Toke Jonsson Email & Phone Number

Vejle, DK

Denmark

• Fertin Pharma is a CDMO specializing in oral dosage forms. I work in the development department for pharmaceutical products, primarily focused on nicotine replacement therapy (NRT). I am responsible for the development.
• Developing pharmaceutical products using Quality by Design (QbD) to ensure compliance with regulatory and customer requirements
• Establishing robust production processes that meet commercial goals for new products before their transition to the Supply Chain
• Building and enhancing the development department’s expertise in tableting technology
• Documenting the development process to establish the CMC/development section of the regulatory dossier

Basel, Switzerland

• As a Formulation Project Leader within the late phase drug product development at Novartis, my focus was to develop their growing pipeline of solid dosage forms. Here I played a key role in the transfer of new products.
• Achieving robust formulations and processes through optimisation, scale-up and validation work
• Providing the required documentation to allow worldwide registration
• Authoring technical reports and protocols to reflect quality and accuracy of data
• Supervising production during transfer to production scale
• Ensuring clear work flows for delivery of projects

Hove, United Kingdom

• Custom Pharma Services is a CDMO specialising in solid dosage forms from pre-formulation through manufacturing, packaging and delivery. As a Technical Project Manager my focus was to progress Custom Pharma Services.
• Achieving robust formulations and processes through optimisation, scale-up and validation work
• Providing the required documentation to allow registration within the UK
• Authoring technical reports and protocols to reflect quality and accuracy of data
• Supervising production during transfer to commercial scale
• Ensuring clear work flows for delivery of projects

Glasgow, United Kingdom

• Bio-Images Research is a CRO that undertakes early phase clinical studies, specialising in gamma scintigraphy as an in vivo imaging method for modified drug release. During the first three years of this employment.
• Carrying out research and development activities for the formulation of a wide range of radiolabelled dosage forms used in scintigraphic clinical studies
• Designing and implementing manufacturing protocols to cGMP
• Supervising manufacture of developed radiolabelled dosage forms
• Assisting with analytical and formulation development activities for novel solid dosage forms
• Providing regular status reports to the Company and University Supervision Team

Norwich, United Kingdom

Working on MSc (Pharm) research project using a model that simulates the human gastric compartment; the Dynamic Gastric Model

Denmark

Practical aspect of my BSc (Pharm) degree involving training in a pharmacy and providing pharmaceutical advice in the dispensary. After completing six months of training at the pharmacy I continued working full time for two months in the dispensary as a trained Pharmaconomist

Copenhagen Area, Denmark

Work experience as a BSc (Pharm) student collating documents and transferring into electronic Common Technical Document (eCTD) formats for submission in registration dossiers

Hong Kong

Paid course-related training abroad with the International Association for the Exchange of Students for Technical Experience (IAESTE), searching literature for a research project involving traditional Chinese medicine

Copenhagen Area, Denmark

Summer vacation job carrying out quality control on imported medicine leaflets and labels on a packing line

Master Of Philosophy (Mphil), Drug Delivery

Thesis entitled: “Small Scale Manufacturing and Scintigraphic Detection of Pellet Formulations”

Master Of Science (Msc), Pharmaceutical Sciences

Thesis entitled: “Effect of food intake on the dissolution of a poorly soluble drug using a novel in vitro system that simulates the human.

Bachelor Of Science (Bsc), Pharmaceutical Sciences

Education record

Education record