Remote Associate Director, Oral Solid Drug Product

Servier Pharmaceuticals; Boston (MA); Hybrid; USD 162,000 - 185,000; Full time

Benefits offered by this job

Hybrid work

Competitive benefits

Incentive programs

Job summary

Servier is seeking an Associate Director for Oral Solid Drug Product in Boston, MA. This role focuses on technical stewardship across the product lifecycle, collaborating with MSAT and external manufacturers to ensure robust processes and compliance.

You will lead cross-functional teams, drive technology transfers, and support regulatory submissions. The ideal candidate has 8+ years of drug product formulation and manufacturing experience, strong GMP/ICH knowledge, and excellent communication

Qualifications

• Bachelor's degree in pharmaceutical sciences or chemical engineering with relevant experience.
• Experience with regulatory submissions and GMP expectations.
• Strong knowledge of oral solid dosage forms and manufacturing processes.

Responsibilities

• Provide technical oversight of manufacturing processes for oral solid products across internal sites and CMOs.
• Lead cross-functional technical teams and manage project timelines, budgets, and risk.
• Support tech transfers, scale-up, PPQ, and lifecycle management activities.
• Prepare and review regulatory documentation and CAPA investigations.

Skills

Strong cross-functional leadership

Excellent communication

Project management

Analytical mindset

Education

Bachelor's in Pharmaceutical Sciences or Chemical Engineering

Master's or PhD in Pharmaceutical Sciences or Chemical Engineering

Tools

Minitab

JMP

Job description

Servier is seeking an Associate Director for Oral Solid Drug Product in Boston, MA. This role focuses on technical stewardship across the product lifecycle, collaborating with MSAT and external manufacturers to ensure robust processes and compliance.

You will lead cross-functional teams, drive technology transfers, and support regulatory submissions. The ideal candidate has 8+ years of drug product formulation and manufacturing experience, strong GMP/ICH knowledge, and excellent communication