Ajankohtaista

Scientists to Product Technology

1.11.2021 | Avoimet työpaikat

https://www.sympahr.net/public/pq.aspx?8236bf3a&lang=en-US

Our growth continues and we are setting up a completely new department to support it. We are now recruiting professionals from all levels to Product Technology department. This department focuses on early stage process and analytical development for the products that come from the research phase to GMP production.

We are now looking for Scientists to start up the Upstream, Downstream and Analytical activities. Your main responsibilities as a Scientist include hands-on lab work as well as documentation. Development work is operated in a pilot or cleanroom environment according to the current GMP guidelines. As a Scientist, you will be working in close collaboration with internal and external stakeholders focusing on developing innovative and scalable solutions for the Cell and Gene Therapy platforms.

You could be the person if…

You are individual with a strong scientific drive and ability to deliver.

You produce clear, easily understandable and accurate documentation in English.

You have good skills in analyzing data, both verbal and numeric. You are also seeking new information to solve challenges and make decisions based on the data.

You are able to innovate new ideas, approaches and views. You also enjoy developing yourself.

Your work approach is precise and you achieve objectives set to you in a timely manner.

As a person, we would like you to be open-minded towards new challenges and obtain a can-do attitude.

In order to succeed, you should have a degree in the field of life sciences, biotechnology, pharmacy, laboratory technology or any other related field of study or sufficient working experience from pharma industry. It is an advantage if you already have some experience in aseptic- or GMP-work and/or you have knowledge on quality systems.

The position is permanent and located in Kuopio, Finland. We hope that you are able to join our team in December-January. This role is new in our organization due to our ongoing growth.

We offer you an active and lively work community with multidisciplinary experts who foster a culture of openness and shared knowledge. We aim to great team spirit and leadership and offer well-being services to enable a good work-life balance. Furthermore, we will support your personal development.

Please send your CV and application via our recruitment system as soon as possible but at the latest by 14 November 2021. We will process applications as they come in, and fill in the position as soon as we find the right candidate.

For further information, please contact Minna Karhinen, minna.karhinen@finvector.com, +358 400 872830 on 25.10 between 2 and 3 pm and on 2.11 between 1 and 2 pm.

Operators to product technology

1.11.2021 | Avoimet työpaikat

https://www.sympahr.net/public/pq.aspx?4bfb36ca&lang=en-US

Lääketehtaamme kasvu jatkuu ja olemme perustamasssa kokonaan uutta osastoa tukemaan toimintaamme. Rekrytoimme nyt Product Technology-osastolle kaikille tasoille huippuosaajia. Osasto keskittyy varhaisen vaiheen prosessin ja analyyttiseen kehitykseen tuotteille, jotka siirtyvät tutkimusvaiheesta GMP-tuotantoon.

Haemme tiimiin operaattoreita käynnistämään GMP tuotanto- ja testaustoimintaa uusille tuotteillemme. Päävastuualueena on tuotantotiloissa ja analytiikan laboratorioissa tapahtuva hands-on työ sekä työn dokumentointi GMP-säännösten mukaisesti.

Taustaltasi voit olla esimerkiksi laborantti tai bioanalyytikko, jolla on joaikaisempaa kokemusta soluviljelystä tai puhdistus- tai analyyttisistä menetelmistä.

Tehtävässä menestyt jos olet työotteeltasi tarkka ja järjestelmällinen etkä pelkää laitteita tai muuttuvia tilanteita.  Meillä on työkielenä englanti, joten sinulla on oltava hyvä englanninkielen suullinen ja kirjallinen taito. Ennen kaikkea etsimme kuitenkin mukavia työkavereita, joilla on avoin ja kehitysmyönteinen asenne tuotanto- ja testaustöitä kohtaan!

Työsuhteesi on toistaiseksi voimassa oleva ja toivoisimme sen alkavan viimeistään tammikuussa 2022. Tarjoamme sinulle dynaamisen ja kansainvälisen työyhteisön. Tuemme hyvinvointiasi työsuhde-eduillamme ja tarjoamme sinulle mahdollisuuden kehittyä ja lisätä osaamistasi urasi aikana. Ennen kaikkea pääset osalliseksi mahtavaa työporukkaa!

Haethan tehtävää viimeistään 7.11.2021. Aloitamme hakemusten käsittelyn ja haastattelut jo hakuaikana.

Lisätietoa tehtävästä antaa Minna Karhinen minna.karhinen@finvector.com tai puhelimitse maanantaina 25.10 klo 14-15 ja tiistaina 2.11 klo 13-14 numerosta +358 400 872830.

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.