Ajankohtaista

Välinehuoltaja

Hae täällä!

Haemme välinehuoltajaa toimitilapalveluihimme Joensuun kampukselle, Itä-Suomen yliopistoon. Tehtävä täytetään 1.3.2023 alkaen tai sopimuksen mukaan. Lue lisää alta, ja hae viimeistään 31.1.2023.

Tehtävä ja palkkaus 

Välinehuoltajan tehtävässä vastaat itsenäisesti luonnontieteiden, metsätieteiden ja tekniikan tiedekunnan tutkimus- ja opetuslaboratorioiden välineiden ja laitteiden pesusta, desinfioinnista ja käyttövalmiudesta. Välinehuollon toiminnot on keskitetty kolmeen eri rakennukseen, joiden välinehuoltopisteisissä tehtävät hoidetaan.

Välinehuoltajan tehtäviin kuuluu: 

• välineistön kerääminen, puhdistaminen, desinfiointi, tarkastaminen, kokoaminen, pakkaaminen ja sterilointi sekä toimittaminen takaisin yksiköihin
• välinehuollossa käytettävien koneiden ja laitteiden puhdistaminen
• työmenetelmien jatkuvaan kehittämiseen ja suunnitteluun osallistuminen

Työpisteen vaihtuminen päivittäin vaatii hyvää organisointikykyä ja työn suunnittelua yksiköiden yhteyshenkilöiden kanssa. Välinehuoltaja vastaa hyvästä ja toimivasta välinehuollosta sekä laadukkaasta asiakaspalvelusta. Työ on fyysistä yksivuorotyötä.

Tehtävä täytetään 1.3.2023 tai sopimuksen mukaan alkaen toistaiseksi. Uuden työntekijän tullessa tehtävään käytetään koeaikaa.  

Tehtävän palkkaus määräytyy yliopistojen palkkausjärjestelmän (muu henkilöstö) mukaisesti. Palkka koostuu tehtäväkohtaisesta palkanosasta ja henkilökohtaiseen suoriutumiseen perustuvasta palkanosasta. Tässä tehtävässä tehtäväkohtainen palkanosa on vaativuustasoluokittelussa tasolla 4. Lisäksi maksetaan henkilökohtaiseen suoriutumiseen perustuvaa palkanosaa, joka on 6 – 50 % tehtäväkohtaisesta palkanosasta. Tehtävään valittavan kokemuksesta ja osaamisesta riippuen palkka työsuhteen alkaessa on noin 2250 – 2350 €/kk. 

Mitä odotamme sinulta

• soveltuvaa toisen asteen ammattitutkintoa tai vastaava tai riittävää tehtävään soveltuvaa työkokemusta
• tietoteknisiä perusvalmiuksia ja riittävää suomenkielen taitoa
• oma-aloitteisuutta ja organisointikykyä
• erinomaista asiakaspalveluasennetta, sekä vuorovaikutus- ja yhteistyötaitoja

Luemme eduksi

• halun kehittyä tehtävässä ja ratkaisukeskeisen asenteen
• itsenäisen ja ennakoivan työskentelytavan ja tiimityötaidot

Tarjoamme sinulle 

• mielenkiintoisen työtehtävän osana kansainvälistä, luovaa, osallistuvaa ja osallistavaa yliopistoyhteisöä 
• nykyaikaiset työvälineet ja työympäristön
• Itä-Suomen yliopiston henkilöstöedut, joihin kuuluvat muun muassa kattava työterveyshuolto, laaja henkilöstökoulutustarjonta, mahdollisuus työsuhdepolkupyörään ja Sykettä-liikuntapalvelut.

Hae näin 

Hakemus tulee jättää viimeistään 31.1.2023 sähköisellä hakulomakkeella:

Liitä sähköiseen hakemukseen: 

• ansioluettelo 
• kopio tutkintotodistuksesta
• muut mahdolliset asiakirjat, joilla haluat osoittaa ansiosi tehtävään

Kysymyksiä? 

Lisätietoja tehtävästä antavat väline- ja laitehuollon lähiesimies Anne Pennanen, puh. 029 445 8265, anne.pennanen@uef.fi  ja toimitilajohtaja Tarja Harjula, puh. 029 445 8068, tarja.harjula@uef.fi

Sales Manager, Life Sciences UK – UPM Biomedicals

https://upm.wd3.myworkdayjobs.com/en-US/Careers/details/Sales-Manager–Life-Sciences-UK_NB6017327?q=upm+biomedicals

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 Sales Manager, Life Sciences UK to join our Biomedicals team in the United Kingdom.

