What Jobs are available for Manufacturing Companies in Caloocan?

JOB QUALIFICATIONS:

• Graduate of any Engineering or four-year degree course
• Detail-oriented with strong analytical and problem-solving skills
• Excellent written and verbal communication and documentation abilities
• Self-motivated, proactive, and adaptable to nightshifts and varying shifting work schedules, including weekends and holidays as needed
• Previous experience in a manufacturing company (at least 6 months) is an advantage but not required
• A teamplayer who can also work independently in ensuring quality and production standards are met
• Willing to be assigned to a fast-paced manufacturing environment

Work Location: Must be willing to be assigned in Meridian Industrial Park Brgy. Maguyam Silang, Cavite

Note: We do not charge any recruitment fee from candidates at any stage of the recruitment process. Please be wary of any individual or organization that asks for a fee in exchange for employment or recruitment assistance as they do not represent our company.

Performs daily monitoring and calibration activities.

Performs sampling and inspection of starting materials and finished goods.

Performs quality inspection of production processes to ensure that they adhere to the established procedures and produce quality products.

Utilizes tools and equipment to verify the functionality and assess the quality characteristics of starting materials and finished products.

Identifies potential issues from the quality requirements.

Validates dispensed Raw Materials and Packaging Material rejects.

Updates Quality Control transactions and reports.

Maintains the detailed records of inspection, testing, and findings.

Ensures that the quality risks are correctly assessed and identified. Leads the Quality Control Team and product development procedures to meet customer expectations.

A. Primary function

• Responsible for the overall Quality Control Program of the Manufacturing which includes scope, frequency, methods of sampling, and testing.
• Knowledgeable in method validation and Multi-point Dissolution.
• Prepare on-time Quality Control report to summarize test results and coordinate with the concerned department for necessary actions.
• Analyzes raw materials, intermediates, bulk products, and finished products as per documented analytical procedures.
• Responsible for providing testing disposition of raw and packaging materials, in-process samples, and finished products according to defined specifications within the agreed lead time.
• Maintain the QC Laboratory to ensure continuous support to the operations and compliance to Good Laboratory Practices (GLP) and review its capacity based on current needs.
• Participate in appropriate technical seminars, conferences, and workshops to develop competency and familiarity with the latest developments in the field of chemical testing.
• Provide statistical input into the development of plans and justification of results using statistical and quality risk management tools (design of experiment, failure mode and effect analysis, hazard analysis, fault tree analysis).
• Assist with test method modifications, development, and validation of new analytical methods.
• Responsible for interpreting complex analytical results, troubleshooting and developing complicated methods and techniques, and completing development, application, and validation of work (protocol drafting, data collection, and preparation of report).
• Recognize results that deviate from established standards, specifications, and trends and independently recommend appropriate actions.
• Perform testing necessary to investigate out-of-specification (OOS) test results.
• Complete OOS reports including corrective and preventive actions independently.
• Support and monitor testing of new formulations and stability products.
• Review and approve testing documentation of other analysts.
• Prepare analytical reports and certificate of Analysis.
• Use strong analytical, problem-solving, and independent decision-making skills.
• Conduct in-house calibration of instruments.
• Perform regular portability tests of process and drinking water to ensure compliance with standards.
• Train and develop other Technical Services Department associates.
• Prepare and revise Standard Operating Procedures by biannual review.
• Update current methods as necessary using the change control system.
• Organize and schedule of work workload for team members.
• Enforce safety procedures and report safety incidents
• Plan, oversee, and implement the departmental objectives in meeting the company's strategic plans.
• Conduct raw material audits.
• Coordinates inter-departmental quality activities

B. Perform other related duties that may be assigned from time to time.

Job Qualifications

• BS degree in Chemistry, and must be a Licensed Chemist.
• At least three (3) to five (5) years experience in QC in a pharmaceutical firm, with a minimum of two (2) to three (3) years in a Supervisory position under Quality Control Management.
• 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, communication and skills.
• Good moral character.

