Consultant I
Syner-G BioPharma Group
WorldwideFully remoteFull TimeMid LevelConsulting Services
No salary statedPosted 10 days ago1w agoApply link checked 1 hour ago
Why we think you can apply
- Hiring model
- Open worldwide · the employer states no country restriction
- Work from
- Anywhere, the UAE included
Posted 10 days ago · apply link checked 1 hour ago
About the role
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.
What we look for
- Bachelor's degree in Life Sciences, Chemistry, Biology, Engineering, or Pharmaceutical Sciences
- 5+ years of project management experience in pharmaceutical development or CMC programs
- Experience in clinical supplies management
- Experience managing CDMOs and CMOs
- Proficiency with Microsoft Project
Project ManagementMicrosoft ProjectGMPPharmaceutical Development
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Syner-G BioPharma Group
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