Consultant I

Remotedxb; Dubai; On-site; AED 350,000 - 550,000; Full time

Job summary

Syner-G BioPharma Group in Dubai seeks a senior Project Manager to lead integrated CMC workstreams across drug substance, drug product, analytics, quality, and regulatory activities. You will coordinate end-to-end clinical supplies, forecast demand, schedule manufacturing, and manage inventory.

The role requires a Bachelor's degree in a life sciences field and at least five years of pharmaceutical PM experience, with strong Microsoft Project skills and vendor oversight.

Qualifications

• Bachelor's degree in Life Sciences, Chemistry, Biology, Engineering, or related field.
• 5+ years PM experience in pharmaceutical development or CMC.
• Experience in clinical supplies management and vendor management.
• Proficiency with Microsoft Project.

Responsibilities

• Develop and manage integrated CMC project plans and timelines across multiple workstreams.
• Coordinate end-to-end clinical supplies operations including demand forecasting and inventory management.
• Oversee packaging and labeling for investigational products ensuring GMP compliance.
• Develop and monitor project budgets, forecasts, and program financials.
• Lead project risk management to mitigate timelines or quality issues.
• Coordinate cross-functional teams and external partners (CDMOs/CMOs).
• Prepare and communicate project status reports and dashboards for clients and internal stakeholders.

Skills

Project management

Pharma development

CMC programs

Vendor management

MS Project

Education

Bachelors in Life Sciences

Tools

Microsoft Project

Job description

Responsibilities

• Develop and manage integrated CMC project plans and timelines across drug substance, drug product, analytical, quality, and regulatory workstreams
• Coordinate end-to-end clinical supplies operations, including demand forecasting, manufacturing scheduling, and inventory management
• Oversee packaging and labeling activities for investigational products ensuring GMP compliance
• Develop and monitor project budgets, forecasts, and program financials
• Lead project risk management efforts to mitigate issues impacting timelines or quality
• Coordinate cross-functional teams and external partners including CDMOs and CMOs
• Prepare and communicate project status reports and dashboards for clients and internal stakeholders

Requirements

• Bachelor's degree in Life Sciences, Chemistry, Biology, Engineering, Pharmaceutical Sciences, or a related scientific discipline
• Minimum of 5 years of project management experience supporting pharmaceutical development or CMC programs
• Demonstrated experience in clinical supplies management and vendor management
• Proficiency with project management tools such as Microsoft Project
• Strong understanding of pharmaceutical development and CMC activities

Preferred Qualifications

• Advanced degree
• PMP or equivalent project management certification
• Experience supporting regulatory submissions and health authority interactions
• Experience with commercial supply chain operations and serialization
• Exposure to small molecules, biologics, and advanced therapies

About the Company

Syner-G BioPharma Group is a strategic biopharma product development and delivery partner that accelerates breakthrough science and the delivery of life-enhancing therapies to patients.