Your new company
Join a multinational pharmaceutical company as CMC Regulatory Affairs Manager, based in Lisbon.
Your new role
This professional will plan, prepare, revise and maintain regulatory CMC documentation for assigned products. Additionally, will develop global CMC strategies in collaboration with internal and external stakeholders, provide regulatory guidance to manufacturing sites, suppliers and partners, and support product lifecycle management. The role also includes assessing product changes, identifying risks and mitigation strategies, and working closely with cross-functional teams and external partners to ensure alignment on product and process changes.
What you'll need to succeed
We are looking for a professional with an academic background in Pharmaceutical Sciences, Chemistry or a related scientific field. At least 5 years of experience in the pharmaceutical industry, including a minimum of 2 years in a CMC role. Strong expertise in CMC lifecycle management, post-approval changes, and a solid understanding of global regulatory requirements (ICH, GMP and international frameworks). Fluency in English, excellent organizational, communication and decision-making skills are essential. Ability to manage complex portfolios, prioritize tasks in a regulated environment and work collaboratively is highly valued.
What you'll get in return
An excellent opportunity to join a global pharmaceutical company offering attractive benefits, career development and a collaborative and dynamic work environment.
What you need to know
If you're interested in this role, click apply now to submit your CV. If this position isn’t the right fit but you're exploring new opportunities, contact us for a confidential career discussion.