Process Engineer at Veraz Inc

Wayne State University; San Diego (CA); On-site; USD 75,000 - 95,000; Full time

Job summary

Wayne State University in San Diego is looking for a motivated Process Engineer to support and optimise operations in packaging, labelling, and distribution. This role requires collaboration with cross-functional teams to ensure compliant production processes within a fast-paced biopharmaceutical environment.

The ideal candidate will have at least a Bachelor’s degree in Engineering, strong analytical skills, and a minimum of one year of applicable industry experience, contributing to operational excellence initiatives.

Qualifications

• Minimum of 1 year experience in process engineering or related role.
• Experience in GMP-regulated environments preferred.
• Ability to manage multiple priorities in fast-paced environments.

Responsibilities

• Support safety by addressing potential safety concerns.
• Assist in planning and executing production schedules.
• Lead continuous improvement initiatives.
• Conduct root cause analyses for production-related issues.
• Generate and close deviations and complaints in compliance with cGMP.
• Create and improve SOPs and training materials.

Skills

Problem-solving

Analytical skills

Organisational skills

Communication

Education

Bachelor's degree in Engineering

Job description

About the Role

We are seeking a motivated and detail-oriented Process Engineer to support and optimise operations across packaging, labelling, storage, distribution, and continuous improvement initiatives. In this role, you will collaborate with cross‑functional teams to drive efficient, compliant, and high‑quality production processes within a fast‑paced pharmaceutical/biotechnology environment.

This position offers the opportunity to work independently while contributing to site‑wide operational excellence initiatives. You will play a key role in production planning, process optimisation, deviation investigations, equipment qualification, and continuous improvement efforts that directly impact product quality, operational reliability, and customer satisfaction.

Key Responsibilities

Support a safe working environment by proactively identifying and addressing potential safety concerns.

Assist in planning, preparing, and executing Traditional and FastChain production schedules to ensure timely packaging and delivery.

Lead and support operational excellence and continuous improvement initiatives across the department and site.

Participate in or lead cross‑functional investigations related to deviations and complaints, identifying root causes and implementing corrective and preventive actions (CAPAs).

Conduct root cause analyses for safety, quality, and delivery events while resolving production‑related issues.

Generate, investigate, and close deviations and product‑related complaints in compliance with cGMP requirements.

Create, revise, and improve SOPs, work instructions, and training materials to ensure operational consistency and compliance.

Collaborate effectively with cross‑functional teams to maintain alignment and support seamless operations.

Drive process optimisation, cost reduction, and innovation through the implementation of new technologies, best practices, and operational learnings.

Support the development, validation, qualification, and optimisation of packaging and labelling equipment and processes.

Monitor and analyse labelling, packaging, and distribution KPIs and implement data‑driven improvements to enhance operational performance.

Support client audits and serve as a subject‑matter expert (SME) for equipment and operational systems.

Perform additional duties as assigned.

Qualifications

Required

Bachelor's degree in Engineering (Mechanical or Electrical Engineering preferred).

Minimum of 1 year of experience in process engineering, manufacturing engineering, or a related role within the pharmaceutical, biotechnology, or GMP‑regulated industry.

A master’s degree in Engineering may be considered in place of prior experience.

Strong problem‑solving, analytical, and organisational skills.

Excellent written and verbal communication skills.

Ability to manage multiple priorities and work effectively in a fast‑paced environment.

Preferred

Experience working in GMP‑regulated manufacturing environments.

Knowledge of pharmaceutical or clinical packaging and supply chain operations.

Experience with process validation, equipment qualification, and deviation investigations.