ALBERT GARCIA
Middle River,MD
Summary
To obtain a position that will enable me to use my strong organizational skills, award-winning work experience, and ability to work well with people.
Overview
13
13
years of professional experience
Work History
Quality Inspector
Johnson & Johnson
Baltimore, MD
11.2021 - Current
- Documented, filed and maintained proper inspection records and quality assurance documents.
- Inspected, tested and measured materials, products and installations against specifications.
- Completed evaluations by properly using various gauges, tools and equipment.
- Measured product dimensions to assess compliance with specifications.
- Recommended corrective actions to minimize rate of product defects.
- Led cross-functional team evaluations of production metrics and test results.
- Reduced costs by avoiding duplication of services.
- Identified and resolved quality issues, escalating critical problems to supervisors.
- Analyzed and interpreted blueprints, data and manuals to determine precise specifications.
- Reviewed blueprints, drawings and other specifications to fully understand project expectations.
- Tracked findings and updated computer tracking system with documented assessments.
Production Associate II
Johnson & Johnson
Baltimore, MD
08.2019 - 11.2021
- Electro Mechanical Assembly, Fabrication and Inspection of medical devices.
- Utilize small hand tools, calibrated instrument, measurement equipment, and test fixtures.
- Work as an integral member of the manufacturing team, working with mechanical, electrical, software, and firmware engineers.
- Maintain clean room integrity by using proper attire and adherence to clean room environment practice and procedures.
- Strictly follow manufacturing and cleaning procedures.
- Maintain accurate records/documentation for quality, inventory and work in progress records.
- Apply workstation practices and line clearance in daily activities.
- Adhere to general safety rules, manufacturing procedures, company policies and procedures, FDA and similar regulatory regulations relating to medical device manufacturing.
- Collaborate with Warehousing on the material movement and storage needs in support of production and testing schedules.
- Maintain accurate records.
- Make suggestions to improve the work systems and processes.
- CGMP and more on Attention to details.
- Completed product assembly according to standardized procedures.
- Inspected and repaired products to meet project expectation
- Inspected plu’s assembly components.
- Inspected oxy-1 assembly components.
Quality Inspector C
Smith Detection
Edgewood, MD
11.2013 - 08.2019
- Executed daily cleaning, sanitizing and sterilization activities in accordance with GMP requirements.
- Developed standard operating procedures for laboratory operations according to GMP regulations.
- Provided support during internal and external audits, ensuring compliance with regulatory standards such as GMP and ISO 9001, 2015.
- Provided training on GMP, ISO 9000, and other relevant regulatory guidelines to staff members.
- Followed industry standards and manufacturer instructions to calibrate measurement tools.
- Oversaw disposal of products, materials and equipment not in compliance with tolerances, safety standards, or quality levels.
- Inspected, tested and measured materials for conformance to specifications and regulatory requirements.
- Created detailed work instructions for inspectors on how to perform their tasks correctly.
- Developed training programs for new employees on proper inspection techniques.Perform inspections on incoming and in-process electronic assemblies and mechanical hardware.
- Conducting of source inspections at vendor facilities.
- Ensure that product is manufactured to the latest applicable configuration documentation.
- Prepare and review data submittal packages for end item deliverables (composed of test data, inspection results, C-of-C's, etc.)
- Prepare Deficiency Reports (DRs) for hardware, software, and documentation issues.
- Maintain, control and process non-conforming material.
- Certify and assists in maintaining ESD stations and monitor employee ESD compliance.
- Participate as a member within Change Control Board (CCB) and Material Review Board (MRB); role is interchangeable with QAE when required.
- Assist in defect tracking and evaluation process, including trend evaluation to reduce recurrences. (As directed by the Q.A.
Manager) - Generate Corrective Action Requests (CARs) for vendor quality rejections.
- Assist in the implementation of ISO 9000, and Procedure Development.Perform inspections on incoming and in-process electronic assemblies and mechanical hardware.
- Conducting of source inspections at vendor facilities.
- Ensure that product is manufactured to the latest applicable configuration documentation.
