Responsibility over the development, scale-up, registration/validation of drug substance, particle engineering and drug development programs in compliance with legislation and regulatory standards of Quality, HSE and cGMP policies. Oversees the manufacturing process for clinical or commercial supplies of materials in cooperation with areas and supports safety/hazard analysis and other technical support areas as required. Promotes the scientific excellence and innovation in the area and contributes with technical expertise to expand the Intellectual Property, product and technology portfolios.
ID
2024-10682
Location
PT-Lisbon
# of Openings
1
Job Family
R&D
Job Post Information* : Posted Date
2 weeks ago(2025/9/1 10:37)
Hovione is a global CDMO dedicated to helping pharmaceutical clients bring innovative therapies to market. We are now hiring a Senior Quality Manager to join our Lisbon-based team. This role is a strategic leadership position with oversight of quality systems, compliance, and regulatory readiness for our manufacturing operations, with a focus on API, raw materials, and drug product environments.
We are seeking an experienced professional from the
ID
2023-9774
Location
PT-Lisbon
# of Openings
1
Job Family
QUALITY
Job Post Information* : Posted Date
2 months ago(2025/7/16 15:20)
- Provide scientific leadership and act as a subject matter expert in analytical development to support R&D process development and other relevant areas.
- Collaborate effectively with internal and external stakeholders to optimize experimental design, troubleshoot technical challenges, perform sample analysis, interpret data, generate reports, and communicate results promptly to key project stakeholders.
- Recommend and oversee the analytical characterization package (chemical, physical, performance) while ensuring the quality and...
