Process Validation Engineer

Must Haves:

• Bachelor's Degree in Engineering, Life Sciences or related field
• 2+ years of process validation experience
• Any experience with sterilize products
• Experience in pharmaceutical manufacturing within a cGMP environment
• Experience authoring technical documentation within a cGMP context

Pluses:

• Experience with responding to regulatory questions with multiple agencies (e.g. FDA, EMA)
• Experience doing a tech transfer
• Cleaning Validation experience
• Experience with sterile injectables

Day to Day:

Insight Global is seeking a Process Validation Engineer in Rocky Mount, NC. You will support a diverse variety of qualification activities for manufacturing processes within a biopharmaceutical manufacturing facility. This role has a heavy focus on process validation and sterilization. You will directly be supporting the manufacturing process validation team for small molecule sterile injectable drug products as they ramp up an new production building.