MSAT Lifecycle Management Data & Process Specialist (Contract)

MSAT Lifecycle Management Data & Process Specialist executes the completeness validation and delivery of commercial manufacturing data for the Manufacturing Science and Technology (MSAT) department throughout the commercial product lifecycle. Operating within the Lifecycle Management (LCM) group this role serves as the functional oversight for department data from CASGEVY manufacturing. The Specialist coordinates verifies and distributes global data to support cross-functional studies regulatory agency responses and technical investigations within the Commercial Manufacturing & Supply Chain network. This position bridges manual data management with advanced analytics partnering alongside Technical Operations and leveraging generative AI technologies to automate internal workflows ensure data integrity and support product commercialization activities.

Key Responsibilities:

Departmental Data Stewardship & Distribution

• Enter and approve manufacturing data from global internal and external manufacturing networks into internal validated databases.
• Provide validated data packages and manufacturing process content for regulatory submissionsand responses including data verification support. Field prioritize and execute routine and ad-hoc requests to provide datasets for various departmental and cross-functional projects.

Lifecycle Management & Regulatory Compliance

• Support Continuous Process Verification (CPV) deliverables and Annual Product Quality Review (APQR) reporting by managing global site data entry assisting with authoring reports and managing completeness of historical data.
• Execute and sign off on Data Verification (DV) protocols for various regulatory submissions and information requests.
• Ensure all data handling complies with cell and gene therapy (CGT) requirements current Good Manufacturing Practices (cGMP) data integrity guidelines and company internal controls.

Process Monitoring & Investigations Support

• Analyze complex manufacturing datasets to identify Out-of-Trend (OOT) and Out-of-Specification (OOS) anomalies proactively flagging processing issues.
• Partner with other MSAT groups by assisting with trend/process investigations and CPV-related quality events.
• Participate in cross-functional manufacturing data review forums to evaluate proactive process performance monitor key metrics and mitigate operational risks through early anomaly detection.
• Synthesize technical data resolve data issues independently and generate metrics/data-driven reports to support compliance efficiency projects and executive decision-making.
• Provide departmental and cross-functional training on data systems/practices

Digital Innovation & Automation

• Utilize generative AI technologies and partner with Automation DTE and QA teams to test integrate and implement digital tools such as electronic Batch Record (eBR) code readers and AI-driven data automation.
• Evaluate emerging data management software (spanning collection preparation storage analysis distribution and visualization) to improve department-wide workflow efficiency and reduce manual errors.

Operational Agility

• Cross-train team members on automated tools and standardized data verification practices to build department-level resilience.

Job Requirements & Qualifications:

Education & Experience

• Bechlors degree in Life Sciences (or engineering with life sciences concentration) with a minimum of 0-2 year of relevant experience or an equivalent combination of education and experience.
• Direct experience managing preparing and verifying data for technical regulatory/agency reports and questions.
• Demonstrated hands-on experience utilizing generative AI technologies to streamline or automate internal processes.
• Strong background working with data management software configurations spanning data collection preparation storage analysis and visualization.
• Basic knowledge of programming or coding using Python SQL C or a similar programming language
• General understanding of statistical concepts and experience interpreting or analyzing data.

Required Knowledge & Skills

• Strong technical background in therapeutic pharmaceutical manufacturing processes with a preference for Cell & Gene Therapy (CGT) cGMP environments.
• Thorough knowledge of current Good Manufacturing Practices (cGMP) and regulatory requirements related to commercial product lifecycle stages.
• Strong problem-solving and critical thinking skills with the ability to analyze complex datasets and make sound data-driven recommendations.
• Excellent written and verbal communication skills with a proven ability to translate complex technical information for diverse stakeholders and cross-functional teams.
• Strong collaborative and leadership skills to contribute to and provide technical data guidance within project frameworks.

Contract length: 6 months with the possibility of extension.

$44/hr. - $54/hr.

MondayFriday Hybrid

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 addition this role will be eligible for overtime pay in accordance with federal and state requirements

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