Nerfe Abante is a QA/QC Engineer from the Philippines seeking a position that promotes professional growth. He has over 10 years of experience in quality control, quality assurance, and product development. His skills include proficiency in MS Office, knowledge of quality standards like ISO 9001 and HACCP, and experience performing inspections, audits, developing documentation, and resolving non-conformances. He holds a Bachelor's degree in Chemical Engineering.
• Competent professional with 10+ years of experience in executing
In-process quality assurance by monitoring complete pharma
manufacturing process in order to comply with the specifications
• Over all responsible for IPQA Activities (both manufacturing and
packing area of solid orals, Nasal spray and Liquid dosage forms)
• Ensure the compliance of quality events like deviation
management, temporary change control, permanent change control, CAPA, Market complaints.etc.
• Active participation in root cause investigation and proposal of CAPA for deviation, market complaint and batch failure.
• Effectiveness check of implemented CAPA in shop floor.
• Calibration Management –ensure calibration of all IPQA instruments as per schedule.
• Skilled in preparation and review of Annual Product Quality Review (APQRs)
• Review of SOPs/work instructions-Gap identification and compliance of the same.
• Conducting in-house cGMP audits to ensure compliance and sound functioning of the process.
• Provide training regarding any changes to existing system and introduction of any new system.
• Knowledge on OOS, OOT, Site Master File.
• Hands-on experience in preparation of Process validations, cleaning validation, hold time study protocols and BMR and BPR preparation.
• Making Sure that products are manufactured according to legal and Customer requirements.
• Diligently Verifies document Completion and Compliance.
• Competent professional with 10+ years of experience in executing
In-process quality assurance by monitoring complete pharma
manufacturing process in order to comply with the specifications
• Over all responsible for IPQA Activities (both manufacturing and
packing area of solid orals, Nasal spray and Liquid dosage forms)
• Ensure the compliance of quality events like deviation
management, temporary change control, permanent change control, CAPA, Market complaints.etc.
• Active participation in root cause investigation and proposal of CAPA for deviation, market complaint and batch failure.
• Effectiveness check of implemented CAPA in shop floor.
• Calibration Management –ensure calibration of all IPQA instruments as per schedule.
• Skilled in preparation and review of Annual Product Quality Review (APQRs)
• Review of SOPs/work instructions-Gap identification and compliance of the same.
• Conducting in-house cGMP audits to ensure compliance and sound functioning of the process.
• Provide training regarding any changes to existing system and introduction of any new system.
• Knowledge on OOS, OOT, Site Master File.
• Hands-on experience in preparation of Process validations, cleaning validation, hold time study protocols and BMR and BPR preparation.
• Making Sure that products are manufactured according to legal and Customer requirements.
• Diligently Verifies document Completion and Compliance.
1. NERFE A. ABANTE
QA/QC Engineer
V I S A S T A T U S : W O R K V I S A E X P E C T E D S A L A R Y : 6 0 0 0 A E D
O B J E C T I V E S
To join a company that promotes excellence and professional
growth among its employees. A company that will enable me to
maximize my potentials and capabilities as a professional, to help me
build my goals.
F U N C T I O N A L I T Y S K I L L S
o Proficient in MS Office Application
o Knowledge in quality assurance principles, including ISO
9001, ISO 14001, and ISO 22000, HACCP and other
Quality Management System standards.
o Knowledge in statistical methods (SPC) and structured
problem solving
o Trained in Food Safety Handling and Internal Quality
Audit.
