- Bachelor's degree in a technical field like computer science, computer engineering, or a related field is a must.
- 2-4 years of experience are necessary.
- Excellent ability to handle different cultures and nationalities.
- Solid knowledge of enterprise information systems such as ERP, PLM, CRM, QMS, etc (e.g., JDE, SAP, Pilgrim) is desirable.
- Familiarity with FDA guidelines for Software Quality and Systems Validation is a bonus.
- Understanding of Good Clinical Practice (GCP), Good pharmacovigilance Practice (GVP), Good Manufacturing Practices (GMP), Good Documentation Practices (GDP), and Good Laboratory Practices (GLP).Experience in creating/reviewing/approving validation documentation.
- Establish and manage software development lifecycle (SDLC) processes.
- 3+ years of SQL experience, capable of writing complex queries such as stored procedures, creating indexes, CTE's, Functions, and query optimization.
- 2+ years of Power BI experience in data usage and export.
- Proficient in Microsoft Excel.
- Demonstrated proficiency in the use of MS Office Suite.
- 2+ years of exposure to python is beneficial. (not mandatory)
- Ability to adjust to a fast-paced environment.
- Capability to map, troubleshoot, and enhance interfaces with multiple systems.
- Background in operating within complex, matrixed, and global business settings.
- Skill in generating and managing business and technical documentation.
- Formulate and implement software test plans, scenarios, and cases.
- Uphold quality assurance standards and ensure products align with customer and industry expectations.
- Recognize, assess, and document software issues.
- Collaborate with engineers and stakeholders to pinpoint areas for enhancement.
- Create and employ test automation tools and methodologies.
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Applications Engineer - Irvine, United States - Cynet Systems Inc.
Description
Qualifications: