Regulatory Document Control Specialist

Bounty Fresh Group Holdings, Inc.; Bulacan; Presencial; PHP 335 000 - 502 000; Tempo integral

Resumo da oferta

Bounty Fresh Group Holdings, Inc. is seeking a Document Control Custodian to maintain organized, current plant documentation and ensure regulatory compliance. You will manage filing, data entry, and monitoring of licenses, permits, and CPRs, while supporting audits and training activities.

Your role includes handling FDA portal applications and enhancing internal communications, contributing to continuous improvement and quality standards in a fast-paced production environment.

Qualificações

• Bachelor’s degree in Industrial Engineering, or any related course.
• A year or more of experience in documentation control or regulatory compliance.
• Familiarity with ISO, IMS, and FDA regulatory requirements is highly desirable.
• Proficient in Word, Excel, and PowerPoint.
• Strong attention to detail and ability to handle confidential information.
• Effective written and verbal communication skills.

Responsabilidades

• Maintain and manage plant documentation to ensure accuracy and accessibility.
• Oversee document control processes including filing, retention, and monitoring permits.
• Coordinate customer satisfaction surveys and audit follow-ups.
• Prepare reports and assist management with continuous improvement initiatives.
• Process FDA applications for product registration and licensing; monitor status.
• Support internal communication and visitor orientation within the plant.

Conhecimentos

Attention to detail

Organizational skills

Written and verbal communication

Confidential information management

Microsoft Office

Formação académica

Bachelor’s degree in Industrial Engineering

Ferramentas

Microsoft Office

Descrição da oferta de emprego

Bounty Fresh Group Holdings, Inc. is seeking a Document Control Custodian to maintain organized, current plant documentation and ensure regulatory compliance. You will manage filing, data entry, and monitoring of licenses, permits, and CPRs, while supporting audits and training activities.

Your role includes handling FDA portal applications and enhancing internal communications, contributing to continuous improvement and quality standards in a fast-paced production environment.