Remote Pharmaceutical Quality Assurance Manager

Placements24; Cape Town; A distancia; ZAR 900.000 - 1.500.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Fully remote work

Health and wellness benefits

Career advancement opportunities

Descripción de la vacante

Placements24 is seeking a highly experienced Pharmaceutical Quality Assurance Manager to join our global team, working remotely from Cape Town. This role will lead the quality management system and QA activities to ensure product safety and regulatory compliance across pharmaceutical operations.

The position focuses on audits, CAPA, change control, and staff training within a multinational environment, requiring strong leadership and remote-work discipline.

Formación

• Bachelor's degree in Pharmacy, Chemistry, Biology, or related life science.
• 8+ years of progressive experience in pharmaceutical Quality Assurance or Quality Control.
• In-depth knowledge of cGMP, ICH guidelines, and regulatory requirements.
• Experience in managing audits, investigations, and CAPA systems.
• Ability to work independently in a remote environment.

Responsabilidades

• Develop, implement, and maintain the Quality Management System (QMS) in compliance with global regulatory standards.
• Oversee and manage all Quality Assurance activities, including batch record review, deviation investigations, and CAPA implementation.
• Conduct internal and external audits of manufacturing sites, suppliers, and partners.
• Ensure compliance with cGMP, GDP, and other relevant pharmaceutical regulations.
• Manage the change control process and risk management activities.
• Provide training and guidance to staff on quality principles and procedures.

Conocimientos

Leadership

Communication

Problem-solving

Remote work

Self-discipline

Educación

Bachelor's degree in Pharmacy, Chemistry, Biology, or related life science

Descripción del empleo

About the Role

Our client is seeking a highly experienced Pharmaceutical Quality Assurance Manager to join their global team, working remotely from Cape Town . This critical role will ensure adherence to stringent quality standards and regulatory requirements across all pharmaceutical operations. You will be instrumental in developing, implementing, and maintaining the quality management system, fostering a culture of quality excellence throughout the organization. This is an exceptional opportunity for a dedicated quality professional to make a significant impact on product safety and efficacy from a flexible, remote setting, ensuring compliance and driving continuous improvement in pharmaceutical manufacturing and distribution.

Key Responsibilities

• Develop, implement, and maintain the company's Quality Management System (QMS) in compliance with global regulatory standards.
• Oversee and manage all Quality Assurance activities, including batch record review, deviation investigations, and CAPA implementation.
• Conduct internal and external audits of manufacturing sites, suppliers, and partners.
• Ensure compliance with cGMP, GDP, and other relevant pharmaceutical regulations.
• Manage the change control process and risk management activities.
• Provide training and guidance to staff on quality principles and procedures.

Requirements

• Bachelor's degree in Pharmacy, Chemistry, Biology, or a related life science field.
• Minimum of 8 years of progressive experience in pharmaceutical Quality Assurance or Quality Control.
• In-depth knowledge of cGMP, ICH guidelines, and regulatory requirements.
• Experience in managing audits, investigations, and CAPA systems.
• Strong leadership, communication, and problem-solving skills.
• Ability to work independently and effectively in a remote environment, demonstrating strong self-discipline.

Benefits

• Competitive salary package with potential for annual bonuses.
• Fully remote work arrangement, offering flexibility and work-life balance.
• Comprehensive health and wellness benefits program.
• Opportunities for career advancement and leadership development within a global organization.
• Contribution to ensuring the safety and quality of vital pharmaceutical products worldwide.