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ZeClinics is HIRING a Laboratory Technician! ZeClinics offers an exciting opportunity for a Laboratory Technician to be part of the team, whose mission is to provide an outsourcing solution for safety and efficacy screenings of novel chemical molecules using zebrafish. The ideal candidate would be responsible for performing experiments and support our Facility Manager in the daily organization of ZeClinics´s Laboratory. Duties of the Laboratory Technician will include: • Perform the experimental tasks related to both scientific services offered by the company to third parties and research and development pipelines., • Analyze the data deriving from experimental approaches., • Ensure the correct use of defined laboratory equipment and maintain them up to date., • Support the Project managers in redacting reports for clients (preparing the text and figures)., • Organize the data derived from the experiments and lab books to ensure full traceability of results., • Support quality validation following GLP-like and GLP regulations and drafting SOPs., • Support in regulatory studies if needed. Studies Holding a Bachelor’s or Master’s degree (and equivalent) in biotechnology, biology, biochemistry, biomedical laboratory science, or a related discipline will be necessary. Experience to value • Proven experience with cellular biology, molecular biology, basic pharmacology, high throughput assays, and other biochemical, molecular, or cellular techniques will be mandatory., • Experience with chemicals administration, microinjection, zebrafish biology, and husbandry will be positively evaluated., • FELASA certification to perform scientific experiments with animals will be a plus. Additional skills • Ability to work independently and interact with several collaborators, • Exceptional organizational skills with strict attention to detail, • Ability to manage multiple projects simultaneously under tight deadlines Languages Good command of Spanish is mandatory, knowledge of English both verbal and written, will be greatly appreciated. The Offer • Duration: Indefinite contract, • Trial period: 3 months, • Estimated annual gross salary: ranging from 23.000 to 25.000 euros per year (depending on experience)., • Flexibility is required to work on weekends during peak service periods, with the preference for having two days per week where weekly and weekend schedules can be interchanged. All applications must include: • A presentation letter addressed to Flavia De Santis and Anna Navarro (Project Managers), • A full CV including contact details, • Two contacts for further references All applications must be sent to the HR DEPARTMENT by e-mail to

¡ÚNETE A NUESTRO EQUIPO EN BARCELONA! 🌟 Posición: Guía Acompañante de Turistas y Gestor de Reservas Tipo de contrato: Indefinido Jornada laboral: Completa (8:30-17:30) Salario: 18.000€ a 20.000€ brutos anuales ¿Quiénes somos? Somos la delegación en Barcelona de un importante touroperador de Tokio, con un equipo entusiasta y dinámico. Buscamos incorporar a un nuevo miembro para apoyar a nuestros viajeros japoneses y brindarles una experiencia única. Requisitos: • Residencia en Barcelona, • Nivel de japonés Noken 3 o superior, con fluidez en la conversación., • Experiencia en atención al público, preferentemente en el sector turístico., • Actitud sociable, proactiva y capacidad para trabajar en equipo., • Titulación preferible en Estudios de Asia Oriental, Traducción e Interpretación, Turismo, entre otras. Funciones: • Asistencia a los turistas y gestión de su experiencia en Barcelona., • Interpretación de patrimonio y cultura local., • Recogida y acompañamiento de viajeros., • Atención personalizada y gestión de reservas y entradas. Si tienes pasión por la cultura japonesa y el turismo, ¡te estamos esperando! Interesados: Enviar CV en castellano y japonés a: ¡Esperamos conocerte pronto y que te unas a nuestro equipo! 💼✨

MAIN DUTIES & RESPONSIBILITIES • Prepare analytical batches to quantify drugs, anti-drugs antibodies or biomarkers in biological matrices by ligand binding assays (ELISA, MSD) according to international guidelines and internal procedures., • Perform the evaluation and treatment of results of analytical batches., • Label proteins with biotin or Sulfo-tag., • Support the Study Director in: (i) the resolution of problems, (ii) the preparation of SOPs and other study documentation., • Carry out maintenance and calibration/verification of laboratory equipment., • Actively support Laboratory Management in evaluating and implementing new processes and equipment. REQUIRED PROFILE & QUALIFICATIONS • PhD, MSc or BSc in biology or related subject., • Minimum 1-year experience in bioanalytical laboratories., • Experience working with ELISA, MSD or other Ligand Binding techniques., • Understanding of international bioanalytical guidelines, and experience working under GLP/GCP regulations., • Experience working with LIMS systems and with cell culture and qPCR techniques will be valued., • Excellent level of English (Spanish – nice to have)., • Proficiency in MS-Office, especially Word and Excel. OTHER REQUIRED SKILLS • Strong communications and organization skills, and capacity to work in teams., • Proactive and hands-on approach., • High level of motivation and enthusiastic personality. WHAT IS OFFERED • Opportunity to work and contribute to the success of an expanding CRO., • Solid scientific team with career growth opportunities., • Cutting edge laboratory with the latest technology., • International and multicultural environment in company based in Barcelona., • Diligent, professional organization, with a human touch. COMPANY DESCRIPTION Anapharm Bioanalytics is a customer-driven Contract Research Organization (CRO) specializing in small and large molecule bioanalysis. With over 30 years of expertise in method development, validation, and sample analysis, the company supports drug development for pharmaceutical and biotechnology industries globally. Anapharm leverages advanced LC-MS/MS and LBA technologies to deliver services such as PK studies, biomarker testing, and immunogenicity assays for preclinical and clinical phases. The organization maintains strict compliance with GLP and GCP standards, having successfully passed multiple regulatory inspections by authorities such as the FDA and EU Health Authorities. Through a global network of partners, Anapharm offers robust full-service solutions for drug development and regulatory approval.

