Project Engineer Job Details

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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!

Job Title: Project Engineer

Job Description:

Position Summary

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.

Essential Functions (ES) and Responsibilities

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.

Job Responsibilities or Job Requirements

Competencies

Ability to follow the cGMP’s and procedures with great attention to detail

Ability to read and understand blueprints

Able to evaluate and interpret regulations and recognize the need for appropriate changes relative to procedures

Able to work in high-pressure, deadline-driven environment

Actively provides feedback to operations management and staff regarding staff performance against SOPs. Works to develop and maintain a collaborative and effective working relationship with operations management

Demonstrated ability to achieve goals, overcome obstacles, and meet deadlines

Demonstrated ability to use computer software including MicroSoft Outlook, Word and Excel.

Exceptional organizational and communication skills required

FDA Adherence

Identifies ways to improve workflow and identify efficiencies while working within constraints of SOPs

Experience Requirements

Minimum of 5 years of engineering experience in a cGMP Pharmaceutical/Biological manufacturing environment.

Education Requirement:
Bachelor's degree in Mechanical, Biochemical, or Chemical Engineering.

Preferred Experience

Compliance Requirements (ES)

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In addition to competitive compensation, we offer a comprehensive benefits package including:401K plan with employer match and immediate vestingMedical, Vision, Life and Dental InsurancePet InsuranceCompany paid STD and LTDCompany Paid Holidays3 Weeks’ Paid Time Off (within the first year)Tuition Assistance (after the first year)Easily accessible to Tri-RailFree shuttle to the Boca Tri-Rail stationADMA 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.