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Hamza Z

@bioavailable

Production Pharmacist

Pakistan
English
About me
I am an experienced Quality Assurance Pharmacist and Production professional specializing in sterile manufacturing. I currently lead the production of peritoneal dialysis fluid, managing automated CIP/SIP systems and ensuring US FDA and cGMP compliance. I have extensive expertise in in-process controls for liquid, dry powder, and lyophilized injections.... Read more

Skills

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bioavailable
Hamza Z
Offline • 
Average response time: 1 hour

See my services

FDA & Food Safety Clearance
I will write pharmaceutical gmp sops, validation protocols and reports
From$35 / projectMore details
Informative & Educational Articles
I will write medical, pharmaceutical and gmp content as a pharmacist
From$10 / projectMore details

Portfolio

Work experience

MTI

quality assurance pharmacist

MTI • Full-time

Feb 2023 - Apr 2026 • 3 yrs 2 mos

Pharmaceutical Manufacturing, Sterile Manufacturing & GMP Documentation Experience I have hands-on pharmaceutical manufacturing experience in liquid, lyophilized, and dry powder injectable manufacturing, with practical involvement in formulation, aseptic processing, process development, equipment qualification, process validation, cleaning and sterilization systems, cleanroom operations, HVAC qualification, filtration systems, and GMP documentation. During my experience in the pharmaceutical injection manufacturing sector, I have worked with multiple sterile pharmaceutical products and manufacturing processes, gaining practical exposure to the complete manufacturing lifecycle from raw material and component handling through formulation, filtration, filling, lyophilization, sealing, sterilization, and finished-product processing. My experience includes both technical manufacturing activities and the development/review of GMP documentation required to support pharmaceutical production, qualification, validation, and regulatory compliance. Sterile Pharmaceutical Manufacturing My core experience includes manufacturing of: * Liquid injections * Lyophilized injections * Dry powder injections * Sterile pharmaceutical products * Small-volume parenteral manufacturing processes * Aseptic processing operations * Terminal sterilization processes * Lyophilization-based manufacturing I have worked with sterile manufacturing areas involving different cleanroom classifications and controlled environments, including Grade/Class A, B, C, and D areas, depending on the specific manufacturing activity. My practical exposure includes: * Vial decartoning * Vial washing * Vial sterilization/depyrogenation * Sterile formulation * Bulk solution preparation * Sterile filtration * Filling operations * Vial stoppering * Vial sealing/crimping * Lyophilization * Terminal sterilization * Material transfer * Personnel movement * Material and personnel airlocks/buffers