Pharmacokinetic Scientist We’re looking for a skilled Pharmacokinetic Scientist to lead key PK activities across our drug development programs. In this role, you’ll design and interpret studies, serve as a principal investigator, guide ADME/DMPK strategy, and play a central role in supporting both internal teams and external partners. Key Responsibilities • Lead assigned studies as Principal Investigator/Study Director, overseeing all PK-related activities., • Design, execute and interpret pharmacokinetic and pharmacodynamic analyses across preclinical and clinical programs., • Conduct non‑compartmental and compartmental analyses using Phoenix WinNonlin., • Prepare protocols and scientific reports describing study objectives, methodology, analysis and results across multiple species and biological matrices., • Analyse and interpret PK data from a broad range of studies (DMPK, ADME, BE/BA, toxicology, SAD/MAD) and refine sampling and dosing strategies., • Provide expert ADME/DMPK input into non‑clinical and clinical study design., • Ensure full compliance with GLP, GCP, SOPs and sponsor protocols., • Engage with clients, support onboarding, contribute to business development, and present study findings directly to sponsors., • MSc or PhD in Pharmacy, Chemistry, Biochemistry, Biology, Biomedicine or a related life science., • Hands-on experience with toxicology studies, bioavailability/bioequivalence, biomarkers and immunogenicity testing., • Advanced proficiency with Phoenix WinNonlin., • Strong understanding of ADME/DMPK regulatory expectations., • Proven ability to work collaboratively in a matrix environment while managing multiple priorities., • Strong interpersonal and communication skills in fluent English., • Proficient with MS Office tools. About Planet Pharma: Planet Pharma is an American parented Employment Business/Agency that provides global staffing services with its head-quarters in Chicago and our EMEA regional office located in Central London. We have invested significantly in creating a robust international platform that enables us to work compliantly in 30+ countries with a current network of 2500+ active contractors globally as well as a very strong permanent / direct hire recruitment offering. Our specialist knowledge and close relationships with our clients and the wider industry really makes us unique in our field. Just recently we were recognised by FORBES as the 17th best professional staffing firm, and have won multiple awards from industry accredited bodies for our commitment to excellence and service delivery. We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing. We are an equal opportunities Recruitment Business and Agency. We welcome applications from all suitably qualified candidates regardless of their race, sex, disability, religion/belief, sexual orientation or age.

Full-time | Remote (CET / GMT preferred) | €40-45k base + equity Reports to: Digital Health Lead About Hyfe Hyfe is a health technology company using AI to turn cough into a continuous, objective health signal. Our technology is used globally in academic research, clinical trials, and pharma-led studies to generate high-quality cough data as a digital biomarker. We work closely with researchers, clinicians, pharma teams, and CROs who care deeply about evidence, rigor, and real-world impact. The Research Partnerships Associate Role This is a science-led partnerships role, designed for someone early in their career with a medical or scientific background who has recently moved, or wants to move, into healthtech. You´ll work with your Hyfe colleagues to build and maintain strong relationships with researchers, key opinion leaders, and industry partners, supporting early conversations, preparing scientific context, and helping turn interest into long-term collaborations. This is not a traditional sales role. It’s about credibility, organisation, and relationship-building in research-driven environments. What You’ll Do Research upcoming studies, funding calls, and institutions where cough monitoring is relevant Build and maintain target lists across academia, pharma, and CROs Support outreach and early conversations with researchers and partners Prepare background research, briefs, decks, and proposals for meetings Join partnership calls with senior team members; support early opportunity qualification Manage and improve our CRM (HubSpot): contacts, pipelines, follow-ups Support Hyfe’s presence at key scientific conferences and run structured follow-up Over time, you’ll take ownership of academic and early research partnerships. What We’re Looking For (Required) A medical, scientific, or technical background (via education or meaningful professional experience) Evidence of ownership and momentum (e.g. a side project, startup experience, independently launched initiative, or sustained project you drove end-to-end) Comfort engaging with research-driven topics and expert audiences Strong written and verbal communication Highly organised, reliable, and detail-oriented Motivated, curious, and comfortable working with autonomy Nice to Have (Not Required) Exposure to academia, clinical research, healthcare, or digital health Experience using CRM, research tools, or automation / AI tools What to Expect Salary: €40-45k base + equity, depending on experience Fully remote within CET / GMT timezones Budget for home work setup Occasional travel for conferences (mainly Europe) Motivated, friendly, “low-ego” colleagues Work on innovation in health/AI How to Apply We’re using LinkedIn Easy Apply. Please ensure your profile clearly shows your scientific or medical background and any experience working with research, healthcare, or technical teams. The next step will be a 30 minute interview with either the Digital Health Lead, or the CEO.