6697 Palma de Mallorca English-speaking jobs in Madrid

Strategic Account Executive will establish and manage a sales pipeline for ByteDance's AI and MaaS solutions across Europe. Responsibilities include developing and executing go-to-market strategies, driving revenue growth, and ensuring customer satisfaction. Requires 5+ years of B2B sales experience, 3+ years in cloud computing, video cloud, or AI/ML, and a strong understanding of AI technologies and business solutions.

The Sales Development Representative / Market Insights Team will collect and organize sales leads for AI products in the Europe and Israel market. Responsibilities include lead generation, lead grading, and distributing leads to Account Executives. The role requires 3+ years of experience in technology-related business development, SDR/Inside Sales, or lead generation.

The Test Development Engineer oversees and conducts battery cell testing to ensure performance, safety, and reliability. Responsibilities include managing test procedures, data analysis, equipment maintenance, and process improvement. Requires a Master's degree in a relevant field and 5+ years of experience in battery cell testing.

The Installation and Commissioning Engineer (I&C) contributes to project success by managing and executing tasks aligned with I&C objectives. The role involves extensive travel within EMEA and to APAC. Assignments include Process Commissioning Engineer, Commissioning Team Leader, or Site Manager, depending on project size and complexity. Responsibilities include installation qualification, operational qualification support, documentation management, performance qualification support, customer training, coordinating commissioning teams, and ensuring project site plan compliance. Minimum qualifications include a graduate degree in a relevant field, 4+ years of experience in process engineering or commissioning, and fluency in English.

RTO Consultant will implement AVEVA Process Optimization (APO) software in Refinery and Petrochemical units. Responsibilities include application maintenance, acting as a technical interface with customers, ensuring project requirements are met, and troubleshooting technical problems. Requires 10+ years of experience in Refinery and/or Petrochemical operations optimization and expertise in rigorous refinery process simulation packages or advanced control. Fluency in English is essential.

Accenture seeks a results-driven SAP manager with experience in High-Tech industries. The ideal candidate will lead end-to-end SAP implementation projects, provide strategic guidance, and build strong client relationships.

Senior SAP Specialist will analyze business needs, design SAP processes, customize modules, execute testing, and provide user training. Requires 4-6 years of SAP PP experience, integration knowledge, and English proficiency.

Lead the development and industrialization of a proprietary, next-generation printing hardware platform. Define the technology roadmap, scale prototypes to production, and lead a multidisciplinary engineering team.

Senior Application Scientist will lead creative application approaches for hard capsule developments using Roquette excipients. Responsibilities include defining specifications, conducting experiments, developing manufacturing protocols, and collaborating with other departments. Requires a Master's degree in a relevant field, 8+ years of experience in Pharmaceutics/Galenic, and proficiency in English and relevant software.

Leads global procurement strategy and execution for Marketing Agencies (Creative, PR, Medical Communications) with a USD 800 million spend. Manages a team of 2-5 professionals and aligns global, regional, and local sourcing strategies. Requires 10+ years procurement experience, global leadership, and expertise in marketing agency procurement.

This role is responsible for site management oversight, clinical monitoring, and central monitoring deliverables with a focus on patient safety, protocol/GCP/regulatory compliance, and data integrity. The Local Sr Clinical Trial Manager (CTM II) oversees site interactions post activation through site closeout. This includes patient recruitment, investigator payments, and other related activities. The CTM II reviews the study scope of work, budget, and protocol content and ensures the clinical project team is aware of contractual obligations and parameters. The CTM II employs strategic thinking and problem-solving skills to propose and implement risk mitigations. The CTM II serves as an escalation point for communications with investigator site staff and may be required to interact on the phone or in person with principal investigators or other site staff members. The CTM II collaborates with other functional leaders to coordinate delivery handoffs and meet expected study milestones. The CTM II is responsible for development and ongoing maintenance of clinical study tools and templates, including the Clinical Monitoring Plan. The CTM II coordinates initial and ongoing training to the study team regarding protocol specificities, Case Report Form (CRF) completion, dashboards, Sponsor Standard Operating Procedures (SOPs), clinical plans and guidelines, data plans, and timelines for the

Clinical Research Associates (CRAs) oversee and ensure the integrity of clinical research studies. Responsibilities include monitoring data and processes, verifying compliance with regulations and protocols, and collaborating with site teams. Requires a bachelor's degree, knowledge of Good Clinical Practice/ICH Guidelines, previous monitoring experience in Spain, and strong communication and computer skills.

This role is responsible for site management oversight, clinical monitoring, and central monitoring deliverables with a focus on patient safety, protocol/GCP/regulatory compliance, and data integrity. The Sr CTM oversees site interactions from activation through closeout, including patient recruitment, investigator payments, and risk mitigation. This position requires a Bachelor's degree or RN in a related field, demonstrated ability to lead teams, and expertise in site management and monitoring. Moderate travel (approximately 20%) may be required.

Manages clinical research studies, ensuring compliance with GCP, SOPs, and regulations. Leads project teams, manages budgets, and coordinates activities with study partners. Develops project plans, presents at meetings, and prepares reports. Requires a bachelor's degree in a life science field and experience in a CRO.

The Veeva Vault (OMP) Subject Matter Expert (SME) for Regulated Activities will provide global OMP Services to platform end-users. The OMP SME will become the first point of contact for other OMP squad members, ensuring compliant, consistent, and high-quality use of OMP.

Serves as Functional Lead for Clinical Data Science, ensuring data quality and alignment with study protocols. Coordinates data cleaning activities, develops data acquisition plans, and monitors project progress. Requires hands-on experience with Veeva CDMS and Veeva CDB.

Clinical Operations roles ensure safe and effective clinical research studies. Responsibilities include site management, protocol adherence, document maintenance, and communication with clinical trial volunteers. Requires a high school diploma, good communication skills, and the ability to learn new technologies. Minimal travel up to 25% may be required.

Manages complex clinical trials, including budget responsibility and cross-functional timelines. Leads and mentors teams, independently manages smaller studies, and contributes to employee performance management.

Supervises material sorting, weighing, and movement within a plant. Requires prior experience in the sector and demonstrable backhoe loader operation experience. A Category C driver's license is preferred.

Lead cybersecurity architect to design, develop, and expand advanced cybersecurity services across Africa. Drive solution architecture, pre-sales engagements, and technical delivery excellence.