and epilepsy. You will be part of an agile cross-functional team and drive patient driven agenda with internal and external stakeholders globally.

We offer an exciting working environment and an opportunity to build the future of Orion. We are striving for excellence in everything we do. We succeed, learn together, and appreciate each other. You’ll be empowered to deliver value. Check Orion for additional information.

Requirements

  • BSc/BA/Masters degree
  • 5+ years in Brand Management / Customer Engagement in global Pharma Rx, New Product experience is advantage
  • Experienced marketeer with extensive local / regional marketing background
  • Knowledge & experience of liaising with local subsidiaries
  • Ability to demonstrate marketing and commercial launch excellence in a variety of areas
  • Deep Omnichannel, Digital and CX knowledge and skillset
  • Data driven mindset, knows how to communicate effectively through data
  • Experience in Dx and Agile methodologies
  • Self-driven individual with a ”can do” mindset
  • Excellent communication and cross-functional collaboration skills
  • Highly proficient in virtual engagements across various platforms.
  • Fluency in English

Additional information

Is this the position you have been waiting for? Please submit your application and CV at the latest on Monday 27 th February 2023.

If you have any questions related to the position, please contact Director Pain Business Unit Camilla Steinby by phone +358 50 966 7823 on Thursday 9 th February between 12.30-14.00

#LI-ORION

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, 3300 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.

Senior Medical Writer (CSR’s & Protocols) – IQVIA Espoo, Uusimaa, Finland On-site

8.2.2023 | Avoimet työpaikat

https://www.linkedin.com/jobs/view/3345693745

About the job

Why IQVIA? Making a positive impact on human health takes insight, curiosity, and intellectual courage. It takes brave minds, pushing the boundaries to transform healthcare. In your role, you will have the opportunity to play an important part in helping our clients drive healthcare forward and, ultimately, improve outcomes for patients.

Role Overview:

  • Acting as Lead Medical Writer on most types of writing projects. Preparing assigned documents in accordance with company Standard Operating Procedures (SOPs) and customer requirements as well as to the agreed timelines. Performs Senior Review of straightforward medical writing deliverables. Negotiates timelines and discusses/resolves customer comments.
  • You will provide written and verbal feedback to junior staff, and to customers when appropriate.
  • You will Keep abreast of current medical and/or technical writing/regulatory knowledge, including Good Clinical Practice (GCP), along with developments and advances in drug development/medical and/or technical writing.

Responsibilities

  • Taking a leading role in preparing assigned documents, including, but not limited to, confirming the scope of the task, confirming templates and specifications, negotiating, and adhering to timelines, organizing document reviews, communicating directly with the customer.
  • Planning and organising workload for assigned projects and tasks: identify project needs, track timelines, and implement customer requests.
  • Leading meetings on more challenging topics independently.
  • You may present on standard Medical Writing processes at full-service bid defence meetings.
  • Assist in the training and development of junior staff, either formally as an assigned mentor or ad hoc for local colleagues or others. May develop and deliver training to the global team on a topic he/she has specific expertise in. May input into and deliver presentations on Medical Writing to other IQVIA groups.
  • May act as Project Manager for a more complex but single Medical Writing project which includes Project Finance/Invoicing responsibilities.
  • Complete project finance activities, including monitoring and forecasting budgeted hours.
  • Propose, review and approve budgets and costings for routine projects, including estimation of hours needed for Medical Writing tasks.
  • May take on a small customer lead role or assist an established partnership lead in their role.
  • May represent region or site on a Medical Writing initiative or cross-functional initiative.
  • Facilitates and brainstorms the identification of new ideas. May represent Medical Writing at a general capabilities audit.

Do you meet the minimum education and expeirnece requirements below?

