Business Wire

Viking Malt Group: Teemu Pohjola is appointed the CFO of Polttimo and Viking Malt Group

3.11.2020 08:30:00 EET | Business Wire | Press release

Share

Teemu Pohjola is appointed CFO of Polttimo and Viking Malt Group effective 3rd of November 2020.

This press release features multimedia. View the full release here: https://www.businesswire.com/news/home/20201102005570/en/

To view this piece of content from mms.businesswire.com, please give your consent at the top of this page.

Teemu Pohjola is appointed CFO of Polttimo and Viking Malt Group effective 3rd of November 2020. Photo: Viking Malt.

Previously Teemu Pohjola held the position of the CFO of Huhtamäki Fiber and Foodservice segment leading an international team of Finance professionals driving its financial strategy and performance since 2017. Prior to that he has worked in international context for 15 years, holding several strategic finance positions in among others Fazer and Salcomp.

“We are pleased to welcome Teemu to our leadership team,” said Kasper Madsen , CEO of Viking Malt Group. “His deep and extensive experience in leading the financial operations in an international context as well as driving the strategic initiatives will be very valuable for us. He will provide strong leadership and is an excellent addition to the team.”

“I am excited to join a company with a strong business model and a proud history and look forward to working with the team to execute the strategy and vision of the company´s priorities.”

As CFO, Teemu Pohjola will lead the finance organization across the five Viking Malt countries and will be responsible for IT as well as accounting, treasury, financial planning, analysis and tax. He is also the Secretary of Polttimo, Viking Malt and Senson.

Teemu holds a Bachelor degree in Business Administration from Mercuria Business School and MBA from Hanken School of Economics.

Background info

Polttimo Group

Polttimo Group, established in 1883, is an international group of companies, specializing in manufacturing raw materials and raw materials solutions for the food and beverage industry around the world. We create new innovative grain-based solutions for our customers. Our main products are malt for brewing, craft brewing and distilling as well as cereal-based ingredients. Our group consists of Viking Malt Group, the leading Nordic malting company, and Senson Oy, manufacturing malt extracts and flours, cereal extracts, enzymes and many other innovative ingredients.

Viking Malt Group

Viking Malt is the number one malting company in Northern Europe, and the world’s leading company of special malts. A dedicated team, good quality malting barley and six efficient production sites with a capacity of 600 000 tons form the basis for our offering to international and local brewers and distillers.

To view this piece of content from cts.businesswire.com, please give your consent at the top of this page.

Contact information

Pia Valve
VP HR & Communications
Viking Malt Oy
Mobile +358-40-7700090
pia.valve@vikingmalt.com
www.vikingmalt.com

About Business Wire

For more than 50 years, Business Wire has been the global leader in press release distribution and regulatory disclosure.

Subscribe to releases from Business Wire

Subscribe to all the latest releases from Business Wire by registering your e-mail address below. You can unsubscribe at any time.

Latest releases from Business Wire

Avanzanite Bioscience’s Partner Agios Announces PYRUKYND® (mitapivat) Approval in the European Union for Adults with Thalassaemia22.5.2026 17:18:00 EEST | Press release

Avanzanite Bioscience B.V., a rapidly growing commercial-stage European specialty pharmaceutical company focused on rare diseases, today reported that its partner, Agios Pharmaceuticals, Inc. (Nasdaq: AGIO), a commercial-stage biopharmaceutical company headquartered in Cambridge, Massachusetts focused on delivering innovative medicines for patients with rare diseases, announced that the European Commission has granted marketing authorisation for PYRUKYND® (mitapivat), an oral pyruvate kinase (PK) activator, in adults for the treatment of anaemia associated with transfusion-dependent and non-transfusion-dependent alpha- or beta-thalassaemia, with an orphan medicinal product designation. This press release features multimedia. View the full release here: https://www.businesswire.com/news/home/20260522186975/en/ Adam Plich, CEO and Co-Founder of Avanzanite Bioscience. “Thalassaemia is a complex, chronic and multisystem disease characterised by anaemia, ineffective erythropoiesis and haemo

ICE Brent and ICE WTI Perpetual Futures to Launch on OKX22.5.2026 15:30:00 EEST | Press release

