BLESELDA RIA G. SIOCO

____________________________________________________

Phase II, Filomena Subd.,San Rafael, Tarlac City,Philippines  |(+63)917-252-5849 |[email protected]

Dear Hiring Manager:

I am writing this letter in response to the job career that you posted on your website to whichever position I may fit in according to my work experiences/knowledge.

My years of experience and knowledge made me say that I am greatly fit for a pharmaceutical job that would extend more of my horizon as I apply for a job on your country. I am greatly interested in applying for the position I have my Curriculum Vitae/ Resume to supplement my profile.

Working in your company would help me enhance more of my potentials and having such a good working environment and people around will eventually provide more stellar service to staff and executives. It would also enhance my communication skills and initiative to a more professional environment as I work in your good company.

Sincerely,

Bleselda Ria G. Sioco

BLESELDA RIA G. SIOCO

Phase II, Filomena Subd.,San Rafael, Tarlac City,Philippines

+639172525849/[email protected]

_____________________________________________________________________________________

PROFESSIONAL SUMMARY

·         Detail oriented pharmacy graduate, Quality Control Admin Assistant working independently with minimal supervision. Efficiently working on incoming samples for testing in the laboratory, allocation of samples per unit, checking of test parameters assigned on each product guided with specification sheets and protocols validated by the company (Unilab.Inc) validation team. Perform analytical assays/testing related to products catered by the company to its consumers most especially HPLC (High Performance Liquid Chromatography) and other physical testing of drugs and accomplish accurate laboratory reports for quality health care.

·         A self-motivated organized professional with over 2 years of experience providing thorough and skillful administrative support to the laboratory (Unilab.Inc).

·         Can work under pressure. Highly organized, analytical thinker with strong communication skills.

·         Excels in multitasking, completing tasks within time.

·         Having general ability and knowledge in handling prescriptions/ medication orders which have been proved after working as Pharmacy Assistant for almost 5 years. Possess excellent customer service and ability to handle customer or patient request with professionalism and efficiency.

·         A graduate with substantial and responsible work experience looking to bring a range of skills and commercial knowledge to a new career in organization in the private or public sector.

·         Possess excellent verbal and written skills with friendly approach.

·         With good working knowledge on standard quality plan in my previous and current experience.

·         I maintain an exceeding functional working environment. I respond to questions and tasks from my leaders and managers in a timely manner and prioritizing multiple on-going projects.

·         In my current work as a team leader, I maintain a quality handed workload and monitoring for the company’s welfare.

HIGHLIGHTS

·         Documentation

·         Filing

·         Understands grammar

·         Quality Control Support

·         Dispensing

·         Patient Counseling

·         Monitoring

·         Packaging of Products- validation as per FDA a.o. 2016

·         Good practice of product detailing

·         Quality Assurance Assay

·         With knowledge to Corel/ Illustrator for packaging materials

PROFESSIONAL EXPERIENCE

v  AMHERST  LABORATORIES. INC (A subsidiaryof UNILAB.INC formerly known as UNITED LABORATORIES)

Address:  UNILAB Pharma Campus, Mamplasan, Binan, Laguna (in front of Brentville Compound)

Length of tenure: October 2015 – December 2017

Position:  Quality Assurance Analyst/Quality Control Admin Assistant

·         Perform analytical tests for Routine/ Stability studies of products guided by analytical procedures and testing protocols.

·         Working on analytical machines such as UPLC (UltraPerformance Liquid Chromatography , HPLC (High Performance Liquid Chromatography), modern analytical balances and other machines for assay in the laboratory.

·         Can do physical testing (Specific gravity and others) of products.

·         Prepare mediums for analytical testing.

·         Evaluation of laboratory reports based on performed assay and its specifications.

·         Receive all incoming products for testing in the laboratory.

·         Encoding of samples in the Incoming Worksheet File as part of the quality and monitoring plan.

·         As per leader’s decision, I represented the laboratory to explain the full quality plan stated in the SOP (Stand Operating Procedures) during the mock U.S. FDA audit- U.S, FDA Consultants mock audit and inspection happened last December 2017.

