Responsibilities:

• Oversee all on-site quality-related activities, including those involving external vendors.
• Develop, verify, and implement quality control procedures to ensure full compliance with statutory GMP and ISO requirements.
• Establish and maintain a comprehensive quality system that adheres to GMP, GDP, SS620, ISO 9001, ISO 13485, and other relevant regulatory standards.
• Lead the implementation of site-level and divisional strategies, fostering a strong quality culture and reliable systems.
• Manage regulatory affairs, including the registration of medical products with relevant health authorities.
• Act as a liaison with regulatory agencies to ensure compliance and support business needs.
• Work closely with stakeholders to drive initiatives in key areas such as energy efficiency, waste management, and sustainable supply chains.

Requirements:

• Bachelor's Degree in Biotechnology, Chemistry, Science & Technology or equivalent
• At least five years of working experience in pharmaceutical industry
• Knowledge of ISO, GMP, GDP and other regulatory authorities
• Proficient in using Microsoft Application
• Good interpersonal skills

Interested candidates who wish to apply for the advertised position, please click on "Apply Now". Alternatively, you may email us an updated copy of your resume (Attn: HUEY) for a confidential discussion.

Job Code: HUEY

EA Reg No: R24122358 (YEO HUEY CHEEN)

EA License: 01C4394 (PERSOLKELLY SINGAPORE Pte Ltd)

We regret that only shortlisted candidates will be notified.

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