  • You have Regulatory Medical Writing expeirnece, typically this would be demonstrated by 3 – 5 years + Writing Clinical Study reports and Protocols. (Required)
  • You have a BSc in a life sciences or related discipline / related field (Required)
  • If you have a MSc or PhD this would be advantages but is not essential.
  • You can effectively review a statistical analysis plan and to identify deficiencies, errors, and inconsistencies in statistical output
  • You can integrate, interpret, and summarize data from a variety of sources in a clear and concise manner.
  • You have an in-depth knowledge of drug development, medical writing, and associated regulations. Good understanding of statistical principles and of medical terminology across a range of therapeutic areas.
  • You have the right to live and work in the UK, EEA, or EU without needed sponsorship.

Skills And Abilities

  • Excellent written and oral communication skills including grammatical/technical writing skills in English.
  • Excellent attention to detail and accuracy.
  • Confident and effective communication and negotiation skills with customers and project managers.
  • Able to deliver difficult messages in constructive manner.
  • Demonstrates initiative and sound judgement when faced with less familiar project/document situations or challenges.
  • Demonstrated abilities in collaboration with others and independent thought.
  • Demonstrates confidence and maturity in most routine medical writing situations.
  • Demonstrates good judgement in requesting input from senior staff.
  • Ability to establish and maintain effective working relationships with co-workers, managers and customers.
  • Ability to effectively manage multiple tasks and projects.
  • Ability to proactively evaluate risks and potential issues and seek solutions and discuss appropriately with colleagues and customers.

IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. Learn more at https://jobs.iqvia.com

IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. Learn more at https://jobs.iqvia.com

Medical Writer 1 – IQVIA Espoo, Uusimaa, Finland On-site

8.2.2023 | Avoimet työpaikat

https://www.linkedin.com/jobs/view/3469423243

About the job

Job Overview

Join our team as a skilled Regulatory Medical Writer I and play a critical role in producing straightforward projects with precision and efficiency. As a valued member of our team, you will create documents that adhere to IQVIA’s Standard Operating Procedures, customer requirements, and project timelines. You will have the opportunity to negotiate timelines and address customer comments with the support of senior team members.

Stay at the forefront of the industry by continuously updating your medical and technical writing knowledge, including GCP, and being aware of the latest developments in drug development and medical writing. With this role, you’ll have the chance to make a meaningful impact and grow your expertise in the field.

Essential Functions

  • Take a leading role in preparing assigned documents, including, but not limited to, confirming the scope of the task, confirming templates and specifications, negotiating and adhering to timelines, organizing document reviews, communicating directly with the customer.
  • Manage day-to-day workload: identify project needs, track timelines and implement customer requests, keeping manager/senior staff abreast of progress on tasks and any potential problems with project work.
  • Attend project team meetings with or without other writers. Participate in/lead comments resolution or similar meetings with external customers.
  • May give simple presentation to an existing customer (e.g. on processes at a Kick-off meeting).
  • Complete project finance activities, including monitoring and forecasting budgeted hours.
  • Awareness of budgets and project finance principles, moving towards review and understanding of budgets relating to assigned projects, including out of scope activities.

Qualifications

  • Bachelor’s Degree Bachelor’s Degree in life sciences related discipline or related field Req
  • Typically requires 1-2 years of prior relevant experience as a Regulatory Medicla writer and related competency levels. Req
  • Familiarity with the structural and content requirements of clinical study reports, protocols, and similar documents.

Req

  • Good understanding of common statistical methods used in clinical trials and/or interpretation of their results.

Req

  • Ability to effectively review a statistical analysis plan and to identify deficiencies, errors, and inconsistencies in statistical output Pref
  • Ability to integrate, interpret, and summarize data from a variety of sources in a clear and concise manner. Req
  • In depth knowledge of drug development, medical writing, and associated regulations. Good understanding of statistical principles and of medical terminology across a range of therapeutic areas. Req
  • Excellent written and oral communication skills including grammatical/technical writing skills.
  • Excellent attention to detail and accuracy.
  • Communicates clearly, effectively and confidently with others.
  • Demonstrated abilities in collaboration with others and independent thought.
  • Demonstrates confidence and maturity in most routine medical writing situations.
  • Demonstrates good judgement in requesting input from senior staff.
  • Ability to establish and maintain effective working relationships with coworkers, managers and customers.
  • Ability to effectively manage multiple tasks and projects.
  • Must be computer literate.

IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. Learn more at https://jobs.iqvia.com

Harjoittelija Integriinien liikennöinti syövässä –projektiin – Turun yliopisto, Turku

8.2.2023 | Avoimet työpaikat

https://duunitori.fi/tyopaikat/tyo/harjoittelija-integriinien-liikennointi-syovassa-projektiin-stsur-16277988?utm_source=loimu&utm_medium=email

Työpaikkakuvaus

Meillä on avoinna harjoittelupaikka 1-3 kuukaudeksi kesän ajalle. Tarjoamme motivoituneelle henkilölle mahdollisuuden kehittää ja hyödyntää osaamistaan kiinnostavassa projektissa tieteellisen tutkimuksen parissa. Tehtävässä pääset oppimaan miten syöpäsolut koordinoivat solunsisäistä liikennöintiä ja aktiinitukirankaa solumigraatiossa.

Harjoittelu on tarkoitettu henkilölle, joka ei aiemmin ole ollut harjoittelussa taikka muuten töissä laitoksella. Harjoittelupaikka soveltuu Biolääketieteen, Biokemian ja Solubiologian opiskelijoille.

Työtehtäviin kuuluu

– Perustekniikat kuten Western blot

– Soluviljely

– Mikroskopianäytteiden valmistus ja kuvantaminen

Työssä tarvittavat taidot

– Työssä vaaditaan hyvät laboratoriotyöskentelyn ja Office-ohjelmien (Word, Excel, PowerPoint) perustaidot

– Eduksi katsotaan kokemus seuraavista menetelmistä ja tekniikoista: Soluviljely, mikroskopia

– Muuta: olethan tarkka, huolellinen ja yhteistyökykyinen

Palkkaus on 1331EUR/kk. Harjoittelussa on yhden kuukauden koeaika, ja harjoittelun kesto on 1-3kk, Toukokuu-Syyskuu 2023 välisenä aikana.

Hakemus

Jätäthän hakemuksesi mahdollisimman pian – viimeistään 15.2.2023 Turun yliopiston sähköisellä hakulomakkeella.

Liitä mukaan motivaatiokirje, opintorekisteriote ja ansioluettelosi. Linkki sähköiseen hakemukseen löytyy osoitteesta: https://www.utu.fi/fi/yliopisto/tule-meille-toihin/avoimet-tehtavat .

Lisätietoja tehtävästä antaa niklas.z.jantti(at)utu.fi ja rekrytointiprosessiin liittyvissä kysymyksissä auttaa biocityhrservices(at)utu.fi.

Harjoittelija – Fimea

8.2.2023 | Avoimet työpaikat

https://www.valtiolle.fi/fi-FI/ilmoitus?id=33-123-2023

Perustiedot
Tehtävän kesto
Määräaikainen

Alkamisaika
1.3.2023
tai sopimuksen mukaan

Tehtävä päättyy
31.8.2023

Määräaikaisuuden syy
Harjoittelu

Työaikamuoto
Virastotyöaika

Työpaikkojen lukumäärä
1

Viran sijoittaminen
Virka on viraston yhteinen.

Lisätietoja tehtävästä
Tiina Karonen
Ylilääkäri, jaostopäällikkö
+358 29 522 3346 (mieluiten/helst klo 8-9)

Sijainti
Lääkealan turvallisuus- ja kehittämiskeskus Fimea/ Helsinki
Mannerheimintie 166
00300
Helsinki

Viran/tehtävän kuvaus
Haemme harjoittelijaa Turvallisuus ja vaikuttavuus vastuualueen Haittavaikutusilmoitusjaostoon. Haittavaikutusilmoitusjaoston vastuisiin kuuluvat mm. haittavaikutusilmoitusten käsittely ja arviointi sekä kansallinen signaalidetektio.

Harjoittelijan pääasiallisiin tehtäviin kuuluu haittavaikutusilmoitusten tulostaminen ja esilajittelu, ilmoitusten esisyöttö haittavaikutustietokantaan, sekä ilmoitusten arkistointi. Harjoittelu suoritetaan paikan päällä Helsingin toimipisteessä.

