Data Entry Control Specialist

-

Carlos Parada

Specialist

Accomplished, result-driven professional with 8+ years of experience in pharmaceutical manufacturing and related industries. Proven expertise in adhering to GMP standards, ensuring product quality, and optimizing production processes to meet and exceed organizational goals. Demonstrates a steadfast commitment to operational excellence, with strong focus on safety, compliance, and efficiency. Skilled in maintaining high levels of technical and product knowledge to enhance team performance, drive customer satisfaction, and support business growth.

INTREST

Field Science

Botany

Disc Golf

Soccer

Tinker

EDUCATION

Bachelor of Science in Biology

University of South Carolina

Aiken

SKILLS

Good Manufacturing Practices

(GMP)

Quality Control Assurance

Batch Record Documentation

Production Processes

Sterile Environments

Standard Operating

Procedures (SOPs)

Data Entry Management

Document Creation

Spreadsheet Analysis

Presentation Design

Excel Automation

+1-706-***-**** ***********@*****.***

Augusta, GA www.linkedin.com/in/carlos-parada

WORK EXPERIENCE

Material Qualification Specialist

Shire Pharmaceutical Covington GA

May 2016 – November 2016

• Collaborated with Stream Support and Internal Audit teams to represent and provide Validation Documents to auditors.

• Created and maintained protocols and reports for raw materials, process components, and final container closures.

• Facilitated global communication with vendors, ensuring alignment and clarity of documentation between the Los Angeles and Lessines facilities.

• Adapted to strict deadlines and shifting priorities, demonstrating strong organizational and problem-solving skills with minimal supervision. Fractionation Department Specialist

Takeda Pharmaceutical Covington GA

May 2018 – February 2022

• Assisted in formatting job aids and site operation procedures for the Fractionation department.

• Managed and implemented activities from the Milestone Tracker and Schedule Reconciliation.

• Led a project to gather and organize facility warranties for the company.

• Applied FDA regulations, Good Laboratory Practices (GLP), and Good Manufacturing Practices (GMP) to ensure compliance.

• Demonstrated strong interpersonal skills and attention to detail, with a proven ability in project management.

Remote Consultant

CallOrange El Salvador

February 2022 – Present

• Supported field technicians by coordinating jobs site logistics and resolving on site issues efficiently

• Collaborated with partner companies to generate job opportunities and managed assignment dispatch to technicians

• Worked alongside a team of remote consultant to ensure exceptional customer service and satisfaction

• Effectively managed operations and communication remotely, demonstrating strong organizational and problem-solving skills in a fast-paced environment COURSES AND CERTIFACTIONS

GMP Certification OSHA Safety Training

HACCP Certification Lean Six Sigma Green/Yellow Belt

Contact this candidate