Biodata |
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| Name of the Candidate | : | [Private] |
| Name of the Post Applied | : | Corporate Quality Assurance |
| Job related skills / software | : | To verify issuance of packaging commodity as per finishing order and inventory requisition, Check the destruction of material against destruction slip, Ensure the waste disposal of material. |
| Category | : | Medical |
| Sub Category | : | Quality Assurance Executive |
| Years of Experience | : | 4 years |
| State | : | Punjab |
| Gender | : | Male |
| Salary Expected per Month(Rs) | : | 0 to 5,000 |
| Highest Qualification attained | : | M.Sc. / MSC : Master of Science |
| Major / Specialization | : | Applied Chemistry & Chemical Technology |
| Email Id | : | [Private] |
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| Are you looking for job now? | : | Yes |
| Can the recruiter contact you? | : | Yes |
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Resume Format / CV Sample Template / Example / Model : |
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Syed Zain Ali
Mobile : 0413 034 099
Email : abidi1988 AT gmail.com
Address : 39 verbena avenue casual 2170 NSW Australia
Skills :
** Time management
** Diagnostic
** Proactive approach
** Problem Solver
** Adoptability
** Collaboration
** Critical thinking
** Ability to develop people
Objective :
Seeking a career with a progressive organization where I can utilize my skills, knowledge and experience in process control and troubleshooting, and most importantly a challenging role that allows for advancement and growth.
Education :
** 2012 – 2013 Masters of Science (Applied Chemistry &Chemical Technology University of Karachi
** 2009 – 2011 Bachelor of Science (Applied Chemistry &Chemical Technology) University of Karachi
Experience :
QUALITY ASSURANCE ( ATCO LABORATORIES LIMITED )
November 2013 – November 2017
Main duties :
** To control in-process checks during the production process.
** To perform in-process checks and assure cGMP follow up for the designated process as per written instructions.
** To check the returned material against manufacturing order and finishing order inventory. To verify dispensing of raw material as per manufacturing order.
** To verify issuance of packaging commodity as per finishing order and inventory requisition.
** Check the destruction of material against destruction slip.
** Ensure the waste disposal of material.
** Check the returned goods against incoming stock receiving report.
** Perform the inspection of first aid boxes and distribution of medicines.
** To check the returned material against manufacturing order and finishing order inventory.
** Preparing and updating list of registered products.
** Participate in the submission of documents for the products registered in exporting countries.
** ** To work as a system coordinator between Quality Assurance / Regulatory / Production / Engineering / Marketing / Material Control department in order to control the technical documents and related is
sues..
** To check and issue the Product Master Formula / Batch Manufacturing Record to control the quality of product during Manufacturing.
** To participate in the issuance & distribution of Standard Operating Procedures.
** To coordinate in Internal Quality Audit & Surveillance Audit of ISO 9001 :2008.
** To coordinate with other departments for allocation of document numbers in order to control the documents.
** To prepare and update the Master List of technical documents of all departments.
** To coordinate in training program to the factory staff related to cGMP.
** To ensure that the QMS standard is being implemented in true spirit for the benefit of the organization
** To assist the manufacturing team in making suitable arrangements so as to ensure the manufacturing of consistent quality products by incorporating GMP and other quality standards.
** To ensure that the production and control operations are clearly written and specified
** To ensure that the GMP requirements are adopted and followed.
** To ensure that the responsibilities are specified in job description.
** To make an arrangement that the starting & packaging materials are manufactured, supplied and used in a correct manner; through supplier audit and quality audit.
** To ensure that the finished drugs are correctly processed and checked according to the defined procedures, if some quality variation observed, investigate and ensure to prevent its recurrence.
** To ensure that the finished drugs are not dispatched before release by the authorized person.
** To ensure that satisfactory storage conditions prevail for the materials.
** Perform self-Inspection, Quality Audit and conduct MRC meetings at appropriate intervals, to re-view and asses the effectiveness of the system
Training Program on Laboratory Experiment of fuel ( Pakistan council of Scientific & Industrial Research )
June 2013 –July 2013
Internship Program ( Macter Pharmaceutical Private limited )
December 2012 – January 2013
Achievements :
** Handled product release programs of the company
** Prepared strategies and plans that results in the development of the organization
** Maintained and managed insternal audit plans
Date :
Place :
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