Apoiar a execução e o controle operacional dos processos de compra internacional, importação e exportação, assegurando a precisão dos registros sistêmicos, o cumprimento dos requisitos legais e a fluidez das etapas com áreas parceiras.
Responsibilities
Gerenciar, atualizar e auditar informações nos sistemas de gestão (ERP) voltadas a compras internacionais e fluxos de comércio exterior
Acompanhar o cumprimento de exigências aduaneiras e operacionais específicas
Identificar riscos operacionais, reportar desvios com clareza nos canais formais, tratar exceções e apoiar a implementação de melhorias processuais
Auxiliar no monitoramento da performance de prestadores da cadeia de suprimentos internacional (agentes de carga, despachantes, transportadores)
Prestar suporte técnico e reportes de status para áreas parceiras (Supply Chain, Jurídico, Financeiro e Comercial) e integrar projetos multidisciplinares corporativos
Requirements
Formação superior completa em Comércio Exterior
Formação superior completa em Relações Internacionais
At the heart of clinical data management lies a critical challenge: turning complex, evolving business needs into precise, actionable system requirements. As a Requirements Engineer for Clinical Trial Systems, you will play a pivotal role in shaping the quality and integrity of a global Operational Data Repository programme — directly enabling faster, more reliable clinical trial execution across the organisation.
Responsibilities
Own the review, improvement, and creation of Functional Requirement Specifications
Identify gaps, resolve ambiguities, and simplify complex business rules
Facilitate structured requirement reviews with cross-functional stakeholders
Drive meaningful improvements to documentation standards, traceability, and requirement governance
Requirements
Degree in Information Technology, Life Sciences, Business, or a related field
Nice to have: Certified Business Analysis Professional
Nice to have: PMI Professional in Business Analysis
Nice to have: International Requirements Engineering Board certification
Entry point for the first level commercial and regulatory questions from internal and external clients regarding Pharma Chemicals and Process Solution Products, acting as an interface between sales, supply chain, and regulatory affairs.
Responsibilities
Deal with requests regarding Pharma Chemicals and Process Solution Products
Act as an interface between sales organization, supply chain, regulatory affairs, and marketing
Support sales representatives in daily activities to meet sales objectives
Handle quotations, enforce price policy, and develop special prices
Oversee handling of commercial documents (brochures, sample requests, literature, product data sheets)
Perform routine and custom GLP/GMP studies, maintaining good housekeeping, equipment maintenance, and stock control to ensure the smooth running of the laboratories, supporting development and manufacturing processes within the pharmaceutical industry.
Locations (2)
Glasgow, Scotland, United Kingdom
Stirling, Scotland, United Kingdom
Responsibilities
Working within the laboratory in accordance with Standard Operating Procedures and relevant compliance regulations
Ensuring routine studies are completed on time and accurately recorded to meet GLP/GMP and scientific standards
Requirements
HND or higher qualification in a Biological Science discipline
In qualità di Therapeutic Area Specialist Oncology, il tuo ruolo si concentrerà sull'area geografica della Romagna e delle Marche.
Compensation
Annual Base Salary (RAL): €50.000 - €75.000
Variable Compensation (SIP)
Responsibilities
attività di informazione scientifica e di presentazione dei farmaci dell'azienda in commercio presso medici, farmacisti, soggetti non prescrittori coinvolti nella somministrazione della terapia (es. infermieri) presso cliniche universitarie, ospedali, case di cura, dispensari, enti ed istituti sanitari e ogni altra struttura sanitaria autorizzata
Illustrare a medici, farmacisti e soggetti non prescrittori coinvolti nella somministrazione della terapia le caratteristiche farmacologiche e terapeutiche dei farmaci dell'azienda al fine di promuoverne la conoscenza, assicurarne il corretto impiego in modo accurato, responsabile ed etico
Guidare e semplificare l'interazione con gli stakeholder esterni coordinandosi con le altre risorse interne per garantire la migliore customer experience, rispettando la distinzione tra attività promozionali e non, in conformità con tutte le normative vigenti e le SOP interne
Agire come Primary Point of Contact – PPOC - degli stakeholder esterni per le attività di informazione scientifica on-label e di gestione delle richieste dell’account (HCO, Organizzazioni Sanitarie)
Collaborare in sinergia con il Medical Science Expert - MSE
Requirements
Medical Manager - Diabetics
The businesses of Merck KGaA, Darmstadt, Germany · Posted Nov 11, 2026
Responsible for ensuring company compliance with pharmaceutical regulations and laws as well as providing expertise on drug safety and medical topics. Provides medical expert advice to ensure accuracy of data to support existing or new product promotion. Develops medical product information and stays informed on scientific trends and competition. Maintains relationships with target opinion leaders and trains local teams on medical topics.
Responsibilities
Act as Local Medical Affairs TA expert in one or more TAs
Co-leading Local TA, Launch and Brand Strategies and lead the Medical Affairs Tactics
Lead Medical Affairs activities in the assigned territory along defined local Medical Launch / Brand strategies
Responsible for assigning, tracking, and monitoring relevant KPIs and metrics for Medical Affairs
Consolidate and communicate trends, market insights, and unmet needs identified in the field
Requirements
Bachelor’s degree of Pharmacist OR Doctor (general)
Act as a medical responsible and clinical representative in global project/regional team, providing medical/scientific input, overseeing clinical documents, monitoring, and supporting regulatory and business development activities.
Responsibilities
Provide medical/scientific input and drive/contribute to the creation of relevant clinical documents
Review and sign off all clinical documents related to the clinical studies
Conduct medical monitoring for responsible project/study
Oversee all medical scientific aspects of the trial and provide guidance
Support the review, analysis and interpretation of study data
As a Service Desk Analyst, you are the first point of contact for users experiencing technical issues across the organization. In this role, you capture and log user issues, categorize and prioritize tickets, and resolve them using prescribed solutions or escalate as required. You ensure timely and accurate updates to users, monitor ticket progress throughout the lifecycle, and contribute to knowledge base improvements, KPI and SLA adherence, and seamless shift handovers.
Responsibilities
Capture and log user issues
Categorize and prioritize tickets
Resolve issues using prescribed solutions or escalate
Ensure timely and accurate updates to users
Monitor ticket progress throughout the lifecycle
Requirements
Graduate degree, preferably in Computer Science or a related field
