Staff Engineer-Site Planner Job in Los Angeles 90012, California US

Staff Engineer-Master Planner 

 

Job Description:

Responsible for: helping develop the overall strategy to improve the efficiency, compliance, and cost of the facility.

 

Ensure the plan adheres to: cGMP and EHS regulation, optimizing space, work centers rationalization, efficiency enhancement. This work should set the foundation for a cost-effective operation and development. Partner with warehouse staff, utilities staff maintenance staff to ensure coordination of the SMP within the teams.  Implement all projects related to the SMP on time on budget. Implement concurrent project assignments, at various levels of completion, requiring several areas of expertise to support manufacturing/operational needs.

Provide support for utility equipment selection, integration, custom design, capital justification, project management, specifications/ acceptance criteria, installation, commissioning, validation, operator training, and maintenance turnover in accordance to good engineering principles, OSHA, FDA/GMP, environmental, etc. Prepare engineering designs, systems integration, floor plans, detailed drawings/schematics, presentations training materials for sanitary and plant utilities (i.e. WFI, USP purified water, clean steam, clean air, steam, air, gases, glycol).

Evaluate equipment, processes, methods and technology on operations and products. Distill technical information and provide presentations to cross-functional management teams. Establish and adhere to budgets and time commitments. Solicit bids and purchase equipment or services from vendors and contractors. Supervise trade contractors for duration of project/s.

Support ongoing business development needs and new product introductions in conjunction with the marketing, Finance, Product Development, Packaging Development and Operations functions. Perform short term assignments within other functional areas in order to implement or affect project goals.

 

Requirements:

·         B.S. in Chemistry or Engineering or Business is required. 

·         8 years of  experience including engineering and technical report writing are required. 

·         Prior pharmaceutical or OTC experience and a thorough understanding of cGMP are required. 

·         3 years of Project Management experience, leading 500K+ projects is required.

·         Experience interacting with vendors and managing contractors in required. 

·         Executed major projects (500K+)  in an FDA regulated/GMP environment

·         Involved in projects from conceptual design through validation and turnover

·         Equipment and system validation knowledge including working knowledge of URS, FS/DS, IQ, OQ

If interested in this excellent opportunity, please send your resume in a word attachment to: Will@Fusion408.com

 

REFERRAL BONUS

 

Do you know a friend or colleague who might be a great fit for this position? Fusion408 has the best referral bonus in the business! Refer a friend or colleague and when we place your referral at this position or any other, you will be handsomely rewarded with a referral bonus of up to $3,000!

 

Have a great day and we look forward to hearing from you soon!