Jaostossa toimintaa kehitetään lean -menetelmin ja uutta haittavaikutusilmoitustietokantaa luodaan ketterän kehittämisen (agile) menetelmin, joita pääset seuraamaan läheltä.
Hakijalta odotamme
• soveltuva korkeakoulututkinto-opiskelija esimerkiksi farmasian tai luonnontieteiden alalta
• valmius itsenäiseen työskentelyyn ja omatoimiseen tiedonhakuun
• tarkka ja huolellinen työskentelyote
• hyvä yhteistyökyky ja vuorovaikutustaidot

Palkkaukseen liittyvät tiedot
1912,65 €

Muut tehtävään liittyvät tiedot
Fimea tarjoaa työntekijöilleen joustavat työajat ja mahdollisuuden etätyöskentelyyn, tuetun lounasruokailun, kattavat työterveyshuollon palvelut, liikunta- ja hyvinvointiedun sekä mahdollisuuksia oman osaamisen kehittämiseen.

Doctoral candidate – DC9, HUMAN doctoral network, Harmonising and Unifying Blood Metabolomic Analysis Networks, Afekta & University of Eastern Finland

8.2.2023 | Avoimet työpaikat

Harmonising and Unifying Blood Metabolomic Analysis Networks

Hosting Institute: Afekta in collaboration with University of Eastern Finland

Gross salary: 4,663 euros (+Family allowance if applicable)

Project description:

The PhD project will focus on assessing the impact of lifestyle intervention on blood microsampling metabolite composition when compared to conventional plasma samples. The aim is to find robust biomarker candidates that would readily reflect the metabolic effect of the intervention and the responsiveness of the individual to the lifestyle intervention. The student will work on optimizing the analytics based on the inter-laboratory comparison of the various blood microsampling home-collection devices. The samples to be collected from the lifestyle intervention will be assessed with the chosen collection method and optimized liquid chromatography mass spectrometry conditions. The impact of the lifestyle will be assessed by the non-targeted metabolite profiling approach, as well as compound-centric investigation of target metabolites that have been linked with dietary and exercise response and reflecting also the composition and function of gut microbiota.

We offer an exciting position and a chance to do research in an intersection between industry and academia. Afekta Technologies Ltd. is a science driven company established in 2017. Afekta offers metabolomics analysis services for various research purposes across life sciences. We have specialized in metabolomics analyses related to food, nutrition, and gut microbiota. Afekta has experience in being a beneficiary in several Horizon 2020 projects including a previous Marie-Sklodowska-Curie Doctoral Network action (MSCA-ITN-ETN-action BestTreat). To learn more about Afekta please visit www.afekta.com.

Academic studies related to the position will be done in the University of Eastern Finland (UEF), which will also award the PhD. UEF is a multidisciplinary university with a strong focus on life sciences. UEF has around 16,000 students and 3,000 staff members. Office and laboratory spaces of Afekta Technologies are right next to the UEF campus in Kuopio. Finland, and Kuopio in particular, is a safe, clean and technology-driven place known for its superb education and welfare know-how. To learn more about UEF and the life in Finland visit https://www.uef.fi/en/life-in-finland.

For further information on the position, please contact CEO Dr. Olli Kärkkäinen (olli@afekta.com, +358 44 2432 322).

Key Requirements:

Applicants should have a strong scientific background in the research field of Chemistry, Biochemistry, Biomedicine, Pharmacy, Toxicology, Pharmacology, or a similar field.

The prospective ideal student needs to have hands-on experience in applying liquid chromatography mass spectrometry -based methods for analysis of compounds in biological samples. Experience in mass spectrometry data analysis and in method optimization and/or data analysis are key requirements as well. Interest towards precise laboratory work and experience in metabolomics data analysis are desirable and will be favourably viewed.

The project will involve international and intersectorial secondments/visits to other project partners in the network for the doctoral candidates to learn new skills and foster collaborations.

