Mister

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Michael Angelo Castor Malate
7 Cadiz St., Intercity Homes Cupang, Muntinlupa City 1771
+63 (917) 831 0223 • mcmalate@gmail.com
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OBJECTIVE:To find a challenging position to meet my competencies, capabilities, skills, education and experience. -------------------------------------------------

PERSONAL INFORMATION:

Nationality:Filipino
Birth date:23 February 1985
Gender:Male
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Marital Status:Single
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EDUCATION:

UNIVERSITY OF THE PHILIPPINES MANILA| Ermita, Manila|
College of Pharmacy * Master of Science in Hospital Pharmacy * GWA 1.9; earned 21 academic units| October 2011|

UNIVERSITY OF SANTO TOMAS| Sampaloc, Manila|
Faculty of Pharmacy * Bachelor of Science in Pharmacy| April 2006|

SAN BEDA COLLEGE| Alabang, Muntinlupa City|
* High School Diploma| April 2002|
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CERTIFICATION:

ATENEO GRADUATE SCHOOL OF BUSINESS| Makati City|
Center for Continuing Education * Six Sigma Green Belt * Project on-going| June 2012| -------------------------------------------------

LICENSE:

PROFESSIONAL REGULATION COMMISSION| Manila|
Pharmacy Licensure Board * Licensed Pharmacist| July 2007|

WORK EXPERIENCE:

SUMMARY:

Highly motivated Quality Assurance & Compliance professional. Strong verbal, listening and written skills. Comfortable in interacting with all levels of the organization and public. Able to negotiate and problem solve quickly, accurately, and efficiently. Adept at multitasking to achieve individual and team goals. Diverse background includes process improvement, customer service and supervision. Committed to quality and excellence. -------------------------------------------------

METRO DRUG, INC. (A Zuellig Pharma Asia Pacific Company) (November 2011 to Present)| Taguig City| Quality Control Supervisor|

Dedicated QA/QC person to ensure compliance and adherence of MDI’s redressing/repacking operation to Good Manufacturing Practices (GMP), ZP RQA Standards, Quality Management System ISO 9001, and compliance to all government/FDA regulatory requirements for repacking/redressing operations.

Repacking/Redressing Operations

* Ensures compliance of the company’s repacking/redressing operation to Zuellig Pharma RQA GMP for Secondary Repacking and Good Storage and Distribution Practices (GSDP) with focus on the following: 1. Master Batch Records

2. Checking and releasing of packaging materials and release of finished products 3. Archiving of product documents
4. Reporting and documentation of non-conformities and/or deviations encountered during checking of packaging materials and products for redressing/repacking operations. 5. Reporting, documentation and addressing customer complaints related to repacking operations 6. Safety handling of cytotoxic products

* Responsible for the day-to-day supervision of repacking/redressing operations in relation to compliance to QA/QC requirements of Principals, FDA, RQA and company policies and standards.

* Responsible in coordinating with Principals and the Warehouse in relation to: 1. Training of personnel for repacking/redressing activities 2. Identifying product specifications
3. Stocks and packaging materials to be used for repacking 4. Repacking/Redressing documentation requirements

* Establish and maintains an updated standard operating procedure for redressing/repacking operation.

* Responsible for the reports required by FDA related to repacking/redressing activities.

* Assists the QMR/QAC Manager and VP-Supply Chain in preparation of reports related to repacking/redressing activities as required by the Principal and other divisions within the company.

Regulatory Functions

* Authorized...
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