OKX, a blockchain technology and trading company serving more than 120 million customers globally,and Intercontinental Exchange (NYSE: ICE), one of the world's leading providers of financial market technology and data powering global capital markets including the New York Stock Exchange, today announced plans for OKX to launch perpetual futures based on ICE's Brent Crude and WTI Crude energy benchmarks. The products are expected to be available to trade on OKX’s platform in jurisdictions where OKX is licensed to offer perpetual futures products. The new OKX contracts represent a major step forward in expanding regulated access to global commodity markets through digital asset infrastructure. This first product collaboration between OKX and ICE comes after the companies established a strategic relationship in March 2026. ICE operates some of the world’s leading exchanges, clearing houses and market data services across energy, commodities, fixed income and equities markets. ICE’s future

Enhertu ® Recommended for Approval in the EU by CHMP for Patients with Previously Treated HER2 Positive Metastatic Solid Tumors22.5.2026 15:00:00 EEST | Press release

Enhertu® (trastuzumab deruxtecan) has been recommended for approval in the European Union (EU) as a monotherapy for the treatment of adult patients with unresectable or metastatic HER2 positive (immunohistochemistry [IHC] 3+) solid tumors who have received prior treatment and who have no satisfactory treatment options. Enhertu is a specifically engineered HER2 directed DXd antibody drug conjugate (ADC) discovered by Daiichi Sankyo (TSE: 4568) and being jointly developed and commercialized by Daiichi Sankyo and AstraZeneca (LSE/STO/NYSE: AZN). The Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency (EMA) based its positive opinion on results from patients with HER2 positive (IHC 3+) tumors in three phase 2 trials including DESTINY-PanTumor02,DESTINY-Lung01 andDESTINY-CRC02 where Enhertu demonstrated clinically meaningful responses across a broad range of tumors. The recommendation will now be reviewed by the European Commission, which has the authority

Future Health Challenge Awards USD 300,000 to Early Detection and Population Health Sensing Tools on Sidelines of World Health Assembly22.5.2026 14:45:00 EEST | Press release

Three global teams developing early detection and real-time population health monitoring solutions have secured a total of USD 300,000 on the sidelines of the 79th World Health Assembly. The winning solutions address critical challenges in early detection, continuous population insight and more timely decision making, signalling a shift in health systems from late-stage treatment to earlier intervention. This press release features multimedia. View the full release here: https://www.businesswire.com/news/home/20260522587414/en/ Selected from 393 submissions across 68 countries, the winning teams were recognised through the inaugural ‘Future Health Challenge 2026: Building Anticipatory Health Systems through Population Sensing’, delivered by Future Health – A Global Initiative by Abu Dhabi in collaboration with MIT Solve. Health systems globally are facing rising costs and persistent delays in diagnosis, with many conditions still identified only after symptoms become severe. At the sam

Pivotal Trial Data for EP0031 (A400), a Next-Generation Selective RET Inhibitor (SRI), in RET Positive Advanced NSCLC, to be Presented at ASCO 202622.5.2026 12:18:00 EEST | Press release

Ellipses Pharma (“Ellipses”), a global oncology drug development company with a pipeline of innovative programmes, announced today that its partner, Kelun-Biotech, is presenting pivotal trial data for EP0031/A400, for the potential treatment of RET-fusion positive Non-Small Cell Lung Cancer (NSCLC), at the 2026 American Society of Clinical Oncology (ASCO) Annual Meeting Chicago, May 29 to June 2. Efficacy and safety of lunbotinib (A400/EP0031), a next-generation selective RET inhibitor (SRI), from a pivotal phase Ⅱ study in patients with advanced RET-fusion positive non-small cell lung cancer (NSCLC), will be presented as an oral presentation scheduled on May 29, 2026, 14:36-14:48 local time (Abstract #8505: Lung Cancer – Non-Small Cell Metastatic). The oral presentation of these data at the prestigious ASCO annual meeting, represents another major milestone in the global development of EP0031/A400 as a next generation SRI. The data were generated in Kelun-Biotech’s Phase 2 study (NCT0

In our pressroom you can read all our latest releases, find our press contacts, images, documents and other relevant information about us.

Visit our pressroom
World GlobeA line styled icon from Orion Icon Library.HiddenA line styled icon from Orion Icon Library.Eye