Job Description

Job description
Site Name: USA - Missouri - St. Louis
Posted Date: Feb 25 2021
Are you looking for an engineering role that allows you to leverage your technical knowledge in a state-of-the-art manufacturing environment? If so, this Project Engineer Professional role could be an ideal opportunity to explore.

As Project Engineer, you will be responsible for implementation and scheduling of a comprehensive predesigned qualification program for the manufacturing plant including its equipment, facilities and utilities.

This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following:

Ensure quality and compliance in accordance with established procedures and standards of the Quality System.
Comply with and support the GSK Environmental, Health and Safety policies and procedures. Follows Project Management SOP and checklists.
Responsible for preparing, estimating, designing, managing, and implementing capital projects up to approximately $1,000,000 and average approximately $200,000 per project.
Develop project feasibility and alternatives. Includes: order of magnitude cost estimate, description of process, process flow diagram, location of process, and comparison of pros and cons of the various alternatives.
Prepares detailed dimensional sketch of equipment layout including final process flow diagram with equipment capacities, rates of production, and materials of construction, and other required specs.
Determine utilities requirement to achieve maximum productivity within project cost constraints.
Provides project justification and writes project description along with final project cost estimate and planned timing of implementation.
Reviews equipment specifications provided by vendors, Selects equipment,
and solicits bids for equipment

Provides technical information (i.e., plans, drawings) and/or expertise to inside maintenance personnel and outside contractors to facilitate installation of equipment or structures. Coordinates installation via communication with manufacturing department to ensure minimal interruption in production and timely installation.
Work with Tech-services to produce the required validation documents: URS, FS, DS, IQ, OQ, and PQ’s.
Routinely monitors equipment performance in Packaging/Manufacturing to ensure performance and minimize downtime, supporting manufacturing day to day as needed.
Promote a safe environment with equipment and process designs. Comply with all operational safety, process safety, environmental permits, Quality policies, procedures and training requirements. Comply with all local and corporate policies and procedures.
Why you?
Basic Qualifications:
We are looking for professionals with these required skills to achieve our goals:

Bachelor’s degree in engineering sciences
2 years of engineering/project management/manufacturing experience
Experience using Programmable logic controllers, Visual Basic, HMI software and AutoCAD or solid works
Preferred Qualifications:
If you have the following characteristics, it would be a plus:

PE , (professional engineer) or PMP (Project management professional)
Prior experience in the design regulations for pharmaceutical/food manufacturing validation to meet FDA requirements
Knowledgeable in cGMP compliance, EHS standards and NIH guidelines.
Demonstrated successes to meet project timelines and budgets.