• Generate and route for approval the Test Scripts required for the computerized systems.
• Generate and route for approval of issues/discrepancies as a result of test scripts

execution. Support engineering, automation, and system owners in theissues/discrepancies resolution, and corrective actions.

• Generate and/or support on the generation of lifecycle documentation, including but not limited to system/risk assessments, URS, specifications, etc. Route for approval lifecycle documentation.
• Generate and route for approval Validation Plan, and Test Plan for the computerized systems.
• Execution and routing for post-approval of the Test Scripts required for the computerized systems.
• Update lifecycle documentation as needed per issues/discrepancies result.
• Generate and route for approval the Test Summary Report and Final Validation reports as required.
• Maintain training current on relevant SOPs.
• Daily accounting of time and activities submitted to Validation Lead/PM weekly.

Requirements:

• Bachelor's degree in engineering, science or related field.
• At least 5 years of experience in CSV activities for Pharmaceutical Industries.
• Primarily experience in Factory talk view site edition (FTView SE) from Rockwell

automation.

• Should have good experience in Automation design.
• Should also have experience in automation embedded in equipment. (Level 2, Level 3 ) SCADA experience is a MUST.
• Experience in reviewing design documents like BOM, Automation / electrical panel, FDS, HDS etc.

Job Types: Full-time, Contract

Pay: $60.00 per hour

Schedule:

• 8 hour shift

Ability to commute/relocate:

• Sanford, NC 27330: Reliably commute or planning to relocate before starting work (Required)

Education:

• Bachelor's (Required)

Experience:

• SCADA: 2 years (Required)
• CSV: 5 years (Required)
• Pharmaceutical Industry: 5 years (Required)
• Validation: 3 years (Required)
• computerizedsystems: 3 years (Required)

Work Location: In person

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