PV/RA/QM Associate (1 Year Contract, Renewable)ID:57707

3,800 MYR ~ 4,500 MYRKota Damansara/Petaling Jaya3 days ago

Overview

  • Salary

    3,800 MYR ~ 4,500 MYR

  • Industry

    Manufacturing(Pharmaceutical/Medical Equipment)

  • Job Description

    Roles & Responsibilities:
    Pharmacovigilance
    • Maintains current knowledge, ensures compliance, and communicates with the relevant global, regional and local functions of the local regulatory requirements.
    • Review, process and forwards safety events (pre-marketing and post-marketing) and/or other medically related information to Global PV and submits such safety events to the local health authority according to relevant global/local SOPs and local requirements.
    • Perform review of abstracts and full articles to identify safety information from literature source.
    • Support creation, management, and oversight of local RMP and all RMP-related PV activities.
    • Support creation and management of local PSMF development.
    • Liaise with investigational site and reporter as necessary regarding safety issues.
    • Develop local PV training material and conduct PV training as per relevant SOPs.
    • Perform reconciliation of safety information with relevant internal and external functions.
    • Supports audits and inspections, including external vendors and ensures execution of deviation and CAPA management.

    Regulatory
    • Support the preparation and archival of registration dossiers to achieve timely regulatory approvals and maintenance of the existing licenses in the local market.
    • Reviewing change requests and assess regulatory impact of product changes.
    • Reviewing proposed labelling for compliance with product branding, global/regional standards and applicable regulations.
    • Provide regulatory intelligence and input, and support the development and implementation of local regulatory strategies.
    • Maintain local label database

    Quality Management/Quality Assurance
    • Support the local GDP inspections from health authority and perform GDP self-inspection.
    • Support in addressing deviations, product complaints from customer to manufacturer, monitor the status until closure.
    • Support in updating SOP and maintaining records in accordance with Good Distribution Practice or any other relevant regulations/guidelines.
    • Support in product imports, redressing and release to local markets.
    • Manage outsourced activities to ensure vendors meet the applicable local and global standards, including auditing vendors.
    • Review and manage promotional materials.

Qualifications

  • Requirement

    • Bachelor’s Degree in Pharmacy, Life Sciences, or a related field.
    • At least 1–2 years of experience in regulatory affairs role in pharmaceutical industry.
    • Strong analytical and problem-solving skills with the ability to interpret complex regulatory requirements.
    • Strong organizational and process management skills.
    • Proactive, detail-oriented, and able to multi-task effectively.
    • Flexible and adaptable to a dynamic regulatory environment.
    • Able to effectively build lasting relationships by demonstrating strong interpersonal and influencing skills throughout all levels of the organization.
    • Teamwork and collaboration with cross functional teams.

  • English Level

    -

  • Other Language

    Malay, English

Additional Information