MSAT Lifecycle Management Data & Process Specialist

Intellectt INC
  • Boston, MA
  • Instant Apply
8 days ago

Job Description

Position: MSAT Lifecycle Management Data & Process Specialist
Location: Boston, MA Hybrid (2 3 days onsite)
Duration: 2+ Years

Job Summary:
This role supports the management, validation, and delivery of commercial manufacturing data across the product lifecycle. The specialist will work with MSAT and cross-functional teams to maintain data integrity, support regulated lifecycle management activities, and execute established data processes accurately.

Key Responsibilities:

  • Enter, review, verify, and approve manufacturing data from global internal and external manufacturing networks using validated databases.
  • Prepare validated datasets and manufacturing process information for regulatory submissions, agency responses, technical studies, and cross-functional requests.
  • Support Continuous Process Verification (CPV) and Annual Product Quality Review (APQR) reporting.
  • Perform Data Verification (DV) for regulatory submissions, agency requests, and technical documentation.
  • Maintain data in compliance with GMP/cGMP, data integrity standards, procedures, and internal controls.
  • Review manufacturing data for trends, discrepancies, OOT, and OOS results.
  • Support process trending, technical investigations, CPV activities, and cross-functional data reviews.
  • Generate metrics, summaries, and reports for compliance and process monitoring.
  • Utilize Microsoft applications, data systems, Power BI, and workflow/automation tools.
  • Support digital improvement initiatives and perform structured data activities with a high level of accuracy.

Qualifications:

  • Bachelor's degree in Life Sciences, Biochemistry, Process Chemistry, Manufacturing, MSAT, or a related scientific discipline.
  • Engineering degrees with a Life Sciences concentration may also be considered.
  • 2 years of relevant professional, internship, co-op, or industry experience.
  • Recent graduates with relevant academic experience may be considered.
  • Exposure to GMP or other regulated environments.
  • Experience with data entry, verification, management, analysis, or reporting.
  • General understanding of statistics and scientific, technical, or manufacturing data.
  • Strong attention to detail, organization, communication, and ability to follow established procedures.
  • Comfortable working with Microsoft applications and learning new digital systems.
  • Basic knowledge of Python, SQL, C++, or similar programming languages is a plus.

Numbers & Facts

LocationBoston, MA

Skills

  • Analysis Skillsunmatched
  • Automationunmatched
  • Biochemistryunmatched
  • Biologyunmatched
  • C++ Programming Languageunmatched
  • Chemical Processesunmatched
  • Cross-Functionalunmatched
  • Current Good Manufacturing Practice (cGMP)unmatched
  • Data Entryunmatched
  • Data Qualityunmatched
  • Data Setsunmatched
  • Detail Orientedunmatched
  • GMP (Good Manufacturing Practices)unmatched
  • Maintain Complianceunmatched
  • Manufacturingunmatched
  • Manufacturing/Industrial Processesunmatched
  • Metricsunmatched
  • Microsoft Product Familyunmatched
  • Power BIunmatched
  • Procedure Developmentunmatched
  • Process Developmentunmatched
  • Process Manufacturingunmatched
  • Product Lifecycleunmatched
  • Product Reviewsunmatched
  • Programming Languagesunmatched
  • Python Programming/Scripting Languageunmatched
  • Regulatory Submissionsunmatched
  • SQL (Structured Query Language)unmatched
  • Statisticsunmatched
  • Structured Dataunmatched
  • Technical Writingunmatched

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