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Do you want to Evolve your professional career and develop your talents? Production Senior Technician. Possession of a science degree will be considered a plus. In Fidia you will have unlimited access to training and coaching programs aligned with market best practices and opportunities for professional development through participation in internal job posting processes, pension fund with company integration and health fund, merit review and referral programs, company canteen, staff discounts and access to the flu vaccination campaign. Fidia Farmaceutici promotes parity and inclusion in all its actions. All people from the status of candidate to that of employee and throughout the duration of their employment relationship are entitled to the same opportunities and protections regardless of gender identity, sexual orientation, ethnicity, migration background, religion, nationality, age. Quality Assurance Expert. The position is also open to candidates belonging to Protected Categories L. With the aim of strengthening the network of medical representatives in the Joint Care area, we are recruiting a. Medical Representative. Who will represent Fidia Farmaceutici and its products, in contact with health professionals and opinion leaders in the following area:. You'll participate in the validation of the computerized systems with a GMP impact, managing the documentation of the QMS linked to the computerized systems especially those documents linked to data integrity and to the serialization. With the aim of strengthening our Corporate Pharmacovigilance Team in Egypt, we are recruiting a. Clinical Safety Physician. The candidate will provide medical advice to the Clinical Project Teams for the planning, conduction and reporting of clinical studies developing study protocols, study reports and discussing with CROs and Vendors the Safety Management Plans and other Study Plans e. Data Management Plans , subject enrolment, subject's safety, responses to Competent Authorities. We are recruiting a. Planning Specialist. Main Responsibilities:. Our offer:. Fidia benefits:. Tecnico Manutentore. Maintenance Technician. Reporting to the direct supervisor the outcome of interventions performed, reporting any anomalies or opportunities for improvement, the candidate will ensure the functionality of pharmaceutical machines and plants, in compliance with safety and GMP regulations. If you login for the first time, we invite you to register and follow the instruction that will allow you to keep your CV updated and submit an application. We kindly ask you to fill all mandatory fields and to attach your CV. Our HR team will contact you in case your profile matches the required skills. Skip to Main Content. Home Privacy More. Log in Account Management. Discover all the opportunities to work with us! Choose Your Filters. With the aim of strengthening the Sterile Liquid Production Department of Fidia Farmaceutici Head Quarter, we are looking for a Production Senior Technician who will assist the department manager and shift leaders with process and plant management tasks, ensuring adherence to the department's technical quality standards including procedures, methods, and handling deviations. Fidia benefits: In Fidia you will have unlimited access to training and coaching programs aligned with market best practices and opportunities for professional development through participation in internal job posting processes, pension fund with company integration and health fund, merit review and referral programs, company canteen, staff discounts and access to the flu vaccination campaign. With the aim of strengthening the network of medical representatives in the Joint Care area, we are recruiting a Medical Representative Who will represent Fidia Farmaceutici and its products, in contact with health professionals and opinion leaders in the following area: Monza, Milano Nord. Main Responsibilities: Provide scientific information about the characteristics, therapeutic indications, efficacy, dosing, and side effects of products in the Fidia portfolio to healthcare professionals, in accordance with applicable policies and laws. Collect feedback on products and forward it to the Pharmacovigilance, Medical Affairs, Marketing and Sales departments. Maintain up-to-date file with information from medical professionals. Ensure proper communication with local colleagues and other relevant team members to better manage the business. Achieve goals within approved deadlines and budget while maintaining constant monitoring of KPI's. Requisitions: Degree in scientific disciplines as required by Legislative Decree of and later amendments. Strong results orientation and ability to plan and analyze. Excellent interpersonal and communication skills. Knowledge of the English language, level B1. Our offer: Open ended contract or a first fixed-term contract, will be evaluated on the basis of seniority in the role. Sales Incentive Plan. Collective Bonus. Company car, fuel card and telepass. Daily allowance. Supervising at local level personnel processes, including position changes, promotions and headcount changes. Coordinating closely with function leaders recruiting, selection and on-boarding programs according with business needs. Implementing people development, career development and compensation processes to support