77 Manufacturing jobs in Trece Martires
Manufacturing Engineer
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Qualifications:
- Bachelor's degree in Electronics, Manufacturing, Industrial, Mechanical & Electrical Engineering
- 3 to 5 years experience in high-volume electronics manufacturing
- Strong knowledge of JEDEC, ISO9001/14001, RoHS standards
- Experience in quality engineering, FMEA, SPC, and process validation
- Proficient in documentation, team collaboration, and training delivery
Job Type: Full-time
Work Location: In person
LOGISTICS ASSISTANT for Manufacturing
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Job Description
• Receives and verifies invoices and delivery orders from warehouse.
• Coordinating with local suppliers in placing orders & ensure timely deliveries & oversee the quality of delivered goods & or services.
Qualification
• Bachelor's degree in Business Administration or other related courses;
• At least 1 year of experience in warehousing and/or Material Control of manufacturing companies or related industries
• Has experience on inventory management (including inventory count process) and related process improvement initiatives
Manufacturing / Production Control Manager (47669)
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- Productivity Improvement
- Operational Improvement
- OEE (Overall Equipment Effectiveness) Analysis
- Identify issues such as time loss, quality defects, and equipment downtime
- Implement specific improvement measures or Execute concrete improvement plans
Job Requirements:
- Extensive experience in productivity and operational improvements in the manufacturing industry.
- Over 3 years of practical experience as a manager.
- Experience calculating and analyzing OEE, as well as problem-solving.
Business level proficiency in both Tagalog and English.
Strong motivation and ability to improve productivity and operations.
- A person who can analyze on-site issues and devise specific countermeasures.
quality control manager
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Job Description:
- 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 collection.
- 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 Deviators- 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
Quality Control Assistant
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Qualifications:
- Graduate of any engineering course. Preferably electronics or mechanical engineers
- Minimum 2 years experience in a quality control or quality assurance role in the manufacturing industry
- Know how to use different measuring tools and equipment
- Skilled in data analysis and report writing
- Knowledgeable in drawing software, 2D or 3D.
- Proficient in Microsoft office
Quality Control Analyst
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Company Description
Sydenham Laboratories, Inc. (SLI) is a pharmaceutical company established in 1971, specializing in the development and manufacture of healthcare products. Certified with ISO 9001:2008, HACCP, and PIC/s GMP compliance, SLI produces oral drug preparations such as tablets, capsules, syrups, and powders for suspension. To ensure zero-cross contamination, non-penicillin, penicillin, and cephalexin products are manufactured in separate buildings with exclusive air-handling systems.
Duties and Responsibilities:
- Performing quality control tests and analyses on raw materials, in-process samples, and finished products according to established protocols
- Documenting test results and maintaining detailed records of all quality control activities
- Identifying and investigating any quality issues, and recommending corrective actions
- Collaborating with the production team to troubleshoot and resolve quality-related problems
- Staying up-to-date with industry regulations and best practices in quality assurance
- Continuously improving quality control processes and procedures
- Performs other duties assigned by Supervisor from time to time
Qualifications:
- Bachelor's degree in a relevant scientific discipline, such as Chemistry, Biotechnology, biology and Pharmacy.
- Chemist and/or Chemical Technician license
- Minimum 2 years of experience as a Quality Control Analyst or in a similar role within the food/pharmaceutical manufacturing industry
- Strong analytical and problem-solving skills, with the ability to interpret data and make informed decisions
- Excellent attention to detail and a commitment to accuracy in all work
- Proficient in using laboratory equipment and software for data analysis and reporting
- Understanding of quality control principles, including standard operating procedures and quality management systems
- Effective communication skills to collaborate with cross-functional teams
Quality Control Inspector
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QUALIFICATION:
- Vocational Course, High school Graduate , College graduate with any related course
- With at least 1 year experience as Quality Inspector
- Can read and interpret mechanical drawing and specifications
- Know how to use measuring tools such as caliper, micrometer, gauges
- Knowledgeable in commuter programming is an advantage
JOB DESCRIPTION:
- Reading blueprints and specifications
- Monitoring operations to ensure that they meet production standards
- Recommending adjustments to the assembly or production process
- Inspecting, testing, or measuring materials or products being produced
- Measuring products with calipers
- Operating electronic inspection equipment and software
- Accepting or rejecting finished items
- Removing all products and materials that fail to meet specifications
- Reporting inspection and testing data such as weights, temperatures, grades, moisture content, and quantities inspected
Job Types: Full-time, Permanent
Benefits:
- On-site parking
- Promotion to permanent employee
- Staff meals provided
Ability to commute/relocate:
- Dasmariñas: Reliably commute or planning to relocate before starting work (Required)
Experience:
- relative: 1 year (Required)
Work Location: In person
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Quality Control Analyst
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Company Description
Sydenham Laboratories, Inc. (SLI) is a pharmaceutical company founded in 1971 by Dr. Eduardo R. dela Cruz. With ISO 9001:2008, HACCP Certification, and PIC/s GMP compliance, SLI specializes in developing and manufacturing healthcare products. The company produces oral drug preparations and food supplements in various dosage forms, ensuring zero-cross contamination through separate buildings with clean room hepa-filtered air-handling systems. SLI is named after Dr. Thomas Sydenham, an advocate of effective illness management and detailed patient observation.
Role Description
This is a full-time on-site role for a Quality Control Analyst located in Dasmariñas, Cavite. The Quality Control Analyst will be responsible for overseeing the quality control processes, performing laboratory tests, ensuring compliance with quality assurance standards, and maintaining laboratory equipment. The role includes analyzing samples, preparing reports, and ensuring products meet specified standards.
Qualifications
- Strong Analytical Skills and Quality Control experience
- Proficiency in Laboratory Skills and handling Laboratory Equipment
- Experience with Quality Assurance processes
- Excellent attention to detail and problem-solving skills
- Ability to work independently and in a team
- Bachelor's degree in Chemistry, and a Chemist and/or Chemical Technician License
- Experience in pharmaceutical or food industry is a plus
Quality Control Manager
Posted today
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Job Description
- 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
Manufacturing Supervisor
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- Responsible for overseeing production operations, ensuring that production lines run at standard speed with minimal rejection rates and maximum efficiency.
- The role also supports the Sr. Operations Supervisor in managing Technicians and Machine Operators, ensuring compliance with maintenance schedules, corrective repairs, and continuous improvement of all machinery and support equipment.