Job Type: Full-time

Benefits:

• Company Christmas gift
• Company events
• Employee discount
• Free parking
• Opportunities for promotion

Ability to commute/relocate:

• Carmona: Reliably commute or planning to relocate before starting work (Required)

Work Location: In person

Key Responsibilities:

1. Implement inspection, testing, and evaluation methods for products and equipment
2. Ensure adherence to internal and external quality standards
3. Collect, analyze, and summarize production data for reporting
4. Oversee food production, packaging, and storage areas to ensure safety compliance
5. Develop and enforce food safety policies and procedures
6. Ensure compliance with HACCP and FDA regulations

• Bachelor's degree in Engineering or Sciences
• Extensive experience in food safety, quality assurance, and lab operations

• Competitive salary and benefits
• Professional development opportunities
• A collaborative and safety-focused work environment

JOB SUMMARY:

Quality Control Engineer is responsible on all aspects of the QC function by establishing necessary controls and ensuring their proper and strict implementation, and in planning, organizing and controlling the quality activities.

QUALIFICATIONS:

• BS in Engineering Degree (IE, ECE, ME)
• With relevant Experience is a MUST.
• Expertise in Microsoft Office: Microsoft Excel, Microsoft Word, Microsoft Power Point and Technical Writing.
• With strong problem solving and analytical skills .
• Quick correlation of cause and effect and improvisation of corrective measures meet unexpected developments needed.
• With knowledge in electronics, and printed circuit board assembly is an advantage.
• Willing to be assigned in Cabuyao or Calamba, Laguna

Job Type: Full-time

Benefits:

• On-site parking
• Paid training
• Transportation service provided

Ability to commute/relocate:

• Tanauan: Reliably commute or planning to relocate before starting work (Required)

Work Location: In person

Job Needs:

The leading supplier of Metal Working Fluids

and Lubricants for the manufacturing industry is in need of…

One (1) Quality Control Analyst- Santa Rosa City, Laguna

to be part of our winning team.

Job Highlights

• Personal and professional growth
• Challenging but fun working environment
• Training

Job Responsibilities

• Prepares reagents, solutions and standards needed for product testing.
• Performs comparisons between our products and competitor's items.
• Conduct product analysis, inventory of chemicals, consumables and spare parts.
• Maintains an organized system of data record keeping and generate test reports.
• Provide input for quality and process improvement for production.

Job Qualifications

• Candidate must possess at least a Bachelor of Science in Chemistry/Chemical Engineering or equivalent.
• At least 1-year proven work experience in the related field is required for this position.
• Fast learner, has initiative, and can blend well in any type of work environment.
• Lives near Santa Rosa City, Laguna

Compensation & Benefits

• Working schedule (Monday to Friday)
• Multiple opportunities for Growth and Development
• Basic salary up to Php 18,000 - Php 22,000
• Rice Subsidy
• Annual salary increases and incentives
• HMO upon one year in service
• Shuttle provided

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

QA/QC STAFF

Job Qualifications:

• Bachelor's degree in engineering (Mechanical, Industrial, Electrical, or related fields)
• 2-3 years of experience in quality assurance, preferably in a manufacturing or production environment, with hands-on experience in defect analysis, product testing, and process optimization.
• Proficient in operating QA testing machinery and conducting dimensional and performance testing.
• Strong understanding of quality standards, tools, and equipment qualification.
• Familiar with statistical analysis software and quality management systems.
• Ability to perform root cause analysis and implement corrective actions effectively.
• Strong skills in failure analysis, defect tracking, and performance optimization.
• A keen eye for detail in monitoring quality metrics, identifying defects, and ensuring compliance with established standards.
• Ability to manage multiple tasks, prioritize effectively, and maintain detailed records of all quality activities, tests, and reports.
• Willing to be assigned at Furukawa Electric Thermal Management Solutions and Products Laguna, Inc., Laguna Technopark, Santa Rosa for Direct Hire.

BENEFITS:

FREE SHUTTLE

FREE UNIFORM

FREE MEDICAL

Job Types: Full-time, Permanent

Benefits:

• Opportunities for promotion
• Paid training
• Promotion to permanent employee
• Transportation service provided

Education:

• Bachelor's (Required)

Experience:

• QA/QC: 2 years (Required)

License/Certification:

• ISO Certificate (Preferred)
• PRC License (Preferred)

Location:

• Santa Rosa (Preferred)

Work Location: In person