MSAT Data & Process Specialist - Hybrid (6Mo)

Vertex Pharmaceuticals LLC; Boston (MA); Hybrid; USD 61,000 - 66,000; Full time

Job summary

Vertex Pharmaceuticals LLC in Boston seeks a MSAT Lifecycle Management Data & Process Specialist to manage, validate, and deliver manufacturing data across the product lifecycle, partnering with MSAT and cross-functional teams to maintain data integrity and support regulated lifecycle activities.

You will work with data systems, Power BI, and associated tools, perform data verification for regulatory submissions, and help generate data-driven reports while following GMP/cGMP standards and

Qualifications

• Bachelor’s degree in a life sciences or related field.
• 0–2 years of relevant experience or internships.
• Experience in GMP-regulated environments or familiar with data integrity concepts.
• Experience with data systems, data entry, verification, management, analysis or reporting.
• Basic knowledge of Python, SQL or C++ is beneficial.
• Solid understanding of statistics and handling scientific/manufacturing data.

Responsibilities

• Enter, review, verify, and approve manufacturing data across global networks.
• Prepare validated datasets for regulatory submissions and cross-functional requests.
• Support CPV and APQR activities with data management and historical datasets.
• Perform data verification for regulatory submissions and technical documentation.
• Generate metrics and data-driven reports to aid compliance and decision-making.
• Follow GMP/cGMP requirements and internal controls in data handling.

Skills

Attention to detail

Communication

Time management

Team collaboration

Data analysis

Statistical understanding

Education

Bachelor’s Degree in Life Sciences, Biochemistry, Process Chemistry, Manufacturing Sciences & Technology, or related field

Tools

Power BI

Microsoft Office

Python

SQL

C++

Job description

Vertex Pharmaceuticals LLC in Boston seeks a MSAT Lifecycle Management Data & Process Specialist to manage, validate, and deliver manufacturing data across the product lifecycle, partnering with MSAT and cross-functional teams to maintain data integrity and support regulated lifecycle activities.

You will work with data systems, Power BI, and associated tools, perform data verification for regulatory submissions, and help generate data-driven reports while following GMP/cGMP standards and