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QA Validation Specialist 3

Sunrise Systems Inc
πŸ‡¬πŸ‡§ United Kingdom | πŸ‡ΊπŸ‡Έ United States
On-site
2 months ago
  • SIP
  • GMP
  • CAPA
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Job Title: Equipment Validation Analyst
Job ID: 26-03440
Location: Portsmouth, NH
Duration: 6 Months

Manager's insight:

  • Role is Equipment Validation and Cleaning Validation
  • Experience with Kneat is absolutely required. Experience with Ellab for Temp Mapping is a plus
  • Manager is looking for candidates with Cleaning Val (CIP, COP, SIP). 95% of equipment is single-use, so the Cleaning Val is limited mostly to Media Hold/Media Fill. Cleaning Val is mostly drafting SOPs
  • Other equipment includes Autoclaves, Parts Washers, and Storage equipment (cold and ambient). Looking for a worker to Build Equipment Requalifications in Kneat.

Job Description:

  • Provide Subject Matter Expert support to Quality Control, Manufacturing, and other departments for the design, operation, and troubleshooting of equipment.
  • Drive/own the validation plans and execution of equipment changes and process improvements.
  • Execution of Installation Qualifications/Operational Qualifications and drafting of Performance Qualifications as required.
  • Perform Equipment Validation activities to include Validation Maintenance Quality Systems review, and requalification to ensure GMP equipment is continuously maintained in a validated state.
  • Program, organize, and maintain Validation equipment and supplies, including dataloggers and probes.
  • Demonstrate a general understanding of biopharmaceutical manufacturing equipment and validation procedures for Installation Verification (IV/IQ), Clean-In-Place (CIP), Steam-In-Place (SIP), Autoclaves, Clean Utilities, Shipping Validation, Temperature Mapping, Controlled Storage Rooms and Equipment.
  • Develop validation protocols from plans and engineering documents.
  • Provide basic technical support when reviewing and approving SOPs, Protocols, Change Controls, Deviations, CAPA, etc.
  • Perform assigned Quality Systems activities within the Document Management System (DMS), TrackWise Quality System (Change Control, Deviation, CAPA)
  • Perform other duties as assigned.

Contact:
Sunny Rajput | sunny.r@sunrisesys.com | URL: www.sunrisesys.com

QA Validation Specialist 3 Β· Sunrise Systems Inc

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