Fermentation and Recovery

Our consultancy is a recognized authority in the field of pharmaceutical manufacturing, with a particular emphasis on Fermentation and Recovery processes, which are integral to the production of Active Pharmaceutical Ingredients (APIs).

Our cadre of seasoned engineers have honed their expertise in both upstream and downstream manufacturing. In the upstream process, they excel in the cultivation of microorganisms that yield the desired therapeutic compounds. They adeptly manipulate and control conditions such as pH, temperature, and aeration to optimize biomass growth and product synthesis.

In the downstream process, our engineers demonstrate proficiency in the recovery and purification of the target product. They are adept at selecting and employing a range of techniques, including filtration, centrifugation, chromatography, and crystallization, to effectively segregate the target compounds from impurities.

Our team is also experienced in the intricacies of providing process support within Fermentation, Recovery, and Purification facilities, ensuring seamless integration and operational efficiency. They possess a comprehensive understanding of equipment functionality and are skilled at troubleshooting and optimizing critical components ranging from bioreactors to separation units.

In addition to these core competencies, our engineers have extensive experience with Clean Utility systems, which underpin the hygienic integrity of the manufacturing environment. They have expert knowledge in the production, distribution, and storage of high-purity water according to the most up-to-date quality standards.

Furthermore, our consultancy also boasts a robust expertise in Black Utility systems, which cater to the non-potable water needs for ancillary purposes. Our engineers are skilled in overseeing the design, operation, and maintenance of these systems, ensuring their reliable performance within the pharmaceutical context.

In conclusion, our consultancy is uniquely positioned to provide unparalleled expertise in the domains of Fermentation and Recovery, underpinned by the exceptional proficiency of our engineers. Through our seasoned acumen, we enable pharmaceutical manufacturers to navigate these critical processes with precision and efficacy, ultimately leading to the production of superior quality APIs and, consequently, enhanced therapeutic outcomes.

We strive to implement simple and operational solutions, and can support the implementation of procedures and training activities that ensure compliance with existing authority requirements and inspection readiness.

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Fermentation and recovery cases

Fermentation and recovery profiles

Experienced in vaccine production, adjuvants, insulin, and antibiotics. Known for driving process improvements, documentation excellence, and cross-functional collaboration in regulated pharma environments. Earlier in my career, I worked as a researcher in Denmark, Germany, and Singapore, focusing on microbial fermentation, enzyme immobilization, and bioprocess development. This foundation strengthens my ability to bridge science and production in complex pharma environments.
Cleaning Validation
Process Technology & Unit Operations
Project management
Qualification/Validation & Comissioning
Quality & GMP documentation & Risk Management
Training & Knowledge Transfer
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Nadja Schultz Jensen

Senior Consultant
Reab, an MSc in Pharmacy graduate from 2020, brings a fresh perspective and dynamic energy to the pharmaceutical industry. Despite being a recent entrant, Reab has swiftly accumulated a wealth of experiences across various facets of the sector.
Aseptic production
Clean Room
Cleaning
GMP
Project Management Support
Upstream/downstream technology
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Reab Jaralla

Process Engineering Consultant
Sema has more than 12 years of experience in the pharmaceutical industry. Working in Xellia with different roles from Compliance specialist, production specialist, GMP documentation specialist, Senior Aseptic processing specialist, has made Sema an experience all round profile around the aseptic processing disciplines.
GMP
Qualification & Validation
Quality
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Sema Oruc

Senior Process Engineering Consultant
Mikael is an experienced person (>15 years) within the pharmaceutical industry who is used to working according to cGMP, working in project form with both leading, driving and being involved in projects and has experience in supporting and leading employees in production.
GMP
Project management
Qualification & Validation
Technology
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Mikael Samuelsson

Process Engineering Specialist
Ann-Rikka has 18 years of experience in the pharmaceutical industry. Working in Novo Nordisk A/S at a fermentation and recovery Pilot plant with hands on operation of the equipment and also reporting.
GMP
Project management
Technology
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Ann-Rikka Søgaard

Process Engineering Specialist

Managing Partner in Process Engineering

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Jonas Højslet

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