Ellab

50 jobs near Columbus, OH

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 ...

Lead CQV Engineer

Concord, NH · On-site

$103K - $135K/yr

Experience with temperature mapping (Ellab a plus) * This role is for 2nd shift. Must be able to work second shift (2-10 PM EST) and weekends

Must have experience with thermal validation using Ellab or equivalent systems, including thermocouple mapping and lethality validation. Must have experience leading or supporting sterilization ...

LeadCQVEngineer

Memphis, TN · On-site

$99K - $131K/yr

Experience with temperature mapping (Ellab a plus). * This role is for 2nd shift. Must be able to work second shift (2-10 PM EST) and weekends. Support and review: * Drawing walkdowns. * Equipment ...

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 ...

Must have experience with thermal validation using Ellab or equivalent systems, including thermocouple mapping and lethality validation. Must have experience leading or supporting sterilization ...

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 ...

Validation Engineer

Athens, GA · On-site

$45 - $48/hr

Experience with validation documentation, CAPA investigations, change control processes, and regulatory requirements including FDA compliance standards; experience using Ellab data loggers and ...

Validation Engineer

Athens, GA · On-site

$45 - $48/hr

Experience with validation documentation, CAPA investigations, change control processes, and regulatory requirements including FDA compliance standards; experience using Ellab data loggers and ...

Validation Engineer

Athens, GA · On-site

$45 - $48/hr

Experience with validation documentation, CAPA investigations, change control processes, and regulatory requirements including FDA compliance standards; experience using Ellab data loggers and ...

Validation Engineer

Athens, GA · On-site

$45 - $48/hr

Experience with validation documentation, CAPA investigations, change control processes, and regulatory requirements including FDA compliance standards; experience using Ellab data loggers and ...

Validation Engineer

Athens, GA · On-site

$45 - $48/hr

Experience with validation documentation, CAPA investigations, change control processes, and regulatory requirements including FDA compliance standards; experience using Ellab data loggers and ...

Certification Tech: * 3-5 years of experience performing certification, calibration, or field service activities in pharmaceutical, biotechnology, laboratory, or other regulated environments.

* 3-5 years of experience performing certification, calibration, or field service activities in pharmaceutical, biotechnology, laboratory, or other regulated environments. * Demonstrated ability to ...

Showing results 21-40

Equipment validation

Portsmouth, NH • On-site

$78/hr

Contractor

Posted 5 days ago


Job description

Description
Job id: 1076
Title: Equipment validation
Location: Portsmouth, NH
Contract: 06 months
Pay rate: $78/hr on W2
Notes from intake - 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 the worker to Build Equipment Requalifications in Kneat.
  1. Provide Subject Matter Expert support to Quality Control, Manufacturing and other departments for the design, operation and troubleshooting of equipment.
  2. Drive/own the validation plans and execution of equipment changes and process improvements.
  3. Execution of Installation Qualifications/Operational Qualifications and drafting Performance Qualifications as required.
  4. Perform Equipment Validation activities to include Validation Maintenance Quality Systems review and requalification to ensure GMP equipment is continuously maintained in a validated state.
  5. Program, organize, and maintain Validation equipment and supplies including dataloggers and probes.
  6. 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.
  7. Develop validation protocols from plans and engineering documents.
  8. Provide basic technical support when reviewing and approving SOPs, Protocols, Change Controls, Deviations, CAPA, etc.
  9. Perform assigned Quality Systems activities within Document Management System (DMS), TrackWise Quality System (Change Control, Deviation, CAPA)
  10. Perform other duties as assigned.