Project Engineer Position Available In Palm Beach, Florida
Tallo's Job Summary: ADMA Biologics is recruiting for a Project Engineer position in Boca Raton, FL. The role involves providing engineering and project management support for GMP manufacturing, troubleshooting, and implementing solutions for existing processes and equipment, as well as designing and commissioning new equipment. A Bachelor's degree in Engineering and 5 years of experience in a cGMP environment are required.
Job Description
Project Engineer
Job Details
Job Location
ADMA Biologics FL – Boca Raton, FL
Position Type
Full Time
Education Level
4 Year Degree
Description ADMA Biologics is a biopharmaceutical company relentlessly committed to creating superior products for immunodeficient patients at risk for infection. It is our devotion to this underserved population that fuels us and our hands-on approach to production and development that sets us apart. If you are looking for a dynamic, innovative, growing company in the biopharmaceutical industry that is committed to excellence and integrity, then consider ADMA Biologics. We currently have an exciting opportunity available for a Project Engineer in Boca Raton, FL! The general purpose of the Project Engineer is to provide engineering, project management, manufacturing and maintenance support to the GMP manufacturing site. Ability to troubleshoot, problem solve and implement engineering solutions for existing manufacturing processes and equipment. Direct, evaluate and assist capital engineering and process improvement projects. Design, procure and commission new process and utility equipment and upgrades to existing systems.
Qualifications Essentials of the job:
Managing small-to-mid sized engineering projects by planning and tracking activities of cross-functional teams and contractors. Develop schedules and performance requirements using appropriate verification tools and techniques to manage project scope, schedule and cost ensuring that project goals are met on time and within budget. Analyze resources and priorities to be applied to assigned projects and perform risk management activities to minimize project risks.
Develop and execute commissioning plans to ensure that process and utility systems and equipment are suitable for their intended use
Develop and review process flow diagrams and piping and instrumentation drawings (P&IDs) for new process and utility systems and modifications to existing systems
Direct and or assist in the design and execution of all capital projects assigned.
Support engineering development with load calculations of flow, heating/cooling capacity, pressures, etc.
Utilize strong technical writing skills to prepare engineering evaluations, change control documentation, testing plans, corrective and preventive actions (CAPAs)
Lead and assist in investigations of process systems and equipment to determine and document root cause and ensure the appropriate corrective actions are initiated and implemented. Use statistical tools in analyzing data to predict trends, measure process capability, improve operating procedures or preventative maintenance procedures, identify bottle necks and equipment reliability.
Help develop efficient PM plans for all key pieces of manufacturing and utilities equipment and provide troubleshooting expertise in all areas of plan operations and maintenance. Create capital expenditure requests and purchase requisitions for approvals prior to procurement of process and utility systems and equipment
Education Requirement:
Bachelor’s degree in Mechanical, Biochemical, or Chemical Engineering.
Experience Requirement:
Minimum of 5 years of engineering experience in a cGMP Pharmaceutical/Biological manufacturing environment.
Other Essential Knowledge:
Able to coordinate and complete complex projects; excellent written and oral communication and presentation skills; computer literate in word processing and data entry; extensive experience with MS Project or Smartsheets, AutoCAD and maintenance planning/scheduling related software; excellent problem-solving skills, detail oriented, and excellent mechanical aptitude, mathematical and statistical analysis skills.
Contacts:
Internal:
Daily contact immediate supervisor, manufacturing managers/personnel and other support groups, and as required other ADMA employees to research, resolve, or provide information.
External:
Frequent contact with vendors and contractors.
Working Conditions:
Physical Demands:
Sit at a desk using a computer. Some heavy lifting required, field verification of equipment and systems in cleanroom and utility spaces, escorting contractors.
Stressors:
Production schedule changes and equipment breakdowns etc., frequent changes in priorities and managing multiple projects with aggressive timelines. In addition to competitive compensation, we offer a comprehensive benefits package including: 401K plan with employer match and immediate vesting
Medical, Vision, Life and Dental Insurance
Pet Insurance Company paid STD and LTD
Company Paid Holidays
3 Weeks’ Paid Time Off (within the first year)
Tuition Assistance (after the first year)
Easily accessible to Tri-Rail
Free shuttle to the Boca Tri-Rail station ADMA Biologics uses E-Verify to confirm the employment eligibility of all newly hired employees. To learn more about E-Verify, including your rights and responsibilities, please visit www.dhs.gov/E-Verify. ADMA Biologics is an Equal Opportunity Employer.