Software Quality Assurance Analyst - Guadalajara, Mexico

Anexinet Blue Bell , PA 19422

Posted 3 months ago

Anexinet specializes in digital business transformation. We empower our clients to grow their customer base and improve workforce efficiency by envisioning, developing, and operating next generation technology solutions. Our core expertise is in digital and mobile applications, analytics, hybrid IT and cloud, enabling businesses to rapidly transform. Our clients partner with Anexinet to support the full lifecycle of their next generation digital business. Our people come and stay at Anexinet because we are a technology focused, team-oriented organization with a culture that is second to none. We are looking for several Quality Assurance Analysts to join our Guadalajara, Mexico team.

Utilizing your manual and automated testing experience, you will join an extensive and talented team that tests mission critical applications and code that we have designed and developed to support the business of our US based clients. In addition to applying hands-on experience with the technical skills listed below, you will be expected to interact effectively with both business and technology clients, share your knowledge and experience with others in a supportive and learning oriented team environment and have a visible and measurable impact on the success of our clients business.

These positions are based in our Guadalajara, Mexico office.

RESPONSIBILITIES:

  • Develop High-Level and Detailed Test Cases from business requirements and technical specifications

  • Participate on a cross-functional team in an Agile environment

  • Participate in software requirements gathering and design sessions.

  • Participate in defining a test approach/strategy for the application.

  • Execute manual test cases.

  • Execute automated test cases.

  • Identify, document and track issues found during testing in a defect management tool

  • Identify, develop, and manage test data

  • Collaborate with team on mobile testing strategy

QUALIFICATIONS:

  • Bachelors degree in Computer Science, Informatics, Electronics, or technical area, from an accredited university.Experience with automated test scripts as QTP, Selenium, SOASTA, Perfecto

  • Experience using Agile software development processes

  • Must have excellent written and verbal communication skills (English required)

  • Ability to travel to US client sites, light travel/meetings with on-site project teams may be required

Interested and qualified candidates should respond to this posting or send a resume to Mike Campo, Vice President of Human Resources and Talent Acquisition to mcampo@anexinet.com.


icon no score

See how you match
to the job

Find your dream job anywhere
with the LiveCareer app.
Mobile App Icon
Download the
LiveCareer app and find
your dream job anywhere
App Store Icon Google Play Icon
lc_ad

Boost your job search productivity with our
free Chrome Extension!

lc_apply_tool GET EXTENSION

Similar Jobs

Want to see jobs matched to your resume? Upload One Now! Remove
Clinical Supply Quality Compliance Coordinator

PRA Health Sciences

Posted 2 days ago

VIEW JOBS 1/15/2020 12:00:00 AM 2020-04-14T00:00 Do you want to be responsible for performing review, coding, and entry of audit report findings, assists with facilitation of Corrective and Preventative Actions (CAPAs), and participates in GCP related projects. Participates in facilitating or co-audits as experience increases and proficiency is demonstrated. Who are we? We Are PRA. We are 16,000+ employees strong, operating in more than 90+ countries. We are committed to saving lives and we are constantly striving to be the best at what we do. Our impact is real and we see it every single day. We help get life-saving drugs into the hands of those who need them most. Who Are You? You are an experience professional with a passion for clinical supplies. You are organized, but flexible and adaptable to unexpected changes. You can easily envision the bigger picture, without losing sight of the day-to-day tasks. You can provide excellent leadership to not only your project teams, but also to clients. You are excited and enthusiastic. You motivate your teams to do great work and collaborate easily with your clients. Most of all, you want to do it in a place where you're more than an employee number. A place you love working. Still here? Good. Because if this is you, we'd really like to meet you. What will you be doing? You will be responsible Quality, Trade Compliance, Environmental Health & Safety requirements within clinical supplies. What do you need to have? * Tracking, managing and reporting of compliance related activities (e.g. training compliance, audit response preparation, SOP periodic reviews, investigations, CAPAs) * Authoring and/or facilitating investigations and assistance in identifying appropriate corrective and preventative actions (CAPAs) * Coordination of inspection activities and assisting areas in maintaining a state of inspection readiness * Coordinate resolution of compliance issues in collaboration with functional areas Documentation * Administration of the SOPs and supporting documentation (e.g. Forms, Job Aids, SOP deviations) in client based system. (Providing draft template, keeping tracking database up-to-date, making docs effective or inactive) * Author / Reviewer / Contributor of SOPs to ensure compliance commitments are appropriately incorporated and ensure timelines are being met * Assure adherence to Records Management and other Documentation system requirements Training * Coordinate development and maintenance of learning plans and assuring consistency across Global Clinical Supply Organization * Administration of the training system (requesting training materials to be uploaded in the system, making and verifying employee, curricula and job position data changes in learning system, running reports) * Monitor that functional area employees have attended mandatory/relevant training and advise management of training compliance status and related training issues Education and Work Experience: * An undergraduate degree or its international equivalent from an accredited institution preferred. * Preferably in the health-sciences or computer sciences Knowledge, Skills, and Abilities: * Experience in clinical research organization is preferred * Basic understanding of ICH GCP, FDA CFR, and EU directive * Read, write and speak fluent English; fluent in host country language required. * Working knowledge of the Clinical Trial Supply process * Working knowledge of project team structure and processes * Proactive approach to work, identifying potential issues well in advance and bringing them to the attention of appropriate personnel for resolution. * Knowledge of project management and Clinical customer relationship building * Knowledge of the 'Customers' team structures and processes * Excellent verbal and written communication skills * Ability to influence others * Ability to multi-tasks * Strong organizational skills * Experience in conflict resolution and negotiation skills * Knowledge of general computer skills (i.e. MS Word, Excel, PowerPoint, MS Project and Access To qualify, applicants must be legally authorized to work in the United States, and should not require, now or in the future, sponsorship for employment visa status. PRA is an EEO/AA employer and is committed to providing opportunities to minorities, women, veterans and individuals with disabilities. PRA Health Sciences Blue Bell PA

Software Quality Assurance Analyst - Guadalajara, Mexico

Anexinet