Ajankohtaista

Manager, Clinical Product Development

1.7.2021 | Avoimet työpaikat

https://www.linkedin.com/jobs/view/2626227355/?refId=D5l5nyXFQWeyuxabnKAGgg%3D%3D

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 Manager, Clinical Product Development to join our Biomedicals team in Helsinki, Finland.

Greetings from your future team leader

We are looking for an experienced, dynamic, open minded individual with a “can-do” attitude. You will be responsible for the wound care products, but also support the developments in regenerative medicine. Since this is a new area for UPM, you will be part of the exciting development phase!” – Johana Kuncová-Kallio, Director, UPM Biomedicals

What You’ll Do

  • You will play a key role in the development of the regulatory route for our existing and upcoming products
  • You act as a product manager for FibDex® advanced wound dressing, and will be responsible for product documentation maintenance and post market surveillance
  • Together with the team, you will be responsible for product development including but not limited to new indications of FibDex® advanced wound dressing and other products for wound healing
  • You will also support new product development for regenerative medicine and pharmaceutical products
  • You will be responsible for regulatory documentation and related quality management processes and reporting

Who You Are

  • You have a university science degree, understanding of wound healing or regenerative medicine mechanisms and a minimum 5 years of relevant work experience, ideally in industry
  • A background in biomaterials is seen beneficial
  • You have a deep understanding and working knowledge of ISO 13485, QC, GMP, MDR practices, document management and associated country registration requirements
  • You have previous experience of medical device product development for the clinical market (strong preference on experience with regulating materials and devices over software) and experience in management of clinical trials
  • Experience from internal auditing, especially medical devices audits, is also an advantage
  • You have proven business acumen and working knowledge of the industry and supplier base
  • You have excellent communication and problem-solving skills and are able to work independently
  • You are a positively thinking, solution oriented, multitasking and proactive team player
  • You are fluent in written and spoken English

This Is What We Offer For You

  • Meaningful job: We are proud of what we do. Saving patients’ lives, developing a new area of UPM, working in a company with high values.
  • Inspired and motivated teams: In the Biomedicals team, you will be working with great people. UPM is a multifaceted, international organization that works as a team to achieve our shared objectives.
  • Development opportunities: We work together on advancing your career. We provide opportunities to support your development throughout every stage.
  • 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 main location for this position is Biomedicum 2U, Tukholmankatu 8, Helsinki. Other locations, where you will work time-to-time, include the headquarters of UPM at Alvar Aallon katu 1, Helsinki and the North European Research Center in Lappeenranta.

For further information about the position, please contact your future manager Kaija Ojala, Business Development Manager, Clinical tel. +358400883440, on Tuesday 29.6.2021 at 9-12 (EET), or Wednesday 30.6.2021 at 11-14 (EET) or your future colleague Kari Luukko, Director, Quality Assurance, tel. +358400259866, on Tuesday 22.6.2021 at 12-15 (EET) or Wednesday 23.6. at 13-16 (EET).

Please send your application via the link by 15.7.2021. We will start going through the applications already during the 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. If you are a UPM employee you can reach us through the UPM Service Portal: [LINK].

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

We deliver renewable and responsible solutions and innovate for a future beyond fossils across six business areas: UPM Biorefining, UPM Energy, UPM Raflatac, UPM Specialty Papers, UPM Communication Papers and UPM Plywood. As the industry leader in responsibility we are committed to the UN Business Ambition for 1.5°C and the science-based targets to mitigate climate change. We employ 18,000 people worldwide and our annual sales are approximately EUR 8.6 billion. Our shares are listed on Nasdaq Helsinki Ltd. UPM Biofore – Beyond fossils. www.upm.com

Follow UPM on Twitter | LinkedIn | Facebook | YouTube | Instagram | #UPM #biofore #beyondfossils

Industry

  • Biotechnology
  • Packaging & Containers
  • Paper & Forest Products

Employment Type

  • Full-time

Job Functions

  • Health Care Provider

Quality Control (QC) Lab Technician

14.6.2021 | Avoimet työpaikat

https://www.recright.com/careers/en/nanoform-finland-oyj/quality-control-qc-lab-technician-60c3483736c0fe5b898dee96

About Nanoform   

Nanoform is an innovative drug particle engineering and nanotechnology company listed on the Premier-segment of Nasdaq First North Growth Market in Helsinki and Stockholm. Nanoform works together with pharma and biotech partners globally to reduce attrition in clinical trials and enhance their molecules’ formulation performance through its nanoforming services. Leveraging our in-house developed AI engine Starmap® we can also predict which customer molecules show most promise for our technology. Nanoform’s capabilities include GMP manufacturing, and its services span the small to large molecule development space with a focus on solving key issues in drug solubility and bioavailability and on enabling novel drug delivery applications.     

Quality Control (QC) Lab Technician  

With the view of developing our organization further, we are now seeking Quality Control Lab Technician to support our quality control team. The position requires availability to integrate shift work regime. The job is located at our facilities in Helsinki, Finland.   

