Sr. Manager, Quality Assurance Compliance

Alcon Indonesia; Batam; On-site; IDR 835.701.000 - 1.169.982.000; Full time

Job summary

A leading global healthcare company based in Indonesia is seeking a Sr. Manager, Quality Assurance Compliance to oversee quality assurance and ensure regulatory compliance. The successful candidate will lead audit preparations, manage quality systems, and facilitate the implementation of the Quality Strategy. This role requires strong leadership and problem-solving skills. Adherence to Good Practice (GxP) regulations is essential. This is an excellent opportunity to impact global eye health.

Qualifications

• Develop and maintain quality programs and procedures for compliance.
• Lead audit preparations and resolve findings.
• Adhere to Good Practice (GxP) regulations and maintain accurate documentation.

Responsibilities

• Oversee teams managing Quality Systems and Supplier Quality processes.
• Facilitate the implementation of the Quality Strategy.
• Ensure compliance with cGMP and ISO standards.

Skills

Leadership

Project Management

Problem-Solving

Communication

Job description

Sr. Manager, Quality Assurance Compliance

At Alcon, we're passionate about enhancing sight and helping people see brilliantly. With more than 25,000 associates, we innovate fearlessly, champion progress, and act swiftly to impact global eye health. We foster an inclusive culture, recognizing your contributions and offering opportunities to grow your career like never before. Together, we make a difference in the lives of our patients and customers. Are you ready to join us?

This role is part of Alcon's Quality & Regulatory Affairs function, a team that ensures our products are in compliance with global, local, and internal regulations and meet the strictest standards of quality as we help people see brilliantly.

The Sr. Manager, Quality Assurance Compliance (Management Path) is primarily responsible for developing and maintaining quality programs, systems, and procedures to ensure compliance with policies and regulations. You will lead audit preparations, resolve findings, and collaborate with auditing groups. Specifics include:

• Oversee teams managing Quality Systems, Complaints, and Supplier Quality processes to ensure compliance with current Good Manufacturing Practices (cGMP), Health Authority, and International Organization for Standardization (ISO) standards
• Facilitate the implementation of the Quality Strategy and support governance processes
• Identify opportunities for improved process efficiencies and implement changes
• Advise on policy, conduct training sessions, and manage quality systems to ensure regulatory compliance
• Make key decisions affecting team operations, requiring advanced leadership, project management, problem‑solving, and communication skills
• Ensure all associates adhere to Good Practice (GxP) regulations by following Standard Operating Procedures (SOPs), maintaining accurate and complete documentation, and completing required training
• Contribute to the overall compliance of the organization and commit to continuous improvement

All associates must adhere to GxP regulations by strictly following Standard Operating Procedures (SOPs), maintaining accurate and complete documentation, ensuring rigorous quality control, and completing all required training. Associates are responsible for meeting their individual job requirements and contributing to the overall compliance of the organization. Compliance with regulatory requirements and a commitment to continuous improvement are essential to our operations.

If you are currently an active employee/contingent worker at Alcon, please click the appropriate link below to apply on the Internal Career site.

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With worldwide headquarters in Atlanta, Ciba Vision is a global leader in the research, development and manufacturing of optical and ophthalmic products and services, including contact lenses and lens care products. Ciba Vision products are available in more than 70 countries worldwide.