Contract Development & GMP Manufacturing for Biopharmaceuticals

We are a leading Contract Development and Manufacturing Organization (CDMO) specialized in the process development and GMP manufacturing of biopharmaceuticals and cell therapy products.

With the unique goal of making your project a success, we offer personalized services for process development and GMP manufacturing of biopharmaceutical products using Microbial and Mammalian expression systems.

Download our current GMP certification.


Keensight Capital, one of the leading European Growth Buyout firms, is committed to supporting entrepreneurs as they implement their growth strategies. For 20 years, Keensight Capital’s team of seasoned professionals has leveraged their knowledge of investment and growth industries to invest for the long term in profitable companies with high growth potential and revenues in the range of €15 million to €250 million.


Drawing on its expertise in the Information Technology/Internet and Healthcare/Wellbeing sectors, Keensight identifies the best investment opportunities in Europe and works closely with management teams to develop and achieve their strategic vision.



People are the heart of our company

We are proud of each one of our more than 250 employees. Our team is composed of highly qualified and skilled professionals working towards a unified goal to offer only the best.


Mr. Molero graduated with a degree in Pharmacy and an Executive MBA degree from the University of Navarra. He has experience spanning more than 30 years in the chemico-pharmaceutical industry in the areas of Operations and Consulting in multinational companies like Glaxo, Roche, Syntex and Shionogi. His brilliant carrier has taken him to the management of plants thereby involving him in major research projects and engineering at the international level. Mr. Molero is leading the company since its beginnings in 2006.

Dámaso Molero

General Manager

Mr. Galan graduated in Business Administration from the University of the Basque Country and is a member of ROAC (Official Register of Statutory Auditors). He has been managing the Financial Departments of many important multinational companies including various areas of automation, like SAS Automotive and TRW, nutrition, construction, and wind power. At 3P he manages the financial and business operation to create the highest level of efficiency.

Ángel Mª Galán

Financial Director

Mrs. San Miguel graduated with a degree in Pharmacy and a Master’s in Research, Innovation and Development of Drugs from the University of Navarra. She joined 3P at 2007 and since then she has been responsible for the certification of biological drug substances, biological drug product and cell therapy products as well as of the management of analytical services area composed by Quality Control and Analytical Method Development. She has successfully managed the regulatory audits from clients and Authorities.

Lucía San Miguel

Quality Control Director & QP

Mr. Cuervo graduated with a degree in Chemical Engineering and a Master’s in Biotechnology Process Engineering, both from Instituto Politécnico Jose Antonio Echeverría (La Habana). He has more than 18 years’ experience in the manufacturing of industrial recombinant proteins leading USP and DSP manufacturing activities under GMP rules. His deep understanding of protein and antibody chemistry has taken him to successfully manage the facility of 3P ensuring the proper operation of each project.

Ruben Cuervo

Plant Director

Mr. Orbara is an electronic Engineer from the University of La Rioja. He holds degrees in programming engineering and robotics. Prior to 3P, he worked, with Volkswagen and Prodinsa Navarra, performing roles in electronic design, installation management, programming and machine mechanics. At 3P he is responsible for the maintenance and control of the manufacturing plant ensuring the effective work of each equipment and technology.

Josu Orbara

Maintenance Director

Mrs. Erroba has a degree in Biochemistry and a PhD in Science from the University of Navarra and she also holds an MBA degree from the CEF Business School. She has been working for more than 11 years in the international biotech industry in different positions such as Strategy Consultant, Business Development and Project Director at ASEBIO. At 3P she leads the Business Development department with three branches of activity: business development, project management and marketing. She develops the international sales plan establishing strategic customer collaborations.

Elena Erroba

Business Development Director

Mr. Alarcon graduated with a double degree in Labour Relations and Work Sciences from the Public University of Navarra and the Rovira i Virgili University. He also holds a master in Human Resources from the Limerick University (Ireland). During his large career he has been managing the international human resources departments of big companies like GESTAMP Renewables Industries, Gamesa or Viscofan. He is responsible to conduct 3P’s human resources strategic planning in order to support and implement strategic plans for high qualified talent acquisition and retention.

Tomás Alarcón

Human Resources Director

He graduated in Biochemistry from the University of País Vasco and has a Master’s degree in Research, Innovation and Development of Drugs from the Center for Research and Applied Pharmacobiology (CIFA), University of Navarra. Prior to joining 3P Biopharmaceuticals, he developed his professional work in the Medical department of Bial Industrial Pharmaceuticals and in the quality assurance unit of CIFA.

Jaime Vaquerizo

Quality Assurance Director

Have you ever thought about what the future will bring?

Living is not about having time, it is about making time. With your work you are creating valuable time and positively impacting the lives of others.

We are an excellent travel companion for your adventure in biologics development, and we are eager to help you make a difference in people’s lives. Our passionate team is constantly pursuing perfection and precision in everything they do, which will ensure rigorous quality for your development or commercial project.

Passion fuels the energy and engagement of our team and all of the work that we do at 3P Biopharmaceuticals. We thoroughly understand your needs and will focus our passion on making your project a success, thereby creating valuable and life changing biopharmaceuticals for patients.


3P Biopharmaceuticals is a business venture whose mission is to provide complete products and services of the highest quality and added value for our customers, as well as achieving the complete satisfaction of our partners and ensuring the welfare of our employees.


Our vision is to become a leading CDMO in the sector of biotechnology in Europe and take on development and manufacturing projects in key international markets in order to contribute to the continual advancement in the health and welfare of people.


  • Careful attention to our customers´ requirements as well as transparency, close collaboration and maintenance of absolute confidentiality and discretion in the development of their projects.
  • A clear focus on quality, performance and a job well done.
  • Clear communication and collaboration with clients, institutions and suppliers. Teamwork coupled with a spirit of continuous improvement and innovation; commitment to our social and environmental surroundings.


3P delivers a broad and profound knowledge of biopharmaceuticals.

Our goal is to exceed our clients´ expectations while providing tailored and successful solutions.

Our flexible, state-of-the art facilities were designed for unilateral flow and are able to produce multiple products at different stages of manufacturing.

Our team is committed and passionate about making your project a success through perfection and precision. At 3P, quality is the core of our daily activities, and it is our DNA. Thanks to our comprehensive Quality System, we are able to ensure the highest level of quality excellence and compliance with regulatory requirements.

3P Biopharmaceuticals has an impressive regulatory track record. We have been successfully inspected more than 70 times for both clients and agencies.

You can be confident that 3P is the committed and trusted partner that you have been searching for, and we are eager to accompany you every step of the way on your biologics journey, from early development to commercial manufacturing.