MS&T Engineer - Part-Time

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

The MS&T Engineer is responsible for supporting site validation and qualification activities within pharmaceutical or medical device manufacturing environments. This role focuses on developing and executing validation strategies, ensuring compliance with regulatory standards, and maintaining documentation throughout the lifecycle of equipment, processes, and systems. The engineer also contributes to risk assessments, deviation investigations, and continuous improvement initiatives. Additionally, the role involves supporting packaging-related projects and collaborating with cross-functional teams and external vendors.

Key Responsibilities

• Coordinate and support validation and qualification activities, including development of validation plans
• Author and execute validation/qualification protocols (IQ/OQ/PQ) in compliance with GMP requirements
• Investigate deviations and implement corrective and preventive actions (CAPA)
• Prepare validation and qualification summary reports
• Perform risk assessments for products, processes, and systems
• Support global packaging changes and act as SME for packaging-related projects
• Collaborate with cross-functional teams and vendors to resolve technical and packaging issues

Required Qualifications

• Minimum 8 years of experience in pharmaceutical or medical device manufacturing
• At least 2 years of experience in creating or approving validation protocols
• Experience in validation/qualification activities and GMP compliance
• Knowledge of deviation management, risk assessment, and CAPA processes
• Experience in packaging validation or labelling review is preferred
• Ability to work effectively in a multidisciplinary team environment

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.