MOHAMMAD SOHAIL ANWAR

CAREER OBJECTIVE:

A challenging position in the required aea which would provide an opportunity for learningand professional advancement.

PERSONAL INFORMATIONAL:

Father's name : Mohammad Moizuddin

Date of Birth : March 4th 1978

N.I.C No. : 421**********

Martial status : Married

Nationality : Pakistani

Religion : Islam

Domicile : Sindh

ACADEMIC QUALIFICATION:

M. Phil 2007 1st Division University Of Karachi

B. Pharmacy 2000 1st Division University Of Karachi SKILLS:

I am well acquainted with the proper and independent use of the following techniquesand equipments.

WAREHOUSE AFFAIRS:

KEY RESPONSIBILITIES:

To Supervise Raw Material, Packaging Material, Samples Stores, Finished Goods, Dispensing of batches & Logistics Store.

To Look after proper receiving & storage of incoming materials, and General Supply items, & Finished Goods in accordance with cGMP and Regulatory requirements and

maintenance of their records.

To ensure proper segregation, Storage of products and Materials according to the required conditions as per cGMP.

To ensure timely and accurate delivery to the customers/distributors. To performCost negotiation with vendor / carriers and provide appropriate solutions for bulk distributions.

Maintaining Bin card of all inventory materials and their data entry through Supply chain Management system.

To ensure receiving of Expired Finished Goods, & their verification from distributors and communicate this to Sales, Distributor & Finance department for claim. Responsible to initiate Destruction document, get it reviewed for Approval and incineration / Disposition as per procedure.

To ensure proper functioning of Cold storage room, Responsible to inform immediately any Malfunctioning of Air conditioning unit in this area to Engineering

& QA department, also responsible to follow up for restoration of Cold storage room.

To ensure proper cleaning and Hygiene conditions of Warehouse. Responsible for timely rectification of Finished Goods complaints received from distributors.

Completes warehouse Operational requirements by scheduling and assigning Employees, following up on work results.

Controls inventory levels by conducting Physical counts, reconciling with Data storage system.

Maintains warehouse Staff by recruiting, selecting, orienting, and training of all employees.

Working on departmental Budget report for Head Count, CAPEX and OPEX. To develop,review, revision and implementation of Departmental SOPs as required. QUALITYASSURANCE AFFAIRS:

KEY RESPONSIBILITIES:

To ensure the GMP compliance in Production area as per GMP checklist on daily basis.

To manage Batch review and Batch release of Products. Ensure the execution of Document Management and Data Control System. To Review & approve of Current and New Products Artworks. To ensure Compliance of Quality systems i.e . Change Controls, Deviations, Customer Complaints and providing CAPA for the same . To develop,review, revision and implementation of QA SOPs as required. Establish and maintain Product Quality Review annually. Handling of Customer and Supplier complaints, Products defects and Recalls. Team member for organizing In house Audits and External Audits of Regulatory bodies, Certification bodies as well as Audits of Exporting countries. Ensures destruction of Rejected products, Packaging components, supplies and returned Goods are being carried out after proper Authorization as per procedure. Working on departmental Budget report for Head Count, CAPEX and OPEX. VALIDATION AFFAIRS :

KEY RESPONSIBILITIES:

Develops Validation Master Plan & Schedule for all production areas, utilities as per Regulatory requirements.

Organizing all Calibration & Qualification activities and prepare the required plans. Timely preparation and approval of Process Validation and Qualification protocols.. Supervise team for different activities related to Process Validation and Equipment Qualificationand Calibration.

Prepare and review SOPs for Validation and Qualification as per requirement.. Preparation of validation summary report for releasing of validation batches. Maintain the product portfolio of plant in validated status according to cGMP rules. To Manage Equipment Qualification of newly installed machines. Handling Thermal Mapping for refrigerators, freezers, incubators, ovens, stability chambers & warehouses.

REGULATORY AFFAIRS:

KEY RESPONSIBILITIES:

Prepare Product registration / Renewal Dossiers according to the regulatory requirements ofMOH

Provide responses to regulatory agencies regarding product information or issues. Develop and maintain Standard Operating Procedures for local working practices. QUALITY CONTROL AFFAIRS:

KEY RESPONSIBILITIES:

To analyze all samples of Finished products, Intermediates, Raw materials and Packaging materials as per requiredstandard.

To prepare testing reports of material and product reports in time and maintain all records as per laid down procedures of the company. Monitoring the Loggingof data in daily logbooks.

Coordinate with production department for timely release of raw materials and finishedproducts.

Handling of Disintegration apparatus, Dissolution apparatus, FTIR, Friabilator, Karl Fisher, Polarimeter. HPLC etc.

WORK EXPERIENCE:

Worked as Management Trainee with Parke Davis Pharmaceutical, Karachi fromMarch 2000 to August 2000.

Worked as an Officer with Aventis Pharma in QA Department from October 2000 to August 2001

Worked as Sr.Quality Assurance Officer with Searle Pakistan Ltd. from September2001 to June 2008.

Worked as a Assistant Manager Quality Assurance in AGP PVT. LTD from July 2008 to December 2013

Worked as a Deputy Manager Warehouse in AGP PVT. LTD from January 2014 to February 2021

Working as Deputy Manager Warehouse in BOSCH Pharmaceutical Pvt. Ltd since March 2021

TRAININGS:

1.Problem Solving and Decision Making (PIM )

2.How to Conduct Audit. ( AGP PVT. LTD. )

3.Importance of Change Control and Deviation Report. ( AGPPVT.LTD.) 4.Validation gives Confidence ( AGPPVT.LTD.)

5.ISO 9001; 2008 QMS awareness and interpretation . ( AGP PVT.LTD.) 6.Process Validation of Sterile Products.( Marriott Hotel ) 7.Lotus Notes Training ( AGP PVT.LTD.)

8.OHSAS Training (Searle Pakistan LTD.)

9.Operational Excellence Using Seven QC Tools .( SMEDA) 10.Change Control Management .( AGP PVT.LTD.)

11.Team Management & Leadership. (OCTARA)

12.Goal Achievement & Task Management . (OCTARA)

13.Power of Positiveness .( AGP PVT.LTD.)

14.Current Trends for Sterile Manufacturing and processing.(Business Link) 15.Attended the Certified Lead Auditor Course conducted by SGS. LANGUAGE PROFICIENCY:

ENGLISH : Good in oral and written communication

URDU : Excellent in oral and written communications COMPUTER KNOWLEDGE:

Run MS OFFICE smoothly

Run SAP smoothly

SKILLS :

Quality Management, Training & Development, Auditing, Problem Solving Continuous Improvement, Qualification, Budgeting, TemperatureMapping, SOP Compliance/Harmonization,InventoryManagement & Project Management

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