Technical Services Executive

Idaman Pharma Manufacturing Sdn Bhd

Perak

On-site

MYR 78,000 - 123,000

Full time

2 days ago

Be an early applicant

Get more replies from employers

Send a job-specific resume in minutes.

Job summary

Idaman Pharma Manufacturing Sdn Bhd - Perak seeks a Validation Specialist to plan, coordinate and execute validation activities in line with GMP, regulatory and quality requirements. You will develop and maintain the Validation Master Plan (VMP) and oversee PV, CV, and product improvement projects.

The role requires strong GMP knowledge, analytical skills and proficient technical report writing, with focus on effective project coordination in a pharmaceutical setting.

Qualifications

Bachelor's Degree in Science or related field.
Minimum 3 years of working experience in Quality Control or Quality Assurance, preferably in the pharmaceutical industry.
Detail-oriented with strong organizational skills.
Knowledge and well verse in PICs, ISPE and ISO Guideline.

Responsibilities

To plan, coordinate and execute validation activities in compliance with GMP, regulatory and quality requirements.
To develop and maintain the Validation Master Plan (VMP).
To execute and oversee Process Validation (PV), Cleaning Validation (CV) and Product Improvement projects.
To apply strong knowledge of GMP, validation principles, analytical skills, and project coordination.

Skills

Validation planning

Coordination

GMP knowledge

Analytical skills

Technical report writing

Project coordination

Education

Bachelor's Degree in Science or related field

Tools

PICs

ISPE guidelines

ISO guidelines

Job description

Jora Malaysia will close on 9th September 2026. Thank you for being with us, we are cheering you on as you continue your career journey.

Idaman Pharma Manufacturing Sdn Bhd - Perak

To plan, coordinate and execute validation activities in compliance with GMP, regulatory and quality requirements.
To develop and maintain the Validation Master Plan (VMP).
To execute and oversee Process Validation (PV), Cleaning Validation (CV) and Product Improvement projects.
To apply strong knowledge of GMP, validation principles, analytical skills, technical report writing, and project coordination.

Job Requirements

Bachelor's Degree in Science or related field.
Minimum 3 years of working experience in Quality Control or Quality Assurance, preferably in the pharmaceutical industry.
Detail-oriented with strong organizational skills.
Knowledge and well verse in PICs, ISPE and ISO Guideline.