Quality Assurance Manager

Agensi Pekerjaan Starec Sdn. Bhd.; Ipoh; On-site; MYR 120,000 - 180,000; Full time

Benefits offered by this job

Bonus

Allowance

Family benefits

Job summary

Our client, a Pharmaceutical Manufacturing Co., is seeking a QA Manager with at least 5 years of QA management experience in the pharmaceutical industry. The role focuses on GMP compliance, QMS governance, and regulatory adherence, with leadership responsibilities across quality, production, and audits.

The successful candidate will lead QA activities, drive continuous improvement, and ensure product quality from raw materials to release, while maintaining strict GMP and regulatory standards.

Qualifications

• Degree in Pharmacy, Biomedical Science, Business, or related fields.
• Registered Pharmacist qualification is preferred but not mandatory.
• Min 5 years of QA management experience within Pharmaceutical (non-medical devices) industry.
• Demonstrate strong knowledge of GMP and regulatory requirements.
• Have proven leadership experience managing quality or production teams.
• Possess excellent analytical, problem-solving, and communication skills.

Responsibilities

• Manage the Quality Management System to ensure GMP compliance.
• Improve quality systems through continuous monitoring and enhancements.
• Represent the QA department in internal and external quality matters.
• Ensure compliance with cGMP, ISO, and GDPMD requirements.
• Plan and conduct internal quality audits regularly.
• Lead GMP inspections conducted by regulators and customers.
• Approve or reject finished products before market release.
• Manage product recalls and customer complaints effectively.
• Oversee raw material qualification and packaging material approval.
• Manage change control, process validation, and Product Quality Reviews.
• Review and approve Batch Manufacturing Records accurately.
• Review and approve Standard Operating Procedures consistently.
• Review and approve deviations and corrective actions promptly.
• Review and approve Change Control documents properly.
• Ensure all quality records remain complete and compliant.
• Manage departmental resources to achieve operational objectives.
• Support production while maintaining required quality standards.
• Lead, coach, and develop the Quality Assurance team.
• Manage recruitment, training, and employee performance effectively.
• Ensure the team complies with all GMP requirements.

Skills

Leadership

Analytical thinking

Communication

Regulatory knowledge

Education

Degree in Pharmacy

Biomedical Science

Business

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.

#Our client is a Pharmaceutical Manufacturing Co.#

Degree in Pharmacy, Biomedical Science, Business, or related fields.

Registered Pharmacist qualification is preferred but not mandatory.

Min 5 years of QA management experience within Pharmaceutical (non-medical devices) industry.

Demonstrate strong knowledge of GMP and regulatory requirements.

Have proven leadership experience managing quality or production teams.

Possess excellent analytical, problem-solving, and communication skills.

Requirement

#Our client is a Pharmaceutical Manufacturing Co.#

• Degree in Pharmacy, Biomedical Science, Business, or related fields.

• Registered Pharmacist qualification is preferred but not mandatory.

• Min 5 years of QA management experience within Pharmaceutical (non-medical devices) industry.

• Demonstrate strong knowledge of GMP and regulatory requirements.

• Have proven leadership experience managing quality or production teams.

• Possess excellent analytical, problem-solving, and communication skills.

Responsibility

#Our client is a Pharmaceutical Manufacturing Co.#

QMS & Compliance

• Manage the Quality Management System to ensure GMP compliance.

• Improve quality systems through continuous monitoring and enhancements.

• Represent the QA department in internal and external quality matters.

• Ensure compliance with cGMP, ISO, and GDPMD requirements.

Audits & Inspections

• Plan and conduct internal quality audits regularly.

• Lead GMP inspections conducted by regulators and customers.

Product Quality

• Approve or reject finished products before market release.

• Manage product recalls and customer complaints effectively.

• Oversee raw material qualification and packaging material approval.

• Manage change control, process validation, and Product Quality Reviews.

Documentation

• Review and approve Batch Manufacturing Records accurately.

• Review and approve Standard Operating Procedures consistently.

• Review and approve deviations and corrective actions promptly.

• Review and approve Change Control documents properly.

• Ensure all quality records remain complete and compliant.

Operations & Team Management

• Manage departmental resources to achieve operational objectives.

• Support production while maintaining required quality standards.

• Lead, coach, and develop the Quality Assurance team.

• Manage recruitment, training, and employee performance effectively.

• Ensure the team complies with all GMP requirements.

Benefits

• Bonus
• allowance
• family benefits