Location: North Carolina
Type: Long-Term Contract

About the Role:

We are seeking an Engineering Manager/CQV Specialist to support biopharmaceutical projects by ensuring compliance, data integrity, and efficient project execution. You will develop reporting tools, lead stakeholder meetings, and optimize workflows while collaborating with cross-functional teams.

Key Responsibilities:

• Develop automated Excel tools for data analysis and reporting.
• Conduct audits of engineering deliverables to ensure data accuracy.
• Lead weekly stakeholder meetings (CQV, Engineering, Vendors) and track action items.
• Create process workflows using Microsoft Visio.
• Maintain project SharePoint sites and ensure documentation compliance (GDP).
• Support system list reviews against P&IDs, AF&IDs, and SLDs.
• Prepare and deliver project updates to stakeholders.

Qualifications:

• Education: Bachelor’s in Chemical Engineering + 2 years’ experience OR Master’s + 1 year.
• Experience: 1+ years in biopharmaceutical projects; liaising with departments/PMs.
• Skills:
  • Advanced Excel (VBA a plus).
  • Proficiency in Word, PowerPoint, Visio.
  • Strong leadership, communication, and problem-solving.
  • Ability to meet deadlines in a fast-paced environment.