25 Food Production jobs in Silang
Quality Control Inspector
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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.
Quality Control Inspector
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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.
Quality Control Inspectors
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What we're looking for
- With or without experience
- Fast learner
- At least college level
- Physically fit
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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Specialist, Quality Control
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Job Position: Specialist, Quality Control (Onsite)
Office Location: Alabang, Muntinlupa
Job Responsibilities:
- Test Planning:
Collaborate with the development team and stakeholders to understand software requirements and design test plans and strategies accordingly. - Test Execution:
Execute test cases and report defects or bugs using bug-tracking tools. Conduct various types of testing, including functional, regression, integration, performance, and usability testing. - Defect Management:
Identify, document, track, and communicate defects found during testing. Work closely with the development team to ensure the timely resolution of issues. - Test Documentation:
Prepare test documentation, including test plans, test cases, test scripts, and test reports. Maintain test artifacts for future reference. - Test Environment Setup:
Collaborate with the development team to set up and maintain test environments, including software installations, hardware configurations, and test data. - Continuous Improvement:
Stay updated with industry trends, new testing tools, and best practices. Suggest and implement process improvements to enhance the quality assurance process. - Collaboration and Communication:
Collaborate with cross-functional teams, including developers, business analysts, project managers, and product owners, to ensure a smooth testing process and timely delivery of high-quality software products.
Job Requirements:
- Candidate must possess at least a Bachelor's/College Degree, Computer Science/Information Technology, Engineering or equivalent.
- Prior experience as a Software QA Tester or in a similar role is desirable. Knowledge of software testing methodologies, tools, and processes is essential.
- Experience in Software QA Testing using Android TV, mobile, and console platforms is a plus .
- Experience with LINUX OS is a plus
- Experience in JIRA Software, Android Studio, and ExoPlayer is a plus
- Demonstrate ability to learn quickly and adapt to a rapidly changing environment.
- Proficiency in test case design, test execution, defect tracking, and test documentation. Familiarity with test automation tools and scripting languages is a plus.
- Strong analytical and problem-solving abilities to identify defects and troubleshoot issues effectively.
- Meticulous attention to detail to ensure comprehensive test coverage and accurate defect reporting.
- Excellent written and verbal communication skills to collaborate with different stakeholders and effectively communicate test results and findings.
- Ability to prioritize tasks, meet deadlines, and manage multiple projects simultaneously.
- Strong team player with the ability to work collaboratively in a cross-functional environment.
- A strong commitment to delivering high-quality software products and ensuring customer satisfaction.
Job Work Setup:
- Onsite
- 8 hours x 5 days a week (Monday to Friday)
- Full Time
Who are we?
Arcadian is your back-office workforce for the streaming video entertainment industry.
As a strategic tech partner, Arcadian seamlessly handles operational tasks, delivering exceptional quality at significantly reduced costs. We provide the perfect blend of talent and technology to bring our customers the best solutions.
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 Analyst
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Job Summary:
We are looking for a motivated and detail-oriented Quality Control Laboratory Analyst to ensure product quality and regulatory compliance. The role involves performing laboratory analyses, maintaining data accuracy, and supporting continuous improvement initiatives. Graduates of BS Chemistry, Chemical Engineering, or Laboratory Technology are encouraged to apply. Prior QC experience is preferred, but fresh graduates with strong academic and laboratory backgrounds are welcome.
Qualifications:
- Graduate of BS Chemistry, Chemical Engineering, or Laboratory Technology.
- Strong analytical and problem-solving skills with attention to detail.
- Preferably with at least one (1) year of laboratory experience in QC/QA; fresh graduates are welcome.
- Proficient in MS Office applications and familiar with laboratory systems (e.g., LIMS).
- Excellent communication and teamwork skills.
- Organized, reliable, and able to work independently under minimal supervision.
Duties and Responsibilities:
- Conduct routine and non-routine testing of raw materials, in-process, finished goods, and stability samples in compliance with QC standards.
- Operate and maintain laboratory instruments such as pH meters, spectrophotometers, and titrators, and report any equipment issues promptly.
- Prepare reagents and calibration standards following proper documentation and safety procedures.
- Record and review analytical data, update laboratory documents, and prepare test reports accurately and on time.
- Assist in method development, validation, and transfers following pharmacopeial guidelines.
- Maintain laboratory cleanliness, safety, and compliance with Good Laboratory Practices (GLP).
- Perform scheduled calibration and verification of instruments and laboratory equipment.
- Monitor and maintain inventory of reagents, standards, and chemicals.
- Participate in internal/external audits, proficiency tests, and continuous improvement activities.
- Coordinate with QA, Production, and R&D to address quality concerns and support investigations or product-related issues.