Microsoft Word, Microsoft Excel, Power Point
Shermandel Suguitan
Head Of Production/ Production Pharmacist
Tanauan City
Summary
Multi-talented Production Manager experienced in diverse industrial environments. Profit-motivated collaborator with ingenuity in troubleshooting complex productivity obstacles. Creative leader with motivational supervisory methods. Smoothly direct employees carrying out manufacturing operations to achieve demanding production goals, schedules and budget targets. Driven leader with excellent analytical, decision-making and project management abilities. Maintain employee focus and achieve quality targets with hands-on supervision. Production management professional knowledgeable about allocating resources, optimizing production and increasing output with hands-on and dedicated approach. Articulate and professional problem-solver with good relationship-building abilities. Proficient in planning and implementing innovative production strategies.
Overview
10
10
years of professional experience
4
4
years of post-secondary education
1
1
Language
Work History
Head of Production/ Production Pharmacist
Vetmate Farma Corporation
294-E Banjo East, Tanauan City
09.2022 - Current
- Supervise the step-by-step process during liquid dosage form compounding (liquid dosage forms ie; syrup and suspension) and solid dosage form compounding (solid dosage forms ie; tablet)
- Find and implement ways to improve production flow and other ways to improve existing company set-up that complies with GMP and GDP
- Responsible for plotting Production Personnel Schedule
- Responsible for plotting Production Products Schedule
- Trouble shoots any problem that occurs during production process and other post-sale customer complaints
- Established a new Batch Manufacturing Record following FDA required form
- Established some forms and improved existing logbooks and tags needed by the FDA during inspections
- Inventory of Finished Goods
- Checking and inspection of Finished Goods for released/ delivery
- Responsible for documenting and filing a written report of newly develop drug product including but not limited to raw material incompatibilities and improper manufacturing process resulting to product incompatibility
- Provide new idea on how to improve manufacturing process and formulation of existing products specifically those products with reported post sale incompatibilities
- Formulations of new drug product that is in-demand and/ or requested by pet owners (some of the products I formulated includes: Papi Doxy 10mg, Papi Doxy 20mg)
Technical Manager/Operations Manager
Vplace Pharma Inc.
Banjo East, Tanauan City
08.2020 - 08.2022
- Liaised between business and technology units to manage delivery schedules for applications.
- Developed suggestions for technical process improvements to optimize resources.
- Managed implementation of new technological improvements resulting in increased efficiency.
- Managed deliverable estimates, negotiated resource conflicts and allocated resources.
- Supervise the step-by-step process during compounding liquid compounding (liquid dosage forms ie; syrup and suspension) and solid compounding (solid dosage forms ie; tablet and capsule)
- Check that all processes and documents (BMR) are complete and properly filled-up as per SOP/ GMP/ GDP.
- Check and reconcile output based on batch manufacturing record.
- Find ways to improve production flow and other ways to improve existing set-up that complies with GMP and GDP
- Responsible for plotting Production Personnel Schedule
- Responsible for plotting Production Products Schedule
- Trouble shoots any problem that occurs during production process and other post-sale customer complaints
- Established a new Batch Manufacturing Record following FDA required form
Head of Production/ Head of Quality Assurance
Vplace Pharma Inc.
Banjo East, Tanauan City
01.2019 - 07.2020
- Standardized production procedures, job roles, and quality assurance guidelines.
- Created streamlined production schedules and collaborated with production employees to communicate objectives and goals.
- Managed continuous improvement initiatives to drive gains in quality, flow, and output.
- Resolved issues quickly to maintain productivity goals.
- Managed internal operational standards and productivity targets.
- Delivered direct feedback to senior management regarding project visibility and status.
- Estimated labor requirements to support anticipated workload.
- Reviewed maintenance and repair problems to determine appropriate action for resolution.
- Supervise the step-by-step process during compounding liquid compounding (liquid dosage forms ie; syrup and suspension) and solid compounding (solid dosage forms ie; tablet and capsule)
- Check that all processes and documents (BMR) are complete and properly filled-up as per SOP/ GMP/ GDP.
- Check and reconcile output based on batch manufacturing record.
- Suggests to the Operations Manager and Head Pharmacist ways to improve production flow and other ways to improve existing set-up that complies with the GMP
- Established some forms and improved existing logbooks and tags needed by the FDA during inspections
- Responsible for documenting and filing a written report of raw materials’ rejection report.
- Contribute on finalizing some checklists including raw material inspection report and revision of QA inspection checklist in packaging materials
- QA inspector on raw materials, packaging materials and retention samples.
- Monitors and checks that all personnels and staffs are following GMP guidelines within the manufacturing premises
- Implements new guidelines release by the PIC/S and FDA to be followed in the process of product handling to improve quality, safety, effectiveness and efficacy of the product
- Provide new idea on how to improve manufacturing process and formulation of existing products specifically those products with reported post sale incompatibilities
Production Supervisor
Azarias Pharmaceutical Incorporation
001 Service Road, Zone 1, Pandayan, Meycauayan
08.2015 - 11.2018
- Established clear priorities and production quality standards.
