 
						Senior Consultant
4 days ago
**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
**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.
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
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