Symbios Orthopédie S.A.

We are currently looking for a Planning Officer The Planning Officer is responsible for the management and optimization of material flows and inventory management for the end-to-end supply chains of the company at the manufacturing site in Switzerland with the its foreign subsidiaries. Key responsibilities : Implementation of a robust S&OP process with our sales force, management of the process in coordination with Marketing and Sales Weekly management of the MRP inputs and outputs, including procurement requests and manufacturing work orders Revamp of product supply strategies – safety stocks, economical quantities, VMI, integration of subsidiary inventories into a global approach Collaborate within the supply chain team and with the other department to manage supply aspects in situations of product launch, growth and discontinuation Risks and bottlenecks assessment and management for internal and external materials flows Sharing of best planning processes with the existing team Enhancing suite of supply chain KPI’s Contribution to MES and VSM implementation projects Profile we are looking for: Bachelor’s degree in SCM, Purchasing, Engineering, or Business Administration 5+ year of experience in a planning or manufacturing controller role within manufacturing industry, with a preference in medical device area Excellent competencies on XLS, ERP/MRP, with a plus if experience with forecasting software / CRM, MES, DDMRP Excellent communication skills, at ease working in teams while able to lead and influence in areas of expertise and responsibilities Curious and analytical mindset, capacity to synthesize information and prioritize situations Languages: Fluent in French and English is a must.

To strengthen our Clinical Affairs team in Switzerland, we are currently looking for a Senior Clinical Trial Specialist Job description: The Senior Clinical Trial Specialist (Clinical Research Specialist) supports the department by coordinating and executing sponsored clinical studies, from planning activities to archiving of study documentation. Its main role is to set-up clinical investigations for Symbios medical devices products, according to EU Medical Device Regulation, ISO 14155 and other applicable regulations. Responsibilities: Support operational execution of global clinical trials following ISO 14155 and GCP requirements Ensure clinical site management and monitoring activities Track, collect and maintain audit-ready trial documentations, including regulatory submission and study specific essential documents. Maintain compliant clinical trial documentation and quality assurance (TMF) Ensure operational support of clinical study teams including the follow up on open action items Support the Clinical Affairs Manager to allow timely responses to Competent Authority (in Belgium, France and Germany), physicians, other requesters for Clinical Studies topics Develop, implement, and maintain global Symbios database on post-marketing studies, including case report form (CRF) design, data validity check specifications Review clinical investigation protocols and other clinical research documents for identification of data collection needs and compliance with applicable regulations Support data analysis and statistical activities for publication purposes Working closely with the Clinical Affairs Manager to define project targets for external partners and ensure work is documented within the contracted project scope Development and implementation of Clinical Monitoring Plan Coordination and oversight of daily operations of the clinical monitoring team (external partner) Management of project milestones and proactively address deficiencies Management of CRA performance (external partner) Qualifications & Required Knowledge, skills & Experience: Bachelor’s or Master’s degree in Medical Technology, Life Sciences, Clinical Affairs (or equivalent work experience in similar function) 5-7 year’s experience as Trial/Study manager or strong background as Lead CRA 1-2 years of experience in a medical device field (MDD/MDR requirements) specially with regulatory, quality and clinical affairs Good knowledge of the ISO 14155: ICH GCP requirements Ability to work autonomously, exercise daily judgment based on above regulatory/clinical knowledge Result oriented and demonstrated organizational/planning skills based on team priority Fluent in English, French and German General Computer skills (PC, Microsoft Word/Excel/PowerPoint, Outlook/Teams) Ability to travel occasionally in Europe