UPM Pharmaceuticals · 22 hours ago
Validation Project Engineer
UPM Pharmaceuticals is an independent contract development and manufacturing organization located in Bristol, Tennessee. The Validation Project Engineer I will assist in validation project work associated with cleaning, process, equipment, facility, and utility qualifications to ensure compliance with Good Manufacturing Practices and UPM’s quality requirements.
BiotechnologyHealthcarePharmaceuticalLife ScienceHealth Care
Responsibilities
Assists in writing, executing, reviewing and summarizing Installation, Operation and Performance Qualifications (IQ/OQ/PQ) for new and existing equipment, systems and utilities under the direction of higher level Validation Engineers
Perform requalification of equipment, systems and utilities as required
Assists in the execution of cleaning and process validations under the direction of higher level Validation Engineers
Identify deviations encountered during protocol execution, write deviation reports and help develop appropriate resolution
Assist in developing, planning and executing Validation Project Plans
Adhere to department and project deadlines, expectations and priorities while developing realistic goals for timely completion of projects
Participate in evaluating and recommending new equipment or process changes
Assess, evaluate and perform testing necessary to close out change controls in a timely manner
Support process and cleaning validation as needed
Other duties as may be assigned
Qualification
Required
Bachelor's degree in a science/engineering related field
At least three years of pharmaceutical validation experience in a GMP environment
Legally authorized to be employed in the United States
Benefits
401(k)
401(k) matching
Dental insurance
Employee assistance program
Employee discount
Flexible spending account
Health insurance
Life insurance
Paid time off
Referral program
Relocation assistance
Retirement plan
Vision insurance
Company
UPM Pharmaceuticals
UPM Pharmaceuticals is a Bristol Tennessee based contract development and manufacturing organization (CDMO) serving the pharmaceutical and biotechnology industries.