Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

The MSAT Advanced Formulation Supervisor is responsible for leading and supporting advanced formulation activities within the Manufacturing Science and Technology (MSAT) organization.
The role focuses on formulation development/technology transfer, optimization, scale-up, execution and lifecycle management of pharmaceutical drug product processes, ensuring robust, compliant, and scalable solutions from development through commercial manufacturing.

This position provides technical leadership, supervises a team of MSAT scientists/specialists, and acts as a key interface between clients and internal cross-functional stakeholders (e.g. Engineering, Manufacturing, Quality etc.).

Key Responsibilities

Technical & Scientific Responsibilities

• Lead advanced formulation activities including development / technology transfer, optimization, and troubleshooting of drug product formulations.
• Support technology transfer, scale-up, and process validation activities from development to commercial manufacturing.
• Provide subject matter expertise in formulation science to support manufacturing deviations, CAPAs, change controls, and continuous improvement initiatives.
• Apply scientific principles (e.g., QbD, DoE, risk assessments) to ensure robust and scalable formulations.
• Support lifecycle management activities, including process optimization and introduction of new technologies.

MSAT & Manufacturing Support

• Act as MSAT technical lead for formulation-related topics during manufacturing campaigns, overseeing critical process steps and supporting real-time decision making.
• Collaborate closely with Manufacturing and Quality to ensure processes are capable, reproducible, and compliant with GMP requirements.
• Serve as a technical escalation point between Manufacturing, MSAT, and Quality during production activities.
• Participate in investigations related to formulation or process performance issues.

Leadership & Supervision

• Supervise, coach, and develop a team of MSAT formulation scientists and/or engineers.
• Allocate resources and prioritize activities to meet project and manufacturing timelines.
• Promote a strong safety, quality, and compliance culture within the team.
• Support knowledge sharing and standardization across MSAT and the broader organization.

Minimum Qualifications

• Master’s degree or PhD in Pharmaceutical Sciences, Chemistry, Chemical Engineering, or related scientific discipline.
• Significant experience in pharmaceutical formulation development and/or MSAT within a GMP environment.
• 7-10 year of experience in Pharmaceutical sector and at least 2 years of people management.
• Strong knowledge of drug product manufacturing processes and regulatory expectations.
• Proven experience in technical problem solving and data-driven decision making.

Preferred Qualifications

• Experience with advanced formulation technologies (e.g., sterile products, lyophilization or complex formulations).
• Experience supporting tech transfer and commercial manufacturing.

Key Competencies

• Technical leadership in formulation and MSAT activities
• Strong communication and stakeholder management skills
• Ability to work effectively in cross-functional and fast-paced environments
• Decision-making capability in a regulated GMP setting
• Coaching and people development mindset