Process Engineer

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

We are looking for a skilled Process Engineer to design, implement, and optimize processes. Key responsibilities include reviewing process design documents, participating in safety and design reviews, managing change control, vendor relations, and quality risk assessments. You will oversee commissioning, qualification, and validation activities while ensuring HSE compliance. Additionally, you’ll troubleshoot process issues, manage deviations, and provide SME input. Collaboration with stakeholders, SOP generation, and completing training on time are essential for success in this role.

Key Responsibilities

• Lead Process Design: Develop and review key process design documents (P&IDs, PFDs, URS, data sheets) to ensure optimal system performance and compliance.
• Drive Safety & Design Excellence: Contribute to safety and design reviews (3D models, HAZOP, DQ) to guarantee robust and safe process designs.
• Manage Project Changes: Oversee site and project change control, ensuring smooth transitions and effective execution of process improvements.
• Vendor Relationship Management: Cultivate strong vendor partnerships, ensuring timely and high-quality deliverables.
• Engage in Quality Risk Assessments: Actively participate in risk assessments to enhance process quality and minimize operational risks.
• Review & Approve Documents: Ensure all relevant technical documents are thoroughly reviewed and approved, maintaining high standards.
• Monitor & Report Progress: Track and report the status of assigned projects and tasks, ensuring transparency and alignment with timelines.
• Coordinate Field Work & Commissioning: Lead and coordinate field work, including commissioning, qualification, and validation activities, ensuring smooth implementation of processes.
• Champion Health, Safety & Environment (HSE): Take full ownership of HSE responsibilities in your designated area, ensuring strict adherence to safety standards.
• Solve Process Issues: Troubleshoot and resolve process-related issues, applying your expertise to maintain smooth operations.
• Manage Deficiencies & Deviations: Effectively address any deficiencies or deviations, working proactively to resolve them.
• Provide Expert Input: Offer Subject Matter Expert (SME) input as needed, driving improvements and operational excellence.
• Support SOP Creation: Contribute to the development and refinement of Standard Operating Procedures (SOPs) to streamline operations.
• Collaborate with Stakeholders: Coordinate with key stakeholders to ensure alignment and successful project outcomes.
• Ongoing Learning: Complete required training on time, keeping up to date with the latest tools, technologies, and industry standards.

Required Qualifications

• Minimum Degree in Engineering or Science Disciplines
• Minimum 3 years’ experience in a related field / Pharmaceutical Industry
• Proven track record in following and promoting Safety in all aspects of your role
• Strong process and automation knowledge, adequate knowledge in utility and HVAC
• Project management / coordination experience
• Proactive and self-motivated
• Adequate knowledge on cGMP and other regulatory requirements, guidelines and industry best practices
• Be IT literate and familiar with Microsoft office suite of applications
• Demonstrated proficiency of written and verbal communication skills in English (including technical writing and presentations) with ability to communicate and collaborate effectively with technical and senior management staff

Why join us?

• Generous Leave Policy including Elderly Care Leave for aging family members, reflecting our commitment to family wellbeing.
• 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.