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Eli Lilly And Company
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Sr. Consultant - Validation

Sr. Consultant - Validation

Eli Lilly And Company

8 - 10 years

9 - 14 Lacs

hyderabad

Posted:2 weeks ago| Platform:

Apply

Skills Required

computer science erp assurance analytical project management clinical trials healthcare life sciences continuous improvement analytics

Work Mode

Work from Office

Job Type

Full Time

Job Description

Drive innovation in validation by exploring and leveraging AI, digital tools, and automation technologies to streamline validation documentation, authoring, and review processes.

Identify opportunities to simplify CSV/CSA activities through adoption of risk-based approaches, automation frameworks, and smart documentation solutions, reducing effort while maintaining compliance.

Continuously evaluate emerging technologies (e.g., AI-assisted authoring, digital validation platforms) and recommend practical use cases for efficiency and quality improvement.

Identify and drive continuous improvement, automation, and simplification opportunities in validation processes using digital tools or AI-enabled solutions.

Project Validation :

Lead and coordinate IT system validation by managing the computer system lifecycle from validation /test planning to reporting and ensure compliance with regulatory requirements , Lilly processes and validation standards .

Responsible for applying appropriate right sizing method/approach and determining the nature and content of d eliverables in scope.

Oversee AI/auto generated validation documents by reviewing and updating content s to ensure accuracy, compliance, and alignment with Lilly s quality management system .

Review all the project validation deliverables authored by the project team (developer, SME etc.) .

Escalate and communicate operational issues , critical compliance findings and risks to the Information System Quality (ISQ) organization and other key stakeholders of the system.

Educate project team members on Lilly IT processes and methodologies.

Collaborate with cross-functional teams to identify and mitigate compliance risks, while providing guidance and training on best practices and regulatory requirements.

Advise project team on implementation of compliance and security control requirements at the appropriate stages of system development .

Contribute to internal and external audits, assessments or inspections .

Change Management :

Ensures IT system change requests (CR) are executed in compliance with Local/ global change control procedures.

Review CRs and e nsure the accuracy and completeness of all change requests.

Review the impacted validation deliverables.

Access Roster , Privacy and Periodic Review :

Facilitate and s upport the system custodian / owner and area management to execute access roster and periodic review followed by respective Corrective and Preventive Action ( CAPA ) closure .

How You Will Succeed:

Achieving measurable improvements in validation efficiency (e.g., reduced cycle time, higher CSA adoption, increased compliance ).

Contributing to continuous improvement for documentation and validation processes for functional area s.

Promoting simplification and harmonization across systems and geographies.

Mentoring and coaching junior validation staff, foster a quality culture across teams.

Driving CSA adoption to simplify and modernize CSV, focusing on risk-based assurance rather than excessive documentation.

What You should Bring:

In-depth knowledge of regulations, guidelines, and industry standards related to CSV, data integrity, and computerized systems like GxP , GAMP 5, FDA 21 CFR Part 820, 21 CFR 210, 21 CFR 211 , 21 CFR Part 11 , EU Annex 11 , ALCOA+ + Principles , etc .

Experience in leading CSV activities across the full system lifecycle (implementation, upgrades, retirement).

Expertise in documents creation which includes , but not limited to validation plan , System Configuration, System Overview, Security Plan and validation report , etc.

Hands-on expertise in preparing, reviewing, and approving validation deliverables.

Strong knowledge of IT system operational compliance processes, including Periodic Reviews and Access Roster Reviews.

Proven ability to apply risk-based validation approaches in alignment with CSA principles to balance compliance with efficiency.

Hands-on experience with commonly used industry tools (e.g., Jira, ServiceNow, Veeva).

Basic Qualifications and Experience Requirement :

Bachelor s degree in computer science, Information Technology, or a related field,

Overall 8- 1 0 + years of experience in CSV in pharmaceuticals or life sciences industry .

Must have extensive knowledge of GxP , regulatory requirements, and IT system validation processes.

Demonstrated expertise in leading compliance initiatives and fostering cross-functional collaboration.

Strong experience in regulatory compliance, validation processes, risk assessment, IT systems change management, stakeholder collaboration, continuous improvement, project management, and analytical problem-solving.

Ability to collaborate with technical and non-technical team members .

Additional Skills/Preferences:

Excellent interpersonal , analytical, problem solving, and investigative skills .

Strong communication and collaboration skills.

Knowledge of Agile principles and frameworks (e.g., Scrum, SAFe ), including related tools (such as Jira) .

Demonstrated leadership skills and effectiveness in the areas of influence, team leadership, articulating and taking a position, negotiation, and conflict resolution.

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