Pharma Validation Specialist (CSV & Stability)

Duopharma Biotech; Selangor; On-site; MYR 60,000 - 80,000; Full time

Job summary

A pharmaceutical manufacturing company in Selangor is seeking a Validation Specialist to execute validation activities and chemical testing. This role involves method validation, documentation management, and coordination to ensure compliance with industry standards. The ideal candidate will have a Bachelor’s Degree in Science, relevant experience in the pharmaceutical sector, and proficiency in laboratory instruments like HPLC and UV-Vis Spectrophotometer. Strong analytical, communication, and documentation skills are essential. This position offers an opportunity to work independently within a regulated environment and contribute to high-quality pharmaceutical production.

Qualifications

• Minimum 3 years of experience in the pharmaceutical industry, preferably in validation.
• Practical experience operating laboratory instruments.
• Ability to work independently in a regulated environment.

Responsibilities

• Execute validation activities including method validation and performance qualification.
• Prepare and maintain validation documentation according to GDP guidelines.
• Coordinate with teams for completion of qualification programs.

Skills

Hands-on experience in Computer System Validation

Strong analytical thinking

Good interpersonal communication skills

Detail-oriented and organized

Proficient in MS Office applications

Education

Bachelor’s Degree in Science or related field

Tools

HPLC

UV-Vis Spectrophotometer

Dissolution Tester

Job description

A pharmaceutical manufacturing company in Selangor is seeking a Validation Specialist to execute validation activities and chemical testing. This role involves method validation, documentation management, and coordination to ensure compliance with industry standards. The ideal candidate will have a Bachelor’s Degree in Science, relevant experience in the pharmaceutical sector, and proficiency in laboratory instruments like HPLC and UV-Vis Spectrophotometer. Strong analytical, communication, and documentation skills are essential. This position offers an opportunity to work independently within a regulated environment and contribute to high-quality pharmaceutical production.