More jobs:
MSAT Lifecycle Management Data & Process Specialist
Job in
Boston, Suffolk County, Massachusetts, 02298, USA
Listed on 2026-09-29
Listing for:
Vertex Pharmaceuticals LLC
Full Time, Contract
position Listed on 2026-09-29
Job specializations:
-
Business
Regulatory Compliance Specialist
Job Description & How to Apply Below
Job Description
The MSAT Lifecycle Management Data & Process Specialist supports the management, validation, and delivery of commercial manufacturing data across the product lifecycle. This role partners with MSAT and cross-functional teams to maintain data integrity, support regulated lifecycle management activities, and ensure accurate and consistent execution of established data processes.
Key Responsibilities:Departmental Data Stewardship & Distribution
- Enter, review, verify, and approve manufacturing data from global internal and external manufacturing networks within validated databases, ensuring information is complete, accurate, and traceable.
- Prepare and provide validated datasets and manufacturing process information to support regulatory submissions, agency responses, technical studies, and routine or ad hoc cross‑functional requests.
- Support Continuous Process Verification (CPV) activities and Annual Product Quality Review (APQR) reporting by managing global manufacturing data and maintaining complete and accurate historical datasets.
- Execute and support Data Verification (DV) activities associated with regulatory submissions, agency information requests, and technical documentation.
- Perform data management activities in accordance with GMP/cGMP requirements, data integrity standards, established procedures, and internal controls.
- Review manufacturing datasets to identify trends, discrepancies, Out-of-Trend (OOT) results, Out-of-Specification (OOS) results, or other potential data or process concerns.
- Support MSAT teams with process trending, technical investigations, CPV-related activities, and cross‑functional manufacturing data reviews.
- Generate metrics, summaries, and data‑driven reports to support compliance, process monitoring, and departmental decision‑making.
- Consistently execute structured and repetitive data processes with a high level of accuracy, organization, and attention to detail.
- Work with Microsoft tools, data systems, Power BI, automation or workflow tools, and other digital platforms used to support data management and reporting activities.
- Support continuous improvement and digital initiatives by learning new systems quickly and utilizing automation, AI‑based tools, and other technologies where appropriate.
- Work effectively in a fast‑paced, team‑oriented environment while managing routine and repetitive activities, adapting to changing priorities, and consistently following established processes.
Requirements & Qualifications:
Education & Experience
- Bachelor’s Degree in Life Sciences, Biochemistry, Process Chemistry, Manufacturing, Manufacturing Sciences & Technology (MSAT), or a related scientific discipline;
Engineering degrees with a Life Sciences concentration may also be considered. - 0–2 years of relevant professional, internship, co‑op, or industry experience; recent graduates with relevant academic experience may be considered.
- Experience or exposure to a GMP-regulated or similarly regulated industry environment.
- Experience working with data systems or performing data entry, verification, management, analysis, or reporting activities.
- Basic knowledge of Python, SQL, C++, or other coding/programming concepts is beneficial.
- General understanding of statistics and comfort working with scientific, technical, or manufacturing data.
- Strong attention to detail with the ability to maintain accuracy while performing structured and repetitive tasks.
- General comfort with digital systems and tools, including Microsoft applications, with the ability to quickly learn new software and internal platforms.
- Strong organizational and time‑management skills with the ability to manage a meaningful workload in a fast‑paced environment.
- Ability to consistently follow established procedures, work reliably within regulated processes, and adapt to changing priorities.
- Strong communication, collaboration, and team‑oriented skills with a willingness to learn and take on new responsibilities.
Contract length: 6 months, with the possibility of extension.
Pay Range$44/hr.
- $48/hr
Monday–Friday, Hybrid
No C2C or Third-Party Vendors
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