attraction and retention in key positions. Supporting head of functions in managing performance management, reward and compensation processes in order to support and maintain a high-performance culture. Ensuring effective labor relations and adherence to local employment law and when necessary, managing industrial relations including relations with external labor organizations. Requirements: Degree and, preferably, a specialization in Human Resources Management. Familiarity with advanced HRIS systems is preferred. Advanced knowledge of written and spoken English and Arabic. Strong results orientation, ability to learn and initiative as well as communication and problem-solving skills. Our offer: Open ended Egyptian contract. Salary between Social and medical insurance. With the aim of strengthening the Quality Department, we are recruiting a Quality Assurance Expert You'll participate in the validation of the computerized systems with a GMP impact, managing the documentation of the QMS linked to the computerized systems especially those documents linked to data integrity and to the serialization. Main responsibilities: Issue the protocols and the validation reports for computerized systems and issue and review quality system procedures. Coordinate the execution of the validation activities envisaged by the VMP by collaborating with the Fidia corporate bodies and with the external companies that carry out the validations themselves. Issue the Validation Project Plan VPP linked to specific projects and coordinate the execution of the defined validation studies. Follow the activities linked to the conformity to the GMP compliance, with special focus to all topics related to data integrity. Review the validation documents issued by the various Fidia corporate bodies and external companies. Issue and keep updated the Plant Document containing the list of computerized systems, Manage software and hardware configuration management by collaborating with the various company functions. Issue quality agreements with SW providers and companies that carry out qualifications and maintenance of computerized systems. Collaborate in carrying out internal and external audits. Requirements: Master's degree in Statistics, Engineering, Biotechnology or other scientific subjects At least 1 year of work experience in the role. Basic knowledge of hardware and software systems e. Problem solving and negotiation skills, as well as ability to learn. Our offer: Open ended contract. Issuing and reviewing quality system procedures with special reference to the raw materials production department. Review of material master records concerning the raw materials production department. Complaint handling of APIs and other raw materials of internal production. Requirements: Master's degree in chemistry and pharmaceutical technology, chemistry, biology, biotechnology, chemical engineering, biomedical engineering or other scientific subjects. Knowledge of the English language at B2 level. Problem solving skills and flexibility, as well as cooperation and teamwork. Belonging to Protected Categories L. Our offer: One-year fixed-term initial contract. Collective Bonus and company Welfare. With the aim of strengthening our Corporate Pharmacovigilance Team in Egypt, we are recruiting a Clinical Safety Physician The candidate will provide medical advice to the Clinical Project Teams for the planning, conduction and reporting of clinical studies developing study protocols, study reports and discussing with CROs and Vendors the Safety Management Plans and other Study Plans e. Main responsibilities: Reviewing and analyzing adverse event reports, clinical trial data, and other safety information related to drugs, medical devices, food supplements and cosmetics under study, identifying and assessing any safety risks associated with study products and making recommendations for managing or mitigating those risks. Contributing to the preparation of regulatory submissions and responding to questions from regulatory agencies regarding the safety and efficacy of products. Participating in ongoing safety surveillance programs to monitor the product safety under development and during the Product Life Cycle Management. Collaborating with Data Monitoring Committees to ensure that data have been reviewed before the review by the Data Monitoring Committees. Acting as a backup for the Risk Management Physician. Requirements: University Degree in Medicine and Surgery years of experience in Pharmacovigilance Knowledge of Clinical Development Processes for drugs and preferably medical devices Knowledge of GVP, PV Legislation and related guidelines Specialization in pharmacology and work experience in clinical research are preferred Proficient knowledge of English language, written and spoken Analytical, communication and team working skills Our offer: Open-ended contract Salary between Ensuring compliance with market requirements. Developing work models and data management useful for measuring and monitoring the planning system in use. At least 5 years of experience in a similar role, with deep knowledge of production planning dynamics and issues in a complex manufacturing company. Good knowledge of English B1 level. Team working, adopting behaviors that favor collaboration. Welcome in our Career page. Preferred Language English US.

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