Sr. Specialist, System Process & Regulatory Innovation

EyeBio
EyeBio

Compliance / Regulatory

Philippines · Petaling Jaya, Selangor, Malaysia

Posted on Jun 27, 2026

Job Description

The Senior Specialist, Regional System Process & Regulatory Innovation (SPRI) is an individual contributor within the Regional Regulatory Operations – Asia Pacific (RRO AP) department, part of our company’s Global Regulatory Affairs and Clinical Safety (GRACS) organization.

This role is responsible for the operational execution and support of regulatory systems, processes, and digital initiatives across the APAC region, while progressively expanding exposure to regional strategy and governance activities within established frameworks.

The Senior Specialist applies technical and functional knowledge of regulatory systems and business processes and works closely with Regulatory Innovation & Information Management (RIIM), Business System Owners (BSOs), and key regional stakeholders to deliver assigned system-related activities and project workstreams.

In addition to core delivery responsibilities, this role contributes to selected regional initiatives, governance activities, and strategic inputs under guidance, supporting alignment with global and regional priorities. The Senior Specialist will progressively build capability in identifying improvement opportunities and supporting change initiatives, while maintaining accountability for execution, data quality, and compliance within defined governance structures.

All activities are performed under established procedures, defined governance, and within regional and global system and process frameworks.

Key Responsibilities

  • Execute and own delivery of assigned system, process, and data-related activities and initiatives end-to-end, including day-to-day operations, project workstreams, and defined improvement efforts.

  • Ensure timely execution, stakeholder alignment, and adherence to governance and compliance requirements.

  • Provide end-user support and enablement across regulatory systems and processes, including:

    • Handling inquiries

    • Supporting data entry and process adherence

    • Contributing to training and communication materials

    • Promoting consistent and compliant system usage across the region

  • Drive data quality and continuous improvement activities, including:

    • Monitoring and root cause analysis

    • Implementing corrective actions

    • Identifying opportunities to enhance workflows, documentation, system usage, and data integrity

  • Support system implementation, enhancements, and change activities, including:

    • Preparation of deliverables

    • Testing, validation, and user acceptance

    • Documentation updates

    • Execution of defined changes to ensure adoption

  • Contribute to governance and strategy activities within defined scope, including:

    • Preparing regional inputs

    • Participating in governance forums

    • Providing data-driven insights for decision-making under guidance

  • Represent the region in selected forums, working groups, or communication platforms as assigned

  • Collaborate with SPRI colleagues and cross-functional stakeholders to:

    • Align activities

    • Share best practices

    • Support regional goals

    • Identify automation and optimization opportunities

Role Scope

  • Individual contributor role

  • No formal people management responsibilities

  • No budget ownership

  • No accountability for regional strategy

Education

  • Bachelor’s degree in Science, Information Technology, Pharmacy, or a related discipline required

Required Experience & Skills

  • Minimum 3 years of experience in:

    • Regulatory Affairs

    • Regulatory Operations

    • System/process-related roles supporting regulatory systems and digital initiatives

  • Working knowledge of regulatory business processes, including:

    • Submission planning and execution

    • Regulatory information management

  • Experience in:

    • System implementation

    • Testing and validation

    • User support activities

  • Ability to manage multiple tasks and priorities in a matrix environment

  • Strong communication and collaboration skills to engage with regional and cross-functional stakeholders

  • Experience in:

    • Data quality initiatives

    • Process improvement

    • System enhancements

Preferred

  • Experience in:

    • Project management methodologies

    • Change management

    • Process re-engineering

    • Analytics and reporting tools (e.g., Cognos, PowerApps, ChatGPT)

    • Training material development and communication strategies

Language Requirements

  • Fluent in English

Required Skills:

Academic Quality Improvement Program (AQIP), Academic Quality Improvement Program (AQIP), Adaptability, Audits Compliance, Business Processes, Business Systems, Change Management, Collaborative Communications, Corrective Action Management, Data Integrity, Data Quality Control, Detail-Oriented, Drug Regulatory Affairs, Employee Training Programs, Global Communications, Information Management, Operational Execution, Pharmaceutical Regulatory Affairs, Pharmacovigilance, Process Improvements, Project Management, Regulatory Affairs Compliance, Regulatory Affairs Management, Regulatory Compliance, Regulatory Operations {+ 2 more}

Preferred Skills:

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Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.

Employee Status:

Regular

Relocation:

VISA Sponsorship:

Travel Requirements:

Flexible Work Arrangements:

Hybrid

Shift:

Valid Driving License:

Hazardous Material(s):

Job Posting End Date:

08/26/2026

*A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.