·         Assist in filing of employee DTR, weekly schedules, training plans, providing and evaluating updates on product’s monthly performance.

·         Working on inventories, database for transmitting samples for third party testing.

v  JECSONS MEDICAL CENTER

Address: Mc Arthur Highway, San Nicolas Tarlac City

Length of tenure: August 2010 – May 2015

Position:  Pharmacy Assistant

·         Assist drug inquiry to patients.

·         Receiving medical prescriptions/physician orders from patients.

·         Working on inventories of stocks in the pharmacy.

·         Documentation of PDEA books (regulated drugs)

·         Dispensing of prescribed drugs both regulated and over the counter.

·         Can provide full patient counseling for product knowledge.

·         Can address physician inquiries about drugs as to pharmacokinetics, pharmacodynamics, dosage, forms and indications.

v  DRUGMAKER’S LABORATORIES, INC.

Address: E & E Industrial Complex, Brgy. San Antonio, San Pedro, Laguna

Length of tenure: January 2018 – February 2019

Position:  Regulatory Staff (Technical 1) – January 2018 to September 2018; Regulatory Team leader (Technical 2) – October 2018 to February 2019

·         Monitoring and checking of LTO (License to Operate) which includes validity, approved changes/ variations.

·         Can access E-Portal of FDA (Food and Drug Administration) for renewal of licenses.

·         Monitoring and checking of CPR’s (Certificate of Product Registration) which includes validity, approved changes/ variation.

·         Monitoring of Initial (ASEAN (ACTD (ASEAN Common Technical Dossier) and NATIONAL) for new product registration, renewal of CPR, variations, PCPR (Principal Certificate Product Registration), CLIDP ( Certificate of Listing of Identical Drug Product) of both the company and TGP (The Generics Pharmacy) and other Clients.

·         Processing of Batch Notifications submitted to FDA.

·         Provides barcodes for new products, CLIDP, renewal of products of non-marketed clients.

·         Encoding/Monitoring of incoming internal/ external letters.

·         Encoding/Monitoring of submitted documents to FDA.

·         Construction of outgoing letters including memos both internal and external.

·         Disseminate FDA updates to management (Posted by FDA).

·         Assign workload to staffs.

·         Checking of packaging materials as per FDA a.o. 2016 memorandum.

·         Acknowledging emails (incoming) with our department regularly (includes emails from FDA, PCPI, TGP, and other manufacturing clients).

·         Attend MANCOMM meetings with the president of the company for updates and monitoring of quality drugs regularly.

·         Intellectual Property of the Philippines-company’s authorized representative for filing/ initial registration of products (patent).

·         QPIRA (Qualified Person in the Industry of Regulatory Affairs) member- 3 years validity (November 2018- November 2021)

·         Do official Business to FDA for drug inquiries and submission of required applications for full drug compliance.

·         Can do Corel/ Illustrator layouts for packaging materials.

·

TRAININGS AND SEMINARS ATTENDED

·         Seminar on proper handling of medical samples

·         6S Seminar

·         Seminar on Patient Counseling

·         Training on salesmanship, pharmacology and Anatomy & Physiology at Zuellig Pharmaceutical under Ms. Ellen Balasa

·         QPIRA (Qualified Person in the Industry of Regulatory Affairs) CFRR (Center for Food Regulation and Research)

CHARACTER REFERENCES

·         LAUREEN JOY MAZON

Quality Control Manager, Amherst Laboratories, Inc. (UNILAB.INC)

+639278500706

·         ELEANOR MENCHAVEZ

Quality Assurance Officer, Amherst Laboratories, Inc. (UNILAB.INC)

+639175713027

·         LADY FATIMA GENESE

Group Leader, Amherst Laboratories, Inc. (UNILAB.INC)

+639175158570

·         REA JAVIER

HR Assistant, Drugmaker’s Laboratories, Inc.

