Validation Engineer
Posted 7 days ago by 1749118488
Negotiable
Undetermined
Undetermined
Location Athens, Georgia, United States
Summary: The Validation Engineer role is a temporary position based in Athens, GA, focused on writing and revising validation documents for a leading medical device company. The engineer will engage in various validation processes, including IQ OQ PQ authoring, while collaborating with operators to gather and organize information. This position requires adherence to internal procedures and templates for documentation. The role is critical in ensuring compliance and supporting non-conformance and CAPAs.
Key Responsibilities:
- Primarily writing validation documents following internal procedures and prescribed templates.
- Revising control documents.
- Writing and executing validation documents and reports as projects progress.
- Authoring and executing IQ OQ PQ and Computer Systems Validation.
- Providing documentation support for non-conformance and CAPAs.
- Routing documents for approval within business applications.
- Gathering information on the floor by speaking with operators and recording data from existing equipment.
Key Skills:
- Experience in writing validation documents.
- Knowledge of IQ OQ PQ and Computer Systems Validation.
- Ability to follow internal procedures and use prescribed templates.
- Strong communication skills for interacting with operators.
- Attention to detail in documentation and reporting.
Salary (Rate): £27.00 hourly
City: Athens
Country: United States
Working Arrangements: undetermined
IR35 Status: undetermined
Seniority Level: undetermined
Industry: Other
We have a current opportunity for a Validation Engineer on a temporary basis. The position will be based in Athens, GA. For further information about this position please apply.
Good morning! I am partnered with a TOP medical device company to find Validation Engineers for locations in Cornelia and Athens. Some details are below. If you (or someone you know) would like to learn more, please respond to this message ASAP - I have interview times available for Fri June 6!
Day to day:
- Primarily writing validation documents; The validation writing is similar across all those things. Follow our internal procedures, prescribed templates used for validations.
- Revising control documents
- As project progresses, writing validation documents, executing documents, writing the reports.
- IQ OQ PQ authoring and executing as well as Computer Systems Validation
- Providing documentation support to non-conformance and CAPAs
- Working within business apps to route documents for approval.
- That person would be on the floor some, gathering information; Speaking with operators to gather information, recording information off of equipment that is existing and organizing all of that information.
EOE Statement: Specialist Staffing Group is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status.
To find out more about Real, please visit www.realstaffing.com
