Technician Quality

Abbott Laboratories; Singapore; On-site; SGD 40,000 - 60,000; Full time

Job summary

A global healthcare leader is seeking a Quality Assurance Inspector for a 1-year contract position, based in Pioneer, Singapore. The ideal candidate will have a Diploma in Science or Engineering and at least 2-3 years of experience in quality inspection, preferably in the medical device industry. Responsibilities include performing inspections, documenting test data, and adhering to FDA regulations. This role requires strong communication and organizational skills.

Qualifications

• Minimum 2-3 years experience in Quality function, especially in medical devices.
• Ability to work in a highly matrixed and geographically diverse environment.
• Strong attention to detail and organizational skills.

Responsibilities

• Perform visual, dimensional and functional inspection and testing.
• Document inspection and test data.
• Comply with FDA regulations and company policies.

Skills

Quality inspection

Knowledge of FDA regulations

Teamwork

Strong communication

Organizational skills

Education

Diploma in Science/Engineering

Job description

Abbott is a global healthcare leader, creating breakthrough science to improve people’s health. We’re always looking towards the future, anticipating changes in medical science and technology.

We’re empowering smarter medical and economic decision making to help transform the way people manage their health at all stages of life. Every day, more than 10 million tests are run on Abbott’s diagnostics instruments, providing lab results for millions of people.

Primary Function:

• Working under minimal supervision, performs inspection and testing of purchased materials, components and products in accordance with policy and procedures.

Major Responsibilities:

• Performs visual, dimensional and functional inspection and testing according to documented policies and procedures.
• Records inspection and test data as prescribed by written instructions and procedures.
• Operates all associated test and measurement equipment as instructed and as documented in procedures.
• Documents non-conformances in Non-Conforming Material Review system.
• Assists in gathering, analyzing, and trending of data.
• Completes and maintains certification/cross-training for all related QA inspection operations.
• Complies with U.S. Food and Drug Administration (FDA) regulations, other regulatory requirements, Company policies, operating procedures, processes, and task assignments.
• Supports all Company initiatives as identified by management and in support of Quality Management Systems (QMS), Environmental Management Systems (EMS), and other regulatory requirements.
• Maintains positive and cooperative communications and collaboration with all levels of employees, customers, contractors, and vendors.

Requirements:

• Diploma in Science/ Engineering or related discipline
• Minimum 2-3 years experience in Quality function, performing inspection, preferably in medical device manufacturing or warehouse operations.
• Knowledge of FDA and Good Manufacturing Practices preferred
• Ability to work in a highly matrixed and geographically diverse business environment.
• Ability to work within a team and as an individual contributor in a fast-paced, changing environment.
• Ability to leverage and/or engage others to accomplish projects.
• Strong verbal and written communications with ability to effectively communicate at multiple levels in the organization.
• Ability to multitask, prioritize and meet deadlines in timely manner.
• Strong organizational and follow-up skills, as well as attention to detail.
• Able and willing to work in third party site location (position will be based in Pioneer)

• Kindly note this role will be based in a third party site location in Pioneer and is a 1 year contract role (renewable based on performance)