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Senior Scientist Quality Assurance

You have several years of experience in a GMP-regulated environment – ideally in Quality Assurance – and are ready for a new challenge in a senior, hands-on role?

As part of our motivated and supportive five-person QA team, you will be responsible for maintaining and further developing our pharmaceutical quality system, with a strong focus on compliance with GMP guidelines to ensure the consistent quality of our manufactured products. With your expertise, you can make a real impact in a dynamic work environment and enjoy opportunities for professional growth and development.

Your responsibilities include:

• Management of deviations, change requests as well as corrective actions and preventive actions
• Review of equipment qualifications, batch documentation, and product release preparations for clinical studies
• Project planning as well as coordination and active participation in interdisciplinary project teams

Scientist Quality Assurance

As part of the Quality Assurance (QA) team, you will be responsible for maintaining and expanding the pharmaceutical quality system. The focus is on compliance with GMP guidelines, which ensure the quality of the manufactured products

Your responsibilities include:

• Management of deviations, change requests as well as corrective actions and preventive actions
• Review of equipment qualifications, batch documentation, and product release preparations for clinical studies
• Project planning as well as coordination and active participation in interdisciplinary project teams

Financial Accountant

In this position, you will oversee all financial transactions of the company and manage the company’s financial reporting.

Your responsibilities include:

• Responsibility for the entire process from general ledger accounting to the preparation of annual reports and its audits
• Creditor and payroll processes
• Social security, tax, and pension declarations
• Selective projects (e.g. simplification and standardization of finance processes, introduction of reporting solutions, business analytics)

Clinical Research Associate / Clinical Scientist

In the Clinical Research department, the main objective is the clinical development of InnoMedica's products in neurology and oncology with the aim of applying innovative drugs in clinical trials to patients and ultimately bringing them to market.

Your responsibilities include:

• Support in the planning of clinical trials and preparation of trial documents as well as documents for the cantonal ethics committee, Swissmedic, and other authorities
• Supervision of clinical trials through close interaction with the clinical trial sites
• Conceptualization and writing of monitoring plans
• Preparation, conduct, and follow-up of regular monitoring visits to trial sites to ensure data integrity through source data review
• Conduct of training activities at the trial sites
• Establishment of clinical trial tools for efficient coordination and communication
• Authoring and/or coordinating scientific publications
• Scientific congress participation and presentation

Clinical Trial Manager

In the Clinical Research department, the main objective is the clinical development of InnoMedica's products in neurology and oncology with the aim of applying innovative drugs in clinical trials to patients and ultimately bringing them to market.

Your responsibilities include:

• Development and design of clinical trials
• Preparation of clinical trial applications in collaboration with our regulatory department and investigators
• Organization and coordination of clinical trials in Switzerland in cooperation with external stakeholders
• Regular visits of clinical sites and monitoring of study results
• Data management
• Participation in routine Pharmacovigilance
• Assurance of GCP compliance

Manager Research and Development

In this position, you will drive the development of our liposomal drug products in the fields of neurology and oncology. You will manage a small, dedicated team while remaining actively involved in hands-on laboratory work. Beyond the lab, you’ll support cross-functional pharmaceutical development project groups.

Your responsibilities include:

• Responsibility for a small team and organization of the department and laboratory
• Design and execution of experiments regarding the formulation and process of existing drug prototypes
• Working towards the discovery of new prototypes in liposomal drug delivery, and their characterization
• Development, characterization, and translation of liposome production processes from laboratory scale to small industrial scale
• Planning and realization of preclinical studies together with external collaborators
• Data analysis and interpretation, report writing
• Development and application of analytical methods for product characterization
• Active involvement in interdepartmental projects (e.g. with regulatory, production, clinical research)