Trabajos facility services en Sant CugatCrear alertas

Ventós Group is an international company specialized in the distribution and production of Essential Oils & Aroma Chemicals, with Headquarters located in Barcelona, Spain. The group has 8 subsidiaries around the world. We believe our people are our most important asset, so we offer a dynamic international working environment with constant opportunities for development. Following our growth and expansion strategy, we are looking to strengthen our Facility & Projects team by incorporating an Infrastructure Project Manager. Responsibilities: • Planning management and coordination of tasks related to facility refurbishment and adaptation, • Coordination and contracting of suppliers and service providers, • Oversight of technical equipment: compressors, generators, scales, pumps, HVAC systems, hot water systems, electrical systems, fire protection systems, loading docks, etc., • Management of services: installers, roofing, masonry, painting, drywall, gardening, flooring, etc., • Review and application of relevant regulations: APQ (chemical storage), local licenses, minimum surface requirements, etc., • Facility management and support for infrastructure improvements, • Approval of expense budgets, • Feasibility studies for investments and budgets, • Providing technical solutions to new proposals, • Managing security and camera systems providers, • Handling environmental activity licenses, • Inspection and monitoring of fire protection systems, odor control systems, and other facility infrastructure, • Providing support to subsidiaries (tanks, installations, warehouse capacity, etc.) Profile: • Degree in Industrial, Civil, or Mechanical Engineering, or similar, • 5 years of experience in construction and facility installations, • Valuable: Additional training in Project Management (PMP), Facility Management, or Occupational Risk Prevention, • Prior experience in infrastructure and facility adaptation projects (industrial buildings, logistics centers, etc.), • Experience coordinating and managing technical suppliers (installation, maintenance, industrial services), • Practical knowledge of technical systems: HVAC, electricity, fire protection, pumps, weighing systems, etc., • Used to working with public administrations for permits and licenses, • Strong knowledge of applicable regulations: APQ, fire safety, urban and environmental norms, • Ability to read and follow technical drawings and blueprints, • Knowledge of preventive/corrective maintenance, inspections, and infrastructure upgrades, • Experience managing budgets and investments using tools such as advanced Excel, ERP systems, or project management tools, • Familiarity with security systems and CCTV What do we expect from you? • A motivated, proactive, and organized person, eager to learn and grow, • Ability to work autonomously and make technical decisions, • Good communication skills for internal and external collaboration, • Comfortable working in multidisciplinary teams and dynamic environments, • Previous experience providing technical support to subsidiaries or other business units is a plus Additional Information: We offer a benefits package which includes: • Remote work: 1 full day and 2 afternoons per week, • Flexible working hours, • Free language classes and access to other training courses, • Health insurance, • Shared spaces for after-work activities, • Subsidized meals and breakfast service, • Corporate paddle tennis court for employees and their families Do you think that your professional profile fits and that this could be a good project for you? Send us your application and tell us why!

Leanbio is a leading Biopharmaceutical CDMO offering end-to-end services in the field of recombinant proteins, mRNA and pDNA. With over a decade of expertise, we have a proven track record in development and manufacturing of therapeutic molecules such as antibodies, Fab fragments, ADCs, enzymes, complex proteins, mRNA and pDNA. Leanbio has already worked with over 100 candidates over these years, some already in late clinical stages. Leanbio is expanding its development and manufacturing capabilities with a new GMP site in Barcelona with over 4,000 sqm. and three manufacturing areas: one for mammalian expression systems up to 2000L, another for microbial and yeast up to 1000L, and a third are for mRNA up to 50L. The new facility includes state-of-the-art development laboratories, oustanding Quality control rooms and warehouse. Leanbio is a global service provider for the development and manufacturing of biologics. Our commitment to excellence is evident in everything we do: • Prioritizing customer satisfaction., • Providing cutting-edge end-to-end services., • Utilizing state-of-the-art facilities., • Offering extensive expertise in biologics. We are looking for a new person to join the QC as an