Senior CQV Lead

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 seeking a Senior CQV Lead to direct commissioning and qualification activities across various systems, ensuring compliance with industry standards. This role involves overseeing the full project lifecycle, from protocol generation to system handover. Ideal candidates will have at least 10 years of experience in the pharmaceutical industry, strong technical knowledge, and a proactive, solution-driven attitude.

Key Responsibilities

• Oversee the commissioning of systems and equipment to ensure they meet specified requirements and are operationally ready.
• Lead, mentor, and manage a team of CQV engineers and technicians. 
• Coordinate with various stakeholders, including project managers, engineering teams, quality assurance (QA), automation engineers, and end-users. 
• Ensure all C&Q activities comply with regulatory guidelines and industry standards.
• Follow commissioning strategy developed by C&Q WPO.
• Review and approve all qualification documentation, ensuring comprehensiveness and compliance.

Required Qualifications

• Minimally a Bachelor of Science/ Bachelor of Engineering or related scientific degree
• At least 10 years of experience in Pharmaceutical industry, preferably within any related production area.
• In-depth technical knowledge in the assigned area and associated regulatory requirements, guidelines, and other industry best practices.
• Ability to work in a fast paced & dynamic work environment.
• Strong knowledge of the CQV process, GMP, and qualification lifecycle documentation.
• Proven success in project management tools and methodologies.
• Exceptional communication, negotiation, and leadership skills.

Why join us?

• 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.