QA Specialist (Pharma) (SG)

Anter Consulting; Singapore; On-site; SGD 60,000 - 90,000; Full time

Job summary

A leading consulting company is looking for a QA Specialist in Singapore to uphold quality standards in pharmaceutical manufacturing. The candidate will be responsible for implementing quality assurance protocols, conducting audits, and ensuring compliance with regulatory requirements. This full-time role requires a Bachelor's degree and relevant experience in the pharmaceutical or biotech industry.

Qualifications

• 3+ years of experience in quality assurance within the pharmaceutical or biotech industry.
• Strong knowledge of cGMP, ISO standards, and regulatory requirements.
• Experience in handling audits and CAPA processes.

Responsibilities

• Oversee and implement quality assurance protocols in line with cGMP and regulatory standards.
• Conduct internal audits and inspections to ensure compliance with quality standards.
• Investigate quality-related deviations and implement corrective actions.

Skills

Attention to detail

Problem-solving

Analytical skills

Communication

Interpersonal skills

Education

Bachelor’s degree in Life Sciences, Chemistry, Pharmacy, or a related field

Tools

Quality management systems (QMS)

Electronic documentation systems

Job description

Join to apply for the QA Specialist (Pharma) (SG) role at Anter Consulting.

We are seeking a detail-oriented QA Specialist to join our team in Singapore, ensuring that quality standards are upheld in pharmaceutical manufacturing and operations. The ideal candidate will be responsible for overseeing quality assurance processes, maintaining compliance with regulatory requirements, and supporting continuous improvement initiatives.

Key Responsibilities

• Oversee and implement quality assurance protocols in line with cGMP and regulatory standards
• Review and approve batch records, validation protocols, and quality documentation
• Conduct internal audits and inspections to ensure compliance with quality standards
• Investigate quality-related deviations and implement corrective and preventive actions (CAPA)
• Collaborate with cross-functional teams to address quality concerns and drive process improvements
• Monitor and ensure compliance with regulatory requirements from agencies such as HSA, FDA, or EMA
• Support training initiatives on quality standards and procedures for staff
• Maintain and manage documentation related to quality systems, audits, and compliance

Required Qualifications And Skills

• Bachelor’s degree in Life Sciences, Chemistry, Pharmacy, or a related field
• 3+ years of experience in quality assurance within the pharmaceutical or biotech industry
• Strong knowledge of cGMP, ISO standards, and regulatory requirements
• Experience in handling quality documentation, audits, and CAPA processes
• Excellent attention to detail and organizational skills
• Strong analytical and problem-solving abilities
• Effective communication and interpersonal skills
• Familiarity with quality management systems (QMS) and electronic documentation systems
• Willingness to work in a fast-paced, compliance-driven environment

Seniority level

• Mid-Senior level

Employment type

• Full-time

Job function

• Quality Assurance

Industries

• Business Consulting and Services