Greetings from your future colleagues

“We are looking for an agile person to join our life science business to direct sales in UK and Ireland alongside our existing and future partners. In UPM Biomedicals, you can experience the start-up environment backed by a solid corporation.” – Dr Johana Kuncova-Kallio, Director, Biomedicals

“You are a team-oriented person with great communication skills and a genuine interest and curiosity for the customer’s needs.” – Tony Kiuru, Senior Manager, Business Development

What you’ll do

• Contribute to the turnover of the UPM Biomedicals with focus to 3D cell culture
• Collect feedback from our customers to generate insights
• Identify, contact and discuss with KOLs
• Develop competitive landscape and market analysis
• Work along our distribution partners and support them in sales activities
• Planning of sales activities for life science field in UK and Ireland
• Support business development in 3D cell culture (GrowDex®), and later also in regenerative medicine
• Support development of the customer experience journey in co-operation with the sales and marketing team

Who you are

• You have a university degree or equivalent lab experience
• You have minimum of 5 years of relevant sales experience (life science instruments or consumables for e.g. HTS, HCS, cell assays) and understanding of relationships between distributor and principal
• You have previously built a network in high content or high throughput screening or related fields
• You have great organizational skills especially when preparing customer visits
• You are diligent in reporting sales activities and have experience with CRM (e.g. SalesForce)
• You have great problem-solving skills
• You are positive thinking, solution oriented, multitasking and motivated team-oriented person
• Cell laboratory skills are considered a benefit
• You are fluent in written and spoken English

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

The job requires 50% of travel time. Besides customer visits and conference participations, once or twice per year, there is a meeting in Finland, where you get to contribute to the development of strategy together with other Biomedicals team members.

The job is home-office based, optionally desk in a life science hub is possible to arrange. Preferable location in the research triangle of London – Oxford – Cambridge.

The recruitment will be done in cooperation with our recruitment partner George James Ltd.

For more information, please contact Tony Kiuru, Senior Manager, Business Development, tony.kiuru@upm.com, or tel +358407085100 on

• December 13th 2022 from 9-11 a.m. EET
• January 10th 2023 from 9-11 a.m. EET

Please send your application via the link latest by January 15th, 2023. We will start going through the applications already during application period so please submit your application as soon as possible.

For support with submitting your application, please contact the HR Service Center at careers@upm.com or tel. +4401723502550.

UPM Biomedicals is the forerunner in producing high quality nanofibrillar cellulose for medical and life science applications. More than 300 patents protect the existing and future products that rely on the Finnish birch pulp. We actively collaborate with universities, research centres and key industrial partners on innovations and products in the field of high throughput drug screening, personalized medicine, advanced cell therapies, 3D bioprinting, tissue engineering and wound care. www.upmbiomedicals.com

#LI-POST

Postdoctoral Researcher in Super-Resolution Microscopy and Microbiology – Helsinki University

https://www.linkedin.com/jobs/view/3413442183

About the job

The University of Helsinki is one of the world s leading universities for multidisciplinary research. HiLIFE Helsinki Institute of Life Science is a research institute that supports high quality life science research across the University campuses and faculties. The research activities at the Institute of Biotechnology consist of several research teams focusing on a specific area of molecular biology, cell biology or biotechnology. For more information, please visit https://www.helsinki.fi/en/hilife-institute-of-biotechnology.TEMPADAPT (Single-molecule visualization of temperature adaptation in sub-cellular dynamics and organization across bacteria) is a 5-year ERC-funded project in the laboratory of Jarno M kel at the Institute of Biotechnology, from 2023 onwards. The project will aim at understanding temperature adaptation at the single molecule level in live bacteria. We will study bacteria thriving at 0 C (psychrophiles), moderate temperatures (mesophiles), and high temperatures up to 100 C (thermophiles). In addition to state-of-the-art super-resolution microscopy, the project will apply single-cell perturbations, machine learning and modelling to analyze, integrate, and make sense of single-cell and molecule level data.

The HiLIFE – Institute of Biotechnology, M kel laboratory of Temperature Adaptation in Bacteria, invites applications for

Postdoctoral Researcher in Super-Resolution Microscopy and Microbiology

starting from May 2023, or as agreed, for a 3-year fixed-term employment contract with the possibility of continuation.

