Senior Director, IT Compliance & Governance (Contract)

Posted Yesterday
Be an Early Applicant
Hiring Remotely in United States
Remote
122-136 Hourly
Senior level
Biotech • Pharmaceutical
The Role
Leads IT GxP and SOX compliance, FDA inspection readiness, audit response, remediation, and evidence management. Owns the IT technology portfolio, including prioritization, roadmap governance, dependencies, reporting, and launch-readiness programs. Coordinates IT governance, procurement, budgeting, policies, SOPs, steering cadences, and cross-functional delivery. Partners with quality, finance, legal, vendors, and managed-service teams to maintain compliant, inspection-ready IT operations across biotech systems.
Summary Generated by Built In

Attention recruitment agencies: All agency inquiries are vetted through 4DMT’s internal Talent Acquisition team. No unsolicited resumes will be accepted. The 4DMT Talent Acquisition team must expressly engage agencies on any requisition. Agencies contacting hiring managers directly will not be tolerated, and doing so may impact your ability to work with 4DMT in the future.


4DMT is a leading late-stage biotechnology company advancing durable and disease-targeted therapeutics with potential to transform treatment paradigms and provide unprecedented benefits to patients. The Company’s lead product candidate 4D-150 is designed to be a backbone therapy forming the foundation of treatment of blinding retinal vascular diseases by providing multi-year sustained delivery of anti-VEGF (aflibercept and anti-VEGF-C) with a single, safe, intravitreal injection, which substantially reduces the treatment burden associated with current bolus injections. The Company’s lead indication for 4D-150 is wet age-related macular degeneration, which is currently in Phase 3 development, and second indication is diabetic macular edema. The Company’s second product candidate is 4D-710, which is the first known genetic medicine to demonstrate successful delivery and expression of the CFTR transgene in the lungs of people with cystic fibrosis after aerosol delivery

GENERAL SUMMARY: 

Reporting to the Sr. VP, IT & Facilities, the IT Compliance & Governance Consultant is a senior IT leader with two mission-critical objectives: as IT’s examiner-facing leader, ensure FDA inspection success by leading IT GxP compliance assessments, remediation plans, evidence readiness, & inspection response; and drive successful delivery of the IT Council-governed technology portfolio, which includes dozens of critical BLA, Inspection & Commercial Launch-readiness projects. 

The role covers three core areas: IT compliance, primarily GxP & SOX; the IT Council project portfolio, including prioritization, status reporting, dependency management, & escalation, with special focus on BLA, Inspection & Commercial launch programs; and IT governance, including IT Council coordination, IT procurement, budget planning/forecasting, policies, SOPs, & cross-functional ways of working.  

RESPONSIBILITIES:  

IT Compliance: 

  • Ensure 4DMT IT meets GxP, SOX & privacy requirements through an auditable control environment & strong evidence management; lead the IT GxP compliance assessment & remediation plan for the upcoming FDA inspection. 
  • Oversee execution of auditable IT activities—system validation, periodic review, backup/restore testing, change control, SOX ITGC reviews & access/inventory management—by internal teams, managed services, consultants & 3rd party service providers to ensure consistent, on-time, right-first-time execution. 
  • Serve as a collaborative partner to QA CSV/CSA, Finance Compliance (SOX) & Legal Compliance (Privacy/Transparency) to align & improve governance & compliance policies/SOPs, & execute audit/inspection preparedness activities (e.g., risk-based storyboarding, control/procedure improvements, evidence readiness drills). 
  • Act as escalation point & examiner-facing interface for IT portions of audits & health authority inspections; explain IT controls & CSV/CSA practices; coordinate IT evidence, storyboards & responses; & manage observations/CAPAs through remediation closure. 

IT Council Project Portfolio: 

  • Own & mature technology portfolio management practices that translate strategy into a clear, funded, executable roadmap with transparent status reporting for leadership decisions; oversee critical implementation programs & drive cross-functional alignment, escalation, dependency management, & delivery discipline. 
  • Run portfolio intake, prioritization, categorization, risk/value assessment, dependency mapping, benefits tracking & portfolio reporting, with special focus on BLA, Inspection & Commercial Launch programs. 

IT Governance: 

  • Coordinate annual planning & IT Council/steering cadences, IT procurement coordination, & budget development/forecasting & BvA spend tracking. 
  • Define, implement, & enforce IT governance across verticals through policies, SOPs, & fit-for-purpose processes, establishing ways of working (e.g., project/program governance, IT cadences, KPI/OKR framework) that improve performance & maturity. 
  • Maintain dotted-line/matrixed governance for IT project managers, IT compliance, IT procurement & system validation staff to drive consistent execution, standard work, & audit/inspection readiness across systems & programs. 

 
QUALIFICATIONS: 

Experience: 

  • 15+ years of IT GxP (e.g. Part 11) compliance responsibility required  
  • 12+ years directly managing or auditing IT operational processes 
  • 10+ years developing, implementing & maintaining SDLC in alignment with principles of GAMP 5 
  • 8+ years of experience in a senior IT leadership position w/demonstrated ability to lead compliance & project teams within the Biotech or Pharma industry. 
  • Direct involvement as IT, compliance, or validation lead for at least one FDA or comparable health authority inspection, including examiner-facing preparation & response 
  • Recent roles demonstrating expertise managing transparent IT project portfolios that enable effective steering committee oversight & portfolio health monitoring 
  • Annual external audits of SOX IT General Control design & effectiveness, Segregation of Duties, & SSAE-18 SOC report reviews a plus 
  • Multiple lab, scientific &/or financial software implementations (SDLC/Change Mgmt) as IT lead or compliance/validation lead.  
  • Direct involvement as IT lead or compliance/validation lead in one or more Data Integrity or Computer System Assurance programs 
  • Experience leading complex, cross-functional technology portfolios or commercial launch programs with dozens of concurrent projects, including roadmap governance, dependency tracking, executive reporting, vendor coordination, & delivery escalation 

Education: 

  • Bachelor’s Degree in a Life Science or Computer Science.   
  • Certifications related to GxP, SOX & Privacy regulations, IT operations & project management strongly preferred. 

