Engineer Process I

Overview

Engineer Process I located in Boca Raton, FL. Job Title : Engineer Process I. Company : BioSpace.

ADMA Biologics is a biopharmaceutical company relentlessly committed to creating superior products for immunodeficient patients at risk for infection. 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.

Job Description

Job Title : Engineer Process I

Company : ADMA Biologics

Location : Boca Raton, FL

Position Summary

The Process Engineer I will provide process development and transfer support for IgG Immunotherapy Production. Provide updates to the Process Development (PD) Management team on a regular basis to ensure compliance issues are being met. Responsible for maintaining compliance in the PD laboratory and executing process development / evaluation studies as well as process validations using a scale-down model. As a key member of the PD group, provide support for Manufacturing, Quality Control / Quality Assurance, and Regulatory departments.

Essential Functions (ES) And Responsibilities

• Provide support for technical issues related to the manufacturing process and product quality.
• Develop new processes as required for production of plasma derived therapies.
• Be familiar with regulatory guidelines to process development / validation as well as implementing manufacturing process changes.
• Optimize and maintain compliance in PD laboratory by ensuring all equipment calibration / IQ / OQ / PM status are current.
• Participate in designing and planning scientific experiments to achieve corporate goals for existing projects.
• Review and / or approve cGMP documentation generated by other PD group members as necessary.
• Lead execution of process development / evaluation studies as well as process validations using a qualified scale down model.
• Be responsible for transferring process changes and / or new processes from PD to Manufacturing.
• Act as a liaison between PD and Manufacturing for supporting deviations and investigations as well as when transferring new and / or optimized processes.
• Maintain and review process development Batch Records for scale down process models.
• Perform other activities as assigned by the PD Managers.
• Support Manufacturing, Engineering, and Quality Management departments with the development and implementation of new process / technology.
• Assist manufacturing personnel in the execution of process development and process validation studies in a cGMP production environment as necessary.

Job Requirements / Competencies

Education Requirements

Experience Requirements

Compliance & Benefits

The minimum compliance expectation for this role entails strict adherence to FDA regulations and company policies governing sales and marketing activities, including completion of required compliance training, accurate documentation of sales interactions, and adherence to data privacy regulations. The role requires proactive participation in compliance reviews, prompt reporting of any potential issues, and ongoing education to stay updated on relevant FDA regulations.

Benefits : In addition to competitive compensation, a comprehensive benefits package includes :

ADMA Biologics, Inc. 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.

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