Position Description

We are looking for enthusiastic and motivated postdoctoral researchers, who are interested in applying (and possibly developing) super-resolution microscopy and single-particle tracking, to join our research group for an ERC-funded project. The project involves planning and executing experimental work including state-of-the-art microscopy, genetic engineering, RNA-sequencing, data analysis, machine learning, and modelling to unravel how bacteria adapt to different temperatures. Our team will work on multiple topics at the interface of physics, chemistry, and biology: intracellular spatial organization, macromolecular crowding, liquid-liquid phase separation, heat- and cold shock protein dynamics, and gene regulation. The postdoctoral researcher will have a key role in contributing ideas, analyzing and interpreting the findings, and writing up the research, in collaboration with the broader project group.

Selection criteria

A successful candidate will have a PhD or equivalent, a strong background in biophysics, microbiology, computational biology, or other relevant fields, and has demonstrated a keen interest in quantitative approaches. Previous experience in wet lab work, genetic engineering, microbiology work, advanced microscopy, Python/R/Matlab coding, bioinformatics, or data analysis is considered an advantage. Excellent communication and writing skills in English and ability to work both independently and collaboratively as part of a multidisciplinary international team are expected. The candidate should have previous research published in peer-reviewed scientific journals, and outstanding organization and time management skills.

Salary And Benefits

The starting salary of the postdoctoral researcher will be 3400-3900 euros/month, depending on the appointees qualifications and experience. A trial period of 6 months will be applied. The University of Helsinki offers comprehensive services to its employees, including occupational health care, supported access to high quality sports facilities, and opportunities for professional development.

How To Apply

Please submit your application as a single pdf file, which includes the following documents in English:

• A motivation letter, clearly stating your research interests and why you consider yourself a good candidate for the position (max 1 page)
• CV (max 2 pages)
• List of publications (max 2 pages)

Include also contact information of two persons who are willing to provide a reference letter by a separate request. Please submit your application, together with the required attachment, through the University of Helsinki electronic recruitment system by clicking on the Apply for job button. Internal applicants (i.e., current employees of the University of Helsinki) submit their applications through the SAP Fiori portal.

The deadline for the applications is 3rd of January, but the position will be filled once a suitable candidate has been identified.

For more information, please contact the Principal Investigator Jarno M kel (jarno.p.makela(at)helsinki.fi) or visit our lab website .

Why work with us?

Finland is a member of the EU, has high quality free schooling (also in English), generous family benefits and healthcare, and was recently ranked as the best country in the world for expat families and in the world s top ten most livable cities. Finland and the Helsinki region possess top expertise in sciences in terms of a vibrant talent pool, leading research, strong support services and functioning collaboration networks. For more information about working at the University of Helsinki and living in Finland, please see helsinki.fi/en/university/working-at-the-university

Helsinki Institute of Life Science

Helsinki Institute of Life Science (HiLIFE) is a new institute established in 2017 that supports high quality life science research across the University campuses and faculties. HiLIFE builds on existing strengths and new recruits and partnerships to create an attractive international environment for researchers to solve grand challenges in health, food, and environment. HiLIFE coordinates research infrastructures in life sciences and provides research-based interdisciplinary training.

University of Helsinki

The University of Helsinki (UH), founded in 1640, is a vibrant scientific community of 40,000 students and researchers. It is one of the leading multidisciplinary research universities and ranks among the top 100 international universities in the world. It is currently investing heavily in life sciences research. UH offers comprehensive services to its employees, including occupational health care and health insurance, sports facilities, and opportunities for professional development.

Mikrobiologi – NextPharma Oy, Tampere

https://www.linkedin.com/jobs/view/3418194537

About the job

Haemme osaavaan ja aikaansaavaan mikrobiologiseen tiimiimme Tampereen tehtaalle ylempää toimihenkilöä toistaiseksi voimassa olevaan työsuhteeseen.

Mitkä ovat tähän toimeen kuuluvat tehtävät?

• vastata lääkevalmisteiden, raaka-aineiden ja vesinäytteiden mikrobiologisesta testauksesta
• vastata poikkeamien selvittämisestä sekä raporttien ja riskiarviointien laatimisesta
• valvoa ja johtaa laboratoriotyötä paikan päällä
• osallistua puhdastilojen mikrobiologiseen olosuhdevalvontaan
• osallistua menetelmänsiirto- ja kehitysprojekteihin, olla vastuussa mikrobiologisten menetelmien kehittämisestä ja validoinnista
• osallistua asiakas- ja viranomaistarkastuksiin

Mitä odotamme hakijalta?

• ylempi korkeakoulututkinto, mikrobiologia tai vastaava
• hyvää suomen ja englannin kielen osaamista
• hyviä vuorovaikutustaitoja, organisointikykyä ja asiakaslähtöisyyttä
• kykyä itsenäiseen työskentelyyn ja päätöksentekoon
• joustavuutta ja positiivista asennetta

Lisäksi arvostamme:

• kokemusta lääketeollisuudesta ja GMP:n tuntemusta tai kokemusta laboratoriotyöstä SFS-EN ISO/IEC 17025 mukaisesti
• kokemusta esihenkilötehtävistä

Kiinnostuitko?

