Open to opportunities

Saif Ul Islam Quraishi

@saifulislamquraishi

Message

Experienced QA pharmacist with 9 years in pharmaceutical quality systems and regulatory compliance.

Pakistan

Message

What I'm looking for

I seek a QA leadership role in a compliance-driven pharma company where I can lead QMS, audits, validation and team development while driving continuous improvement.

I have approximately nine years of experience in the pharmaceutical industry with a Pharm‑D background and a strong focus on quality assurance and compliance.

I lead and support QMS activities including internal audits, CAPA management, documentation control, batch review and release using SAP, and data analysis with Minitab.

I played leading roles in regulatory and third‑party inspections, ISO 17025 accreditation, FSSC 22000 audit activities, and implementation of GMP, HACCP and risk‑based inspection approaches; I also design and deliver GMP and technical training.

I am driven to continuously improve processes, mentor colleagues, and implement robust systems that ensure product quality and regulatory compliance.

Experience

Work history, roles, and key accomplishments

Current

Deputy Manager QA

Current

Remington Pharmaceutical Industries

Sep 2023 - Present (2 years 3 months)

Supervise QMS, production QA (O&C) and QC lab operations; led WHO PQ inspection activities and secured ISO 17025 accreditation while supporting FSSC22000 readiness and clinical-trial document control.

WHO PQ Inspections Minitab Training Development FSSC 22000

Assistant Manager QA

Remington Pharmaceutical Industries

Sep 2021 - Sep 2023 (2 years)

Managed QMS operations including internal, vendor and remote audits, CAPA and change-control tracking, and SAP-based batch release; led validation reviews and performed risk assessments using FMEA and HACCP.

Internal Audit CAPA Validation SAP HACCP Minitab Change Control

Sr. Officer QA (SE&D)

Remington Pharmaceutical Industries

Feb 2019 - Sep 2021 (2 years 7 months)

Supported execution of QMS and WHO PQ inspection activities, developed and reviewed GMP documentation, and managed CAPAs and risk assessments while performing product quality reviews using Minitab.

SOP Development WHO PQ CAPA Minitab Documentation Management

Officer QA

CSH Pharmaceutical Industries

Dec 2017 - Feb 2019 (1 year 2 months)

Reviewed and released batch documentation via SAP, managed IPQC records and product quality reviews using Minitab, and prepared and maintained GMP documentation while driving deviations and CAPA closure.

Root Cause Analysis Batch SAP IPQC Minitab SOPs CAPA

QA Inspector

Himont Pharmaceutical Industries

Nov 2015 - Nov 2017 (2 years)

Performed batch documentation review and IPQC verification, prepared quality documentation and led root cause analyses and GMP training to support manufacturing compliance and change control closure.

Batch IPQC SOPs Root Cause Analysis Minitab