- Set and enforced performance-oriented production approach, significantly increasing worker output and reducing safety incidents.
- Prepared in advance for and addressed production problems, material deficits, equipment failures, and unavoidable delays.
- Achieved on-time shipments goal by empowering employees to continued success.
- Resolved issues quickly to maintain productivity goals.
- Evaluated team member performance regularly to identify and resolve productivity concerns.
- Managed team of 50 production associates, overseeing productive production processes and meeting all deadlines.
- Supervise the step-by-step process during compounding (liquid dosage forms ie; syrup and suspension).
- Check that all processes and documents (BMR) are complete and properly filled-up as per SOP/ GMP/ GDP.
- Coordinated with other departments to maintain smooth and efficient product flow.
- Evaluated existing production processes and identified areas for improvement.
Dispensing Pharmacist/Head of Production/Quality Assurance Inspector
Azarias Pharmaceutical Incorporation
001 Service Road, Zone 1, Pandayan, Meycauayan
07.2013 - 07.2015
- Responsible for documenting and filing a written report of raw materials’ rejection report.
- Contribute on finalizing some checklists including raw material inspection report and revision of QA inspection checklist in packaging materials
- QA inspector on raw materials, packaging materials and retention samples.
- Monitors and checks that all personnels and staffs are following GMP guidelines within the manufacturing premises
- Responsible for documenting and filing a written report of newly develop drug product including but not limited to raw material incompatibilities and improper manufacturing process resulting to product incompatibility then reporting it to the R&D Manager
- Helps to provide new idea on how to improve manufacturing process and formulation of existing products specifically those products with reported post sale incompatibilities
- Dispense all the right raw materials for production use.
- Checks incoming raw materials as per checklist.
- Initiates sampling of all materials for Q.C. analysis.
- Assures that all raw materials to be dispensed are with dispensing labels and are approved by Quality Control.
- Inventory of Raw materials
- Dispensing of Raw materials needed for production use
Education
Bachelor of Science - Pharmacy
Mariano Marcos State University
City Of Batac, Ilocos Norte, Philippines 06.2009 - 04.2013
Skills
Production optimization
Additional Information
PROFESSIONAL ELIGIBILITY
January 2015
Pharmacy Board Examination, Manila Philippines
PRC Reg. no.: 0066785
SPECIAL SKILLS
Product inventory and monitoring following first-in first-out process to prevent and minimize loss due product expiration. Able to make forms necessary to improve product monitoring and release. Knowledgeable in drug compounding (on various dosage forms syrup, suspension, tablet and capsule) following Good Manufacturing Practices, can perform QA checking, inspection and review of documents of the in-process of pharmaceutical products which I gained from my previous work experiences. Computer literate. Has management related skills and people management training. Goal oriented and able to work and finish assigned tasks with minimum supervision.
PERSONAL INFORMATION
Nickname: Sherman, Man-man, Man
Date & Place of Birth: November 04, 1992 / MMMH and MC, Batac, Ilocos Norte
Gender/Age/Civil Status: Male / 31 years old/ Single
Height / Weight: 5 ft. and 3 inches / 150 lbs.
Citizenship/ Languages: Filipino / English, Filipino, Ilocano
References :
1. Antonio Nabong – Chief Operations Officer/ Co-owner, Vplace Pharma Inc. - Address: 155A Aurora St., Brgy. Maytunas, San Juan City, Philippines
2. Lusbelia Barrera – HR Manager, Vplace Pharma Inc. - Address: 155A Aurora St., Brgy. Maytunas, San Juan City, Philippines
3. Jovilyn De Leon, RPh – Production Manager, Azarias Pharmaceutical Lab., Inc. - Address: Upper Northern Hills, Meycauayan, Bulacan, Philippines
4. Jeruthel G. Samulde – OIC-HR Dept. - Azarias Pharmaceutical Laboratories Inc. - Address: 01 Villacor Village Martha St., Langka Meycauayan, Bulacan
Software
Timeline
Head of Production/ Production Pharmacist
Vetmate Farma Corporation
09.2022 - Current
Technical Manager/Operations Manager
Vplace Pharma Inc.
08.2020 - 08.2022
Head of Production/ Head of Quality Assurance
Vplace Pharma Inc.
01.2019 - 07.2020
Production Supervisor
Azarias Pharmaceutical Incorporation
08.2015 - 11.2018
Dispensing Pharmacist/Head of Production/Quality Assurance Inspector
Azarias Pharmaceutical Incorporation
07.2013 - 07.2015
Bachelor of Science - Pharmacy
Mariano Marcos State University
06.2009 - 04.2013
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