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KategoriaFarmasia, tutkimus ja kehitys
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Työpaikan tunniste00055660
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SopimusMääräaikainen
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SijaintiKuopio
Are you looking for new career opportunities in the field of chemistry, biochemistry or biotechnology and are you particularly interested in documentation? Great! New pharmaceutical factory Finport is nearing completion in Kuopio, and we are now looking for Quality Control Validation Specialist for a fixed term employment relationship. A warm welcome to be a part of the international growth organization of the pharmaceutical industry, where your work has a greater meaning for everyone and everywhere!
Your role
As part of Quality Control team, you will play a part ensuring the quality and patient safety of our product. In your role you generate, review and approve GMP documents, and maintain and develop the quality system in the area of expertise according to good documentation practice. In addition, you participate in analytical investigations and approve QC release and in-process test results. The work is largely screen terminal work, documentation, writing work instructions and quality control. The work will start on September 11th or according to the agreement. QC team works Mon-Fri in one shift. The employment relationship is initially fixed term for one year.
In order to succeed you will need to have:
In term of your working style, you are self-directed, precise and systematic. You are good at communicating and you bring joy and good spirit to the work community. You also easily adjust to changing situations and be interested in developing your skills. The working language in your team is English so the be successful, good command of both written and spoken English is a must.
What FinVector offers you
One year fixed term employment realtionship in a organization where your work truly matters for people's health and where your work is valued. High competenxe, quality, teamwork and transparency are emphasized in everything that is done at Finvector. In international organization you have great opportunities to grow and develop.
In addition to great colleagues and meaningful work, you get comprehensive personnel benefits, such as extensive occupational healthcare services, ePassi benefits (support for physical and cultural free-time activities), free parking and access to the bonus model.
The application process and selections
Send your application and resume in English via the attached application link by 3.9 at the latest and tell us why you would be the most suitable person for the position. Please note that we are processing applications within the application period. Adecco Finland is responsible for the recruitment process. You will be employed directly to our partner FinVector for a fixed term employment. For more information, please contact Adecco's Recruitment Consultant Heidi Hämäläinen by email Heidi.hamalainen@adecco.fi.
FinVector is an internationally renowned biopharmaceutical company that manufactures viral-based gene therapy products. We believe in delivering to market innovative medicines and therapies, which bring renewed hope, purpose, and a true sense of belonging to individuals battling major illnesses. Our state-of-the-art manufacturing facility is located in the beautiful and thriving science and technology area of Savilahti in Kuopio, Finland. Our vibrant and multinational working community consists of hundreds of professionals representing nearly 50 different nationalities, fostering a diverse and collaborative environment. FinVector is a subsidiary of Ferring Ventures S/A.
Learn more: www.finvector.com
Instagram: @finvectorians - https://www.instagram.com/finvectorians
LinkedIn: FinVector Oy - https://linkedin.com/company/finvector/
Key words: laadunvalvonta, lääketeollisuus, biolääketeollisuus, laboratorio, dokumentaatio, kemianala, biotieteet, quality & control, specialist, pharmaceutical production, biopharmaceutical industry, laboratory, documentation
Your role
As part of Quality Control team, you will play a part ensuring the quality and patient safety of our product. In your role you generate, review and approve GMP documents, and maintain and develop the quality system in the area of expertise according to good documentation practice. In addition, you participate in analytical investigations and approve QC release and in-process test results. The work is largely screen terminal work, documentation, writing work instructions and quality control. The work will start on September 11th or according to the agreement. QC team works Mon-Fri in one shift. The employment relationship is initially fixed term for one year.
In order to succeed you will need to have:
- Good understanding and experience of analytical methods, techniques and equipment (e.g. spectrophotometers, flow cytometer, pH/Conductivity meters, cell counters, PCRs)
- Degree in Chemistry, Biochemistry, biotechnology or equivalent
- Previous in-vitro experience is considered as an advantage
- Motivation to learn new, accuracy and orderliness
- Independent and accurate working style
- Ability to easily adjust to changing situations and be interested in developing your skills.
- Good command of both written and spoken English is a must
In term of your working style, you are self-directed, precise and systematic. You are good at communicating and you bring joy and good spirit to the work community. You also easily adjust to changing situations and be interested in developing your skills. The working language in your team is English so the be successful, good command of both written and spoken English is a must.
What FinVector offers you
One year fixed term employment realtionship in a organization where your work truly matters for people's health and where your work is valued. High competenxe, quality, teamwork and transparency are emphasized in everything that is done at Finvector. In international organization you have great opportunities to grow and develop.
In addition to great colleagues and meaningful work, you get comprehensive personnel benefits, such as extensive occupational healthcare services, ePassi benefits (support for physical and cultural free-time activities), free parking and access to the bonus model.
The application process and selections
Send your application and resume in English via the attached application link by 3.9 at the latest and tell us why you would be the most suitable person for the position. Please note that we are processing applications within the application period. Adecco Finland is responsible for the recruitment process. You will be employed directly to our partner FinVector for a fixed term employment. For more information, please contact Adecco's Recruitment Consultant Heidi Hämäläinen by email Heidi.hamalainen@adecco.fi.
FinVector is an internationally renowned biopharmaceutical company that manufactures viral-based gene therapy products. We believe in delivering to market innovative medicines and therapies, which bring renewed hope, purpose, and a true sense of belonging to individuals battling major illnesses. Our state-of-the-art manufacturing facility is located in the beautiful and thriving science and technology area of Savilahti in Kuopio, Finland. Our vibrant and multinational working community consists of hundreds of professionals representing nearly 50 different nationalities, fostering a diverse and collaborative environment. FinVector is a subsidiary of Ferring Ventures S/A.
Learn more: www.finvector.com
Instagram: @finvectorians - https://www.instagram.com/finvectorians
LinkedIn: FinVector Oy - https://linkedin.com/company/finvector/
Key words: laadunvalvonta, lääketeollisuus, biolääketeollisuus, laboratorio, dokumentaatio, kemianala, biotieteet, quality & control, specialist, pharmaceutical production, biopharmaceutical industry, laboratory, documentation
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