Ofertas de emprego de fda
26-50 de 79 vagas de emprego
- Lisboa 41
- Porto 7
- Coimbra 5
- Sintra 3
- Torres Vedras 3
- Amadora 2
- Maia 2
- Oeiras 2
- Portalegre 2
- Castelo Branco 1
- Lisboa 52
- Porto 11
- Coimbra 5
- Portalegre 2
- Aveiro 1
- Castelo Branco 1
- Gerente De Marketing 11
- Monitor 7
- Designer 4
- Director 4
- Engenheiro de Qualidade 4
- Analista de dados 3
- Software Tester 3
- Analista De Negócios 1
- Consultor 1
- Consultor de Pmo 1
- hovione 7
- critical manufacturing 4
- bial 2
- Autônomo 4
- Efetivo
- Estágio 2
- Não definido
- Prestador de Serviço
- Temporário
- 12x36
- A combinar
- Jornada flexível
- Período integral 8
- Tempo parcial
- Último dia 29
- Última semana 45
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Associate Director, Global Regulatory Affairs
novo Organon Lisboa, Lisboa
...for their assigned products, in order to optimize label and obtain shortest time to approval by regulatory agencies, including but not limited to US-FDA...
Há 8 h 34 minutos em Talent.comRelatório -
Global regulatory affairs strategy manager
novo ZEISS Group Portalegre, Portalegre
...fda, ema, pmda, nmpa, notified bodies). Proficiency in English; additional languages are a plus. Our Benefits. Opportunities for professional growth and...
Há 17 h 2 minutos em jobs.searchRelatório -
Senior and Principal Biostatistician - FSP
Fortrea Oeiras, Lisboa
...fda, ema) and industry standards. Excellent communication skills, with the ability to effectively collaborate and present complex data to. Technical...
Há 2 dias em Vagas.ptRelatório -
Regulatory Affairs, Senior Specialist/Manager
novo Ergomed Lisboa, Lisboa
...complex technical/scientific/legal documentation. Ensure preparation, collection, review of regulatory information and documents to support submissions to FDA...
Há 8 h 45 minutos em Talent.comRelatório -
Supervisor, Production
novo Hikma Pharmaceuticals Sintra, Lisboa
...manufacturing schedules are developed and executed with no interruptions in the manufacturing processes and in full compliance with SOPs, cGMPs, EU and FDA...
Há 15 h 33 minutos em Talent.comRelatório -
Sr. ITOT Project Manager
novo Hovione Lisboa, Lisboa
...FDA 21 CFR Part 11, EU Annex 11, and data integrity standards. Collaborate with Manufacturing, Quality Assurance, Engineering, and Automation teams to align...
Há 8 h 29 minutos em Talent.comRelatório -
Industrial Equipment & Medical Devices Industry Manager
novo Critical Manufacturing Maia, Porto
...FDA 21 CFR Part 11 for med device), and market dynamics Comfortable drafting whitepapers, articles, or conference presentations tailored to the needs and...
Há 8 h 37 minutos em Talent.comRelatório -
Production transfer specialist
Tecnimede Group Lisboa, Lisboa
...(EMA/FDA). Experience in evaluating CMOs (Contract Manufacturing Organizations) and monitoring compliance. Strong project management and coordination skills...
Há 2 dias em LifeworQRelatório -
Trainee Validation and Qualification Engineer
Hovione Loures, Lisboa
...be responsible to: Performs assembly, qualification and automation of facilities, equipment and utility systems according to regulatory demands (cGMPs, FDA...
Há 6 dias em Vagas.ptRelatório -
Engenheiro Mecânico (M/F)
novo Fortil
...FDA / EMA Experiência com sistemas HVAC, sistemas CIP/SIP, bombas, trocadores de calor, compressores, etc. Capacidade de leitura e elaboração de P&ID...
Há 8 h 44 minutos em Talent.comRelatório -
Senior Regulatory Writing Specialist
novo Med Communications International Lisboa, Lisboa
...in more than 1 therapeutic area. Manages at least 3 single-document projects simultaneously. Working knowledge of: Relevant regulatory guidance (eg, ICH, FDA...
Há 8 h 44 minutos em Talent.comRelatório -
Quality Assurance Specialist
Randstad II - Prestação de Serviços Limitada Vale de Cambra, Aveiro
...de ações corretivas e preventivas (CAPAs) decorrentes de auditorias ou inspeções regulatórias; Garantir a conformidade com os requisitos e diretrizes da FDA...
Há 10 dias em Vagas.ptRelatório -
Fraud Data Analyst
Axians Portugal Lisboa, Lisboa
...Nos o seu currículo, de preferência em inglês -------------------------@axians.comcom o subject "FDA. MM.PL”. Saber mais sobre a Axians#J-18808-Ljbffr
Há Mais de 30 dias em Vagas.ptRelatório -
Project manager – pharmaceutical r&d
Tecnimede Group Lisboa, Lisboa
...EMA/FDA guidelines and quality standards; Deliver progress reports to executive committees and global stakeholders, focusing on risk management and go/no-go...
Há 2 dias em LifeworQRelatório -
Fraud Data Analyst (J)
Axians Portugal Amadora, Lisboa +1 Localização
...Nos o seu currículo, de preferência em inglês -------------------------@axians.comcom o subject "FDA. MM.PL”. Saber mais sobre a Axians#J-18808-Ljbffr
Há 17 dias em Vagas.ptRelatório -
Career Opportunities: Quality Assurance Operations Specialis
BIAL Porto, Porto
...FDA approved manufacturing site (preferential). Solid English skills (B2 minimum); Excellent communication skills and ability to enhance partnerships with...
Há 10 dias em Vagas.ptRelatório -
Medical Consultant - Freelance KOL / SME for Neurology (Pain
novo TFS HealthScience Lisboa, Lisboa
...(FDA/EMA). Excellent communication and stakeholder engagement skills; strong presentation, negotiation, and interpersonal skills for engaging stakeholders...
Bruto/anual: 60.000€
Há 1 dia em JobleadsRelatório -
GxP CSV Specialist. Healthcare
Trinetix Lisboa, Lisboa
...fda, mhra) or audit preparation. Working knowledge of data integrity principles and ALCOA+ framework. Certification in CSV, QA, or GxP compliance (e... ispe...
Há 21 dias em Vagas.ptRelatório -
Senior Regulatory Writing Specialist
Med Communications International Lisboa, Lisboa
...in more than 1 therapeutic area. Manages at least 3. Document projects simultaneously. Working knowledge of: Relevant regulatory guidance (eg, ICH, FDA...
Há 8 dias em Vagas.ptRelatório -
Production Transfer Technician
novo Tecnimede Group Lisboa, Lisboa
...(EMA/FDA). Experience in evaluating CMOs (Contract Manufacturing Organizations) and monitoring compliance. Strong project management and coordination skills...
Há 1 dia em LifeworQRelatório -
Senior Compliance & CQV Engineer
Hovione Lisboa, Lisboa
...FDA guidelines. Key ResponsibilitiesBody of Knowledge & StandardsDevelop and maintain CQV standards, SOPs, and technical guidelines. Provide expert feedback...
Há 21 dias em Vagas.ptRelatório -
Director, Delivery (Europe)
ValGenesis Lisboa, Lisboa
...Director, Delivery (Europe) leads. Centric consultative. Based technical delivery of projects primarily, but not exclusively, across Europe. The position is responsible for managing a. Performing services team, driving life sciences customers’ success, and ensuring that every client achieves value through the adoption of ValGenesis’ solutions. This role requires a strong background in SaaS implementation, life sciences regulations (GxP, FDA...
Há Mais de 30 dias em Vagas.ptRelatório -
Senior Medical Writer - Europe - Remote
Worldwide Clinical Trials
...in Worldwide preparing and leading the development of Pre-IND documents, synopsis, briefing books for all authorities (FDA, EMA, MHRA, Health Canada
Bruto/anual: 40.000€
Há 3 dias em JobleadsRelatório -
Full Stack Engineer
Atomic Talent Porto, Porto
...stage and looking to bring on their first Python Full Stack Engineer. They have patented diagnostic technology already making a difference to patients, and FDA...
Há 10 dias em Vagas.ptRelatório -
Quality Assurance Operations Specialist
BIAL Trofa, Porto
...FDA-approved manufacturing site (preferential); Excellent communication skills and ability to enhance partnerships with internal and external stakeholders...
Há 10 dias em Vagas.ptRelatório
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