Duration: 12 Months Contract (Possible Extension)
Remember to check your CV before applying Also, ensure you read through all the requirements related to this role.
Description
About the role.
Provide engineering support, direction, and project management for all facilities areas, systems, and infrastructure supporting medical device manufacturing, lab, and office space. Collaborate cross-functionally to design, construct, commission, qualify, and maintain all controlled environments and facilities systems utilized by manufacturing. Lead cross-discipline facilities infrastructure projects of varying sizes and timelines.
Job Responsibilities include:
Responsible for planning facilities equipment layouts for economy of operation and maximum utilization of facilities and equipment.
Reviews and estimates design costs including equipment, installation, labor, materials, preparation, and other related costs.
Develops criteria and performance specifications for facilities infrastructure and equipment required to meet unique operating requirements and building/safety codes.
Developing and driving new process changes to improve efficiency and compliance
Coordinates with architecture/engineering firms in developing design criteria and preparing layout and detail drawings.
Manages commissioning and qualification of controlled environment areas and bulk systems used in the manufacturing of medical devices
Achieve detailed mechanical understanding of all infrastructure supporting medical device manufacturing and lab areas.
Prepares bid sheets and contracts for construction projects supporting competitive bid process.
Effectively collaborate cross-functionally in order to provide project recommendations for diverse group of customers.
Effectively manage construction projects to tight timelines and costs
Inspects or directs the inspection of construction and installation progress to ensure conformance to established drawings, specifications, and schedules.
Gathers and reviews data concerning facility or equipment specifications, company or government restrictions, required completion date, and construction feasibility.
May be responsible for scheduling, coordinating, and planning preventative maintenance.
Plans and coordinates shutdown of manufacturing areas for updates, modifications, and critical maintenance
Responsible ensuring quality compliance of controlled areas and systems in alignment with FDA regulations, global standards, site processes, and industry standards
Create systematic decision assessments ranging from high-level budgetary reviews to detailed design reviews
Required Qualifications:
Bachelor's degree in engineering
Must have 3+ years of experience
Highly self-motivated
Proven history of leadership
Excellent communication skills (written and verbal)
Ability to collaborate across many disciplines
Comfortability working through and within change
Experience working in a large business setting across many departments and disciplines
Ability and interest in a fast-paced role that changes priorities quickly
Preferred Qualifications:
Experiencing managing complex engineering design projects
Ability to distill complex topics into simplified and digestible summaries
Experience working for a Fortune 500 organization
Experiencing qualifying facilities infrastructure used for medical device manufacturing
Experience utilizing lean manufacturing tools
Experience driving and managing process change
About US Tech Solutions:
US Tech Solutions is a global staff augmentation firm providing a wide range of talent on-demand and total workforce solutions. To learn more about US Tech Solutions, please visit www.ustechsolutions.com.
US Tech Solutions is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.
Recruiter Details:
Name: Kanika
Email: ******
Internal Id: 24-23443