Muhammad Noman Subhan

Manager QA

Talent

R-432 Sector 16-A Bufferzone North Karachi, Karachi, PakistanMember since June 25, 2026

Technical TransferCleaning ValidationProcess ValidationMethod ValidationCAPAProduct ComplaintsQuality Systems AuditsVendor EvaluationAnnual Product ReviewChange Control ManagementOut of SpecificationLocal and Export DossiersInstrument ValidationQuality Management SystemGMPStability StudiesHPLCSpectrophotometerMicrobiological TestingLAL TestFT-IRKarl-FischerDisintegration ApparatusDissolution ApparatusMS OfficeInternetBusiness Management SystemISO 2200:2008ISO 9001:2008

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Technical TransferCleaning ValidationProcess ValidationMethod ValidationCAPA

About

A designation rewarding assignment, where my professional skills will be of value and innovation of skills and my qualifications will be appreciated through challenges.

Experience

Manager QA - Pakistan Pharmaceutical Products (Pvt.) Ltd.

(2019-01-01)

Joining this company 1st jan 2019 of Manager QA in Pakistan pharmaceutical Products(Pvt.)Ltd.

Preparation and review technical transfer of protocol and reports.
Ability to handle analytical method, cleaning and process validations.
Handling of product complaints and providing CAPA for the same.
Assist in Internal and External Quality Systems Audits and the CAPA implementation.
Vendor evaluation and qualification for starting materials and raw materials.
Preparation of Annual Product Review (APR).
Logging and handling the investigations for deviations, OOS and providing CAPA for the same.
Change control management.
Provide support to the various divisions for effective and efficient implementation of the Quality Management System.
Upgrade Quality Control process.
Co-ordinate with Production, QC, warehouse and Maintenance regarding non-conformance & corrective action for the same

Manager QA - Maple Pharmaceutical (PVT)LTD

(2015-12-01 - 2019-01-01)

About 3 years' experience of manager QA in Maple pharmaceutical.

Compilation of Local and Export Dossiers.
Preparation and review technical transfer of protocol and reports.
Ability to handle analytical method, cleaning and process validations.
Handling of product complaints and providing CAPA for the same.
Assist in Internal and External Quality Systems Audits and the CAPA implementation.
Vendor evaluation and qualification for starting materials and raw materials.
Preparation of Annual Product Review (APR).
Logging and handling the investigations for deviations, OOS and providing CAPA for the same.
Change control management.
Provide support to the various divisions for effective and efficient implementation of the Quality Management System.
Upgrade Quality Control process.
Co-ordinate with Production, QC, warehouse and Maintenance regarding non-conformance & corrective action for the same

Deputy Manager QA/ Validation - Maple Pharmaceutical (PVT)LTD

(2008-12-01 - 2015-12-01)

Managing validation planning.
Managing Method Validation
Managing Process Validation
Managing Cleaning Validation
Managing Validation sample collected.
Managing Validation protocol.
Managing Validation SOP,s.
Managing Validation reports.
Managing Validation testing
Managing Instrument Validation IQ/OQ/PQ Protocol & Report
Managing Validation of HVAC System
Dossiers of local and export
To maintain the quality manual
To maintain the Quality management system
To maintain Safety Manual
Approval of all testing matter in QC(Finished Product
Method Development of new product
Responsible all QC and QA Matter
Supervise of all Microbiological activity
Preparation of stability product Protocol
Responsible of SOP'S & report of APR
Responsible of Collected Date APR
Responsible of APR established annual schedule
Responsible of APR reports maintain
Responsible of CAPA activities
Responsible of Change Control activities
Responsible of NCMR report.
Responsible of deviation activities.
Responsible of Out of specification activities
Responsible of Quality Control Budget preparation
Responsible of trial batch and R&D work.
Responsible of all QA & QC work
Reviewing and up date of specification and SOP's
Approved Art work and packaging material
Responsible Internal audit of plant
Procurement of equipment, chemical and other items preparation comprising sheet and purchase order.
Responsible to order and maintain Inventory
Management representative of ISO 2200:2008 and ISO 9001:2008
Responsible of all documentation
Like Site master file
Quality manual
Safety manual
Environmental system
GMP system
Trial batch of soft gel
Trial batch of Cranberry Sachet
Trial batch of Tablet
Trial batch of herbal syrup

Assistant Manager Q.C - Lexicon pharmaceutical private limited

(2004-01-01 - 2008-01-01)

Three years experience.

Responsible of finished product
Responsible of trial batch manufacturing
Responsible of raw material testing
Responsible of New Method development of new product
Responsible Validation Activity.
To plan and carry out stability studies of trial batches.
To plan and prepare formulation and manufacturing for trial batches of new product.
To plan manufacturing of trial batches.
Registration of product for local, and export.
To initiate and proof reading of art work for new products.
Stability protocol
Supervise of All Microbiological Activities

Senior Quality Control Analyst - Elko organization private limited

(2002-01-01 - 2004-01-01)

Three years experience.