Application Testing - CSV Specialist with Pharmaceutical cGMP exp

APPLICATION TESTING - CSV SPECIALIST WITH PHARMACEUTICAL cGMP TAMPA, FL Location opens to New Brunswick, NJ or Tampa, FL. Local Candidates only Required Skills:

• Bachelor of Science degree or equivalent work experience with IT/IM background, Chemistry, biology, life sciences, or related fields a significant plus.
• 3+ years with SDLC.
• 3+ years of Computer System Validation.
• 3+ years of Application Testing.
• Must have a good understanding of GMP, GxP, and 21 CFR part 11 regulations
• Candidate should have a range of technical skills and strong understanding of Software Development Life Cycle (SDLC).
• Ability to interact with users and translate needs into requirement for configurations and customizations.
• Ability to design, author, edit and execute test scripts using automated testing tool.
• Ability to author SDLC documentation, including user requirements, design documents and summaries.
• Must be customer focused and team oriented, possessing good interpersonal, oral and written communications skills.

• Knowledge of the pharmaceutical industry, especially experience in supporting systems/applications in a regulated environment
• Experience with Citrix, SharePoint, Web, GUI Application Support/Developer
• Management of Master Data in LabWare LIMS systems; examples include updates to product templates, product specifications, analysis, user management etc.
• Experience with LabWare LIMS configuration preferred.

• Application Testing specialist/ Validation consultant role is responsible for supporting an IT project within Global Product Development and Manufacturing Services group.
• Participation in creating system testing scripts to validate scientific applications using automated testing tool like HP ALM.
• Participation in collecting user requirement and creating user requirement specification and functional specifications.
• Participation in creating design documents, training document.