+639178810695/ 556-7738

BLESELDA RIA G. SIOCO

____________________________________________________

Phase II, Filomena Subd.,San Rafael, Tarlac City,Philippines  |(+63)917-252-5849 |[email protected]

Dear Hiring Manager:

I am writing this letter in response to the job career that you posted on your website to whichever position I may fit in according to my work experiences/knowledge.

My years of experience and knowledge made me say that I am greatly fit for a pharmaceutical job that would extend more of my horizon as I apply for a job on your country. I am greatly interested in applying for the position I have my Curriculum Vitae/ Resume to supplement my profile.

Working in your company would help me enhance more of my potentials and having such a good working environment and people around will eventually provide more stellar service to staff and executives. It would also enhance my communication skills and initiative to a more professional environment as I work in your good company.

Sincerely,

Bleselda Ria G. Sioco

BLESELDA RIA G. SIOCO

Phase II, Filomena Subd.,San Rafael, Tarlac City,Philippines

+639172525849/[email protected]

_____________________________________________________________________________________

PROFESSIONAL SUMMARY

·         Detail oriented pharmacy graduate, Quality Control Admin Assistant working independently with minimal supervision. Efficiently working on incoming samples for testing in the laboratory, allocation of samples per unit, checking of test parameters assigned on each product guided with specification sheets and protocols validated by the company (Unilab.Inc) validation team. Perform analytical assays/testing related to products catered by the company to its consumers most especially HPLC (High Performance Liquid Chromatography) and other physical testing of drugs and accomplish accurate laboratory reports for quality health care.

·         A self-motivated organized professional with over 2 years of experience providing thorough and skillful administrative support to the laboratory (Unilab.Inc).

·         Can work under pressure. Highly organized, analytical thinker with strong communication skills.

·         Excels in multitasking, completing tasks within time.

·         Having general ability and knowledge in handling prescriptions/ medication orders which have been proved after working as Pharmacy Assistant for almost 5 years. Possess excellent customer service and ability to handle customer or patient request with professionalism and efficiency.

·         A graduate with substantial and responsible work experience looking to bring a range of skills and commercial knowledge to a new career in organization in the private or public sector.

·         Possess excellent verbal and written skills with friendly approach.

·         With good working knowledge on standard quality plan in my previous and current experience.

·         I maintain an exceeding functional working environment. I respond to questions and tasks from my leaders and managers in a timely manner and prioritizing multiple on-going projects.

·         In my current work as a team leader, I maintain a quality handed workload and monitoring for the company’s welfare.

HIGHLIGHTS

·         Documentation

·         Filing

·         Understands grammar

·         Quality Control Support

·         Dispensing

·         Patient Counseling

·         Monitoring

·         Packaging of Products- validation as per FDA a.o. 2016

·         Good practice of product detailing

·         Quality Assurance Assay

·         With knowledge to Corel/ Illustrator for packaging materials

PROFESSIONAL EXPERIENCE

v  AMHERST  LABORATORIES. INC (A subsidiaryof UNILAB.INC formerly known as UNITED LABORATORIES)

Address:  UNILAB Pharma Campus, Mamplasan, Binan, Laguna (in front of Brentville Compound)

Length of tenure: October 2015 – December 2017

Position:  Quality Assurance Analyst/Quality Control Admin Assistant

·         Perform analytical tests for Routine/ Stability studies of products guided by analytical procedures and testing protocols.

·         Working on analytical machines such as UPLC (UltraPerformance Liquid Chromatography , HPLC (High Performance Liquid Chromatography), modern analytical balances and other machines for assay in the laboratory.

·         Can do physical testing (Specific gravity and others) of products.

·         Prepare mediums for analytical testing.

·         Evaluation of laboratory reports based on performed assay and its specifications.

·         Receive all incoming products for testing in the laboratory.

·         Encoding of samples in the Incoming Worksheet File as part of the quality and monitoring plan.

·         As per leader’s decision, I represented the laboratory to explain the full quality plan stated in the SOP (Stand Operating Procedures) during the mock U.S. FDA audit- U.S, FDA Consultants mock audit and inspection happened last December 2017.

