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.
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
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
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.
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.
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.
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.
Laittakaa kalenteriin päivämäärä 31.3.2023 ylös, sillä jälleen kerran saamme järjestää yhdessä Suomen Sidekudostutkijoiden kanssa yhteisen seminaarin. Biomedicum täyttyy mitä mielenkiintoisimmista puhujista ja ilta huipentuu yhteiselle illalliselle. Halukkaille on mahdollisuus päästä pitämään oma lyhyt esityksensä, joten muistathan lähettää abstraktisi viimeistään tiistaihin 28.2. mennessä. Rekisteröidy tapahtumaan 17.3. mennessä! Helsingissä nähdään!
Once again we are proud to inform that the 2nd joint meeting together with Finnish Matrix Biology Society will be held on Friday 31.3.2023 in Biomedicum, Helsinki. There will be great speakers and interesting talks, and finally a dinner that ends the whole seminar day. For short talks, remember to submit your abstract by 28.2. Remember to register for the seminar by 17th March! See you in Helsinki!
Puissan Biotech, with operations in China and Finland, is a rapidly growing high-tech company, who develops and provides in silico methods for life science industry. Our goal is to reduce the cost and time of R&D by reducing experimental work and animal testing with advanced computing aided methods such as simulation and data analytics.
We are now looking for Business Development Manager based in Helsinki.
This position is mainly responsible for growing revenue by developing new clients for Puissan
Establishing new customer projects and relationships at companies in hospital, pharmaceutical, personal care and drug delivery industries etc.
Proactively call on prospective clients to develop understanding of their needs and identify new business opportunities.
Strengthen the brand name of Puissan and drive our leadership in the marketplace by effective marketing and PR activities.
Develop and implement sales forecasts, strategy and plans designed to achieve new business goals.
Maintain a new business pipeline for Puissan’s products and services.
Close new business transactions by effectively negotiating pricing and contract terms and conditions.
THE REQUIREMENTS:
At least 3 years working experience in pharmaceutical, biomedical or personal care industry or CRO preclinical R&D, preferably hands-on experience in In silico methods (PBPK, QSAR).
At least Master’s degree in pharmacology/biomedicine/biochemistry/medical/bio IT.
Fluency in English, and excellent written communication and presentation skills.
Strong interpersonal and communication skills with a confident and articulate style.
Positive attitude, initiative and enthusiasm.
Strong work ethic and ability to work with a high degree of autonomy.
Biovian on vahvasti kasvava turkulainen bioteknologiayritys. Tarjoamme sopimusvalmistusta, -analysointia ja prosessikehitystä biotekniikkayrityksille, jotka kehittävät innovatiivisia geeniterapia tai biofarmaseuttisia tuotteita. Saatamme asiakasprojekteja laboratoriosta kliiniseen potilaskäyttöön asti taidolla, innolla ja sydämellä.
Scientist tai Senior scientist
Yhtiön kasvaessa haemme henkilöä tuotanto- ja laboratoriotehtäviin. Tehtävässäsi tulet keskittymään lääkeaineiden puhdistusprosesseihin, jossa työtehtäväsi on proteiinien ja geeniterapiatuotteiden puhdistuksen suunnittelu ja toteuttaminen. Puhdistusprosessit toteutetaan pääasiassa kromatografia ja suodatus (TFF) -menetelmillä.
Tehtävissä työ muodostuu yksilöllisesti osaamisalueittesi ja kokemuksesi mukaan.
Päätehtäväsi on:
Toimia asiantuntijana lääkeaineiden puhdistusprosesseissa.
Osallistua lääkeainetuotannon työhön, eli proteiinien ja geeniterapiatuotteiden puhdistukseen, ja sen suunnitteluun. Työ tehdään kehityslaboratoriossa ja/tai puhdastiloissa.
Työhön ja projekteihin liittyvä raportointi ja dokumentointi.
Työssä onnistuaksesi
Odotamme sinulta tehtävään soveltuvaa akateemista loppututkintoa (esim. biokemisti tai vastaava) tai pitkän linjan kokemusta vastaavasta työstä. Odotamme käytännön kokemusta laboratorio- ja/tai puhdastilaympäristöstä.
Toivomme sinulta kokemusta lääketeollisuudesta ja lisäksi vahvaa osaamista jollakin alla mainitusta osa-alueesta sekä asiantuntemusta useimmista niistä:
Aseptinen työskentely
Puhdastilatyöskentely
Laboratoriotyöskentely
Rekombinanttiproteiininen tai virusvektorivalmisteiden puhdistaminen ja käytännön kokemus kromatografialaitteistoista
Kokemus GMP:stä
Olet työskentelytyyliltäsi tarkka, järjestelmällinen, reipas ja toimelias henkilö. Sinulla on myös hyvät vuorovaikutus- ja ryhmätyötaidot.
Sinulla on hyvä suomen kielen taito. Työohjeet ja dokumentointi tehdään englanniksi, joten toivomme sinulta myös hyvää englannin kielen taitoa.
Mitä sinä saat meiltä?
Tarjoamme sinulle merkityksellisiä ja vastuullisia työtehtäviä lääkkeiden ja biologisten prosessien parissa.
Pääset osaksi huipputiimiämme, joka koostuu monialaisista asiantuntijoista. Saat hyvän perehdytyksen tehtävään ja mahdollisuuden ammatilliseen kehittymiseen.
Työtehtävä on kokoaikainen ja vakituinen. Työtä tehdään Turussa Kupittaalla, jossa toimipisteemme sijaitsee.
Saat viihtyisän työpaikan, sekä hyvät henkilöstöedut – tarjoamme työntekijöillemme esimerkiksi laajan työterveyshuollon, terveysvakuutuksen sekä hyvinvointi- ja liikuntaedun.
Lisätietoja tehtävistä saat tuotantojohtaja Johanna Silvolalta (puh nro 040 350 8585). Parhaiten tavoitat Johannan 30.1.2023 klo 15:30-16:30.
Kiinnostuitko?
Lähetä hakemuksesi (suomeksi tai englanniksi) palkkatoiveineen viimeistään keskiviikkoon 8.2. mennessä.
Tule mukaan työskentelemään kanssamme tulevaisuuden biologisten lääkkeiden parissa ja muuttamaan ideoita tuotteiksi!