Say yes to what’s next: Lisätietoja antaa Head of QC Päivi Waris paivi.waris@nextpharma.com / +358 40 838 9070. Lähetä hakemuksesi nettisivujemme https://careers.nextpharma.com/ kautta viimeistään 13.1.2023. Ilmoitathan hakemuksessasi palkkatoiveesi sekä ajankohdan, jolloin voisit aloittaa työt. Niittyhaankatu 20, Tampere.

Olemme yksi johtavista lääketeollisuuden, biotekniikan ja terveydenhuollon sopimusvalmistajista Euroopassa, ja meillä on noin 2000 työntekijää Saksassa, Ranskassa ja Suomessa. Meille seuraava askel on aina se tärkein. Nopea tempomme vie meitä eteenpäin, tuo työympäristöömme elämää ja kannustaa kasvuun. Avaimemme menestykseen on innostus ja haluamme tarjota erinomaista palvelua asiakkaillemme ympäri maailman. Tervetuloa NextPharmaan.

Tehtaamme Suomessa sijaitsee Tampereella ja on erikoistunut aseptiseen silmälääkkeiden tuotantoon, josta meillä on pitkä kokemus. Tampereen tehtaalla valmistamme ja pakkaamme nestemäisiä silmälääkkeitä BFS (Blow Fill Seal), MD (Multi dose) three piece (korkki, tiputin, pullo) ja PFMD (preservative free multi dose) tuotteina. Tuotantomme tuotteet ovat globaaleja ja ne ovat markkinoilla useissa maissa.

Postdoctoral Researcher / Project Researcher / Doctoral researcher, Translational Immunology – University of Eastern Finland

https://rekry.saima.fi/certiahome/open_job_view.html?did=5600&jc=16&id=000014296&lang=en

The University of Eastern Finland is inviting applications for a Postdoctoral Researcher/Project Researcher/ Doctoral Researcher (Translational Immunology) position in Kuopio. The position will be filled for 1 March 2023 to 31 August 2024 (or as agreed). Please find more information below and submit your application no later than 16 January 2023. 

Role and salary 

As our new Postdoctoral, Project or Doctoral Researcher in Translational Immunology, you will be working in the School of Medicine in the Faculty of Health Sciences, Kuopio Campus.

Our research focuses on the immunological disturbances in autoimmune diseases, with a special emphasis on CD4+ T cells. We utilize a state-of-the-art single-cell methodology to study clinical samples from children with type 1 diabetes and juvenile idiopathic arthritis. More details on the research group and research interests can be found at https://uefconnect.uef.fi/en/group/translational-immunology-group/.

The successful candidate will work on a project funded by the Academy of Finland aiming to analyse CD4+ T cell phenotypic alterations related to autoimmunity in type 1 diabetes. The candidate may also participate in projects studying immune responses in patients with juvenile idiopathic arthritis and in patients undergoing immune checkpoint inhibitor therapy for cancers.

A person to be appointed to the Postdoctoral Researcher or Project Researcher position is required to hold a suitable doctoral degree. If you have been awarded your doctoral degree less than five years ago, the post will be one of a Postdoctoral Researcher. If the doctoral degree has been awarded more than five years ago, the post will be one of a Project Researcher. In this context, five years is the net period of time, which does not include maternity leave, parental leave, military service, etc. The position of postdoctoral researcher and project researcher shall always be filled for a fixed term (UEF University Regulations, Section 31). 

A person appointed to the Doctoral Researcher position shall be qualified to pursue postgraduate studies, i.e., they are required to have completed a suitable higher university degree or an equivalent education abroad that would qualify the person for similar academic studies. The positions of doctoral researcher shall always be filled for a fixed term (UEF University Regulations, Section 31).

The position will be filled for 1.3.2023-31.8.2024 (or 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 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. For a Postdoctoral Researcher/Project Researcher, the job requirement component is 3,044,00 euros/month, based on level 5 of the job
requirement chart for teaching and research staff. For a Doctoral Researcher, the job requirement component is 2,108,40 -2,628,85 euros/month, based on levels 2-4 of the job requirement chart for teaching and research staff. The personal performance component can be a minimum of 6 % and a maximum of 50 % of the above-mentioned sum. At the beginning the salary will be between 3,348-3,866 € (as post-doctoral/project researcher) or 2,319-3,339 € (as doctoral researcher).

