Validation Engineer AT Jacksonville, FL
Product, process, equipment, software, validation, change control, reports, documentation.
Validation Engineer5-9 years industry experience working in medical device and / or pharmaceutical manufacturing, Quality Assurance or Regulatory fields
- Must have : Working experience in Product, equipment, process, software validation
- Validation reports / documentation preparation
- Change control
- Working experience in medical device and / or pharmaceutical manufacturing, Quality Assurance or Regulatory fields
- Facilitates complex validation activities within product, process, equipment, software, and facilities changes and ensures all activities are consistent with regulations and validation policies and procedures.
- Represents Project in validation for multi-departmental meetings, change control, and project teams as needed.
- Compiles data and provides reports to project team on a periodic basis.
- Review and support updates to quality documentation and procedures.
- Works independently on complex issues; serving as a subject matter expert within validation area.
- Technical expert for job function.
- Prioritize tasks to meet deadlines.
- Must have very good written and verbal communication skills.
- Customer support experience preferred.
- Ability to multitask, including ability to understand customer requirements, retrieve relevant information, and provide responses satisfactorily and with immediacy is required.
- Employee must be able to effectively prioritize and manage multiple activities and responsibilities.
- Ability to function in a team environment and deliver on team objectives is required.
- Ability to make decisions and solve problems while exhibiting situational judgement.Bachelor's Degree - Science / Engineering / BusinessMaster's degree preferred