445 Quality Control jobs in Muntinlupa City

The Megawide Group has a vision of a First-World Philippines. This vision united all its businesses, driven by a mission to deliver engineering excellence and innovation in its diverse assets throughout the Philippines.

We are a proud Quadruple A contractor in the Philippines, an exceptional innovator in Engineering, Procurement, and Construction (EPC), and infrastructure development through proprietary engineering methodologies.

Megawide is currently seeking an innovative and results-driven Quality Control Engineer who will oversee quality policies, systems, and procedures, and will be responsible for ensuring construction services meet set standards of quality, project specifications, and customer requirements.

Job Qualifications:

• Graduate of BS Civil Engineering; must be a licensed Civil Engineer.
• Minimum of three (3) years of experience in quality control in construction projects, preferably in infrastructure or civil works.
• Knowledge of QA/QC procedures, ITPs, and material testing.
• Detail-oriented, with strong organizational skills; able to multitask, prioritize workload, and work independently to meet deadlines with minimal supervision
• Must have strong oral and written communication skills

We are looking for a detail-oriented Audio Quality Control to oversee the quality and accuracy of audiobook narrations. This role requires a keen ear for detail, strong organizational skills, and the ability to manage multiple projects efficiently.

Job Type: Full-time

Pay: Php28,000.00 per month

Benefits:

• Free parking
• On-site parking
• Pay raise

Ability to commute/relocate:

• Taguig: Reliably commute or planning to relocate before starting work (Preferred)

Education:

• Bachelor's (Preferred)

Language:

• English (Required)

Work Location: In person

Expected Start Date: 10/07/2025

Job Description:

*Responsible for the regular conduct of the food safely compliance inspection of assigned stores and distribution centers to validate compliance of establishment to food safety management and product handling standards

*Candidates must possess at least a Bachelor's/College Degree in Food Technology/Nutrition/Dietetics or its equivalent

*With at least 1 year work experience handling quality and regulatory related dunction from a food manufacturing or retail industry

*Experience in Food Safety Compliance Inspection, Quality Management Program Accreditation, and Health and Safety Compliance is an advantage

• Inspect and verify incoming raw and packaging materials against specifications, COAs, and supplier documents.
• Check identity, labeling, and physical attributes (color, odor, texture, appearance) of materials and products.
• Quarantine and report non-conforming or suspect materials/products to the QA/QC Specialist
• Collect, label, and store retention samples with proper documentation.
• Ensure production areas, equipment, tools, materials, and personnel comply with GMP requirements before and during operations.
• Monitor employee hygiene and grooming practices.
• Conduct repacking process checks, including fill weight verification, at defined intervals.
• Perform 100% QC verification of finished goods to confirm compliance with packaging, labeling, and quality specifications.
• Document all inspection findings, discrepancies, activities and inspection reports.
• Escalate issues, recommend corrective actions, and issue GMP tickets for violations.
• Conduct weekly GMP audits in the warehouse and monthly GMP audits in production.

QUALIFICATIONS:

Education:

• College level/graduate with any related science course.

Experience:

• Minimum of (6) months relevant experience in QA/QC or related role.

Knowledge:

• Calibration and verification of measuring devices.
• Knowledge of GMP, HACCP, and quality inspection practices.
• Sampling procedures and retention handling.
• Non-conformance reporting and corrective actions.
• Computer literate (MS Office, email, data entry)
• Document literate (record-keeping, reporting, filing)

Other Qualification:

• Flexible and willing to perform cross-functional tasks when needed

Job Types: Full-time, Permanent, Fresh graduate

Benefits:

• Additional leave
• Company Christmas gift
• Company events
• Employee discount
• Health insurance
• Opportunities for promotion
• Promotion to permanent employee

Education:

• Senior High School (Preferred)

Experience:

• Quality Control: 1 year (Preferred)
• Food Manufacturing: 1 year (Preferred)

Work Location: In person

• Graduate of BS Chemistry
• Licensed Chemist
• With or without experience
• Knowledgeable in performing laboratory techniques and chemical analysis
• Good analytical thinking and decision-making skills
• Has keen attention to details.

Job Types: Full-time, Permanent, Fresh graduate

Pay: Php19, Php21,000.00 per month

Benefits:

• Additional leave
• Free parking
• Health insurance
• On-site parking
• Opportunities for promotion
• Pay raise
• Promotion to permanent employee
• Staff meals provided
• Transportation service provided

Work Location: In person

What we're looking for

• With or without experience
• Fast learner
• At least college level
• Physically fit

Job Description

Responsible for verifying the activities done during the In-house inspection of finished products and ensuring FDA requirements and company objectives are met.

