Process Engineer at Veraz Inc

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.

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

Assist in planning, preparing, and executing Traditional and Fast Chain 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.

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.

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.