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Quality Technician 1

3 weeks ago

Singapore Illumina Full time

Join to apply for the
Quality Technician 1
role at
Illumina
Join to apply for the
Quality Technician 1
role at
Illumina
Get AI-powered advice on this job and more exclusive features.
What if the work you did every day could impact the lives of people you know? Or all of humanity?
At Illumina, we are expanding access to genomic technology to realize health equity for billions of people around the world. Our efforts enable life-changing discoveries that are transforming human health through the early detection and diagnosis of diseases and new treatment options for patients.
Working at Illumina means being part of something bigger than yourself. Every person, in every role, has the opportunity to make a difference. Surrounded by extraordinary people, inspiring leaders, and world changing projects, you will do more and become more than you ever thought possible.
Summary
Position Summary:
The individual will work as part of the Quality team to support QC Operations. The QC Technician will be performing routine quality activities for outgoing inspection/review of the Batch Record (BR) or Device History Record (DHR) electronically or in hardcopy forms of a semi-finished or finished products and executes the final release for downstream processes or customer shipment. Functional responsibilities include ensuring that product was made according to the procedure and regulatory requirements as well accurate and timely maintenance and review of manufacturing BR/DHR documentation.
Position Responsibilities
Review and approval of label/cosmetics check on a finished product.
Review and approval of Batch Record (BR) or Device History Record (DHR).
Responsible for the disposition of the inspected/ reviewed semi-finished or finished products in MES and/or SAP system.
Review logistic team's execution on Country Specific Labelling activities and provide disposition for shipment.
Documents the executed inspection/ review and timely recording of data in compliance to Quality Systems specification.
Performs the review and closure of Return Material Authorization (RMA) activities.
Reports abnormalities detected during the inspection/ review and raise a non-conformance record (NCR) when required.
Generates Certificate of Conformance (CoC) or Certificate of Analysis (CoA) to finished product when required.
Assists to Customer Care Team requests on CoC, CoA, or product label request.
Attends team daily meeting and production standup meeting and shares the information or update to the team.
Contributes to the team's goal on target KPI for Turn-Around-Time and First Pass Yield.
Highlight within the QC and/or functional team for any issues that will delay the release of a semi-finished or finished products from BR/ DHR review.
Listed responsibilities are an essential, but not exhaustive list, of the usual duties associated with the position. Changes to individual responsibilities may occur due to business needs.
Position Requirements
Must have a computer skills and competent in Microsoft Office applications (Word, Excel, Powerpoint, Outlook).
Good written and oral communication skills with clarity and accuracy within the QC team and/or cross-functional team when communicating information such as findings during BR/DHR review.
Ability to read, understand, and follow work instructions or procedures with minimal guidance and executes associated tasks.
Self-starter, self-initiative, organized, and have attention to detail and accuracy.
Ability to work well with a team as well as ability to work independently with minimal supervision.
All listed requirements are deemed as essential functions to this position; however, business conditions may require reasonable accommodations for additional task and responsibilities.
Preferred Experience/Education/Skills
Preferably diploma holder or higher.
Minimum 1 to 2 years Quality Role related work experience or internship preferably in biotech or medical device industry.
We are a company deeply rooted in belonging, promoting an inclusive environment where employees feel valued and empowered to contribute to our mission. Built on a strong foundation, Illumina has always prioritized openness, collaboration, and seeking alternative perspectives to propel innovation in genomics. We are proud to confirm a zero-net gap in pay, regardless of gender, ethnicity, or race. We also have several Employee Resource Groups (ERG) that deliver career development experiences, increase cultural awareness, and offer opportunities to engage in social responsibility. We are proud to be an equal opportunity employer committed to providing employment opportunity regardless of sex, race, creed, color, gender, religion, marital status, domestic partner status, age, national origin or ancestry, physical or mental disability, medical condition, sexual orientation, pregnancy, military or veteran status, citizenship status, and genetic information. Illumina conducts background checks on applicants for whom a conditional offer of employment has been made. Qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable local, state, and federal laws. Background check results may potentially result in the withdrawal of a conditional offer of employment. The background check process and any decisions made as a result shall be made in accordance with all applicable local, state, and federal laws. Illumina prohibits the use of generative artificial intelligence (AI) in the application and interview process. If you require accommodation to complete the application or interview process, please contact To learn more, visit: The position will be posted until a final candidate is selected or the requisition has a sufficient number of qualified applicants.
Seniority level
Seniority level Not Applicable
Employment type
Employment type Full-time
Job function
Job function Quality Assurance
Industries Biotechnology Research, Research Services, and Medical Equipment Manufacturing
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