·         Assist in filing of employee DTR, weekly schedules, training plans, providing and evaluating updates on product’s monthly performance.

·         Working on inventories, database for transmitting samples for third party testing.

v  JECSONS MEDICAL CENTER

Address: Mc Arthur Highway, San Nicolas Tarlac City

Length of tenure: August 2010 – May 2015

Position:  Pharmacy Assistant

·         Assist drug inquiry to patients.

·         Receiving medical prescriptions/physician orders from patients.

·         Working on inventories of stocks in the pharmacy.

·         Documentation of PDEA books (regulated drugs)

·         Dispensing of prescribed drugs both regulated and over the counter.

·         Can provide full patient counseling for product knowledge.

·         Can address physician inquiries about drugs as to pharmacokinetics, pharmacodynamics, dosage, forms and indications.

v  DRUGMAKER’S LABORATORIES, INC.

Address: E & E Industrial Complex, Brgy. San Antonio, San Pedro, Laguna

Length of tenure: January 2018 – February 2019

Position:  Regulatory Staff (Technical 1) – January 2018 to September 2018; Regulatory Team leader (Technical 2) – October 2018 to February 2019

·         Monitoring and checking of LTO (License to Operate) which includes validity, approved changes/ variations.

·         Can access E-Portal of FDA (Food and Drug Administration) for renewal of licenses.

·         Monitoring and checking of CPR’s (Certificate of Product Registration) which includes validity, approved changes/ variation.

·         Monitoring of Initial (ASEAN (ACTD (ASEAN Common Technical Dossier) and NATIONAL) for new product registration, renewal of CPR, variations, PCPR (Principal Certificate Product Registration), CLIDP ( Certificate of Listing of Identical Drug Product) of both the company and TGP (The Generics Pharmacy) and other Clients.

·         Processing of Batch Notifications submitted to FDA.

·         Provides barcodes for new products, CLIDP, renewal of products of non-marketed clients.

·         Encoding/Monitoring of incoming internal/ external letters.

·         Encoding/Monitoring of submitted documents to FDA.

·         Construction of outgoing letters including memos both internal and external.

·         Disseminate FDA updates to management (Posted by FDA).

·         Assign workload to staffs.

·         Checking of packaging materials as per FDA a.o. 2016 memorandum.

·         Acknowledging emails (incoming) with our department regularly (includes emails from FDA, PCPI, TGP, and other manufacturing clients).

·         Attend MANCOMM meetings with the president of the company for updates and monitoring of quality drugs regularly.

·         Intellectual Property of the Philippines-company’s authorized representative for filing/ initial registration of products (patent).

·         QPIRA (Qualified Person in the Industry of Regulatory Affairs) member- 3 years validity (November 2018- November 2021)

·         Do official Business to FDA for drug inquiries and submission of required applications for full drug compliance.

·         Can do Corel/ Illustrator layouts for packaging materials.

·

TRAININGS AND SEMINARS ATTENDED

·         Seminar on proper handling of medical samples

·         6S Seminar

·         Seminar on Patient Counseling

·         Training on salesmanship, pharmacology and Anatomy & Physiology at Zuellig Pharmaceutical under Ms. Ellen Balasa

·         QPIRA (Qualified Person in the Industry of Regulatory Affairs) CFRR (Center for Food Regulation and Research)

CHARACTER REFERENCES

·         LAUREEN JOY MAZON

Quality Control Manager, Amherst Laboratories, Inc. (UNILAB.INC)

+639278500706

·         ELEANOR MENCHAVEZ

Quality Assurance Officer, Amherst Laboratories, Inc. (UNILAB.INC)

+639175713027

·         LADY FATIMA GENESE

Group Leader, Amherst Laboratories, Inc. (UNILAB.INC)

+639175158570

·         REA JAVIER

HR Assistant, Drugmaker’s Laboratories, Inc.

+639178810695/ 556-7738