Process Technician

About No deviation

At No deviation, we are dedicated to delivering patient-centric solutions that revolutionize the pharmaceutical landscape. As a dynamic expert in engineering consultancy, Commissioning Qualification Validation (CQV), and Quality, Compliance, and Regulatory services, we are looking for individuals who are excited to contribute to impactful projects and drive innovation.

We believe that great things happen when Empathy, Integrity, and Transparency guide our actions. That's why we foster a culture of collaboration, inclusion, and continuous development – empowering our team members to grow personally and professionally.

Position Overview

This role is part of a dynamic engineering team supporting a high-volume, multi-product life science manufacturing environment. The position focuses on assisting process engineers with product characterization, metrology, and continuous improvement activities. Working cross-functionally with manufacturing, quality, facilities, analytical sciences, and supply chain teams, the role supports new product introductions, process sustainment, and optimization efforts within a regulated biotech or medical device setting.

Key Responsibilities

• Support process engineers with data analysis related to yield, defects, and process performance
• Assist in the design, execution, and documentation of controlled experiments
• Support investigations related to nonconforming materials and process deviations
• Coordinate equipment and process validation activities, including execution, data collection, and reporting
• Assist engineering teams in developing and sustaining manufacturing processes for new and existing products
• Prepare, review, update, and release engineering documentation and work instructions
• Collaborate cross-functionally to support new product releases and process improvements
  

Required Qualification

• Diploma or Bachelors degree in Engineering, Science, or a related technical field
• Understanding of manufacturing processes within a regulated biotech, medical device, or life science environment
• Ability to execute test plans for components, materials, systems, and processes
• Knowledge of product and process feasibility studies, validation, qualification, and production optimization
• Proficiency in Microsoft Word, Excel, and PowerPoint
• Strong teamwork, interpersonal, and communication skills
• Well-developed technical documentation and report-writing abilities
• Ability to work effectively under pressure, manage multiple tasks, and collaborate across functions
• Proactive, self-motivated, and continuous-improvement mindset
• Experience in a manufacturing or FDA-regulated environment is an advantage

Why join us?

• Generous Leave Policy.
• Comprehensive Health & Wellness Coverage: Receive robust medical and dental coverage to support your health needs.
• Professional Development Opportunities: Access continuous learning programs and resources for career growth within the company.
• Inclusive Culture: Work in an environment where innovation, collaboration, and diverse perspectives are encouraged and celebrated.
• Shape the Future: Make a real difference in the pharmaceutical industry while advancing your career.

How to apply

Are you ready to play a key role in shaping the future of pharmaceutical solutions? If you're passionate about making an impact, we want you on our team!

Please submit your resume, outlining your qualifications and experience relevant to the role, here.