QC Analyst (Fixed-Term Contract)
Haleon Careers
Description
Haleon is a world-leading consumer health company that is driven by the unique combination of deep human understanding and trusted science. We are now looking for a Quality Control Analyst to join our team in Jakarta Timur, Indonesia.
As Quality Control Analyst, you will be responsible for conducting tests and evaluating results to ensure that our products meet GMP and company standards. You will analyze samples, record data, and report your findings. You will also be expected to take on additional tasks as required. This is a 12-month contract position. We offer a rewarding and collaborative work environment with a competitive compensation package. If you are looking for an opportunity to help improve everyday health for billions of people, we invite you to join our team.
This role will provide YOU the opportunity to lead key activities to progress YOUR career, these responsibilities include some of the following:
- • Conduct chemical and physical testing for finished product effectively and efficiently in compliance to valid analytical method and record the results in laboratory report, as per testing plan prepared by Quality Control Lead.
- • Conduct stock opname and management of analytical working standard.
- • Immediately report any OOS results and deviations during the analysis in Quality Control Lab to Quality Control Lead.
- • Record, store, inspect and destroy finished product samples.
- • Control the preparation, use, storage and expiration date of the reagent and reference standard used in the testing process and ensure it is used in accordance with a valid procedure.
- • Record the use of reagent and reference standard and notify Quality Control Lab Support or Reference Standard Responsible Person, if any reagent or reference standard is out of stock or expired.
- • Check the date of calibration of instrument in the Quality Control Laboratory before use, record its use and report to Quality Control Lead if any nonconformance is found.
- • Ensure Good Documentation Practice and data integrity is always shown on all GxP activities.
- • Maintain the cleanliness of glassware and other instruments and work areas in the Quality Control laboratory.
Why you?
Basic Qualifications:We are looking for professionals with these required skills to achieve our goals:
- • Vocational school for Chemical Analyst or associated science
- • 4 years in pharmaceutical or associated industry
Preferred Qualifications:
If you have the following characteristics, it would be a plus:
- • Understanding of basic manufacturing processes, laboratory activities and basic quality system
- • Good knowledge of analytical/ inspection techniques, precision and accuracy
- • Good knowledge of cGMPs and local regulatory requirements especially in good laboratory practices and good documentation practices.
- • Skillful to operate laboratory instrument related with the work assignment.
- • Good knowledge of troubleshooting analytical problems.
- • Able to use MS office and internet.
- • Able to have basic communication in English both verbal and written.
- • Good team work and interpersonal skills.
- • Result oriented, good reporting skill, strong analytical and numerical skills.