Quality Assurance Management
Resume:
MUHAMMAD UMAIR SADIQ
Quality Assurance Professional
PROFILE
Self-motivated, energetic and persuasive
professional backed by almost 10 years of
demonstrated expertise in Quality
Assurance IPC,QMS and validation with
extensive knowledge of FDA guidelines,
GMP (Good Manufacturing Practice) &
GDP(Good Documentation Practice), QMS
(Quality Management System), Quality of
solid dosage form, Quality of sterile
products, Quality of liquid and suspension,
In process control, Noncompliance,
CAPA(Corrective and Preventive Action),
Investigation, Sampling of raw material,
APQR (Annual Product Review),Releasing
of products,SAP
Task-focused professionals with expertise
in all facets of Quality Assurance skilled in
collaborating with all members of the
organization to achieve Quality related
objectives. Instrumental in streamlining
and improving processes, enhancing
productivity with Quality and implementing
QMS, cGMP, GLP and GDP.
CONTACT
**************@*****.***
LinkedIn;
https://www.linkedin.com/in/umair-
sadiq-37a471168
Address: House No F54 Quetta Avenue
Schem Quetta
Quetta Town near jan japan
EDUCATION
University of Baluchistan Quetta, Pakistan
2007 - 2013
PHARM -D (Pharmaceutics, industrial pharmaceutics, instrumentation, bio pharmaceutical, Pharmacology Etc.)
Tameer-e-Nou college Quetta, Pakistan
2004 - 2006
Intermediate (Biology, chemistry, Physics)
WORK EXPERIANCE
MARTIN DOW MARKER – PHARMACEUTICAL, QUETTA, PAKISTAN SENIOUR ASSOCIATE MANAGER VALIDATION
April 2025 - Currently
Responsibilities
Process validation Protocol PVP, Process Validation Report PVR, Master Validation Plan, sampling of process validation and cleaning validation. Performance Qualification, Installation Qualification, Operational Qualification. Sterile Area Qualifications’ ASSOCIATE MANAGER QUALITY ASSURANCE
April 2022 – March 2025
Responsibilities
VALIDATION: Currently working in the Validation department. Process Validation Protocol PVP, Process Validation Report PVR, Master Validation Plan, Sampling of process validation and cleaning validation since September 2022. IN PROCESS CONTROL /QMS: Maintain GMP, cGMP, GDP. Assign the duty to subordinates according to sections/Departments. Validation of Product, validation of sterile areas after every 6 months, Area Qualification. Maintain and communicate Quality vision for safe and efficient production of APIs and GMP compounds. Documentation according to GDP, Annual product Quality Review (APQR), CAPA Investigation including, Market complain review with investigation. Line clearance of Area and Machine on floor. Ensure the Quality of products according to SOP.
Major Achievement: IQ, OQ, PQ of Compact line Syrup filling, Implementation of Power BI based APQR.
ASSISTANT MANAGER QUALITY ASSURANCE
January 2017–March 2022
Responsibility
Maintain GMP, cGMP, GDP, GLP. Assign the duty to subordinates according to sections/Departments. Validation of Product, validation of sterile areas after every 6 months, Area Qualification. Maintain and communicate Quality vision for safe and efficient production of APIs and GMP compounds. Documentation according to GDP, Annual product Review
(APR), CAPA Investigation including OOT, OOS, Market complain review with investigation. Line clearance of Area and Machine on floor. Ensure the Quality of products according to USP. Maintain the Record room and Reference storeroom according to SOPs. Sampling of Raw Material, tablet, Liquid. Sterile products. Major Achievement: implemented QMS.
Successfully done validation of Sterile Area according to PQE. Successful Audit of PQE 2019 SAP implemented.
HOBBIES
Cricket
Reading books
Hiking
Net surfing
CORE STRENGTHS &
ENABLING SKILLS
Leadership, Management, Teamwork,
English, French
Office Microsoft,
Honesty,
Good listener,
Observer,
Good Learner, and SAP etc.,
Merck PVT Ltd
Quality Assurance Officer
September 2013–December 2016
Ensure the Quality of products like solid, liquid, and sterile products. Line clearance of Area, machine, or room according to SOPs. In process control according to SOPs. Annual Product Review as per SOPs. Validation of sterile areas, IQ, OQ, PQ. Autoclave validation, filling line validation, filter integrity validation, product validation. To make a CAPA for nonconference. Sampling of Raw material according to SOPs, Sampling of solid liquid and sterile products for QC analysis,
Contact this candidate