Genetix Biotherapeutics: Developing and commercializing curative gene therapies for rare diseases.
7+ YOE7+ years in industry with 5+ years in CSV within a GxP environment; degree in computer systems/engineering; change control experience; regulatory inspection readiness; Veeva Vaults preferred.
GxP, CSV, GAMP 5, 21 CFR Part 11, EU Annex 11, ICH Q9, ICH Q10, CSA, Veeva Vaults
12+ YOEBachelor's in Engineering/IT/CS, minimum 12 years in pharmaceutical quality/QA/CSV/IT compliance, leadership experience, expertise in 21 CFR and GAMP standards, GMP IT oversight, documentation and regulatory interaction skills.
Veeva Vault RIM Test & Validation Lead (CSV / QEA)
Boston, Massachusetts, United States
$71k-$113k/yrHybridFull Time
CognizantNASDAQ: CTSH: Provides IT consulting and technology services to global enterprises.
3+ YOE3–5 years Veeva Vault RIM configuration/support; 8+ years CSV; life sciences with GxP; regulatory affairs knowledge; experience with regulatory submissions.
Veeva Vault RIM Test & Validation Lead (CSV / QEA)
Boston, Massachusetts, United States
$71k-$113k/yrHybridFull Time
CognizantNasdaq: CTSH: Provides global information technology and business process outsourcing services.
8+ YOE3–5 years Veeva Vault RIM configuration; 8+ years CSV experience; Life Sciences with GxP; Regulatory Affairs and eCTD knowledge; regulatory submission experience.
Bristol Myers SquibbNew York Stock Exchange: BMY: Develops and distributes innovative medicines for serious diseases.
12+ YOEBachelor's in Engineering/IT/Computer Science, 12+ years in pharmaceutical quality/CSV/IT compliance, leadership experience, expertise in 21 CFR and GAMP, QA and validation knowledge, strong technical writing and problem-solving skills.
Verista: Provides compliance, automation, and validation services to life sciences.
5+ YOEBachelor's degree required; 5+ years GMP document control/validation document management; ValGenesis preferred; Autodesk Forma experience; GDP and electronic records fluency; strong organization and communication.
Senior Quality Engineer, Computer System Validation (CSV)
Northbridge or Watertown
$142k-$179k/yrHybridFull Time
EyePoint PharmaceuticalsNASDAQ: EYPT: Clinical-stage developing sustained-delivery treatments for retinal diseases.
3+ YOEBachelor's degree and 3+ years GxP computerized system validation experience in pharma/biotech/medical device; knowledge of GAMP 5, 21 CFR Part 11, EU Annex 11, ICH Q9/Q10 and FDA CSA; strong documentation, risk management, and project leadership skills.
GxP, GAMP 5, 21 CFR Part 11, EU Annex 11, ICH Q9, ICH Q10, FDA Computer Software Assurance (CSA), RCA, FMEA, VSM, ERP
Alegeus: Provides technology platforms for managing healthcare benefit accounts.
End-user technical support experience, SQL and CSV file handling, BS in technical discipline or equivalent, strong analytical and communication skills.
NTT DATA: Global provider of IT and business consulting services.
5+ YOE5+ years NetSuite functional experience with full-cycle implementations as functional lead focused on Manufacturing, PO, Order Management, SuiteFlow, CSV data migration; undergraduate degree in supply chain/manufacturing/business/IS required.
NetSuite, NetSuite WMS Lite, SuiteFlow, SuiteScript, SuiteQL, CSV, Microsoft Word, Microsoft Excel, Microsoft PowerPoint
ModernaNasdaq: MRNA: Develops and manufactures messenger RNA medicines and vaccines.
9+ YOE9+ years experience in pharmaceutical/biotech automation; Bachelor's in engineering (or equivalent); expertise with DeltaV, PLCs, SCADA, AVEVA PI, OPC/Kepware, RESTful APIs, CSV and regulatory requirements (21 CFR Part 11, Annex 11).
OpenExchange: Secure video platforms and managed services for financial communications.
0+ YOEBachelor's in Computer Science required; 0–2 years technical experience; Python/scripting, SQL and database familiarity, APIs and JSON/CSV; strong communication and client-facing skills; ability to work flexible hours and be forward deployed.
Tata Consultancy ServicesNational Stock Exchange of India: TCS: Global provider of IT services, consulting, and business solutions.
8+ YOE8+ years IT and QA experience, 5+ years supporting pharma/life sciences, experience leading global testing delivery, knowledge of GxP/CSV/CSA and 21 CFR Part 11, stakeholder management, test strategy and data validation.
Veeva SystemsNYSE: VEEV: Cloud-based software solutions for the global life sciences industry.
5+ YOE5+ years software consulting experience; 3+ years configuring Veeva Network MDM or similar MDM; strong SQL, ETL, APIs, CSV/FTP skills; bachelor’s degree or equivalent; ability to travel 20–30%; authorized to work in the US (no visa sponsorship).
Computer System Validation - Senior Consultant - Life Sciences
New York or Boston or Chicago or Hoboken or McLean or Pittsburgh or Philadelphia or Washington
$94k-$155k/yrHybridFull Time
EY: Global firm providing audit, tax, and professional consulting services.
3+ YOEBachelor's degree in a technical field and 3+ years life sciences validation experience; strong CSV, SDLC/Agile, GxP/regulatory and risk-based validation knowledge.
Associate Director, Lab Computing and Facilities Technology
Cambridge or Norton
$172k-$233k/yrHybridFull Time
Alnylam PharmaceuticalsNASDAQ: ALNY: Develops RNAi therapeutics to treat rare and common diseases.
10+ YOEBachelor's in CS/Engineering/Life Sciences (or equiv), 10+ years in lab computing/operational technology in biotech/pharma, CSV/GAMP5 expertise, LIMS/ELN support, and leadership of technical teams.
LIMS, ELN/LES, Computer System Validation (CSV), GAMP 5, FDA 21 CFR Part 11, EU GMP Annex 11, ALCOA+
Candel TherapeuticsNASDAQ: CADL: Develops viral immunotherapies for the treatment of cancer.
10+ YOEBachelor's in life sciences,10+ years biotech/pharma QA with GxP systems, vendor oversight, CSV, audits, and Part 11 compliance; experience with eQMS/EDMS and regulated clinical workflows.
Syner-G BioPharma Group: Provides CMC and regulatory services for life sciences companies.
4+ YOEBachelor's in life science or engineering, 4–7 years in biotech/pharma/medical device, strong knowledge of FDA cGMP, FMEA, CSV, and hands-on IQ/OQ/PQ validation experience.
Mariana OncologyNYSE: NVS: Developing precision radioligand therapies for solid tumors.
3+ YOEBachelor's in engineering/chemistry/life sciences/pharmacy; 3+ years GMP validation/QA in biotech or pharma aseptic manufacturing; experience with equipment, utilities, CSV, commissioning, and global GMP/regulatory requirements.