analyst to work in our brand new facilities in Sant Quirze del Vallès: MAIN RESPONSIBILITIES: • Perform routine and non-routine physicochemical analyses of raw materials, intermediates, and finished products using techniques such as:HPLC (High-Performance Liquid Chromatography), Karl Fischer titration (moisture determination), FTIR / IR (identification of materials), Loss on Drying (LOD), Potentiometric titrations, Residue on Ignition (ROI), pH, conductivity, osmolality, TOC, etc., • Carry out sampling and analysis of water systems, including:Water for Injection (WFI), • Support environmental monitoring activities, including:surface and air sampling in classified areas., • Ensure strict adherence to GMP and ALCOA++ data integrity principles, maintaining complete, accurate, and traceable documentation., • Document all activities clearly and contemporaneously in lab notebooks, logbooks, or electronic systems (e.g., LIMS), in compliance with internal SOPs., • Participate in quality system activities, such as investigation of OOS / OOT results reporting of deviations and support in CAPA implementation., • Maintain and calibrate laboratory equipment, performing routine checks and informing of any malfunction or need for maintenance., • Follow safety protocols and contribute to keeping the lab in a clean condition at all times., • Collaborate with cross-functional teams, including QA, production, and validation, when needed. REQUIREMENTS: • Advanced Training in Laboratory Analysis and Control with 2–5 years of experience in Quality Control in a GMP-regulated pharmaceutical environment., • Practical experience in physicochemical testing including HPLC, Karl Fischer, IR, Loss on Drying, potentiometric titrations, and Residue on Ignition., • Skilled in sampling and analysis of pharmaceutical water systems (WFI, Purified Water) following USP/EP methods., • Familiarity with environmental monitoring in cleanroom environments is an asset., • Strong knowledge of ALCOA++ principles and GMP documentation practices., • Experience with quality systems (OOS, deviations, CAPAs, change control)., • Proactive team player with good organizational skills and the ability to work independently., • Fluent in Spanish with basic to intermediate English communication skills (reading/writing preferred).

Leanbio is a leading Biopharmaceutical CDMO offering end-to-end services in the field of recombinant proteins, mRNA and pDNA. With over a decade of expertise, we have a proven track record in development and manufacturing of therapeutic molecules such as antibodies, Fab fragments, ADCs, enzymes, complex proteins, mRNA and pDNA. Leanbio has already worked with over 100 candidates over these years, some already in late clinical stages. Leanbio is expanding its development and manufacturing capabilities with a new GMP site in Barcelona with over 4,000 sqm. and three manufacturing areas: one for mammalian expression systems up to 2000L, another for microbial and yeast up to 1000L, and a third are for mRNA up to 50L. The new facility includes state-of-the-art development laboratories, oustanding Quality control rooms and warehouse. Leanbio is a global service provider for the development and manufacturing of biologics. Our commitment to excellence is evident in everything we do: • Prioritizing customer satisfaction., • Providing cutting-edge end-to-end services., • Utilizing state-of-the-art facilities., • Offering extensive expertise in biologics. We are looking for a new person to join the QA as a Specialist to work in our brand new facilities in Sant Quirze del Vallès: MAIN RESPONSIBILITIES: • To build, with the Head of Quality Assurance oversight, the Quality Management System creating and/or approving Standard Operating Procedures to support GMP manufacturing activities., • To build and manage the Documentation Management System and associated training., • To lead the supplier qualification program, approving new suppliers and managing supplier status during its life cycle., • To review Technical Agreements between the company and suppliers/clients., • To review batch documentation for release purposes., • To support facility, utilities and equipment qualification activities, approving protocols and final reports as well as managing related change control records. REQUIREMENTS: • Bachelor’s degree in a Science field with proven experience in GMP Quality Assurance roles., • In-depth knowledge managing Quality Management Systems (deviations, CAPA, change controls, audits and supplier qualification)., • Experience in batch release activities acting as QP deputy will be a plus., • Experience in facilities, utilities and equipment qualification., • Outstanding problem-solving and decision-making skills., • Team player, excellent verbal and written comunication skills (both Spanish and English) and strong analytical and organizatonal skills.

