Document Controller: Cement Manufacturers Association of the Philippines, (CeMAP) Inc.

Name of Company / Institution:

Cement Manufacturers Association of the Philippines, (CeMAP) Inc.

Work Location:

1 Corporal Cruz St. cor. E. Rodriguez Jr. Ave., Bagong Ilog Pasig City

Company Brief Description:

The CeMAP, as the association of the cement manufacturers of the Philippines, promotes and looks after the interests of its members in the following areas:

  1. Consistency in the production of high quality cement.
  2. Development of products and cement based products for the consumers.
  3. Prevent unfair competition and ensure a level playing field for the manufacturers.
  4. Leadership in the implementation of sustainable development initiatives.
  5. Data source for the association members and for government and non-government construction stakeholders.
  6. Public Relations for the cement industry.

Job Title:

Document Controller

Job Responsibilities:

  • Assist the QMO to ensure that the CTC meet the requirement of PNS ISO/IEC 17025:2017.
  • Ensure that the CTC’s quality procedures and standards are adhered to.
  • Support the Chemical Testing Group, Physical Testing Group and Technical Services Group in the preparation of the quality system documentation.
  • Coordinate, implement and maintain the CTC’s document control system.  Maintain a list of documents and forms (Master List) and identify location of electronic data and printed copies.
  • Check, review and organize all copies of the quality system documentation to ensure that the quality manual, procedures, work instructions, forms and other references are consistent and updated and controlled (no unauthorized distribution or reproduction).  Ensure easy retrieval of official documents and records when requested by internal or external party, upon approval of the QMO.
  • Respond to user requests for documentation.
  • Support accurate management of equipment labeling.
  • Investigate and implement corrective actions related to document control.
  • Assist QMO with new employee inductions especially in proper orientation on document handling and control.
  • Participate in trainings as required to achieve the level of competence for the document controller.
  • Ensure all documents and records are disposed properly according to the established retention period.
  • Prepare minutes of the laboratory meetings and coordinate issues arising/pending for action to person in-charge.  Provide copies of the minutes to all groups within one week after the meeting.
  • Ensure that all employees of CTC/CeMAP as well as external parties who come to the laboratory to witness/observe/supply/service/audit/assess/undergo training have signed the confidentiality and impartiality agreement.
  • Review test certificates for error in customer details based on sample receiving report.
  • Assist CTC’s Secretary in proper filing and organization of all official test reports and test certificates.
  • Coordinate with IT consultant on the proper and complete back-up of all electronic data.
  • Inform all concerned group of the revision/changes in documents and forms.
  • Comply with the CTC’s Health & Safety Policies.

Job Qualifications:

  • Graduate of BS Chemistry or any science related course
  • With at least one year experience in an accredited laboratory for ISO/IEC 17025:2017 or 2005
  • Adept with the documentation requirement of ISO/IEC 17025:2017
Immediate Supervisor:Quality Management Officer
Type of Employment:Full-time
Available Slots:1
Monthly Salary Range:PHP 20,001 to PHP 25,000

Contact Person / Details:

Joan Domingo
02-70929389
hr@cemap.org.ph

QA Analyst (Chemical Technician): Purebev International Corporation

Name of Company / Institution:

Purebev International Corporation

Work Location:

Km. 42, Governors Drive, Brgy. Hugo Perez, Trece Martires City, Cavite

Company Brief Description:

PUREBEV INTERNATIONAL CORP. IS A FOOD MANUFACTURING PLANT THAT PRODUCES ASEPTICALLY PACKED BEVERAGES LIKE MILK, CHOCOLATE- MILK AND FRUIT JUICE DRINKS.

Job Title:

QA Analyst (Chemical Technician)

Job Responsibilities:

  • Analyzes CIP concentration of cleaning chemicals during CIP and pH of water final rinse after CIP.
  • Conducts routine package integrity evaluation from Filling Machine.
  • Checks correctness of top codes of packs and carton boxes at specified frequency.
  • Ensures that non-conforming packs during filling operations are not included in good packs.
  • Gets aimed samples from Filling Area while Filling Machines are running and labels them accordingly for microbial evaluation.
  • Records every event in Filling operators in Package Integrity Monitoring Form.
  • Conducts routine checking of hydrogen peroxide concentration and peroxide residue test the finished product upon filling in aseptic packaging.
  • Conducts routine calibration of QA Station Lab instruments.
  • Prepares reagent (ink solution).
  • Conducts routine swab test on production personnel and equipments and routine air exposure test in processing areas.
  • Performs aseptic sampling of rinse water from identified sampling points or microbial analysis.
  • Conducts checking of concentration of submitted concentrated CIP chemicals.
  • Assists Production and Maintenance Departments in water test runs by performing package integrity evaluation.
  • Maintains cleanliness in the QA Station Lab.
  • Records chemical consumption for every chemical usage.
  • Maintains QA retention samples of evaluated empty packs from routine in-line packaging integrity evaluation.
  • Assists in troubleshooting activities by isolation of visible defective packs from identified pallets.
  • To uphold all Company Rules and Regulation, Health, Safety and Environmental Procedures and the company’s Food Safety Policy

