Aqiff Azmi

Pharmaceutical Manufacturing Executive with 3 years of experience in solid dosage manufacturing, specializing in tablet compression, capsule filling, coating, sorting and GMP-compliant production operations. Experienced in equipment qualification (IQ/OQ/PQ), process optimization, batch documentation, production troubleshooting, and cross-functional coordination with QA, Engineering, Maintenance and Warehouse teams. Proven ability to supervise production personnel, support validation activities, improve operational efficiency, and maintain compliance with GMP, GDP, PIC/S, HALAL, and regulatory requirements.

Strong leadership, problem-solving, and project coordination skills with hands-on involvement and continuous improvement initiatives.

Jr Executive, Production at Noripharma Sdn Bhd (2024-07 – Present)

• Ensure manufacturing operations comply with GMP, GDP, BMR, SOP, HALAL, PIC/S, and regulatory requirements.
• Supervise daily production activities across tablet compression, capsule filling, coating and sorting departments to achieve productivity, quality and delivery targets within 22 production personnel.
• Coordinate manpower allocation, machine readiness and material availability to support execution of over 100 batches per month while ensuring uninterrupted production schedules.
• Collaborate closely with QA, Engineering, Maintenance, Warehouse and Planning departments to resolve production issues and minimize downtime.
• Lead investigations and troubleshooting activities related to equipment, process deviations and operational challenges.
• Ensure accurate completion and review of batch manufacturing records, equipment logbooks and production documentation.
• Conduct routine inspections of production facilities and equipment to ensure operational readiness and compliance contributing to improved equipment reliability and a 20% reduction in production downtime.
• Provide technical guidance, GMP coaching, and on-the-job training to operators and line leaders to improve competency and compliance awareness.
• Participate in equipment qualification, validation activities and commissioning projects for new equipment.
• Managed cross-functional production projects by working closely with Supply Chain, Purchasing, Quality Control and Maintenance departments to ensure material availability, equipment readiness and on-time batch execution.

Executive, Regulatory Affairs at Herbal Science Sdn Bhd (2023-10 – 2024-01)

• Managed regulatory compliance activities for health supplements, traditional medicines, and cosmetic products by preparing and submitted product registration, variation, renewal, and notification applications to NPRA and relevant regulatory authorities.
• Liaised with regulatory agencies including NPRA, MITI, BKKM, and KPDN to ensure compliance with local and export market requirements.
• Supported documentation review and compliance verification for product commercialization activities

Internship trainee in Quality Control department at Duopharma HAPI Bhd (2023-03 – 2023-10)

Continued as Protégé at Duopharma HAPI in Protégé Programme.

• Performed analytical testing of finished products, in-process samples, raw materials, and stability samples according to approved specifications and procedures.
• Assisted in laboratory investigations involving OOS (Out-of-Specification) and OOT (Out-of-Trend) results.
• Maintained compliance with GMP and data integrity requirements through accurate documentation practices.
• Collaborated with QC analysts and supervisors to ensure timely completion of testing activities.

Bachelor of Manufacturing Engineering Technology (Pharmaceutical) with Hons in Manufacturing Engineering Technology (Pharmaceutical) – Universiti Malaysia Pahang (2019-09 – 2023-09)

Pure Science Module 1 in Pure Science – Kolej Matrikulasi Negeri Sembilan (2018-05 – 2019-04)

Sijil Pelajaran Malaysia – Sekolah Sultan Alam Shah (2013-02 – 2017-12)