Product Manager, Life Sciences – UPM, The Biofore Company

8.2.2023 | Avoimet työpaikat

https://www.linkedin.com/jobs/view/3436245060

About the job

Are you looking to join a dynamic, innovation-driven, international company, building a better future for us all? UPM leads the forest based bioindustry into a sustainable, innovation-driven, and exciting future. The competence, integrity and drive of our people make us unique. We live by our values – trust and be trusted, achieve together, renew with courage.

We are now looking for a Product Manager, Life Sciences to join our Biomedicals team. The job is based in Helsinki, Finland and/or in Switzerland.

Greetings From Your Future Manager

“We are looking for a team player with great communication skills to join our agile start-up like team within a large corporation. You are able to capture sharp customer insights, translate them into business and product strategy and take actions to solve our customer’s challenges.” – Tony Kiuru, Senior Manager, Business Development

What You’ll Do

  • Collect feedback from our customers to generate insights
  • Discuss with KOLs to seek product improvements
  • Support development of the customer experience journey in co-operation with the sales and marketing team
  • Develop and implement the strategic plan for GrowDex, GrowDase and GrowInk product groups globally
  • Create and maintain the business cases for strategically important products/product groups and key customers
  • Gather requirements from prospects, evaluators, and customers, and use those inputs to lead product development plans. Conduct quantitative and qualitative analysis on variety of sources to understand business trends and support business initiatives.
  • Provide expert advice and support on assigned products to sales and marketing and operations
  • Translate deep understanding of customer workflows and customer needs into sharp customer insights. Use these insights to shape product development pipelines
  • Liaise with sales and marketing to design product launches, sales campaigns and sales collateral for the product that are effective and appropriate for the target audience
  • The job requires 25-40% of travel time. Besides customer visits and conference participations, you will also be visiting the manufacturing site and participating in UPM Biomedicals strategy meetings.

Who You Are

  • You have a minimum of 3 years of relevant experience from life science section as a product manager or similar, and you have an understanding of the relationships between manufacturing and sales
  • You have previously supported product development or product sales in the life science sector, preferably with a focus in cell-based assays. You have experience developing deep understanding of customer workflows and customer needs into sharp customer insights.
  • You have a university degree
  • You have excellent organizational and project management skills. You are a good listener with ability to influence across teams and stakeholders, internally and externally.
  • Cell laboratory skills are considered as an asset
  • You are fluent in written and spoken English. Finnish and German language skills are considered a plus.

This Is What We Offer For You

  • Meaningful job: Our work impacts the quality of healthcare in future. We highlight the expertise of our personnel, the high quality of our products and the company values.
  • Inspired and motivated teams: We have highly skilled workforce. We are a multifaceted, international organization that works as a team to achieve our vision.
  • Development opportunities: With us you can build up your expertise. We provide opportunities to support your development throughout every stage of your career.
  • Responsibility for people and environment: Our ethical principles embrace people as well as the environment. We are always striving to build a more sustainable future.

Additional Information

For more information, please contact Senior Manager, Business Development Tony Kiuru at +358407085100 during the following time slots: 23rd of January 9.00-10.00 or 30th of January 9.00-10.00. All times in Finnish time zone (EET).Please send your application via the link latest by February 12th, 2023.For support with submitting your application, please contact HR Service Center at careers@upm.com or tel. +358204146600.A security background check may be performed for those selected to UPM positions, in accordance with the company recruitment guidelines and the Security Clearance Act 726/2014.UPM is a non-smoking workplace in Finland

UPM Biomedicals is advancing the healthcare with innovative products combining the know-how in natural materials with research results in regenerative medicine. We are the first company to manufacture plant nanocellulose in ISO 13485 quality and are protected with more than 400 patents. Currently, we have five product families – GrowDex® for 3D cell culture, GrowInk™ for bioprinting, GrowDase™ for gentle release of cells, FibDex® advanced wound dressing and OEM nanocellulose for custom formulations in life science and clinical fields.

UPM Biomedicals is part of UPM-Kymmene Oyj, a company with more than 100 years of history, 10 billion euros turnover and 17,000 employees in 46 countries.