Our requirements and expectations 

• A PhD in immunology or a related discipline (Postdoctoral/Project Researcher) or an MSc in biosciences or a related discipline (Doctoral Researcher)
• Good knowledge of written and spoken English
• Able to work independently and supervise students
• Be willing to contribute to writing peer-reviewed publications and applications for research funding

Previous experience in some of the following techniques is considered highly advantageous:

• High-parameter flow cytometry with experience in panel design and analysis
• Magnetic and flow-cytometric cell sorting
• T-cell culture
• Single-cell omics
• Biostatistics/bioinformatics (e.g. FlowJo, Graphpad Prism, SPSS, SeqGeq, R)

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.

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

You will have an opportunity to work in an interesting 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 16 January 2023 (by 24.00 hours Finnish time).

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

– CV (http://www.tenk.fi/en/template-researchers-curriculum-vitae)
– list of publications (https://www.aka.fi/en/research-funding/apply-for-funding/how-to-apply-for-funding/az-index-of-application-guidelines2/list-of-publications/)
– copies of your academic degree certificates / diplomas, and copies of certificates / diplomas relating to your language proficiency, if not indicated in the academic degree certificates/diplomas
– motivation letter
– recommendation letter(s) (if available) 

Questions?

For further information on the position, please contact: Professor Tuure Kinnunen, +358 29 4454980, tuure.kinnunen@uef.fi.

For further information on the application procedure, please contact HR-secretary Sanna Partanen, +358 29 4454634, sanna.partanen@uef.fi.

University of Eastern Finland and the Faculty of Health Sciences 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 Health Sciences operates at the Kuopio Campus of the University of Eastern Finland. The Faculty is research-intensive, and its internationally recognised research activities are closely linked to the strategic research areas of the University. There are approximately 3 090 degree students and about 580 PhD students in the Faculty. The faculty has 800 staff members. http://www.uef.fi/en/ttdk/etusivu

Manager, Quality – UPM, The Biofore Company, Helsinki

https://www.linkedin.com/jobs/view/3391738490

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 Quality Manager to join our Biomedicals team in Helsinki or Lappeenranta, Finland.

Greetings from your future colleagues

“We are looking for a diligent professional with a solid experience in ISO 13485 to maintain our QMS and also to help leading the implementation of FDA and GMP compliance.” – Johana Kuncová-Kallio, Director, Biomedicals

“UPM proprietary nanocellulose technologies open a wide range of business opportunities in the biomedical field. Together with our professional and enthusiastic team, you will play a key role in securing the product quality and regulatory compliance and also have a possibility to participate in new business development.” – Kari Luukko, Director, QA Biomedicals

What You’ll Do

• You share the vision for our products and for your part are responsible for its high-quality execution, the strategy implementation, and the roadmap development
• You maintain and develop our ISO 13485 quality management system (QMS) in accordance with applicable regulations
• You manage and develop QMS processes such as annual planning, non-conformities (NC) treatment, CAPA, change control and supplier management
• You manage the process of legislation and standards monitoring
• You maintain and develop UPM Biomedicals’ QMS database
• You support and steer the team members in daily quality operations such as quality control, document management, NC and CAPA processes, design and development
• You plan and co-ordinate management reviews, personnel trainings, as well as internal and external audits
• You are the main contact for our notified body
• You will be responsible for regulatory compliance on general level and support our teams in product-specific compliances. You will also participate in risk management processes of our products
• You manage the regulatory strategy process of our products’ global market expansions and collaborate with our business developers and product managers

Who You Are

• You have a university science degree and minimum if 5 years in a managerial role within quality management systems and regulatory affairs with focus to medical devices, ideally biomaterials rather than diagnostics or software
• You have a deep understanding and working knowledge of ISO 13485, QC, GMP, MDR and FDA practices and document management. Your documentation practices are exact and persistent
• You have proven business acumen and working knowledge of the industry and supplier base
• You have excellent communication and problem solving skills
• You are positive thinking, solution oriented, multitasking, persistent and proactive team player
• You are fluent in written and spoken English. Finnish is seen as a benefit
• Seen as a benefit:
  • You have previous experience of medical device or in vitro medical device product development for the Clinical market
  • You have previous experience in management of clinical trials
  • You know medical device registration processes in different territories

This Is What We Offer For You

• Meaningful job: We are proud of what we do. Our work highlights the expertise of our personnel, the high quality of our products and the company’s values.
• Inspired and motivated teams: We have highly skilled workforce. We are a multifaceted, international organisation that works as a team to achieve our shared objectives.
• 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

