Quality Technician

Singapore; Singapore; On-site; SGD 30,000 - 60,000; Full time

Job summary

Join a forward-thinking company dedicated to transforming vital organ therapies and enhancing patient care. This role offers an exciting opportunity to engage in essential audits and quality assurance processes that ensure the highest standards in kidney care. You will be part of a passionate team committed to making a meaningful impact on patients' lives. If you are driven, detail-oriented, and eager to contribute to innovative healthcare solutions, this position is perfect for you. Embrace the chance to grow professionally while helping to extend lives and expand possibilities in a supportive environment.

Qualifications

• Minimum 5 years experience or fresh diploma in relevant fields.
• Strong communication skills and knowledge of quality systems.

Responsibilities

• Conduct audits on product specifications and machine parameters.
• Ensure compliance with GMP and quality documentation.

Skills

Interpersonal communication

Quality System knowledge

SPC (Statistical Process Control)

Metrology

Blueprint reading

Education

Diploma/NITEC (NTC/ITC)

GCE 'O' level/Form IV (Mechanical)

Certified Quality Inspector (CQI)

Job description

Vantive is a vital organ therapy company on a mission to extend lives and expand possibilities for patients and care teams everywhere. For 70 years, our team has driven meaningful innovations in kidney care. As we build on our legacy, we are deepening our commitment to elevating the dialysis experience through digital solutions and advanced services, while looking beyond kidney care and investing in transforming vital organ therapies. Greater flexibility and efficiency in therapy administration for care teams, and longer, fuller lives for patients—that is what Vantive aspires to deliver.

We believe Vantive will not only build our leadership in the kidney care space, it will also offer meaningful work to those who join us. At Vantive, you will become part of a community of people who are focused, courageous and don’t settle for the mediocre. Each of us is driven to help improve patients’ lives worldwide. Join us in advancing our mission to extend lives and expand possibilities.

Essential Duties and Responsibilities:

1. Process Audit:
   1. Review machine parameters per Specs & SOPs and challenge sensors, testers etc per Specs & SOPs.
   2. Review PM/ records and activities and whether operators are performing tasks/ Assembly per Specs, SOPs, JIBs.
   3. Gauges are calibrated.
2. Product Audits:
   1. Check whether product meets specs.
3. Labels Audit:
   1. Check barcode equipment, ink jet equipment and correct printed materials.
4. GMP Audit:
   1. Check area for housekeeping, cleaning logs, material segregation, compliance to GMP on people machines, materials.
5. Batch document Audit:
   1. Check Batch records to see whether they are accurate.
   2. Sub assembly logs are accurate and specs are ‘official copy.
   3. Verification of quality documents and ensures documents for batch release are submitted timely.
6. Operation issues:
   1. Coordinate on- status memo, raised retention and documentation of activities.
   2. Audit reworked/ 100% inspection procedure and signed off on batch records.
7. Special projects:
   1. Perform mold approvals and protocol testings.
8. Responsible for compliance to EHS procedure and requirement.

Qualifications/ Education:

• Diploma/ NITEC (NTC/ ITC) GCE ‘O’ level/ Form IV (Mechanical) or equivalent and Certified Quality Inspector (CQI) preferred

Skill Set and/or Experience:

• NITEC (NTC/ ITC) with at least 5 years/Fresh Diploma
• Good Interpersonal communication skill
• Working knowledge of following preferred- Quality System, SPC, metrology, blue print reading

Reasonable Accommodation

Vantive is committed to working with and providing reasonable accommodations to individuals with disabilities globally. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please click on the link here and let us know the nature of your request along with your contact information. Form Link