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CMC Specialist in Regulatory Affairs

In this versatile position, you will support the development of InnoMedica's products in the areas of formulation/process development, production, and quality control. In doing so, you ensure that each development step and its related submission meet regulatory requirements to be approved by the authorities.

Your responsibilities include:

• Identification of product-specific regulatory requirements, development of regulatory strategies, and clarification of open questions in collaboration with the authorities
• Participation in interdisciplinary working groups and contribution of regulatory expertise in the area of CMC (Chemistry, Manufacturing, and Control)
• Management and updating of regulatory quality documentation (PQD/IMPD-Q) for products

HR & Communication Specialist

In this multifaceted role, you bring together exceptional communication flair and strong HR expertise. As an HR Specialist, you will be responsible for the entire employee lifecycle – from recruiting and onboarding to employee support, development, and offboarding processes. As a Communication Specialist, you represent InnoMedica externally and ensure effective information flow with both internal and external stakeholders (investors, medical professionals, employees, etc.).

Your responsibilities include:

• Recruitment activities, including candidate sourcing and interview coordination
• Operational HR support and management of employee records
• Organization of onboarding and offboarding processes
• Creation of key messages and content for the website, newsletters, investor documents, and product brochures in close collaboration with various internal departments
• Planning and execution of internal and external events (scientific conferences, investor events, employee events, etc.)

Laboratory Technician Quality Control & Analytics

As part of our Quality Control & Analytics team, you will be responsible for the performance, documentation, evaluation and assessment of analytical tests for raw materials and finished products in a GMP environment.

Your responsibilities include:

• In-process controls, release and stability tests using HPLC-based analytical methods
• DLS-based analyses; pH, IR, and wet chemical analyses
• Visual appearance test of finished drug product for batch release and stability
• Coordination with contract laboratories for routine testing and method development
• Reporting and investigation of OOS results; documentation of events or deviations
• Authoring of change requests and CAPAs
• Responsibility for stock management and logistical tasks in the laboratory
• Qualification, maintenance and calibration of laboratory equipment; technical troubleshooting
• Assistance in the development and validation of HPLC methods

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

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