- Prepare and review data submittal packages for end item deliverables (composed of test data, inspection results, C-of-C's, etc.)
- Prepare Deficiency Reports (DRs) for hardware, software, and documentation issues.
- Maintain, control and process non-conforming material.
- Certify and assists in maintaining ESD stations and monitor employee ESD compliance.
- Participate as a member within Change Control Board (CCB) and Material Review Board (MRB); role is interchangeable with QAE when required.
- Assist in defect tracking and evaluation process, including trend evaluation to reduce recurrences. (As directed by the Q.A.
Manager) - Generate Corrective Action Requests (CARs) for vendor quality rejections.
- Assist in the implementation of ISO 9000, and Procedure Development.
- Assist in coordination of failure analysis effort.
- Perform inspections on incoming and in-process electronic assemblies and mechanical hardware.
- Conducting of source inspections at vendor facilities.
- Ensure that product is manufactured to the latest applicable configuration documentation.
- Prepare and review data submittal packages for end item deliverables (composed of test data, inspection results, C-of-C's, etc.)
- Maintain, control and process non-conforming material.
- Certify and assists in maintaining ESD stations and monitor employee ESD compliance.
- Participate as a member within Change Control Board
- (CCB) and Material Review Board (MRB); role is interchangeable with QAE when required.
- Assist in defect tracking and evaluation process, including trend evaluation to reduce recurrences. (As directed by the Q.A.
Manager) - Generate Corrective Action Requests (CARs) for vendor quality rejections.
- Assist in the implementation of ISO 9000, and Procedure Development.
Inventory Control Associate
Under Armour Company
Baltimore, Maryland
11.2011 - 11.2013
- The inventory associate is responsible for monitoring the shipment, production, and ensuring that the data remains maintained and updated in the system.
- Assists in the preparation of all the inventory related reports, answers all the routine queries and provides the much needed support for the operations, logistics, accounting, and quality departments.
- Reviews all the shipment documents and verifies the details to make sure that they are complete and accurate.
- Reviews the shipment transactions and ensures that the receipts are posted in a timely manner.
- Accountable for reconciliation activities so that the inventory records are validated and are actively involved in the resolution of issues.
- To take daily inventory of the assigned supply, requisitions, and to restock supplies to par levels.
- To rotate the stock and ensure that the stored area is clean and maintained up to date in accordance with the regulatory requirements.
- To monitor the usage of the stock, create reports related to utilization, and coordinate with the other departments and recommend changes in inventory.
- To be the key person responsible for cycle counts as well as the physical inventories.
- To conduct a keen research and resolve all the inaccuracies in inventory and complete audits of the internal processes.
- To handle all the activities related to data entry, scheduling, customer service, etc., and perform all the other related duties as well.
Education
High School Diploma -
Montessori School of ST.Nicholas
Pampanga, Philippines 04-1997
Some College (No Degree) -
Community College of Baltimore County
Baltimore, MDSkills
- Quality control
- Assembly procedures
- Loading and unloading protocols
- Documentation ability
- Mechanical aptitude
- Hand tools
- Machine setups
- Quality assurance standards
- Batch production
- Equipment operation
- Product packaging
- Shipment preparation
- Tolerances measurement
- Product assembly
- Quality inspections
- Equipment calibration
- Temperature restricted production
- RFID tools
- Aseptic and sterilization techniques
- Medical device soldering
- Compliance with GMPs
- CGMP regulations
- CGMP compliance
- Outstanding clerical abilities
- Reporting abilities
- Decision-making
- Work ethic
- Team building
- Relationship building
- Troubleshooting
- Problem resolution
- Friendly, positive attitude
- Leadership
- Communication
- Working collaboratively
Timeline
Quality Inspector
Johnson & Johnson
11.2021 - Current
Production Associate II
Johnson & Johnson
08.2019 - 11.2021
Quality Inspector C
Smith Detection
11.2013 - 08.2019
Inventory Control Associate
Under Armour Company
11.2011 - 11.2013
High School Diploma -
Montessori School of ST.Nicholas
Some College (No Degree) -
Community College of Baltimore County
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