QC Chemist at Elite Advanced Materials Sdn Bhd

Elite Advanced Materials Sdn Bhd

Rawang

On-site

MYR 31,000 - 39,000

Full time

14 days+

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Benefits offered by this job

Maternity leave

Opportunities for promotion

Professional development

Job summary

Elite Advanced Materials Sdn Bhd is seeking a QC Chemist to ensure raw materials, in-process products and finished goods meet quality standards. You will manage analytical data, quality systems and lead improvements in the QC function.

The role requires a Bachelor’s in Chemistry or related field and at least 5 years’ QC experience within regulated manufacturing, with ISO/GMP exposure. Strong leadership, documentation and problem-solving skills are essential.

Qualifications

Bachelor's Degree in Chemistry or related discipline.
Minimum 5 years experience in Quality Control within chemical, pharmaceutical, medical device, diagnostics or related manufacturing industries.
Experience working under ISO quality systems.
Experience supervising laboratory personnel is preferred.

Responsibilities

Perform and review chemical analysis of raw materials, intermediates and finished products.
Review analytical data and ensure compliance with approved specifications.
Approve or reject materials based on established quality requirements.
Conduct routine production quality inspections (AQL).
Prepare Certificates of Analysis (COA), analytical reports and technical reports.
Ensure all laboratory work complies with Good Laboratory Practices (GLP).
Lead investigations into Out of Specification (OOS) and Out of Trend (OOT) results.
Investigate customer complaints and quality incidents.

Skills

Wet chemistry

Instrumental analysis

Analytical method validation

Data interpretation

Root Cause Analysis

Statistical Process Control

CAPA

Internal auditing

Technical report writing

Education

Bachelor's Degree in Chemistry or related discipline

Tools

FTIR

GC-FID

Karl Fischer Titrator

pH Meter

Conductivity Meter

Density Meter

Refractometer

Moisture Analysis Equipment

Job description

This Full time on site position offers great opportunities for career growth.

About Us

Elite Advanced Materials (EAM) is a science driven chemical manufacturer specialising in high purity solvents, specialty chemicals, medical and diagnostic reagents, cleaning and disinfection technologies, and advanced manufacturing solutions. We serve pharmaceutical, medical device, diagnostics, food, laboratory, and industrial customers across Asia with a strong focus on quality, innovation, and regulatory compliance.

Position Summary

The QC Chemist is responsible for ensuring that raw materials, in process products, and finished products consistently meet quality standards. This role combines laboratory analysis, quality system management, technical problem solving, instrument management, and team leadership. The successful candidate will play an important role in maintaining ISO compliant laboratory operations while driving continual improvement across the quality function.

Key Responsibilities

Laboratory Operations

Perform and review chemical analysis of raw materials, intermediates and finished products.
Review analytical data and ensure compliance with approved specifications.
Approve or reject materials based on established quality requirements.
Conduct routine production quality inspections (AQL).
Prepare Certificates of Analysis (COA), analytical reports and technical reports.
Ensure all laboratory work complies with Good Laboratory Practices (GLP).

Analytical Instrumentation

Operate, troubleshoot and maintain laboratory instruments including:
FTIR UV-Visible Spectrophotometer
GC / GC-FID
Karl Fischer Titrator
pH Meter
Conductivity Meter
Density Meter
Refractometer
Moisture Analysis Equipment
Other analytical instruments as required
Coordinate calibration, preventive maintenance and verification of laboratory equipment.

Quality Management System

Support and maintain the company's Quality Management System, including:
ISO 9001
ISO 14001
ISO/IEC 17025
ISO 13485 (where applicable)
GMP
HACCP
Halal Assurance System (HAS)

Internal audits
Corrective and Preventive Actions (CAPA)
Root Cause Analysis
Change Control
Risk Assessment
Documentation control
SOP development and revision
Investigation & Continuous Improvement
Lead investigations into Out of Specification (OOS) and Out of Trend (OOT) results.
Investigate customer complaints and quality incidents.
Support production during process deviations.
Identify opportunities to improve laboratory efficiency and analytical methods.
Drive continuous improvement initiatives within QC.

Team Leadership

Supervise QC Chemists and Laboratory Technicians.
Train and mentor new laboratory personnel.
Review work performed by junior chemists.
Support competency development within the laboratory.

Inventory & Laboratory Management

Monitor laboratory chemical inventory.
Manage laboratory consumables.
Ensure laboratory housekeeping and safety compliance.
Support laboratory budgeting and purchasing activities.

Qualification & Experience

Education

Bachelor's Degree in Chemistry, Analytical Chemistry, Applied Chemistry, Chemical Engineering or related discipline.

Experience

Minimum 5 years experience in Quality Control within chemical, pharmaceutical, medical device, diagnostics or related manufacturing industries.
Experience working under ISO quality systems.
Experience supervising laboratory personnel is preferred.

Technical Skills

Wet chemistry
Instrumental analysis
Analytical method validation
FTIR GC UV-Vis Karl Fischer Laboratory troubleshooting
Data interpretation
Root Cause Analysis
Statistical Process Control
CAPA
Internal auditing
Technical report writing

Personal Attributes

Highly analytical with strong attention to detail
Hands on and practical in laboratory work
Able to solve technical problems independently
Strong in documentation and report writing
Organised and systematic
Good communicator with leadership capability
Able to work in a fast paced manufacturing environment
Committed to quality and continuous improvement

Authority

Place raw materials, intermediates or finished products on quality hold.
Recommend release or rejection of products according to approved procedures.
Stop testing or production activities where quality risks are identified.
Initiate investigations into quality issues.
Recommend corrective and preventive actions.
Supervise QC laboratory personnel.
Liaise directly with suppliers and customers on technical quality matters.
Approve laboratory documentation within delegated authority.

Why Join EAM?

Work with advanced analytical technologies and modern laboratory equipment. Exposure to pharmaceutical, medical, diagnostics and specialty chemical industries. Opportunity to work on innovative R&D and manufacturing projects. Continuous learning and career development. Collaborative and science driven working environment. Attractive remuneration based on experience.

Benefits