Regulatory Affairs Pharmacist — Compliance & Dossier Lead

Cosmetique Asia Corporation

Bulacan

On-site

PHP 600,000 - 1,000,000

Full time

6 days ago
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Job summary

Cosmetique Asia Corporation in Bulacan is seeking an experienced Regulatory Affairs Pharmacist to ensure compliance with local and international regulations for cosmetics, food, and drugs. You will bring 5–7 years of relevant experience and leverage your expertise to navigate complex regulatory environments.

Responsibilities include preparing regulatory dossiers, approvals, and licenses; acting as a primary liaison with authorities during inspections and meetings; reviewing labels and packaging

Qualifications

  • Licensed Pharmacist with 5–7 years of relevant experience.
  • Experts in regulatory compliance for cosmetics, food, and drugs.
  • Strong knowledge of local and international regulations and solid project management.
  • Detail-oriented and able to manage complex regulatory situations.
  • Excellent communication and interpersonal skills.
  • Proficient in MS Office (Word, Excel, PowerPoint).

Responsibilities

  • Ensure compliance with regulatory requirements for materials, manufacturing processes, labeling, and finished products.
  • Prepare, submit, and maintain regulatory dossiers, approvals, change notifications, and licenses.
  • Act as the primary liaison with regulatory authorities, supporting inspections, audits, and regulatory meetings.
  • Review labels, packaging, and marketing materials to ensure regulatory and claims compliance.
  • Monitor regulatory changes, manage audits, and support ongoing compliance throughout the product lifecycle.

Skills

Regulatory compliance
Project management
Communication skills
Interpersonal skills
Detail-oriented

Education

Licensed Pharmacist

Tools

MS Office (Word, Excel, PowerPoint)

Job description

Cosmetique Asia Corporation in Bulacan is seeking an experienced Regulatory Affairs Pharmacist to ensure compliance with local and international regulations for cosmetics, food, and drugs. You will bring 5–7 years of relevant experience and leverage your expertise to navigate complex regulatory environments.

Responsibilities include preparing regulatory dossiers, approvals, and licenses; acting as a primary liaison with authorities during inspections and meetings; reviewing labels and packaging

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