Senior MS&T Manager, Commercial Pharmaceutical Manufacturing

Veloxis Pharmaceuticals, Inc.; Cary (NC); Hybrid; USD 160,000 - 175,000; Full time

Job summary

Veloxis Pharmaceuticals, Inc. in Cary, NC is seeking a Senior Manager for Manufacturing Sciences & Technology (MS&T) to lead the science strategy for a high-volume commercial program.

The role emphasizes coating robustness, dissolution performance, and CPV across the network and requires regular on-site collaboration with a CDMO partner. The position oversees process development, PPQ validation, lifecycle management, and cross-functional leadership across QA, QC, regulatory, and supply, while

Qualifications

• 10+ years of pharmaceutical or biotech manufacturing experience.
• Experience with technology transfer, process validation, CPV, and change controls.
• Experience with film-coated, modified-release dosage forms and dissolution testing.
• Experience supporting a high-volume commercial program and parallel scale-up.
• Experience supporting regulatory inspections and global submissions.
• Ability to mentor junior staff in a global organization.

Responsibilities

• Lead MS&T product strategy for a high-volume commercial program (100+ batches/year).
• Act as MTO lead for inspection readiness and activities.
• Develop and execute manufacturing science strategies ensuring regulatory compliance and operational excellence.
• Provide technical leadership for campaigns and scale-ups at the CDMO.
• Ensure robust, compliant, validated processes with strong dissolution performance.
• Drive continuous improvement across the program.

Skills

Fluent English

Technical leadership

Coaching

Cross-functional

Problem solving

Education

Bachelor's degree in Engineering or related

MS/PhD/MBA preferred

Job description

Veloxis Pharmaceuticals, Inc. in Cary, NC is seeking a Senior Manager for Manufacturing Sciences & Technology (MS&T) to lead the science strategy for a high-volume commercial program.

The role emphasizes coating robustness, dissolution performance, and CPV across the network and requires regular on-site collaboration with a CDMO partner. The position oversees process development, PPQ validation, lifecycle management, and cross-functional leadership across QA, QC, regulatory, and supply, while