E X P E R I E N C E
QUALITY CONTROL/ DOCUMENT CONTROLLER
– UNICAP, Jebel Ali Fze
June 2013 to present
DUTIES & RESPONSIBILITIES
o Review and update Quality Manual for any improvements,
updates and changes in the process and procedure.
o In-charge of the safe keeping and distribution of the
updated procedures, forms, records and official documents
of the Company Manual.
o In-charge of the Internal Food Safety Quality Audit.
o Monitors daily cleanliness and sanitation of the plant.
o Performs quality inspection and evaluate the incoming raw
materials
o Performs quality inspection and generate data report of the
formed products. Visual checking, dimensional and
functional evaluation.
o Performs hourly on-line quality inspection of the produce
formed products.
o Performs calibration of the IMD camera
o Performs quality inspection and issue evaluation report for
the outgoing finished products.
o Assists in internal and external customers in addressing
technical and quality-related inquiries regarding the
company’s products, processes or procedures.
o Responsible for handling the internal and external product
non-conformities.
PRODUCT DEVELOPMENT ASSOCIATE(D.A.)
- United Graphic Expression Corp
April 2012 – Feb 2013
DUTIES & RESPONSIBILITIES
o Coordinates with the Client/Customer for the Product
Specifications of developmental products thru the
Account Officer
o Creates a Product Development Protocol for the
developmental Product
o Arrange an alignment meeting with the Logistics,
Production, QA and Account Officer for the pilot run
or trial production of the developmental product.
o Monitor process flow, functional and physical
attributes of the developmental product.
o Creates Inspection Protocol, Quality Plan, Technical
Specification, and HACCP Plan as required.
o Records monitoring and submits the final documents
such as Inspection Protocol, Quality Plan, and
Technical Specification to the Document Controller for
archiving and future reference.
SR. QUALITY ASSURANCE INSPECTOR -
United Graphic Expression Corp
July 2004 –April 2012
DUTIES & RESPOSIBILITIES
o Ensure the quality of all incoming raw materials and
other related materials intended for manufacturing
operations.
o Performs sampling, quality inspection, testing and
evaluation of all incoming raw material deliveries
according to established quality standards covering
issuance of appropriate disposition and NCR as
applicable.
o Performs sampling, quality inspection, testing and
evaluation of contracted services according to
established quality standards including informing
relevant function of deviations found and issuance of
NCR as required.
o Perform quality inspection of finished goods covering
issuance of NCR as applicable, preparation of
certificates of inspection and other required reports
ensuring accuracy, completeness and timeliness.
o Assist in reviewing laboratory test procedures and
tolerances for materials used in manufacturing
operation.
o Responsible for managing the use, calibration and
compactness of test, measuring and all other
equipment in the QA laboratory.
Rm 33 Bin Hayder Blg. Salahuldin Rd. Deira Dubai, UAE
+971-566255916
faye_absin@yahoo.com.ph
0
100
RELIABILITY CREATIVITY COMMITMENT FLEXIBILITY
COMPETENCY
2. o Assist in analyzing product performance data and
participate in problem solving and process improvement
projects within the manufacturing environment.
o Assist internal and external customers in addressing
technical and quality-related inquiries regarding the
company’s products, processes or procedures.
o Responsible for documents, records and samples
safekeeping and maintenance.
LABORATORY ANALYST- Fountain Dept. Coca-
Cola Bottler’s Philippines
May 2003 - June 2004
DUTIES AND RESPONSIBILITIES
o Prepare solutions for laboratory usage.
o Analyzed and record test results as required.
o Performed safety checks regularly.
o Assisted in writing test results, and reviewed them as
needed.
o Performed other lab-related duties as assigned.
o Performed and assisted in various laboratory analyses.
o Performed a variety of analytical testing techniques.
o Minimized and prevented errors when executing
laboratory testing.
o Obtained and prepared samples to study at processing
period from raw materials to completed products.
o Deftly maintained testing equipment in suitable working
order.
E D U C A T I O N
Bachelor of Science in Chemical Engineering
1999 - 2003
Technological Institute of the Philippines
1996-1999
Adamson University
P E R S O N A L I N F O R M A T I O N
Age : 35
Date of birth : July 28, 1979
Citizenship : Filipino
Religion : Catholic
Civil Status : Married