Senior Process Engineer

ZipRecruiter; Philadelphia (Philadelphia County); On-site; USD 80,000 - 110,000; Full time

Job summary

An innovative firm is seeking a Senior Process Engineer to revolutionize biopharmaceutical manufacturing. This critical role involves spearheading process optimization, ensuring compliance with strict regulatory standards, and collaborating with cross-functional teams to drive advancements in cell therapy. With a focus on operational excellence, you will lead the charge in implementing cutting-edge technologies and refining processes that will shape the future of the industry. If you are passionate about making a significant impact in the biopharma sector and possess strong leadership and analytical skills, this opportunity is perfect for you.

Qualifications

• 5+ years of experience in BioPharma Life Sciences.
• Hands-on GMP experience and knowledge of cell therapy manufacturing.

Responsibilities

• Lead process optimization and integration of new technologies.
• Ensure compliance with FDA, EMA, and ISO regulations.

Skills

Process Optimization

CQV (Commissioning, Qualification & Validation)

GMP Compliance

Cell Culture Processes

Analytical Skills

Leadership Skills

Education

Degree in Chemical Engineering

Degree in Mechanical Engineering

Degree in Biochemical Engineering

Job description

Job Description

Senior Process Engineer Biopharma Manufacturing (Philadelphia, PA Area)

Are you ready to shape the future of biopharmaceutical manufacturing?

Workforce Genetics is seeking a Senior Process Engineer to drive innovation and operational excellence within a cutting-edge cGMP facility. This is an exciting opportunity to lead process improvements, support strategic growth, and influence groundbreaking advancements in cell therapy and biopharma manufacturing.

What You'll Do:

• Spearhead process optimization, ensuring the seamless integration of new equipment and technologies.
• Lead CQV (Commissioning, Qualification & Validation) efforts for state-of-the-art process equipment.
• Develop and refine technical transfer documents, supporting next-generation biopharma manufacturing.
• Collaborate with senior leadership to align process and facility engineering strategies with long-term growth objectives.
• Ensure compliance with FDA, EMA, and ISO regulations while upholding GMP standards.
• Work cross-functionally with automation, facility design, and mechanical teams to drive innovation.

What You Bring:

• Degree in Chemical, Mechanical, or Biochemical Engineering (BS/MS)
• 5+ years of experience in BioPharma Life Sciences, with expertise in process simulation and safety reviews.
• Hands-on GMP experience, including change controls, deviation management, and CAPAs. Strong knowledge of cell culture processes and cell therapy manufacturing.
• Exceptional communication, analytical, and leadership skills to drive impactful results.