Dunicom company is engaged in project engineering for pharmaceutical and biotechnological industry and design of sophisticated manufacturing facilities for the highest safety and quality standards – from the initial stages of project concept development, through manufacturing and construction to the commissioning stage. Our core values are defined by orientation towards meeting client’s needs and requirements, as well as implementation of service with highest level of quality and reliability.
As an engineering and consulting company, we are able to identify applicable strategies and provide optimal solutions and compliance with current manufacturing practices, along with taking into consideration client’s guidelines and realization of their wishes and demands. Having knowledge of state-of-the-art bioprocess technologies we are able to provide options and alternative solutions to support the decision-making process of designing a biopharmaceutical manufacturing plant. To provide the best service in the initial project phase that includes plant design.
Our design team will ensure to deliver polished and proficient CAD designs of pipelines, vessels, skids, package units and more, showcasing our engineering skills. We are proud to have high-skilled professionals who can navigate through demanding software, increasing at the same time engineering knowledge and applying years of experience in virtual reality. Whether installing small, but complicated machines or decommissioning old, redundant process plants, Dunicom owns a long-term track record of successful projects. By always respecting time and financial limits, we make sure to provide process system design, commissioning and validating, GMP compliance and state-of-the-art cleaning technologies to pharmaceutical, biotechnological and other regulated process and manufacturing industries.
We can execute following tasks:
Dealing with responsibilities which include making major strategic corporate decisions, managing the overall operations and resources of the company, while achieving high quality of work.
Always making sure to lead the development of the company’s short – and long-term strategy.
Head of Development and Manufacturing with many years of experience in pharmaceutical, biotechnological and chemical industry. Responsible for coordinating and managing the project from basic design to plant start-up.
With his extensive knowledge, experience and professional attitude towards business, easily solves all the challenges that may be found on the way to the realization of the project.
Head of Quality assurance with experience in establishing and managing ISO 9001:2015 standard. Making the most out of her role to provide reliable and durable service while maintaining a positive reputation among clients.
In charge of reviewing client’s initial requirements, suggests design improvements, monitoring and implementation of qualification procedures.
New Contract Development and Manufacturing Organization (CDMO) production facility.
Expansion of existing biopharmaceutical facility, Croatia.
US Boston Northway Biotech New automated cGMP manufacturing site, USA.
New Facility for Mammalian Process Drug Substance Manufacturing, Estonia.
New biopharmaceutical facility, Lithuania.
Consulting services and development of the flowchart for construction of the New Facility, Croatia.
Expansion of USP area in STA6 Facility, Lithuania.
Vessel Skirtings for providing required room cleanliness levels.
Expansion of existing biopharmaceutical plant-modular construction, Lithuania.
Join our team