MSAT Lifecycle Management Data & Process Specialist (Contract)
Vertex Atriumworks
·Yesterday
- Salary
- $44+
- Location
- Boston, MA, US
- Type
- Contract
- Department
- Management
- Closing date
- Today
- Source
- iCIMS
Description
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.
Lifecycle Management & Regulatory Compliance
- 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.
Process Monitoring & Investigation Support
- 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.
Digital Innovation & Systems Support
- 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.
Operational Agility
- Work effectively in a fast-paced, team-oriented environment while managing routine and repetitive activities, adapting to changing priorities, and consistently following established processes.
Job 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.
Required Knowledge & Skills
- 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
Shift/Hours
Monday–Friday, Hybrid
Requisition Disclaimer
This job posting is for a temporary role with a third-party agency partner on assignment at Vertex Pharmaceuticals (“Vertex”). The individual selected for this role will be offered the role as an employee of a third- party agency partner; compensation, medical benefits, fringe benefits and other terms and conditions of employment shall be presented by the third-party agency partner upon offer. The pay rate range provided is a reasonable estimate of the anticipated compensation range for this job at the time of posting. The actual pay rate will be based on a number of factors, including skills, competencies, experience, location and/or being pursued and other job-related factors permitted by law. In addition, this role will be eligible for overtime pay, in accordance with federal and state requirements
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