Leanbio is a leading Biopharmaceutical CDMO offering end-to-end services in the field of recombinant proteins, mRNA and pDNA. With over a decade of expertise, we have a proven track record in development and manufacturing of therapeutic molecules such as antibodies, Fab fragments, ADCs, enzymes, complex proteins, mRNA and pDNA. Leanbio has already worked with over 100 candidates over these years, some already in late clinical stages. Leanbio is expanding its development and manufacturing capabilities with a new GMP site in Barcelona with over 4,000 sqm. and three manufacturing areas: one for mammalian expression systems up to 2000L, another for microbial and yeast up to 1000L, and a third are for mRNA up to 50L. The new facility includes state-of-the-art development laboratories, oustanding Quality control rooms and warehouse. Leanbio is a global service provider for the development and manufacturing of biologics. Our commitment to excellence is evident in everything we do: • Prioritizing customer satisfaction., • Providing cutting-edge end-to-end services., • Utilizing state-of-the-art facilities., • Offering extensive expertise in biologics. We are looking for a new person to join the team as a Marketing Manager in our brand new facilities in Sant Quirze del Vallès: MAIN RESPONSIBILITIES: • Marketing strategy development and execution., • Lead generation and campaign management (digital, events, etc)., • Measure ROI and performance of all marketing activities using KPIs and analytics., • Content Creation & Brand Messaging. Create compelling, scientifically accurate content for web, social media, brochures, whitepapers, case studies, and videos. Maintain brand consistency across all platforms and communications., • Digital Marketing & Website Management., • Plan and manage company participation in events and fairs. Coordinate logistics, branding, promotional material, and follow-up activities with BD. Fairs preparation, assistance and follow-up., • Work creatively and analytically in a problem-solving environment demonstrating teamwork, innovation and excellence., • Market Intelligence & Competitive Analysis: Monitor market trends, customer needs, and competitor positioning in the DS/CDMO space. Provide insights and strategic recommendations to BD and leadership teams., • Business Development Support: develop marketing collateral (presentations, flyers, technical overviews) for the BD team., • Budget & Vendor Management: Manage the marketing budget, external agencies, designers, and other vendors to deliver cost-effective campaigns., • Stakeholder Collaboration: Work closely with internal teams (BD, Technical, PM, Regulatory) to ensure accurate, aligned messaging., • Act as the marketing voice within cross-functional planning and client targeting., • Collaborate on RFP responses and client-specific materials, if needed., • Participate in establishing practices, templates, policies, tools and partnerships to expand and mature these capabilities for the organization., • Develop and deliver progress reports, proposals, requirements documentation and presentations to various audiences, including project team, BD Director, sponsors, and other key stakeholders., • Deliver appropriate and effective executive level communication., • Continue professional development in order to keep abreast of emerging technologies, methods and best practices., • Support in Business Plans. REQUIREMENTS: • Bachelor's Degree in Marketing, Communications, Life Sciences or equivalent work experience., • MBA or master’s in marketing, Life Sciences, or Business is a plus., • 5+ years of marketing experience for complex services. At least 2 years in CDMO, pharma, or biotech industry., • 5+ years of experience working with business stakeholders within a cross-functional matrix environment., • 3+ years of previous experience with Market research and analysis, Digital Marketing (SEO, social media, content marketing, etc), and Data-Driven Decisions to measure ROI and performance., • Technical skills are also desirable. It will be highly desirable Industry-Specific Knowledge and deep understanding of the pharmaceutical value chain, regulatory environment (e.g., FDA, EMA), and B2B marketing dynamics in a CDMO setting. Ability to grasp and communicate technical aspects of drug development, manufacturing, and analytical services., • High English level to understand complex technical and business discussions (written and spoken), communicate fluently and effectively in professional settings. Write clear, well-structured messages, communications, and emails. Present ideas for marketing activities and adapt the communication style for different audiences (scientific, commercial, regulatory)., • Intermediate level of proficiency with CRMs (PipeDrive, Salesforce, etc), MS Project, Excel, Visio, PowerPoint and SharePoint with experience presenting to stakeholders and / or Senior Leadership., • Proven ability to demonstrate a drive for results and accountability of business needs., • Proven ability to work in an ambiguous environment and collaborate across multiple areas in order to achieve a common business objective., • Interpersonal skills to influence and spur change, facilitate and enhance performance within a cross - functional environment., • Demonstrate decisiveness in resolving business problems, making decisions and identifying priorities.