Quality Control Specialist | Biopharma Quality & Compliance (MNC) #HDCA

Recruit Express Pte Ltd; Singapore; Presencial; SGD 55 000 - 85 000; Tempo integral

Resumo da oferta

Recruit Express Pte Ltd invites applications for a Quality Control professional in Singapore. The role focuses on ensuring GMP-compliant QC activities within a biopharmaceutical manufacturing setting, maintaining documentation, and supporting equipment qualification to meet regulatory standards.

Ideal candidates will bring hands-on QC experience, strong GMP knowledge, and meticulous documentation skills to uphold product quality and continuous improvement across teams.

Qualificações

• Must have hands-on QC experience in pharmaceutical/biopharmaceutical or related regulated industry.
• Strong knowledge of GMP requirements and quality systems.
• Hands-on experience with equipment qualification and document control.

Responsabilidades

• Perform quality control activities in accordance with GMP and established procedures.
• Conduct quality checks, review documentation and ensure compliance with quality standards.
• Support equipment qualification to ensure fit-for-use and regulatory compliance.
• Prepare, review and maintain QC records, reports and technical documentation.
• Investigate deviations and support CAPA activities.
• Collaborate with cross-functional teams to sustain a strong quality culture.

Conhecimentos

QC experience

GMP knowledge

Equipment qualification

Documentation practices

Analytical

Organisational skills

Descrição da oferta de emprego

Job Highlights

• Opportunity to contribute to quality and compliance within a biopharmaceutical manufacturing environment
• Play a key role in maintaining product quality and upholding GMP standards
• Office hours Mon - Fri
• Ideal for candidates with hands-on QC experience and equipment qualification expertise

Job Responsibilities

• Perform quality control activities in accordance with established procedures and Good Manufacturing Practice (GMP) requirements
• Conduct quality checks, review documentation and ensure compliance with relevant quality standards
• Support equipment qualification activities to ensure equipment is fit for intended use and meets regulatory requirements
• Prepare, review and maintain accurate QC records, reports and technical documentation
• Investigate deviations, identify potential quality issues and support corrective and preventive actions (CAPA)
• Work closely with cross-functional teams to support continuous improvement and maintain a strong quality culture

Requirements

• Relevant experience in Quality Control (QC) within the pharmaceutical, biopharmaceutical or related regulated industry
• Strong working knowledge of GMP requirements
• Hands-on experience in equipment qualification is essential
• Good documentation practices and attention to detail
• Strong analytical, problem-solving and organisational skills