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Validation Specialist

Company: Gill's Process Control, Inc.
Location: Rocky Mount
Posted on: August 10, 2019

Job Description:

Qualifications and Skills3 or more years or more experience in pharmaceutical manufacturing environmentIn-depth understanding of all system lifecycle deliverables from Commissioning & Qualification (C&Q) and Computer System Validation (CSV) documentsExperience with Automated Systems (PLC, HMI)Experience with pharmaceutical manufacturing systems and equipment such as: Commodity Tunnel Sterilizers, Isolator technology, Fillers, HVAC systems, and Utility systemsMust be proficient in the ability to write validation protocols and reports.Skilled in technical writing and document control.Must have a project management mentality and excellent communication skillsMust have organizational skills to maintain data and documentationAbility to work independently without direction but also able to work within a teamProficient with MS Word and ExcelDaily ResponsibilitiesDraft, execute and close out qualification and validation (IQ, OQ, PQ) projects for plant utilities, facilities, equipment, or computer systems projectsEstablish/Write validation plans using MS WordExecute validation strategies and acceptance criteria based on established site, industry and regulatory standards.Schedule meetings and lead meetingsCommunicate project status to management and client project managersComplete time sheets for time trackingBenefitsPaid Time Off (PTO)VacationHealth CareRetirement IRA planShort term disabilityJob Type: Full-timeSalary: $65,000.00 to $95,000.00 /yearExperience:Pharmaceutical Validation: 3 years (Required)Location:Rocky Mount, Wilson, Greenville NC (Required)Language:English (Preferred)Work authorization:United States (Required)

Keywords: Gill's Process Control, Inc., Rocky Mount , Validation Specialist, Other , Rocky Mount, North Carolina

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