At the beginning (first 2 years), the job requires intensive presence in Finland (Lappeenranta or Helsinki) to adapt Biomedicals operations, later the location is negotiable in UPM sites in Europe.The recruitment will be done in cooperation with our recruitment partner George James Ltd.For more information, please contact Kari Luukko, Director, QA Biomedicals on +358400259866 at the following times:

• December 15th 2022 9-11 a.m. EET
• January 5th 2023 from 9-11 a.m. EET
• January 12th 2023 from 9-11 a.m. EET

Please send your application via link latest by 15.01.2023. We will start going through the applications already during application period so please submit your application as soon as possible.For support with submitting your application, please contact the 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 the forerunner in producing high quality nanofibrillar cellulose for medical and life science applications. More than 300 patents protect the existing and future products that rely on the Finnish birch pulp. We actively collaborate with universities, research centres and key industrial partners on innovations and products in the field of high throughput drug screening, personalized medicine, advanced cell therapies, 3D bioprinting, tissue engineering and wound care. www.upmbiomedicals.com

Field Application Specialist, Forensics (m/f/d), Russian Speaker – Thermo Fisher Scientific Finland

https://www.linkedin.com/jobs/view/3401232509

About the job

When you’re part of Thermo Fisher Scientific, you’ll do challenging work, and join a team that values performance, quality and innovation. As part of a successful, growing global organization you will be encouraged to perform at your best. With revenues of more than $40 billion and the largest investment in R&D in the industry, we give our people the resources and chances to create significant contributions to the world.

Location/Division Specific Information

Location: – Remote / Field within EuropeDivision: Genetic Sciences Division – Human Identification (HID)

Discover Impactful Work:

Join us as a Field Applications Specialist (FAS) and assist us in our mission to become the world leader in serving science. This multifaceted position involves providing scientific training, guidance, application support and troubleshooting for our customers in Russian-speaking countries.

A day in the Life:

• Deliver on-site and remote scientific application support & training support to our customers on our HID products.
• Supporting our customers with the implementation of new products, applications or workflows.
• Diagnose & resolve product performance problems and customer queries/complaints by phone, email or onsite.
• Work with sales representatives on sales calls to customer laboratories to provide technical and applications assistance in response to customer inquiries.
• Assist the regional sales team in the development of accounts by giving technical seminars and presentations that promote the use of our products.
• Providing pre-sales support activities like product demonstrations, user meetings or seminars.
• Visit and represent our company on scientific or commercial meetings, conferences, trade shows, congresses, etc.
• Establish contacts to key opinion leaders in the field and develop local references.
• Maintain up-to-date technical expertise and in-depth knowledge of our product portfolio and scientific developments in the forensic DNA-identification workflow.
• Become a strong internal Voice of Customer by providing customer feedback on our products to local and European Sales & Marketing.
• Build trust with our customers and excel in customer service.

Keys to Success:

Education

• Degree in Biology, Biotechnology, Biomedical Sciences, Genetics, Molecular Biology, Biochemistry or similar (Masters or PhD preferred)

Experience

• Extensive technical hands-on experience (+5 years) in a forensics lab environment such as data analysis and/or research & development.
• Previous experience in a support / training-related position or hands-on experience with Thermo Fisher Scientific HID technology is appreciated.

Knowledge, Skills, Abilities

• High degree of technical competence & confidence.
• Able to connect with and support people optimally with varying levels of technical knowledge and expertise.
• Customer-centricity with the emotional intelligence to understand customer concerns and aware of markets, trends and competitors.
• Good computer (especially MS Office) and/or IT skills and have an interest for groundbreaking innovation and technology.
• Excellent communication & presentation skills.
• Fluent Russian and English language skills – oral and written.
• Willingness to travel internationally (mainly Russian-speaking countries / CIS with the exception of Russia and Belarus; and within Europe).
• Valid driver’s license.

We are offering an employment with an innovative, growing organisation with outstanding career and development prospects and an exciting company culture which stands for integrity, intensity and innovation. The role comes with a competitive salary plan, company pension scheme, bonus plan, company car and further employee benefits.

Interested? Please apply in English language.

Our Mission is to enable our customers to make the world healthier, cleaner and safer. Watch as our colleagues explain 5 reasons to work with us. As one team of 100,000+ colleagues, we share a common set of values – Integrity, Intensity, Innovation and Involvement – working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need. #StartYourStory at Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued.Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.

APEX Clinical Research Associate – Parexel, Helsinki

https://www.linkedin.com/jobs/view/3331544730

About the job

Additional Job Description

Join the APEX CRA Program!

