Quality Manager

3 days ago

Kabupaten Bintan, Riau Islands, Indonesia Esco Full time

At Esco, we strive to make human lives healthier and safer by committing to invent, discover and commercialize enabling technologies in the life sciences arena globally. A leading manufacturer of laboratory equipment, bioprocessing tools and state-of-the-art IVF medical devices, we pride ourselves as a life sciences ecosystem builder comprising of over 30 companies in 43 office locations, with proprietary products and services sold in more than 100 countries worldwide.

We continuously challenge ourselves to break new grounds in the life sciences arena and we succeed by leveraging on the diverse expertise of our talented individuals from all walks of life. In exchange, we provide opportunities for them to reach their potentials. Let's work together to deepen our global footprint and pursue our mission in making human lives healthier and safer

Main Responsibilities


•Create and approve standards based on industry and customer needs.


•Develop quality control processes.


•Review and implement product specifications.


•Ensure products meet legal, regulatory and safety requirements.


•Supervise staff and track performance.


•Check the quality of raw materials.


•Monitor and assess internal production processes.


•Set quality control criterias.


•Gather feedback from customers about products.


•Generate reports on quality standards.


•Report on factory quality performance to management.


•Evaluate product recalls.


•Improve production efficiency and manage waste.


•Work with senior management to set quality goals.


•Manage customer, regulatory, and third-party audits.


•Create and report on internal audits to senior management.


•Track and report ISO goal data to senior management.


•Support Global Esco Entities with quality and ISO matters.


•Set targets and KPIs for the quality department.

Qualifications:


•Bachelor's degree in Engineering, Life Sciences, or a related field.


•Previous experience as a manager in a manufacturing environment.


•Experience in automotive, high-tech electronics, or medical devices industries.


•Familiar with quality standards, processes, and company/industry regulations, including medical devices.


•Proficient in technology and computer systems.


•Good understanding of Microsoft Office applications.


•Strong leadership and management skills.


•Excellent analytical and problem-solving abilities.


•Able to positively influence others.


•A great team player with strong interpersonal skills.


•Strong background and experience in Quality.


•Background and experience in implementing ISO 9001, 14001, 13485, 17025, and CPAKB.

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