Sr. Infrastructure Qualification

2 weeks ago

Newark, United States Adept Source Full time

Title: Sr. IT Infrastructure Qualification / CSV Consultant
Type of role: Contract 6++ Months
Location: Newark, CA 94560 (Hybrid - 3 days onsite/week)

*****Candidate must be a W2*****
No 3rd party accepted

Our direct client is looking for a Sr. IT Infrastructure Qualification consultant. This person will be a part of the IT R&D Department and will perform and/or direct IT Infrastructure Qualification projects in compliance with cGMP, 21 CFR Part 11 and Annex 11. This individual will ensure that GxP systems & underlying IT infrastructure meets the intended use and comply with applicable regulations, current industry practices, and company’s policies and procedures. Qualification or Validation projects will primarily include IT Infrastructure but may include projects from other departments that support GxP operations.

Job Description:
Provide independent technical leadership and accountability for overall IT Infrastructure Qualification and CSV efforts.
Ensure quality and compliance is met in accordance with established procedures and standards of the Quality Systems by applying critical thinking on qualification and validation work.
Plan, generate, review and/or approve qualification or validation packages for IT Infrastructure or GxP systems in support of compliance activities.
Develop or assist with change controls, CAPAs, deviations, exceptions required as part of qualification/validation efforts.
Engage with IT stakeholders in supporting continuous improvements to the existing procedures and policies in relation to compliance and update those as necessary.
Perform gap analysis & necessary remediation efforts on current IT Infrastructure to ensure compliance with Part 11 and Annex 11.
Collaborate/lead/participate in decision making and make recommendations regarding best options for qualification of computerized systems. Maintain close communication with stakeholders and team members to keep apprised of IT Infrastructure needs, & impact on GxP processes or operations.
Collaborate with company’s approved vendor personnel in coordinating qualification or validation efforts to ensure successful system implementations.
Perform system assessments based on version upgrades/release updates on SaaS/Cloud based GxP systems and ensure all the required verification and validation efforts are performed per the assessments conducted.
Facilitate the computer system validation risk assessments i.e. System level, Requirement level risk assessments, & System and Data Audit Trail assessments etc.
Assist IT staff with business process deliverables such as process flows, data flows, user/operating procedures, work instructions and forms for GxP computerized systems.
Perform System Periodic Reviews ensuring that the systems are maintained in their validated state.
Support Regulatory inspections and internal and partner audits, and implements corrective actions as needed in CSV.

Requirements:7+ years or more in the pharmaceutical industry with GMP experience
Understanding of Validation Life Cycle approach and practical working knowledge of computer system validation/computer software assurance requirements
Knowledge of infrastructure qualification or validation of computerized systems within an FDA regulated environments with a strong understanding of industry standards and best practices for computer validation such as GAMP 5, 21 CFR Part 11 and Part 211, EudraLex Volume 4 and Annex 11, and ICH Q7, Q8, Q9 and Q10
Demonstrate ability to effectively manage multiple projects/priorities and good understanding of SDLC phases and phase gates
Experience with EDMS, VLMS, LMS and working knowledge of IT Infrastructure systems (AD, Backups, VMware, Monitoring at minimum)
Demonstrate excellent written and oral communication skills.
Effective time management and interpersonal skills.
Must work effectively within teams with rapidly changing priorities.
Demonstrates analytical problem-solving skills.


Preferred:
Relevant validation experience with Quality Systems, Manufacturing Systems, or Laboratory systems used within the pharmaceutical industry is a plus.

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