Are you a recent graduate and do you have less than 6 months clinical experience? Did you study in the life sciences/data sciences/data analytics/clinical/nursing area?

The Accelerated Program of Education, Exposure, and Experience for CRAs (APEX CRA) provides foundational clinical research training – including project and system experience – to new CRA hires who are recent college graduates and have less than a year of monitoring experience.

Through this program, you’ll transform into a credible and experienced CRA I. As you progress, APEX CRAs perform billable project tasks to support the CRAs and Clinical Operations Leads (COLs) with a focus in three developmental areas: Project Support, Initiation CRA support, and Site Facing support. You’ll be required to complete the ACRP Entry Level Knowledge Assessment and are enrolled in a 1-year membership to the ACRP.

You’ll also work closely with CRAs to gain exposure to and experience with the CRA role and its responsibilities across a period of three to six months. During this experience, you’ll have the opportunity to practically apply in-class concepts with day-to-day application by working with clinical systems including Clinical Trial Management Systems (CTMS), Electronic Data Capture, Safety Information Systems, and TMF platforms, and benefit from both instructor-led trainings and ongoing coaching and support of Line Managers and COLs.

Finally, APEX CRAs accompany CRAs for observational and co-monitoring support on-site or during remote visits which combines learning for the APEX CRAs and workload aid for their CRA colleagues. Upon completion of the program, you’re well-positioned to independently function within the CRA role and to immediately begin successful monitoring!

Minimum Bachelor’s degree in life sciences/data sciences/pharmacy/nursing or other related discipline

• 1 year or less of monitoring/clinical experience
• Complete Finnish language proficiency
• Strong interpersonal, written, and verbal communication skills within a matrixed team
• Experience working in a self-driven capacity, with a sense of urgency and limited oversight
• A client-focused approach to work and flexible attitude with respect to assignments/new learning
• The ability to manage multiple tasks, evaluate unpredictable scenarios and achieve project timelines while applying your understanding of study protocol(s)An honest and ethical work approach to promote the development of life changing treatments for patients
• Strong computer skills and aptitude to learn quickly

Medical Monitor – Aurealis Therapeutics, Kuopio

https://www.linkedin.com/jobs/view/3397551502

About the job

Aurealis Therapeutics is a Swiss-Finnish private biopharmaceutical company focusing on the development of a 4-in-1 synthetic biology, cell and gene therapy platform to address unmet medical needs in three therapy areas: chronic wounds, oncology, and inflammation.

We at Aurealis Therapeutics are looking for aMedical Monitor for a permanent-term contract in Kuopio or potentially other location in Finland, the Netherlands, Germany, or Switzerland. The start date of the job is negotiable, but we wish you could start during the first quarter of 2023. You will be working full-time.

We are looking for a team player for the medical monitoring and drug safety management of the company. As a Medical Monitor, you are responsible for medical and safety aspects of clinical development, advising and consulting on safety event evaluation, providing physician-level opinions on multiple trials and sites, consulting on protocol design, patient safety concerns, deciding if a specific adverse event requires un-blinding, mediating between sponsor, CRO and trial sites, reviewing whether concomitant medications and adverse events are coded and reported properly, examining the protocols of a clinical study, planning and initiating a trial, dealing with the data (analysis, interpretation, exploration). You are also responsible for pharmacovigilance/drug safety (Drug Safety Officer).

Your previous work experience and knowledge defines your position and responsibilities, so you have the opportunity to affect your role. Successful candidate for this role must be able to communicate efficiently in English.

We hope that you have at least +2 years of experience in similar roles and in depth, hands-on experience and understanding of clinical trial execution and follow-up. You have a degree in Medicine (MD). Working experience in chronic wound indications is an advantage, but not a must. You would be reporting to our Chief Medical Officer, and working closely with the clinical and regulatory teams and with external service providers (CROs). You are collaborative, highly organized and enjoy working with different systems. If so, you might be our new colleague!

Experience and skills required:

• Overall knowledge and experience of the drug development process, clinical trial conduct, data management, drug safety, and biostatistics
• Deep knowledge of relevant regulations e.g., ICH/GCP/GVP, EMA, and FDA guidelines
• Excellent organizational, decision making and project management skills
• Experience in working with software programs (EDC, eTMF, etc.)

We will offer you a position in an international and dynamic working environment where you have the opportunity to develop your career path. Join our team!

If you are interested in the position, please fill-in the application at https://aurealistherapeutics.com/medical-monitor/. We will be interviewing during the application time.

