1-year contract
Based in Tuas, Singapore
Transportation provided at selected MRT locations to and fro Plant.
ABOUT US
Pacific Refreshments Pte Ltd (The Coca-Cola Company) is a strategic concentrate manufacturing plant in Asia. We are an export facility, specializing in the manufacturing of concentrates and beverage bases, with a complex portfolio, supporting the ASEAN, South Pacific and Southwest Asia business units. We are on a journey of growth - having completed the construction and expansion of our site towards doubling our manufacturing capacity in recent years. We have also embarked on our digital transformation journey, striving to be the Lighthouse for the Consumer Products Supply (CPS) plants in Asia and to be a leader in digital transformation.
Pacific Refreshments Pte Ltd is a winner of the ‘2020 HR Asia Best Companies to Work For’ Award.
Position Overview
Responsible for evaluating conformance to Company specifications for all ingredients from receiving to work in process to finished beverage bases, including processes, whether at Plant or at suppliers.
Ensure compliance with good laboratory (GLP) practices and good manufacturing practice (GMP), thereby adding value to the Company’s business.
Responsibilities
- Evaluate ingredients, work in process, and finished beverage bases with physical-chemical, microbiological and sensory evaluation test procedures to ensure conformance to specification and in accordance to Company ‘s Quality system.
- Complete the approval and release procedures for ingredients, packaging materials and finished product and ensure quality data are transacted in SAP/Sample Manager (Laboratory Integrated Management System (LIMs)).
- Ensure ingredients have all pertinent documentation (Certificates of Analysis, pre-shipment approvals, etc. before their final release.
- Sample ingredients, packaging materials, intermediate and final products both within the premises and at external storage if required.
- Calibrate analytical equipment accordingly.
- Conduct laboratory testing of equipment /processes/methods to ensure accuracy and repeatability of quality data through process capability studies, control charting, methods validation, out of specification/out of trend analysis demonstrating that GLP is practiced consistently. Document and maintain records of laboratory procedures, process and test data.
- Keep record of chemicals, glass wares, reagents inventories and MSDS for all chemicals. Support the purchase of laboratory item.
Requirements
- Diploma in Applied science or Food science related discipline.
- Minimum of 1 years’ experience in food/beverage or pharmaceutical multinational organization’s quality control department/laboratory operations.
- Good Manufacturing Practices (GMP) experience would be considered as an advantage.
- Good Laboratory Practices (LGP) experience would be considered as an advantage.
- Demonstrated ability of executing food industry analytical testing.
- SAP knowledge would be considered as an advantage.
- Able to support shift work (7:30am - 4pm / 3:30pm - 12mn).
If this sounds like something you're interested to explore further, we look forward to meeting you in our Happiness Factory!
