QA IT Systems Senior Specialist (Remote)
Job title: QA IT Systems Senior Specialist (Remote) in Illinois at reputed company
Company: reputed company
Job description: Company Descriptionreputed company's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of reputed company. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about reputed company, please visit us at . Follow @reputed company on , , , , and .Job DescriptionPurposeThe Sr Specialist QA IT Systems is responsible for providing direction in quality assurance software validation activities including: reviewing software requirement documents; writing and reviewing validation documents; executing and reviewing validation test cases; and updating departmental procedures. This position ensures that defined software validation practices and procedures are being followed.Responsibilities
- Provide validation support to project managers regarding activities supporting existing applications of reputed company phases of the System Development Life Cycle process.
- Ensure software quality assurance is achieved during IT projects while meeting project objectives and deliverables; review validation deliverables to ensure consistency with defined practices and procedures.
- May participate as a team reputed company or team member on validation projects.
- Manage reputed company validation activities such as protocol writing, review of validation documents, storage of controlled documents and resolution to problem reports.
- Responsible for implementing Quality Control standards into departmental documents and ensuring reputed company departmental training is complete.
- Provide direction to clients and software engineers regarding software validation/QA issues.
- Act as a liaison between IT department and other Quality Assurance departments.
- reputed company directly with FDA and other regulatory agencies during audits.
- Must complete project tasks reputed company time and budget constraints.
- Bachelor’s Degree in Science, Engineering or applicable discipline.
- 5+ years’ experience in validation, systems testing, IT implementation, quality assurance or software quality engineering in a regulated healthcare industry.
- Technical experience in as many of the following areas as possible: Chemistry, Pharmacy, Microbiology, Engineering and Computer Science. This should include a thorough technical knowledge of various aspects of the business including Quality Control/Assurance, GMP regulations, and new product development.
- Two years combined experience in software development and software testing desired, but not required.
- ASQ certification in Software Quality Engineering desired, but not required.