Track This Job
Add this job to your tracking list to:
- Monitor application status and updates
- Change status (Applied, Interview, Offer, etc.)
- Add personal notes and comments
- Set reminders for follow-ups
- Track your entire application journey
Save This Job
Add this job to your saved collection to:
- Access easily from your saved jobs dashboard
- Review job details later without searching again
- Compare with other saved opportunities
- Keep a collection of interesting positions
- Receive notifications about saved jobs before they expire
AI-Powered Job Summary
Get a concise overview of key job requirements, responsibilities, and qualifications in seconds.
Pro Tip: Use this feature to quickly decide if a job matches your skills before reading the full description.
Tecnimede Group is a 40 years Portuguese multinational company that wants to improve and preserve human life and health through the development, production and marketing of pharmaceutical products with a strong focus on quality and technological innovation. The group covers the entire life cycle of the medicinal products for human use with a strong investment in research and development.
Exporting to more than 100 countries worldwide, it is present in 6 countries (Portugal, Spain, Italy, Morocco, Colombia and Brazil) with a strong focus in expanding internationally and building strategic partnerships.
We are currently recruiting an experienced Project Manager for Pharmaceutical R&D (m/f) to join our team, in Torres Vedras.
If you are looking for innovation and continuous improvement in pharmaceutical processes, this is your opportunity to make a significant impact across our research and development center .
Key Responsibilities:
- Lead end-to-end management of pharmaceutical R&D projects, ensuring adherence to regulatory timelines, scientific milestones, and budgets (including public/private funding applications);
- Coordinate cross-functional teams (CMC, Clinical Operations, Regulatory Affairs, Biostatistics) and optimize collaborations with CROs, academic institutions, and external partners;
- Ensure compliance with ICH-GCP, EMA/FDA guidelines and quality standards;
- Deliver progress reports to executive committees and global stakeholders, focusing on risk management and go/no-go decisions;
Ideal Profile:
- Master’s/PhD in Life Sciences, Biomedical Engineering, Pharmacy, or related field;
- 5+ years of project management experience in pharmaceutical R&D including knowledge of the drug development lifecycle (preclinical to Phase III);
- PMP certification (preferred);
- Fluency in technical English and with experience in global matrix environments;
- Key competencies: transversal leadership, data-driven critical thinking, proficiency in Smartsheet, MS Project, Veeva;
What We Offer:
- Opportunity to work on innovative therapies with real global health impact;
- Access to leadership development programs;
- Competitive compensation package and premium healthcare benefits;
Submit your CV (in English) to:
"In accordance with the provisions of the GDPR and other legislation in force on personal data protection, the contracting company guarantees that the processing of your personal data is lawful, fair, transparent and limited to the purposes for which your data was collected."
Key Skills
Ranked by relevanceReady to apply?
Join Tecnimede Group and take your career to the next level!
Application takes less than 5 minutes