Job Qualifications:

  • Must possess a Bachelor’s degree in Chemistry, Food Science, Food Technology or any related allied courses
  • Must be a Licensed Chemical Technician (Passed Board/Professional License Exam)
  • With or without experience in the food manufacturing industry
  • Flexible, hardworking, willing to work in shifting schedule and computer literate.
  • With basic knowledge in good laboratory practices, laboratory safety
  • Knowledgeable in various laboratory analysis and operation of various laboratory equipments
  • With knowledge on GMP, HACCP and Food Safety Standards
  • Good communication skills and computer literate
  • Good Analytical skills
  • With good leadership skills and ability to related well in all levels of the organization
  • Willing to relocate in Trece Martires Cavite or in nearby place
Type of Employment:Full-time
Available Slots:1
Monthly Salary Range:PHP 12,001 to PHP 15,000

Contact Person / Details:

Anne Loqueloque
09069165549
maria.anna.loqueloque@gmail.com

QC Analyst: Medi-Rx, Inc.

Name of Company / Institution:

Medi-Rx, Inc.

Work Location:

11 Mindanao Avenue Bagong Pag-asa, Q.C.

Company Brief Description:

Medi-Rx Inc., is a Filipino-owned local pharmaceutical manufacturing company that has over 41 years
experience in marketing and manufacturing pharmaceutical healthcare products.

Job Title:

QC Analyst

Job Responsibilities:

  • Analyze and inspect incoming raw materials, in-process, and finished products.
  • Set up, operate and maintain laboratory equipment.
  • Perform good laboratory practices in the performance of laboratory activities.

Job Qualifications:

  • Licensed Chemist
  • Pharmaceutical laboratory experience as analyst is preferred.
  • Licensed fresh graduates are welcome to apply.
Type of Employment:Full-time
Available Slots:1
Monthly Salary Range:PHP 20,001 to PHP 25,000

Contact Person / Details:

Estrella E. Nicor
84269765
zonie_medirx@yahoo.com

Quality Services Analyst: VIBELLE MANUFACTURING CORPORATION

Name of Company / Institution:VIBELLE MANUFACTURING CORPORATION
Work Location:18 JP BAUTISTA AVENUE, POTERO MALABON CITY
Company Brief Description:Vibelle Manufacturing Corporation, local licensee of Jergens, skin care products and the maker of pioneering Filipino Brand Caronia.
Job Title:Quality Services Analyst
Job Responsibilities:
  1. Performs evaluation of raw materials, packaging materials, in-process and finished products to ensure conformance with technical specifications through established physical and chemical test procedures.
  2. Provides technical support to operations by enforcing strict cGMP compliance;
  3. Ensures that all products produced are in compliance with regulatory requirements prescribed by the Food and Drug Administration (FDA) and Philippine Drug Enforcement Agency (PDEA) and other applicable regulatory agencies.
Job Qualifications:
  1. Must be a licensed Chemist, or Chemical Engineer;
  2. Adept in using standard laboratory equipment and instruments;
  3. Knowledgeable in audit procedures and accreditation processes such as cGMP and ISO.
  4. Must be Filipino citizens or hold relevant residence status;
  5. Preferably has at least one year prior work experience in quality assurance and control;
  6. Preferably has prior work experience in the personal care or cosmetic industry;
  7. Highly analytical, has good attention to details, and can work with minimal supervision;
  8. Proficient in Microsoft Office or equivalent software;
  9. Has above average written and oral communications skills;
  10. Willing to work and to be based in Potrero, Malabon City.
Type of Employment:
Available Slots:
Monthly Salary Range:
Contact Person / Details:Email Add: hrd@vibelle.com
Contact #: 361-8049/364-1101
Contact Person: Romina L. Gabriel