If you have any questions regarding the position, please contact Maija Rusi, our Financial and Administrative Director, by email at maija@aurealistherapeutics.com

Analytical Scientist – Biovian Oy, Turku

https://duunitori.fi/tyopaikat/tyo/analytical-scientist-stse-16084415?utm_source=loimu&utm_medium=email

Työpaikkakuvaus

Biovian on vahvasti kasvava turkulainen bioteknologiayritys. Tarjoamme sopimusvalmistusta, -analysointia ja prosessikehitystä biotekniikkayrityksille, jotka kehittävät innovatiivisia geeniterapioita tai biofarmaseuttisia tuotteita. Saatamme asiakasprojekteja laboratoriosta kliiniseen potilaskäyttöön asti taidolla, innolla ja sydämellä – tämä on meillä Manufacturing Happiness.

Haemme Analytical Scientistiä HPLC-tiimiimme

Yhtiön kasvaessa haemme vahvistusta laadunvalvontalaboratoriomme. Analytical scientist tehtävässä päävastuusi on HPLC analyysien suunnittelu, validointi, tarkastaminen, tulosten raportointi ja työn ohjaus. Lisäksi osallistut analyysimenetelmien kehittämiseen, laboratorion yleistoimintoihin ja toimit asiantuntijana asiakaspalavereissa. Analysoitavat tuotteet ovat pääasiassa proteiineja, joten aikaisempi työskentely vastaavien tuotteiden parissa on eduksi.

Päätehtäväsi on

– Toimia HPLC-analytiikan asiantuntijana ja kehittää työtä.
– Projekteihin liittyvä raportointi, dokumentointi ja työohjeiden kirjoitus.
– Vastata työn aikatauluttamisesta ja tarkastaa analyysien tulokset.
– Opastaa HPLC-analyysien tekijöitä.
– Toimia GMP-ohjeistuksen mukaisesti.
– Osallistua asiakaspalavereihin asiantuntijana.

Työssä onnistuaksesi

Odotamme sinulta laajaa työkokemusta HPLC-analytiikasta. Sinulla on soveltuva ylemmän korkeakoulun tutkinto (esim. biolääketieteestä tai biokemiasta) sekä käytännön kokemusta analytiikasta. Olet tottunut dokumentoimaan ja kirjoittamaan raportteja englanniksi.

Toivomme, että sinulla on vahvaa osaamista jollakin alla mainitusta osa-alueesta sekä asiantuntemusta useimmista niistä:

– GMP
– Proteiinianalytiikka
– Lääketeollisuus
– Laboratoriotyöskentely
– Tietotekniset taidot / LIMS

Olet työskentelytyyliltäsi tarkka, järjestelmällinen, reipas ja toimelias henkilö. Sinulla on myös hyvät vuorovaikutus- ja ryhmätyötaidot. Toivomme sinulta myös joustavaa työotetta sekä kykyä työskennellä itsenäisessä tehtävässä.

Työohjeet ja dokumentointi tehdään englanniksi, joten toivomme sinulta hyvän suomen kielen taidon lisäksi 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 monipuolisten tehtävien kautta.
– Saat viihtyisän työpaikan, jossa työntekijöitä arvostetaan, sekä hyvät henkilöstöedut – tarjoamme työntekijöillemme esimerkiksi laajan työterveyshuollon, terveysvakuutuksen sekä hyvinvointi- ja liikuntaedun.

Työtehtävä on kokoaikainen ja vakituinen. Työtä tehdään Turussa Kupittaalla, jossa toimipisteemme sijaitsee. Jatkossa sinun on mahdollista työskennellä myös etänä, toivomme kuitenkin, että olet paikan päällä noin neljä päivää viikosta.

Kiinnostuitko?

Lähetä hakemuksesi (suomeksi tai englanniksi) palkkatoiveineen viimeistään maanantaina 16.1.2023.

Lisätietoja tehtävästä antaa QC Manager Anne Rokka, 050 576 3192 9.1.2022 klo 12-13 ja 12.1. klo 9-10.

Käymme hakemuksia läpi hakuaikana ja haastatteluja voidaan aloittaa jo ennen hakuajan umpeutumista.

Tule mukaan työskentelemään kanssamme tulevaisuuden biologisten lääkkeiden parissa ja muuttamaan ideoita tuotteiksi!

WWW-osoite https://biovian.com/
Yhteystiedot Riikka Laine, riikka.laine@biovian.com
Työpaikan osoite Tykistökatu 6 A, 20520 TURKU
Työ alkaa Sopimuksen mukaan
Työaika kokoaikatyö
Työn kesto yli 12 kuukautta
Haku päättyy 16.01.2023 klo 23:59
Ilmoitus jätetty 29.12.2022
Ilmoitusnumero 11766715