Skills: 

  • Strong knowledge of the IT implications of cGMP, GCP & ICH guidelines, Part 11/Annex 11, Computer System Assurance, Data Integrity guidelines for US, Canada & EU markets, SOX, & privacy/transparency regulations 
  • Strong skills designing, enabling & auditing compliant IT operational processes, including SDLC, Change, Access, Inventory, Data Protection/Backup, & Service Continuity Management 
  • Strong skills using & administering GRC, QMS & LMS tools required 
  • Skills with Smartsheet, SharePoint, Box & Veeva Vault a plus. 
  • Collaborative Communication Skills: 
  • Ability to work with a diverse group of personalities & individuals at all levels  
  • Excellent document authoring, review & writing skills 
  • Strong verbal communication skills 
  • Ability to work independently, multitask, and maintain strong attention to detail & accuracy 
  • Proven ability to set schedules & meet deadlines 

Physical Requirements and Working Conditions:

  • Physical Requirements - Sedentary work: Exerting up to 10 pounds of force occasionally and/or a negligible amount of force frequently or constantly to lift, carry, push, pull or otherwise move objects, including the human body. Sedentary work involves sitting most of the time. Jobs are sedentary if walking and standing are required only occasionally and all other sedentary criteria are met.
  • Working Conditions - The worker is not substantially exposed to adverse environmental conditions (as in typical office or administrative work).

Hourly compensation range: $122.00 - 136.00/hr

Please note, the hourly compensation range offered to the final candidate depends on various factors: candidate’s geographical location, relevant work experience, skills, and years of experience.  



4DMT provides equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, gender, sexual orientation, national origin, age, disability, genetic information, marital status, status as a covered veteran, and any other category protected under applicable federal, state, provincial and local laws.
 
Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities

Skills Required

  • 15+ years of IT GxP compliance experience, including Part 11 requirements
  • 12+ years directly managing or auditing IT operational processes
  • 10+ years developing, implementing, and maintaining SDLC processes aligned with GAMP 5
  • 8+ years in a senior IT leadership position within the biotech or pharmaceutical industry
  • Experience leading compliance and project teams
  • Direct involvement as an IT, compliance, or validation lead in at least one FDA or comparable health authority inspection
  • Experience with examiner-facing inspection preparation and response
  • Experience managing transparent IT project portfolios and steering committee oversight
  • Experience with complex, cross-functional technology portfolios or commercial launch programs involving roadmap governance, dependency tracking, executive reporting, vendor coordination, and delivery escalation
  • Experience leading Data Integrity or Computer System Assurance programs
  • Experience implementing multiple laboratory, scientific, or financial software systems as an IT, compliance, or validation lead
  • Bachelor's degree in Life Science or Computer Science
  • Knowledge of cGMP, GCP, ICH guidelines, Part 11, Annex 11, Computer System Assurance, Data Integrity, SOX, and privacy/transparency regulations
  • Experience designing, enabling, and auditing SDLC, change, access, inventory, data protection, backup, and service continuity processes
  • Strong skills using and administering GRC, QMS, and LMS tools
  • Strong document authoring, review, writing, verbal communication, organization, multitasking, and deadline-management skills
  • Annual external audits of SOX IT General Control design and effectiveness
  • Segregation of Duties and SSAE-18 SOC report review experience
  • Certifications related to GxP, SOX, privacy regulations, IT operations, or project management
  • Experience with Smartsheet, SharePoint, Box, and Veeva Vault
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The Company
HQ: Emeryville, California
164 Employees
Year Founded: 2013

What We Do

4DMT is a clinical stage biopharma company inventing and developing innovative products to unlock the full potential of genetic medicine to treat large market and rare diseases. Our vector discovery platform Therapeutic Vector Evolution harnesses the power of directed evolution, a Nobel Prize-winning technology, with approximately one billion synthetic AAV capsid-derived sequences to invent customized and evolved vectors with improved therapeutic profiles compared to wild-type vectors. Our product design, development and manufacturing engine empowers us to efficiently create our valuable and diverse product pipeline. This combination of bold innovation and relentless execution gives 4DMT the capability to revolutionize genetic medicines and to strive for potential curative therapies. We have built a deep portfolio of genetic medicine product candidates, with five product candidates in clinical trials for seven patient populations. We are taking genetic medicine to new heights and into new disease areas to overcome challenges not addressed by existing medicines. This incredible challenge drives our relentless and talented team. Our people are the essence of our inspiring, innovative and collaborative environment that encourages individual contributions and provides opportunities for career development. We seek the best in the industry who identify with our mission and our bold and innovative results-driven approach. Our 4 Guiding Principles drive the way we work together: - Dare to Cure - Break Boundaries - Beyond Yourself - Prepare & Executive Relentlessly

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