You will be responsible for    

  • Ensure that all QC analysis are carried out in an effective and accurate manner according to company standard procedures (SOPs). 
  • Implement and develop new methods.
  • Maintain and calibrate laboratory equipment.
  • Manage reagent, material, and standards stock levels to ensure lab work continuity.
  • Ensure that records are done in an accurate manner as per company standards and procedures.
  • Support the GMP laboratory activities as per company standard procedures and Quality system. 
  • Support current R&D projects by running appropriate analysis and sampling.
  • Maintain QC Databases and others relevant for QC operations
  • Communicate efficiently with the production and technical teams to discuss QC outcomes and improvements

Ideal experience     

  • You have a Bsc or Msc degree in pharmacy, chemistry, microbiology, biotechnology or in an equivalent field. 
  • You have been working with biomolecules (especially with proteins).
  • Experience from some of the analytical techniques: SDS-PAGE, HPLC-(SEC), immunoassays, DLS.
  • Working knowledge of SOPs, Pharmacopeias and GXP Regulations.
  • Good technical knowledge and understanding of laboratory procedures, methodology and standards.
  • Capacity to work independently in a laboratory environment 
  • Capacity to produce clear records and data reports.
  • Experience in working in GXP environments. 
  • Preferred experience in using electronic Quality systems (LIMS, QMS, CDS, CAPA, others).  
  • You are used to work with MS Office programs.

Personal qualities we are looking for 

  • You are a doer and have an accurate working style 
  • You are flexible in working in a team as well as independently 
  • You have an ability to work in a high-performance environment 
  • Good English level, both written and spoken   

What we offer to you  

  • A great team to join with skilled and highly motivated colleagues
  • Encouraging and forward-looking team spirit
  • You will be part of a team that invents world-class solutions for the pharmaceutical industry
  • We provide extensive learning opportunities. You are able to utilize your skills and competencies widely as we continuously create something new
  • We like challenges and want everyone to enjoy solving them together
  • Competitive compensation package with broad employee benefits selection

You will get to be part of a unique start-up in the pharma industry.   

Interested?   

To apply for this position, please supply a covering letter and CV by 21st of June, 2021. Please note that we may already start the interviewing process during application period.   

Quality Control Lab Technician

14.6.2021 | Avoimet työpaikat

https://www.recright.com/careers/en/nanoform-finland-oyj/quality-control-lab-technician-60c35a7336c0fea0d68df604

About Nanoform 

Nanoform is an innovative drug particle engineering and nanotechnology company listed on the Premier-segment of Nasdaq First North Growth Market in Helsinki and Stockholm. Nanoform works together with pharma and biotech partners globally to reduce attrition in clinical trials and enhance their molecules’ formulation performance through its nanoforming services. Leveraging our in-house developed AI engine Starmap® we can also predict which customer molecules show most promise for our technology. Nanoform’s capabilities include GMP manufacturing, and its services span the small to large molecule development space with a focus on solving key issues in drug solubility and bioavailability and on enabling novel drug delivery applications.   

Quality Control (QC) Lab Technician  

With the view of developing our organization further, we are now seeking Quality Control Lab Technician to support our quality control team. The position requires availability to integrate shift work regime. The job is located at our facilities in Helsinki, Finland.   

 You will be responsible for    

  • Ensure that all QC analysis are carried out in an effective and accurate manner according to company standard procedures (SOPs). 
  • Implement and develop new methods.
  • Maintain and calibrate laboratory equipment.
  • Manage reagent, material, and standards stock levels to ensure lab work  continuity.
  • Ensure that records are done in an accurate manner as per company standards and procedures.
  • Support the GMP laboratory activities as per company standard procedures and Quality system. 
  • Support current R&D projects by running appropriate analysis and sampling.
  • Maintain QC Databases and others relevant for QC operations
  • Communicate efficiently with the production and technical teams to discuss QC outcomes and improvements 

Ideal experience     

  • You have a Bsc or Msc degree in pharmacy, chemistry, microbiology, biotechnology or in an equivalent field. 
  • Working knowledge of SOPs, Pharmacopeias and GXP Regulations.
  • Good technical knowledge and understanding of laboratory procedures, methodology and standards.
  • Experience in all or some of the following analytical techniques: HPLC, UPLC, DSC, XRPD, Laser Diffraction, DLS, Karl Fisher, FTIR, SEM, AFM.
  • Capacity to work independently in a laboratory environment 
  • Capacity to produce clear records and data reports.
  • Experience in working in GXP environments. 
  • Preferred experience in using electronic Quality systems (LIMS, QMS, CDS, CAPA, others).  
  • You are used to work with MS Office programs.

