Overview
On Site
Full Time
Skills
Regulatory Compliance
Leadership
Communication
Management
Pharmaceutics
Medical Devices
IQ
OQ
Documentation
Pharmaceutical Industry
Electrical Engineering
Mechanical Engineering
Chemical Engineering
Job Details
Responsibilities:
- Responsible for preparing, executing commissioning and qualification documents for a variety of utilities, facility, and process equipment.
- Develop and execute a variety of validation and FDA compliance related documents/protocols for pharmaceutical equipment.
- Make an impact day-to-day with your skills and expertise, strengthening that relationship with our clients and team.
- Excellent leadership skills include the ability to simultaneously organize, and successfully execute multiple project responsibilities.
- Candidates need to possess good communication and interpersonal skills and the ability to interact with all levels of management, clients, and vendors.
- Strong computer skills are also required.
- Minimum 5 years of demonstrated experience with validation of pharmaceutical or medical device processes and equipment.
- FAT, SAT, IQ and OQ documentation development and execution on Automated Systems in the Pharmaceutical Industry.
- Validation experience in the areas of automation, packaging, cleaning, Computer systems, utilities and/or facilities is desired.
- Willing and able to travel as necessary for project requirements to include but not limited to project installation and start-up activities, client meetings, company sponsored meetings, trainings, industry related seminars, forums, or conventions, etc.
- Bachelor's degree in electrical engineering, Mechanical Engineering, Chemical Engineering, or equivalent technical degree.
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