
Principal Scientific Manager
4 weeks ago
About Aragen Life Sciences:
Aragen is a trusted partner to the global life sciences industry, offering end-to-end discovery, development, and manufacturing solutions. As a leading Contract Research Organization (CRO) , we are committed to scientific excellence, innovation, and client success.
Role Overview:
We are seeking a highly experienced and motivated Senior/Principal Scientific Manager to lead our Peptide Synthesis function. This leadership role involves managing high-impact peptide synthesis projects, ensuring client satisfaction, optimizing resource utilization, and fostering a high-performance scientific culture.
Key Responsibilities:
Client & Project Management:
- Manage and grow global client relationships; serve as the primary technical contact
- Plan, lead, and deliver multiple peptide synthesis projects on time and within budget
- Drive collaboration, project retention, and client satisfaction
Scientific & Technical Leadership:
- Provide deep scientific guidance in solid-phase and solution-phase peptide synthesis
- Troubleshoot complex synthetic challenges and optimize purification strategies
- Drive innovation through adoption of advanced analytical and purification technologies
Team Development & Leadership:
- Mentor and guide scientific staff; foster continuous learning and development
- Conduct performance reviews and implement recognition and engagement programs
- Build a strong pipeline of scientific talent within the peptide synthesis function
Operational Excellence:
- Optimize usage of manpower, infrastructure, and materials for cost-effective delivery
- Ensure adherence to GLP, safety, IP confidentiality, and data integrity protocols
- Lead continuous improvement initiatives and contribute to business unit growth
Key Qualifications:
- Ph.D. / Postdoctoral Fellowship in Organic or Medicinal Chemistry
- Senior Scientific Manager (M2): 5–8 years of relevant experience
- Principal Scientific Manager (M3): 7–11 years of relevant experience
- Expertise in peptide synthesis (SPPS, solution phase) with hands-on troubleshooting
- Prior experience in CRO/CDMO setups highly desirable
- Strong people management, client handling, and cross-functional collaboration skills
- Research publications in peer-reviewed journals preferred
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