Requirements:
- 3+ years performing validation activities.
- Experience in custom engineered solutions, Medical Devices, or Life Sciences is preferred.
- Experience working with electrical design drawings.
- Proficient in Microsoft Office.
- Experience working in a GAMP 5 based validation model.
- Excellent presentation skills and ability to mentor without direct authority.
- Ability to work in a team environment. Self-starter, able to work with minimal guidance.
- Experience with Rockwell Automation PLC Control Systems is preferred.
- Experience debugging/working with custom machines is preferred.\
Responsibilities:
- Provide validation experience and guidance during equipment design, software design, build, debug, and qualification phases of a project.
- Write overall project quality (validation scope) plans.
- Organize, guide, and write requirement specifications as necessary.
- Review qualification/requalification packages for completeness and accuracy, sound rationale, compliance with validation policies.
- Interface with internal and client validation and engineering teams to secure document approvals.
- Oversee and execute validation qualifications at our facility and at the customer’s site.
- Organize, guide, and write qualification plans and protocols as necessary.
- Work through validation documentation in a timely manner to meet project schedules.
- Create validation summary reports. Provide input to address validation deviations and/or change requests and identify qualification requirements to ensure compliance to system’s current validated state and all cGxP's.
- Drive a quality approach into the organization, change control, and documentation for the equipment design, software, and documentation.
- Support all aspects of the Validation Life Cycle, from design through operation and improvement.
- Develop pertinent document templates tailored to customer SOP’s.
Regards,
Mohammed ilyas,
PH - 229-264-4024 or Text - 229-469-1455 or you can share the updated resume at Mohammed@vtekis. com
All your information will be kept confidential according to EEO guidelines.