Contractor, Quality Systems - Software QA
- Contractor
- Full-Time
- Remote, OR
- Splintpharma
- Prefferd visa: OPT, CPT, F1, H4, Have H1 Visa, Need H1 Visa, EAD
- Posted 1 year ago – Accepting applications
-
Offerd Salary $ 25 - $ 35
-
Required Position 2-4 hires
-
Experience 0-3 Years Required
Job Opening for Contractor, Quality Systems - Software QA
We are currently working on the job opening i.,e. Job Opening for Contractor, Quality Systems - Software QA. Please let me know if you are interested in applying for the same.
Contractor, Quality Systems - Software QA is responsible for supporting QA review of software development lifecycle documentation with a specific focus on validation/implementation of new software systems.
Primary Responsibilities Include:
• Review/Approve Test Scripts
• Review Validation Summary Reports, Installation Qualification, Operational
Qualification, Perfformance Qulaification, and Trace Matrices, escalate issue to management
• Support the development of training content
Qualification:
• 5+ years relevant Quality Assurance experience in a pharma/biotech company, working within a regulated GMP environment.
• Prior experience with implementing software systems and/or continuous improvement initiatives focused on software systems
• Ability to partner cross functionally and integrate feedback during development and implementation of quality systems
• Ability to work independently to meet objectives and timelines
• Has an awareness of cGMP and ICH regulations/ guidelines and GAMP-5
• Prior experience with electronic test systems preferred (e.g. Valgenesis, Kneat)
Job Opening for Contractor, Quality Systems - Software QA
We are currently working on the job opening i.,e. Job Opening for Contractor, Quality Systems - Software QA. Please let me know if you are interested in applying for the same.
Contractor, Quality Systems - Software QA is responsible for supporting QA review of software development lifecycle documentation with a specific focus on validation/implementation of new software systems.
Primary Responsibilities Include:
• Review/Approve Test Scripts
• Review Validation Summary Reports, Installation Qualification, Operational
Qualification, Perfformance Qulaification, and Trace Matrices, escalate issue to management
• Support the development of training content
Qualification:
• 5+ years relevant Quality Assurance experience in a pharma/biotech company, working within a regulated GMP environment.
• Prior experience with implementing software systems and/or continuous improvement initiatives focused on software systems
• Ability to partner cross functionally and integrate feedback during development and implementation of quality systems
• Ability to work independently to meet objectives and timelines
• Has an awareness of cGMP and ICH regulations/ guidelines and GAMP-5
• Prior experience with electronic test systems preferred (e.g. Valgenesis, Kneat)