Personal qualities we are looking for 

  • You are a doer and have an accurate working style 
  • You are flexible in working in a team as well as independently 
  • You have an ability to work in a high-performance environment 
  • Good English level, both written and spoken   

What we offer to you  

  • A great team to join with skilled and highly motivated colleagues
  • Encouraging and forward-looking team spirit
  • You will be part of a team that invents world-class solutions for the pharmaceutical industry
  • We provide extensive learning opportunities. You are able to utilize your skills and competencies widely as we continuously create something new
  • We like challenges and want everyone to enjoy solving them together
  • Competitive compensation package with broad employee benefits selection

You will get to be part of a unique start-up in the pharma industry.     

We are looking forward to hear from you!

To apply for this position, please supply a covering letter by 21st of June,2021.

Please note that we may already start the interviewing process during application period.   

Tutkija, genotoksikologia

13.5.2021 | Avoimet työpaikat

https://duunitori.fi/tyopaikat/tyo/tutkija-stse-13186637?utm_source=loimu&utm_medium=site

Työterveyslaitos on työhyvinvoinnin asiantuntija, joka tutkii, palvelee ja vaikuttaa. Visiomme on ”Hyvinvointia työstä”, sillä terveellinen, turvallinen ja mielekäs työ luo hyvinvointia. Kehitämme asiakkaidemme kanssa hyviä työyhteisöjä ja turvallisia työympäristöjä sekä tuemme työntekijöiden työkykyä. Asiakkaitamme ovat työpaikat, päättäjät, kansalaiset, työterveysyksiköt sekä muut työhyvinvointia kehittävät organisaatiot. Toimipisteemme sijaitsevat Helsingissä, Kuopiossa, Oulussa, Tampereella ja Turussa. Työntekijöitä on noin 500. Lisätietoja: www.ttl.fi @tyoterveys

Työturvallisuus-yksikön genotoksikologian tutkimusryhmään haetaan

TUTKIJAA


määräaikaiseen työsuhteeseen tutkimaan mikro- ja nanomuovien ympäristölle altistumisen genotoksisia vaikutuksia in vitro, in vivo ja ihmisryhmissä. Tehtävä on osa EU:n H2020 PlasticHeal -tutkimushanketta, jonka kesto on kaksi vuotta. Tutkijana osallistut myös ryhmän muihin projekteihin.

Työssä suoritat kokeita ja analyyseja näytteistä ja tuloksista sekä kirjoitat raportteja ja tieteellisiä artikkeleita. Tehtäviisi kuuluu myös tukea projektien teknisessä koordinoinnissa ja toteuttamisessa, mukaan lukien osakokonaisuuksien johtaminen. Osallistut myös hankkeiden tulosten levittämiseen.

Olet etsimämme henkilö, mikäli sinulla on tehtävään soveltuva tohtorin tutkinto biologian, toksikologian tai siihen liittyvältä alueelta. Sinulla on asiantuntemusta in vivo- ja in vitro -malleissa geneettisen toksikologian alalla. Tehtävässä toimiminen vaatii hyvää englannin kielen kirjoitus- ja viestintätaitoa. Etuna pidetään aikaisempaa kokemusta virtaussytometrianalyyseistä, mikroskopiasta, in vitro syöpämenetelmistä ja ihmisen biomonitorointitutkimuksista.

Tehtävä on kokoaikainen ja määräaikainen työsuhde kahden vuoden ajaksi. Työ alkaa 15. elokuuta tai sopimuksen mukaan. Noudatamme työsuhteessa 6 kuukauden koeaikaa. Palkkaus ja työsuhteen ehdot määräytyvät Työterveyslaitoksen työehtosopimuksen mukaan. Työ sijoittuu Työterveyslaitoksen Helsingin toimipisteeseen.

Tarjoamme sinulle monipuolisen ja haasteellisen työn moniammatillisessa työyhteisössä sekä hyvät mahdollisuudet kehittää omaa osaamistasi. Henkilöstöetumme tukevat työhyvinvointiasi. Käytössäsi ovat laajat työaikaliukumat (klo 6-21) ja etätyömahdollisuus. Lisäksi tarjoamme muun muassa lounas-, kulttuuri-, liikunta- ja hierontaedun, laajan työterveyshuollon sekä mahdollisuuden käyttää työajasta tunti viikossa liikuntaan.

Kiinnostuitko? Jätä hakemuksesi TTL:n verkkosivujen kautta osoitteessa www.ttl.fi/rekry 31.5. mennessä. Lisätietoja tehtävästä antavat vanhempi tutkija Julia Catalán (julia.catalan@ttl.fi, 0503528521) ja johtaja Tommi Alanko (tommi.alanko@ttl.fi).

WWW-osoite http://www.ttl.fi
Yhteystiedot Lisätietoja tehtävästä antavat vanhempi tutkija Julia Cataln (julia.catalan@ttl.fi, 0503528521) ja johtaja Tommi Alanko (tommi.alanko@ttl.fi).
Työpaikan osoite 00250 HELSINKI
Työ alkaa 15.8. tai sopimuksen mukaan
Työaika kokoaikatyö
Työn kesto yli 12 kuukautta
Haku päättyy 31.05.2021 klo 23:59
Ilmoitus jätetty 10.05.2021
Ilmoitusnumero 10748871