Pharmaceutical and Healthcare Jobs Pharma
Advertise  |  Tell a Friend  |  About  |  Contact Us  |  Home
Careers in PharmacyFind Jobs Post Your Resume
Science Jobs Medical Device Jobs
Medical Sales Jobs Biotech Jobs
Pharmaceutical Sales Jobs Pharmacy Tech
Biotechnology Jobs  Health Care Jobs
Pharmacy Technician Jobs Healthcare Careers


Home >> View Job 

Career Tools
Get a Job Winning Resume
What's Your Former Boss Say About You?
Blast Your Resume
Free Magazines
Find Job Fairs
My Network
Find Training Courses
Pharma Talk Blog
Find Service Providers

Featured Jobs
Biotech Jobs
Director, Regulatory Affairs
Emergent BioSolutions
Pharmaceutical Jobs
Director/Sr Director, VPoC BioPharm DPU (2 positions)
GlaxoSmithKline
Director, Internal Communictions, Global Oncology Business
GlaxoSmithKline
Healthcare Jobs
Apply online for the Lead Validation Project Engineer position and advance your career in the Pharmaceutical industry today.
Lead Validation Project Engineer : E-Technologies Group
Employee Type Full Time
Company Name E-Technologies Group
Location West Chester
Ohio
45069
Salary (year) $70000 - $110000
Experience 6 to 9 Years
Industry Pharmaceutical
Job Type Validation
Relocation Required
Travel Requirement 25%
E-Technologies Group  
View all jobs from E-Technologies Group 

      
What Does Your Boss Say About You?
Description
E-Technologies Group is seeking to fill a direct hire position for a Lead Validation Project Engineer. Essential job duties include leadership of teams in the development, review, approval, and execution of validation documentation including VP, Trace Matrices, IQ, OQ and Summary Reports to maintain processes, systems, and equipment in a validated state per URS and DDS information. This position also requires providing guidance and training to internal and external departments on the development and execution of validation protocols. Ideal candidates will have some combination of the following skill sets.
Requirements
All candidates should meet the following minimum requirements: • BS or MS in Engineering, computer sciences or physical/life sciences or equivalent experience • Computer System Validation Project Management/Leadership experience • Must have minimum 7 years experience in leading the validation of and/or validating automated/PLC controlled equipment and processes • IQ and OQ documentation development and execution on Automated Systems • Ability to read/interpret electrical schematics, P&ID’s, AF&ID’s, and related design material • Understanding of Project Scope, Schedule and Budget development with Project Forecasting and Reporting for successful project implementation is desirable • Knowledge of cGxP requirements • Self starter with excellent written and oral communication skills • Ability to manage personnel and projects while exercising excellent decision making and time management skills Desirable attributes include: • GAMP 5/SDLC expertise • Working knowledge of 21 CFR Parts 210 and 211, and 21 CFR Part 11 • Integrated C&Q methodology experience • PLC/HMI/Batch programming experience • SOP development experience • Experience with validating: CIP & SIP Processes, RSBatch recipes, Filling Lines and/or Packaging Lines
Contact Info

To apply for this position directly, please Click Here.
Find More Pharmaceutical Jobs in the Pharmaceutical industry.