Quality Specialist

Role – QA Specialist

Location – Pennsylvania

Working type – Permanent

Hours – 9-5 (Monday to Friday)

Company:

Scienta are proud to be partnering with Philadelphia’s leading CDMO in their Quality expansion. They focus on developing and manufacturing Cell and Gene Therapy products which are marketed across the globe and want an ambitious Quality Specialist to join their teams!

What You’ll Do:

• Perform documentation and records review to ensure compliance with GMP standards
• Update and manage all Quality topics related to the QMS
• Investigate quality-related incidents, customer complaints, and develop corrective and preventive action plans.
• Maintain accurate records of quality assurance activities, including incident reports, corrective actions, and Standard Operating Procedures (SOPs).

What You’ll Bring:

• 1 – 2 years Quality experience
• Knowledge of GMP and related standards
• QMS Experience (Veeva OR TrackWise preferred)
• Relevant working experience / Scientific Degree
• Must have the Right to Work in the US