• Monitors compliance of all staff with the requirements of GMP
• Ensures that the products comply with the specifications as per approved artwork or finished product specifications
• Signs Batch Inspection Records after every activity is done
• Counterchecks damages and non-conformances
• Ensures that the products are inspected and stored accordingly, to obtain the required quality
• Ensures strict implementation of instructions (SOPs) to QC procedures.
• Makes new SOPs, revises or updates existing SOPs
• Performs activities related to Pharmaceutical Quality System (such as Product Quality Review, Quality Risk Management, Change Control, Deviations, OOS and CAPA)
• Ensures initial and continuing training of QC staff is carried out and adapted according to need
• Ensures communication with the concerned departments to raise quality issues to the appropriate levels of management
• Coordinates with the Production, Warehouse, Sales, and Regulatory Departments regarding quality issues
• Generates inspection reports, or other reports, as needed
• Ensures that all measuring and monitoring devices (weighing balances, thermohydrometers, data loggers, bio ref, thermal gun, etc.) used by the company are calibrated; ensures proper coordination with other concerned departments (ex. Production and Warehouse) regarding calibration schedules and maintains an updated calibration master plan as needed
• Performs and/or supervises daily and monthly internal calibration of weighing balances in the Production/QC Area
• Other responsibilities that are deemed necessary by the Management

Job Qualification

• A Licensed Pharmacist with active license
• Knows how to operate Microsoft Office Applications
• Knowledge of the Good Manufacturing Practices and FDA guidelines
• Highly self-motivated, goal-oriented, and committed to pursuing a long-term career
• Can work under minimal supervision

• Ensure Compliance- Make sure products meet specifications and comply with regulations
• Supervise Inspectors- train and oversee inspectors who perform quality checks
• Schedule Inspections- plan inspections, audits and data collections
• Follow-up on programs- make sure programs are being followed, such as Good Manufacturing Practices (GMPs).
• Resolve Issues- take corrective actions for non-compliant items.
• Review Documentations- check production records and other documents to verify compliance.
• Coordinate with clients- work with clients to ensure inspections are timely
• Document Deviations- record any deviations from quality standards.

Qualifications:

• must be College Graduate of BS in Industrial Engineering
• with 3-5 years experience in Managerial Position
• with experience in handling Ceramics Manufacturing Industry.

Job Types: Full-time, Permanent

Work Location: In person

Collect information about the composition of chemical substances, and process and communicate this information through the principles of science, engineering, and mathematics. Develop and improve processes, equipment, and formulas, and prepare compounds and solutions to conduct tests.

• Sampling and testing of raw materials, intermediates, and finished products
• Preparing Quality reports, including analytical reports (for raw materials and finished products)
• Calibrating analytical equipment when required.
• Creating and executing method development and validation test protocols for finished products and generating the appropriate analytical methods.
• Perform routine and non-routine chemical analysis of products using standard operating procedures.
• Write and execute chemical testing procedures.
• Maintain up-to-date documents for chemical testing methods and activities.
• Operate laboratory equipment safely and effectively to conduct testing.
• Record, analyse and report test results to Managers.
• Maintain inventory of chemicals and supplies in the laboratory.
• Supporting all Quality Control activities.
• Ensuring good relations and communications with all members of the team and responding politely and in a timely fashion to internal and external customers.
• Perform various techniques like HPLC.
• Observing and complying with Good Manufacturing Practices (GMP) and Good Distribution Practices (GDP).
• Perform other related duties that may be assigned from time to time.

Job Qualifications:

• BS degree in Chemistry, Chemical Engineering, or Chemical Technology/Pharmacist
• At least two (2) years of direct lab experience in an FDA-regulated pharmaceutical firm as an advanced but not required.
• Must be a Registered Chemical Engineer or Registered Chemical Technician.
• Strong knowledge of Standard Operating Procedures and compliance with Good Laboratory Practices, Good Documentation Practices, and Current Good Manufacturing Practices.
• Strong working knowledge of technical and quality concepts of the manufacturing and testing of pharmaceutical products.
• Experience in participating in deviation investigations, determining root cause, and developing corrective action plans.
• Team player with strong interpersonal, organizational, and communication skills.
• Willing to work in Bancal, Carmona Cavite
• Working schedule will be from Mondays to Fridays

Job Type: Full-time

Benefits:

• Company Christmas gift
• Employee discount
• Free parking

Ability to commute/relocate:

• Carmona, Cavite: Reliably commute or planning to relocate before starting work (Preferred)

Experience:

• Manufacturing: 2 years (Preferred)

License/Certification:

• Licensed Chemist (Preferred)

Work Location: In person