ROSITA MASIGLAT SISON
PHONE: 0905-434-5465; 0921-795-4210
EMAIL: [email protected]
ADDRESS: 9055 D. Governor’s Drive Bancal Carmona Cavite
BIRTHDAY: October 10, 1970
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CAREER SUMMARY: An experienced Research and Development/Quality Control and Assurance
Specialist with demonstrated work of history in the field of food, pharmaceutical
and veterinary feeds industry.

TECHNICAL SKILLS
• Laboratory Quality Control Analyst/Quality Assurance Inspector
• Knowledge and skills on instrumentation Titrimetry, Spectrophotometry and Liquid Chromatography
• Quality auditing skills for an ISO certified company
• Research and Development Specialist
• Product Formulation Specialist
• Method Development
• Wet Chemistry
• Sample Preparation
• Good Laboratory Practice
• Equipment Calibration
• Investigation and Analysis

PERSONAL SKILLS
• Effective in communication skills, both verbal and written
• Excellent interpersonal skills and demonstrated ability to work with others effectively
• Creative ability to conceptualize and articulate to new approaches and solutions
• Proven analytical and problem-solving skills
• Time Management
• Customer Service
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EDUCATION
Bachelor of Science in Chemistry
Pamantasan ng Lungsod ng Maynila
Intramuros, Manila

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ACHIEVEMENTS/RESPONSIBILITIES
• Internal Quality Auditor for ISO (Quality Management System

PROFESSIONAL EXPERIENCE

• AM-EUROPHARMA CORPORATION
Product Innovation Specialist
August 2018 – February 2019

JOB RESPONSIBILITIES
1. Formulates new products, from development to commercialization, within defined company,
industry, and regulatory parameters
2. Leads research activities for new product development, product enhancements and product
redesign as assigned
3. Establishes guidelines and criteria for acceptance and testing of all raw and packaging
Materials to be used for new product development or technology transfer
4. Creates technical specifications for raw and packaging materials, in-process and finished
products
5. Coordinates testing and evaluation of raw/packaging materials, in process and FP with
the group
6. Creates project timelines in accordance with Business Development priorities, sets
milestones/critical paths and ensures on time project completion
7. Participates in team-driven activities to facilitate on-going production improvements or
new product development projects
8. Coordinates and collaborates with production n and planning regarding pilot batch run
and process validation schedule to meet project timelines
9. Performs trials to modify existing formulations to improve product quality and or
reduce product cost
10. Coordinates and monitor stability study programs for new products and products for
Improvement
11. Coordinates and collaborates with regulatory affairs pertaining to technical and documentary
requirements for product registration
12. Prepares product registration documents and product dossiers/packages compliant to
regulatory requirements

• PHIL. UNITED PHARMA CORPORATION
Research and Development Specialist
January 2018 – May 2018

JOB RESPONSIBILITIES
1. Perform high quality research activities
2. Provide technical support to the pharmaceutical research and training teams
3. Be responsible for maintenance and preparation of the pharmaceutical research and equipment
4. Participate in innovative research and development programs
5. Maximize the academic research profile of the pharmaceutical by actively participating and
organizing international conferences and workshops
6. In collaboration with the Regulatory Affairs, contribute to the development, implementation
of the pharmaceutical plan of R&D projects under his/her responsibility
7. Design the clinical development plan of all R&D projects of the growth in accordance with
current regulatory guidelines
8. Manage the budget of R&D projects under his/her responsibilities

• REFAMED RESEARCH LABORATORY CORPORATION
Senior Process Research and Development Specialist
2012 – 2017

Quality Control Analyst/Quality Assurance Inspector/Chemist
2004 – 2012

JOB RESPONSIBILITES (Senior Process Research and Development Specialist)
1. In-charge of the manufacturing process, trouble-shooting activities
2. Conducts study, review and pre-qualification of alternative sources of applicable raw material
substitution to existing component in the product formulation as a resolution to the identified
trouble-shooting made and recommends accordingly
3. Perform research activities, the collation and orderly safe-keeping of the researched data,
information, hand-outs, or related dossiers that supports the commercial trouble-shooting or
the recommended product enhancement or fortification of the existing product formula
4. Conducts supporting trial testing parallel to the commercially-identified trouble to rule out
root cause and recommends appropriate corrective actions
5. Prepares Master Production Documentation of all Re-processing formulation and the
applicable registration to the Document Control Center
6. Plays vital role for the developmental projects
7. Responsible for the updating of file record of the Master Batch Production Record (MBPR)
and assures the complete attachment of the relevant supporting documents
8. In-charge of the Monthly Developmental Progress Report and the need to call for any related
coordination meeting
9. Facilitates the conduct of continual study of updated quality assured and innovative
development of processes and products and its implementation
10. Authorized signatory for the following documents in the absence of Department Head

JOB RESPONISBILITES (Quality Control Analyst)
1. Responsible for testing and analysis of incoming raw materials, source sample, advance sample
Needed for manufacturing use or other related pre-qualification
2. Ensures that analysis are completed according to established Standard Operating Procedures,
Good Laboratory Practices
3. Validates analysis and instrumentation
4. Prepares documents and reports
5. Responsible for minor equipment/tools troubleshooting and repair
(Quality Assurance Inspector)
1. Read and analyzes product specifications
2. Monitor operations to ensure that they meet production standards
3. Recommends adjustment to production process
4. Inspect, test, or measure produced products
5. Accept or reject finished products
6. Report inspection and analysis of data results

• ISO PACKAGING CORPORATION
Quality Control Analyst/Quality Assurance Inspector
2003 – 2004

JOB RESPONSIBILITIES
1. Responsible for checking of incoming corrugated box delivered from a client (moisture content
and comply with set standards and specifications
2. Physical and visual inspection of newly produced corrugated box based on parameter
requirements.
3. In-process checking during production, tests moisture content, temperature and size
4. Prepares certificate of analysis of all product batch for delivery

• MEDICAL GENERICS LABORATORY
Quality Control Analyst
2002 – 2003

JOB RESPONSIBILITIES
1. Testing and control of in process pharmaceutical products (physical and chemical assay)
2. Check incoming raw materials for testing and analysis
3. Inspect finished goods for quality assurance before delivery

• MORNING STAR MILLING CORPORATION
Quality Control Analyst/Quality Assurance Inspector
1998 – 2002

JOB RESPONSIBILITIES
1. Physico and chemical analysis of in process flour milled sample
(moisture content, ash, protein, pH, particle size)
2. Interpret and evaluate protein quantity versus quality, absorption determination, dough
properties using Farinograph and Extensograph which will be applied to mill operations
and management
3. Ensure accurate and timely reporting of quality measures

• KAMERAWORLD INC.
Head Photo Printer/Photographer
1993 – 1998

DUTIES AND RESPONSIBILITIES
1. Evaluate prepress separations and mark up color for print of assigned print publications
And products
2. Troubleshoot reproduction problems related to prepress and printing processes
3. Work directly with internal customers to understand needs and ensures expectations are met
4. Consistently performs at a level that meets or exceeds performance standards

• UNITED LABORATORIES INC.
Laboratory Technician/Chemist
1992 – 1993

DUTIES AND ROLES
1. Ensure quality compliance in manual inspection of liquid parenteral finished product division
2. Defects and detects categorization in the manual visual inspection of vials and ampoules
3. Reports non-compliance finished goods to immediate superior

REFERENCES

• Available upon request