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Quality Assurance Specialist (Lab)

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Job Description

Why Ansell

Ansell is a world leader in providing superior health and safety protection solutions that enhance human well-being. The world's need for better protection never stops, so Ansell is constantly researching, developing and investing to manufacture and distribute cutting edge product innovation and technology, marketed under well-known brands that customers trust. Operating in two main business segments, Industrial and Healthcare, Ansell is the market leader that continues to grow, employing 14,000 people worldwide.

For more information about our Company, our People and our Values, please follow the link https://www.ansell.com

Ansell is looking for Specialist QA lab to be based in Seremban, Malaysia. This position is responsible to conduct lab testing for raw material, in-process material, finished goods, and other required testing for waste water, city incoming water ensure all readings are according to the parameters and specifications.

What you can expect from Ansell

  • Work for a world leader in the health and safety protection solutions industry.
  • A secure workplace with competitive remuneration and annual bonus based on own and company performance.
  • Inclusive, collaborative, and supportive work atmosphere.
  • A diverse and international work environment.

What your role will be in details

Reporting to the Assistant QA Manager, you will:

1) In-coming Raw Material Quality Control.

  • To review all the in-coming raw material records and to take action accordingly when there's any issue regarding the receiving, checking and inspection.
  • To evaluate supplier/new supplier based on conformance or deviation from the new material quality specification.

2) In-process Materials Quality Control

  • To ensure that procedures for in-process inspection and testing activities are documented and adequate.
  • To ensure that in-process inspection and testing are in accordance to quality plan and records of verification are maintained as per quality plan.
  • To ensure that in-process material is not used or processed (except due to urgency which shall then positively identified and recorded to permit recall) until it has been inspected/verified as conforming to the specified requirements.

3) Finished Gloves Properties Testing

  • To ensure that procedures for finished glove physical properties/chemical properties testing are documented and adequate.

4) Equipment Calibration/Verification

  • To ensure that inspection, measuring and test equipment that could affect quality are identified, control and calibrate/verify at appropriate intervals.
  • To ensure that the process and procedure for equipment calibration/verification are documented and adequate.
  • To ensure that the status of calibration/verification is suitably identified on the equipment/appropriate means and calibration/verification records are maintained.
  • To ensure that the environmental conditions are suitable for the calibrations/verifications, inspection, measurements and test being carried out.
  • To ensure that the handling, preservation and storage of inspection, measuring and test equipment is such that the accuracy and fitness for use are maintained.
  • To ensure adjustable equipment is safeguard by suitable means to prevent adjustment.
  • To ensure external calibration is carried out as schedule and calibration certificate is properly maintained.

5) New Supplier Assessment on Raw Materials

  • To monitor and evaluate the existing supplier quality performance and identify needs for new supplier assessment.
  • To compare the product specification of materials supplied by existing and new supplier.
  • To evaluate supplier based on conformance or deviation from the new material quality specification.

6) Quality System

  • To periodic review Laboratory procedure and activities to ensure meeting ISO9001 Quality Management system requirement.
  • To revise Lab SOP to reflect actual practice.

7) Support Environment Testing

  • To carry out lab testing of wastewater and other testing on discharge from production lines

What will you bring

  • Bachelor's Degree in Chemistry, Polymer Science, Rubber Technology, Chemical Engineering or its equivalent
  • Good communication and interpersonal skills
  • Good written and spoken English and ability to communicate in a language other than English and Malay or a foreign language will be an added advantage.
  • Well organized and with capability to make good reporting.
  • Prior medical device experience, or other regulated industry
  • Ability to formulate responses to common inquiries or complaints from customers.
  • Have good understanding of the Quality Assurance functions and its related disciplines.
  • Possess foundation level knowledge of glove dipping processes and on product defectives and quality.
  • Possess knowledge in analytical techniques, good knowledge in relevant computer software such as SPC software etc.
  • Has good understanding of safety, health and environment practices, good manufacturing practices.
  • Good work & time management skills and applies good project management skills.
  • Competent in systematic and statistical data analysis, as well as presentation of results.
  • Good understanding of Quality Management Systems, in particular for ISO 13485.
  • Good understanding of Good Lab Practices.

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About Company

Job ID: 146466915