Careers

Process Engineer
June 21, 2021

Job Responsibilities

  • Supervises the whole production process;
  • Acts as production liaison with Research and Development, Quality Assurance Department on new manufacturing processes;
  • Responsible for proper orientation of personnel on manufacturing process;
  • Conducts Time and Motion study for each product during first production and submits recommended direct labor cost for approval.
  • Improves process capability and production volume while maintaining and improving quality standards.
  • Maintains record of machine equipment inventory and monitors preventive maintenance schedule as well as coordination with suppliers and maintenance staff for machine breakdown.
  • Ensures equipment works to its specification and appropriate capacity.
  • Strictly implements Current Good Manufacturing Practice regulations in the production area enforced by FDA ensuring safe working conditions and compliance with health and safety legislation.

Qualifications:

  • Must be a graduate of BS Industrial Engineering or Chemical Engineering degree; Professional license is not a requirement but an advantage;
  • With 1 -2 years relevant experience as Supervisor/Officer or at least 4 years relevant working experience in an FMCG environment;
  • Team player with strong interpersonal skills;
  • Proficient in MS Office Application especially in MS Excel;
  • Experience with Lean Manufacturing is an advantage;
  • Performs tasks that may be assigned by his/her Supervisor and Department Head from time to time.
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Nurse/Pollution Control Office
June 21, 2021

Job Responsibilities

  • Helps develop and implement health and safety programs;
  • Provides emergency treatment in the workplace, but not limited to providing assistance to injured person to the nearest hospital in emergency cases; administer over the counter medication to employees;
  • Documents all employee injury and illness in the workplace and maintain health records.
  • Monitors mental/physical health conditions, coordinates with HMO and provide immediate assistance if needed; promotes healthy eating and wellness programs;
  • Documents and evaluates Annual Physical Examination and ensures that the company is up to date with public health and employment legislations.
  • Performs the main tasks of a Pollution Control Officer:
  • Processing of Accreditation Documents for Chic Centre
  • Submission of Quarterly Reports and Renewal of Permits for Department of Environment and Natural Resources, Laguna Lake Development Authority;
  • Handling of the disposal of Hazardous Waste and Waste Water Disposal;
  • Representing Chic Centre in meetings, seminars in DENR, LLDA.
  • Sees to it that the Accredited Third Party Hauler and Treatment Facility is compliant to all the Environmental Law set by the Government; monitors the Permit to Transport and Renewal of Accreditation;
  • Coordinates with other department in terms of Waste Disposal and standardization of SOPs
  • Performs tasks that may be assigned by his/her Supervisor and Department Head from time to time.
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Quality Control Analyst
June 21, 2021

Main Functions: The QC Analyst is directly responsible on the analysis and release of all incoming Raw and Packaging Materials, Bulk Products and Finished Goods

Primary Job Responsibilities:

  1. Conducts evaluation, analysis and release of Raw and Packaging Materials, Bulk Products and Finished Goods
  2. Examines, checks, releases status and recommend approval/rejection of Raw and Packaging material as well as Bulk and Finished Products, Products manufactured or packed or held under control by the company or third party
  3. Ensures equipment to be used in production are cleaned or sanitized prior to usage
  4. Ensures proper documentation of the test results in the Quality Control Logsheets and Batch Manufacturing Record (BMR) and ensure proper tagging of all tested materials stored at Warehouse
  5. Checks for completeness of data entries on the submitted Batch Manufacturing Record (BMR) prior to release of the tested bulk products to filling
  6. Prepares reports e.g. Rejection, Approval, Certificate of Analysis or Certificate of Inspection of Finished Goods, Raw and Packaging Materials and other necessary reports
  7. Collects retention samples and conducts product stability testing and prepares necessary reports. Ensures proper labeling, storage and recording of data in the QC Logsheets
  8. Prepares and conducts Raw Material Audit and Self-Plant Audit in compliance to cGMP/GMP
  9. Helps establishes Test Method and Specifications of Intermediate Bulk, Raw and Packaging Material and Finished Goods together with the Technical Team Lead;
  10. Assists Technical Team Lead/Head in handling customer complaints, feedback and inquiries.

General Job Responsibilities

  1. Ensures implementation of Good Laboratory and Housekeeping Practices, Good Manufacturing Practices and Good Documentation Practices
  2. Monitors, requests and conducts inventory of laboratory and office supplies.
  3. Monitors and requests calibration and maintenance of instrument and equipment to ensure good quality of analytical results according to schedule
  4. Prepares other necessary reports or Memo regarding non-compliance to standard procedures or any issues with product quality related Provides assistance and should also perform extended Quality Control duties in the absence of co-workers under supervision of the Technical Team Lead/ Technical Head.

Qualifications:

  • Team player with strong interpersonal skills;
  • Keen to details, good organizational and decision making skills.
  • Preferably with 1 - 2 years of experience in similar position in a manufacturing setting;
  • Graduate of BS Chemistry with Professional License is required.
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Research and Development Assistant
June 21, 2021

Primary Job Responsibilities

  1. Manages activities in line with new product development and reformulation for existing products.
  2. Prepares laboratory batch in accordance with product profile.
  3. Develops packaging materials and establishes specification for new products.
  4. Conducts product evaluation e.g. usage test, stability test to establish shelf life and other parameters.
  5. Validates process to be employed for the new product and the equipment suitable for the process.
  6. Prepares Master Formula, Packaging/Product Specification Sheet and other necessary documents prior to production of new or reformulated products.
  7. Requests and monitors pilot production run (if necessary)
  8. Responsible on monitoring of products during initial production run.
  9. Retains production samples for monitoring and stability testing of new products
  10. Prepares Product Information File of new products and endorse to Regulatory Affairs Officer.
  11. Assists QC analyst for the analysis and/or acceptance of new incoming raw and packaging materials.
  12. Conducts investigation on products with quality issue and recommends corrective actions.
  13. Performs trade check for product quality checking and prepare necessary reports.

General Job Responsibilities

  1. Ensures implementation of Good Laboratory and Housekeeping Practices, Good Manufacturing Practices and Good Documentation Practices
  2. Monitors, requests and conducts inventory of laboratory and office supplies.
  3. Request calibration and maintenance of instrument and equipment to ensure good quality of analytical results according to schedule
  4. Prepares other necessary reports or Memo regarding non-compliance to standard procedures or any issues with product quality related
  5. Provides assistance and should also perform extended Quality Control duties in the absence of co-workers.

JOB QUALIFICATIONS:

  • Bachelor’s degree required, preferably Bachelor of Science in Pharmacy.
  • Professional license is required.
  • Team player with strong inter personal skills; keen to details
  • Good organizational and decision-making skills;
  • Preferably with 2 years of experience in similar position in manufacturing setting;
  • Experience in Personal Care manufacturing company is an advantage;
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