Senior Consultant

3 days ago


Tuas, Singapore Nityo Infotech Full time

**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

**Experience**:

- GMP- regulated: 5 years (required)
- CSV (computer system Validation): 5 years (required)
- DeltaV: 5 years (required)

Work Location: In person


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