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Cleaning Validation (Atlanta, GA)

Duluth, GA, United StatesRemoteFull-time

AI Summary

Responsible for cleaning validation and commissioning/qualification activities in medical device manufacturing, applying risk-based approaches, equipment qualification, process validation, and computerized system validation.

About this role

Cleaning Validation (Atlanta, GA)

Validation & Engineering Group, Inc. is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, among other services.

  • Cleaning Validation is a must
  • Expertise in “Risk Based Approach” for Commissioning and Qualification practices
  • Planning and Integration of Commissioning and Qualification activities in medical device manufacturing (Class II preferred)
  • Risk Management practices (i.e. Assessments, Functional Risk Documents, pFMEA, etc.)
  • Equipment qualification and process validation
  • Computerized System Validation (PLC, HMI, etc.)
  • 21 CFR Part 11 requirements and how to incorporate these requirements into an efficient testing strategy
  • Assist in deviation investigation and resolution for problems and issues encountered during field execution activities

Qualifications

  • B.S. Engineering (e.g. Computer Science, Chemical, Mechanical, Electrical, etc.)
  • 3-5 years hands-on validation experience (writing and execution of validation protocols)
  • Capable of working independently with minimal supervision, and communicating with project team members to assure timelines are met
  • Great technical writing and communication skills
  • Proficiency in Microsoft Office application (Word, Excel and Project)
  • Effective interpersonal and problem solving skills
  • Demonstrate excellence in good documentation requirements and attention to detail

Additional Information

Validation and Engineering Group, Inc is an Equal Employment Opportunity employer.

Skills

21 CFR Part 11CommissioningComputerized System ValidationFMEAHMIIQ OQ PQMedical Device ManufacturingPLCRisk ManagementValidation

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