Senior Consultant - Manufacturing

Key Responsibilities

• Lead and support MSAT-related projects in GMP-regulated environments
• Develop and manage detailed project plans, protocols, and reports
• Identify and resolve issues proactively, ensuring project timelines are met
• Engage with clients and internal teams through effective communication
• Oversee document lifecycle: creation, review, approval, and archival
• Conduct data analysis and risk assessments to support project decisions
• Collaborate with cross-functional stakeholders to ensure alignment on deliverables
• Apply systems thinking to troubleshoot and solve technical or operational issues

Required Qualifications

• Experience: Minimum 3 years in a pharmaceutical or GMP-regulated environment
• Background: Experience in one or more of the following:
• Quality Systems & Operations
• Quality Control
• Manufacturing
• Engineering
• Technology Transfer

Regulatory Knowledge: Familiarity with ICH Q7, Q8, Q9, ISO 14644, ANSI Z1.4, etc.

Job Type: Full-time

Pay: $4,500.00 - $7,000.00 per month

Benefits:

• Health insurance

Schedule:

• Monday to Friday
• Shift system

Experience:

• GMP- regulated: 3 years (Required)

Work Location: In person