Quality and Regulatory Affairs Specialist

Majeton Pte. Ltd.; Singapore; On-site; SGD 60,000 - 80,000; Full time

Job summary

A health product company in Singapore is seeking an experienced Quality & Regulatory Affairs Specialist to ensure regulatory compliance and uphold product quality. This role involves managing regulatory affairs, conducting audits, and maintaining documentation. Candidates should have a Bachelor’s degree in Life Sciences or a related field and at least 2 years of relevant experience. The company offers competitive salaries, performance bonuses, and professional growth opportunities.

Benefits

Competitive salary and performance-based bonuses

Opportunities for professional growth and development

Coffee treats from management

Team-oriented work environment

Qualifications

• At least 2 years of experience in pharmaceutical or medical device QA or RA.
• Familiar with Singapore HSA regulations including GDP and Medical Device Regulations.
• Experience in SOP writing and Quality Management Systems.

Responsibilities

• Manage local GDPMDS and GDP inspections and maintain records.
• Handle AE intake for all products and manage compliance of PV SOPs.
• Support inspection readiness and regulatory support in RA activities.

Skills

Regulatory compliance

Quality assurance

Documentation skills

Communication skills

Training and mentorship

Education

Bachelor’s degree in Life Sciences, Pharmacy, or related discipline

Job description

Overview

At Majeton, we are driven by our commitment to deliver “The Right Product for Health”. Our team of researchers and clinical experts utilize clinic feedback from practitioners, scientifically researched literature and top quality manufacturing as the foundation for all products.

We are seeking a meticulous and experienced Quality & Regulatory Affairs Specialist to join our team and ensure regulatory compliance, uphold product quality, and oversee vigilance reporting for all of our marketed products.

Responsibilities

Quality Assurance (QA)

• Handle and manage local annual GDPMDS and GDP inspection; support inspection readiness

• Maintain and manage all controls of documents and records

• Manage and maintain local GDPMDS and GDP SOP and system records, including but not limited to all product complaints, returns, disposal, internal inspection/audit, deviation, CAPA management, etc

• Manage new and existing supplier management activities

• Perform personnel training to ensure regulatory and quality compliance

Regulatory Affairs & Pharmacovigilance (RA & PV)

• Manage and process AE intake for all products

• Perform signal detection

• Manage compliance of all PV SOPs

• Provide regulatory support in RA activities

Qualifications

• Holds a Bachelor’s degree in Life Sciences, Pharmacy, or a related discipline

• Has at least 2 years of experience in pharmaceutical or medical device QA or RA, with some exposure to PV

• Is familiar with Singapore HSA regulations, including Health Supplements Guidelines, Medical Device Regulations, and GDP

• Has experience in SOP writing, inspection preparation, and Quality Management Systems (QMS)

• Demonstrates strong documentation, regulatory filing, and communication skills

• Is eager to grow with the company and open to cross-functional learning and development

• Is ready to take on more responsibilities within the Quality & Regulatory Affairs domain; training and mentorship provided

• Is adaptable and willing to support the team with ad hoc tasks when required.

Nice to have

• Knowledge or exposure to US FDA biologic regulations and pharmacovigilance systems

• Experience in SME distribution companies or startup environments

• Experience in preparing for inspection readiness

What we offer

• Competitive salary and performance-based bonuses

• Opportunities for professional growth and development

• Coffee treats from our generous bosses

• A team of hard-working colleagues who work hard and play hard