Senior QC Scientist, Program Management

Catalent Pharma Solutions; Glen Burnie (MD); Presencial; USD 110.000 - 120.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Medical/Dental/Vision

Tuition Reimbursement

Paid Time Off

8 Holidays

Descripción de la vacante

Catalent Pharma Solutions seeks a Senior QC Scientist - Program Management to coordinate testing workflows and serve as the primary QC liaison with clients and internal teams onsite in Harmans, MD. The role emphasizes maintaining testing timelines, regulatory compliance, and strong cross‑functional collaboration.

The position demands 4–8 years in QC, GMP/ICH knowledge, and excellent communication. Onsite work with potential off-hours to support campaigns and deadlines.

Formación

• Bachelor’s degree in a life sciences or related field with 4–8 years in QC.

Responsabilidades

• Serve as the primary QC liaison for clients and internal teams, aligning testing requirements, deliverables, and timelines.
• 2: Coordinate QC activities across Project Management, Process Development, Analytical Development, QC, and QA for GMP readiness.
• 3: Manage internal and external testing execution, including method transfers and outsourced testing.
• 4: Oversee sample management, reagents, shipments, and logistics.
• 5: Establish and coordinate stability programs with clients and internal teams.
• 6: Generate and maintain sampling plans and testing schedules.
• 7: Develop project trackers to monitor QC milestones and progress.
• 8: Align manufacturing schedules with QC testing activities for timely reporting.
• 9: Communicate QC updates and results to clients and stakeholders.

Conocimientos

GMP knowledge

Cross-functional collab

Project coordination

Communication skills

Analytical thinking

Regulatory understanding

Educación

Bachelor’s degree in Biology/ Chemistry/ Engineering/ Pharmacy/ IT

Herramientas

MS Office Suite

Microsoft Project

Smartsheet

Descripción del empleo

Catalent Pharma Solutions seeks a Senior QC Scientist - Program Management to coordinate testing workflows and serve as the primary QC liaison with clients and internal teams onsite in Harmans, MD. The role emphasizes maintaining testing timelines, regulatory compliance, and strong cross‑functional collaboration.

The position demands 4–8 years in QC, GMP/ICH knowledge, and excellent communication. Onsite work with potential off-hours to support campaigns and deadlines.