Primary Responsibilities

You are responsible for ensuring the quality and consistency of gypsum board products by conducting rigorous testing and analysis. This role involves collaboration with cross-functional teams to maintain adherence to quality standards, identify areas for improvement and contribute to the overall success of the manufacturing process.

Value Expectations ...

Problem Solving

People Management

Critical Thinking ...

Assist QC team to maintain SDS folder, keep raw material and Finished goods SDS updated Assist QC team on product or sample monitoring, update monitoring report Assist QC team on new lab blend request, sample retrieval request

Assist QC team on lab retain sample management and record Manage trading goods arrangement to ensure all ready for customer collection or ready for loading Bi-weekly stock count, update stock report to Production Controller

All workers PPE safety check especially weekend work day Supervise and manage on production blending processes Pre-arrangement of packaging for production ...

Assist QC team to maintain SDS folder, keep raw material and Finished goods SDS updated Assist QC team on product or sample monitoring, update monitoring report Assist QC team on new lab blend request, sample retrieval request

Assist QC team on lab retain sample management and record Manage trading goods arrangement to ensure all ready for customer collection or ready for loading Bi-weekly stock count, update stock report to Production Controller

All workers PPE safety check especially weekend work day Supervise and manage on production blending processes Pre-arrangement of packaging for production ...

Requirements Minimum Diploma in Chemistry or relevant courses Minimum 2 years of experience

Able to work independently with minimal supervision Able to write and communicate in English Knowledge in Excel and word

Knowledge in SAP will be an added advantage

Testing of finished products against specifications and to notify for any out of specifications

Maintenance of manufacturing facility as per GMP requirements

Prepare products for testing from external laboratories ...

Assist QC manager in daily operations

Testing of finished products against specifications and to notify for any out of specifications

Maintenance of manufacturing facility as per GMP requirements ...

As Our Product Executive You Will

Coordinate product development

: Assisting the Assistant Manager. Product Development in coordinating and managing product development projects, including writing specifications for features and performance, defining product testing standards, and conducting field testing to gather feedback on performance. ...

Responsible for developing effective laboratory management systems that include workload prioritizing, overtime allocation, good housekeeping, laboratory inventory control, analytical equipment maintenance, minimizing laboratory waste generation and disposal.

Set up and maintain the highest standard of QA laboratory quality system such as to ensure raw materials and finished goods meet specification, technical competence of QA laboratory staff and analytical results.

Carry out laboratory scale blending, issue work-off recommendation and seek the approval from management and President for write-off if not workable. ...

To responsible loading and unloading works on incoming & outgoing goods in the warehouse.

Maintain up to date stock record.

To practice regular stock check to ensure the physical stock quantity tallies with updated stock record in the system. ...

Purpose

To provide an effective testing and analytical service to the plant ensuring that products manufactured are tested

to specification on time and plant quality and safety goals are met. ...

To maintain records and manage all aspects of testing activities.

To verify accuracy of all chemical testing results.

To develop and verify new methodologies; ensure accurate and consistent testing procedures through the validation of current procedures and by developing, validating and implementing new procedures. ...

Ensure that all raw material, in-process and finished product testing and method transfer testing is carried out per

schedule and per gmp. Ensure that records are maintained to appropriate requirements.

Major Responsibilities:Responsible for housekeeping duties in the lab. ...

schedule and per gmp. Ensure that records are maintained to appropriate requirements.

Major Responsibilities:Responsible for housekeeping duties in the lab.

Responsible for the timely completion of chemical testing of raw material, intermediates, in-process ...

As Our Product Executive You Will

Coordinate product development

: Assisting the Assistant Manager. Product Development in coordinating and managing product development projects, including writing specifications for features and performance, defining product testing standards, and conducting field testing to gather feedback on performance. ...

Document & sample preparation

Provide technical support to Sales Department

Perform calibration and maintenance of lab equipment's ...

Wednesday: Morning, Evening, Afternoon

Thursday: Morning, Evening, Afternoon

Friday: Morning, Evening, Afternoon

Basic Salary: $3200

Allowance: $450 + daily transport claim

Job Description: ...

Execute analytical method transfers, validations, verifications, and equivalency studies according to Standard Operating Procedures (SOPs)

Conduct precise and efficient analytical testing in compliance with Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP) standards.

Engage in 5S team initiatives and maintain excellent housekeeping practices to ensure adherence to safety protocols. ...

The Role:

Entegris is seeking a 1st shift QA Analytical Chemist for our KSP facility. Wednesday-Sunday 8:00am-5:00pm.

The QA Chemist is responsible for QA testing and will provide analytical support for production of our Micro-Contamination Control and Membrane products. The QA Chemist will prepare and test samples using ICP-MS, Ion Chromatography, TOC analysis, NVR, LC-CAD, GC-MS and GC-FID/MS. ...

Ensures that analyses are carried out for the purpose of having reliable results available in a timely manner

Calculates, checks, and reports the analysis results so that correct decisions can be made for the validation and release process

Escalates in the event of deviations, takes the necessary measures, and draws up the associated reports ...

The Senior R&D Chemist is responsible for designing and developing products to meet quality standards and regulatory requirements (cGMP, 21 CFR Part 211, EU MDD/MDR, ISO 13485). He/she coordinates and conducts testing in compliance with SOPs, ISO standards, and global market regulations for physical, chemical, and microbiological aspects.

Responsibilities:

Lead and oversee a team of chemists in R&D, Technology Transfer, and Projects. ...

Working Hours: Mon to Fri 8.30am -5.30pm

Basic Salary: $3200

Allowance: $450 + daily transport claim ...

Analyses

Ensures that analyses are carried out for the purpose of having reliable results available in a timely manner

Calculates, checks, and reports the analysis results so that correct decisions can be made for the validation and release process ...

What You Will Achieve

You will be a member of Pfizer’s dedicated and highly effective quality assurance and control team. You will be responsible for analyzing chemical, biological or microbiological products to support our quality programs. Your contribution to environmental testing, utility monitoring, analytical testing, microbial identification and sterility testing will help Pfizer provide safe drugs to patients.

Your understanding of Quality Control instruments will help us meet their accuracy specifications against established standards. You will also be relied on for setting requirements for the transfer of methodology from R&D. ...

evaluate adequacy of quality assurance standards

devise sampling procedures and directions for recording and reporting quality data

review the implementation and efficiency of quality and inspection systems ...

What You Will Achieve

You will be a member of Pfizer’s dedicated and highly effective quality assurance and control team. You will be responsible for analyzing chemical, biological or microbiological products to support our quality programs. Your contribution to environmental testing, utility monitoring, analytical testing, microbial identification and sterility testing will help Pfizer provide safe drugs to patients.

Your understanding of Quality Control instruments will help us meet their accuracy specifications against established standards. You will also be relied on for setting requirements for the transfer of methodology from R&D. ...

Responsibilities

Review lab data, validation and stability protocols/documents, batch records, specifications, and manufacturing orders for compliance

Support manufacturing through timely process of deviations, change controls, and investigations to ensure quality products ...