Global CMC Strategy Lead I

Zoetis Inc; Zaventem; On-site; EUR 60,000 - 90,000; Full time

Job summary

Zoetis Inc in Belgium seeks a Regulatory CMC professional to develop global CMC strategies for pharmaceutical dosage forms and support regulatory submissions across development and post-approval changes. You will collaborate with manufacturing sites and contract manufacturers, delivering compliant CMC sections for registration and launch. Strong communication and regulatory experience are required.

Travel is possible (<10%). A Bachelor’s degree with 3+ years in regulatory activities is required, with a focus on biologics or pharmaceutical products.

Qualifications

• Bachelor’s degree with at least 3 years in analytical, manufacturing, or regulatory activities supporting biologics, biopharmaceutical, or pharmaceutical products.
• Strong written and verbal communication; regulatory experience preferred.

Responsibilities

• Develop global Regulatory CMC strategies for pharmaceutical dosage forms.
• Support CMC activities for new product development teams, including post-approval changes and site transfers.
• Prepare responses to global health authority questions and information requests.
• Maintain awareness of emerging global CMC regulations; support Zoetis regulatory positions.
• Build relationships with Zoetis manufacturing sites and contract manufacturers for the portfolio.
• Provide regulatory support as a technical liaison to deliver high-quality CMC sections for registration, approval, and launch.

Skills

Regulatory CMC

CMC strategy

Regulatory submissions

Cross-functional collaboration

Regulatory liaison

Education

Bachelor’s degree

Job description

Zoetis Inc in Belgium seeks a Regulatory CMC professional to develop global CMC strategies for pharmaceutical dosage forms and support regulatory submissions across development and post-approval changes. You will collaborate with manufacturing sites and contract manufacturers, delivering compliant CMC sections for registration and launch. Strong communication and regulatory experience are required.

Travel is possible (<10%). A Bachelor’s degree with 3+ years in regulatory activities is required, with a focus on biologics or pharmaceutical products.