Senior C&Q Engineer

Roles & Responsibilities

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 C&Q Engineer to lead 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 7 years of experience in the pharmaceutical industry, strong technical knowledge, and a proactive, solution-driven attitude.

Key Responsibilities

• Lead the protocol generation and review for the assigned areas (i.e. process equipment, facilities, utilities and laboratory equipment)
• Review vendor or construction turnover document
• Review construction walkdowns to assure compliance with design
• Lead or direct execution of full C&Q project lifecycle, including URS, Design Verification, FAT, SAT, DQ, IQ, OQ and PQ etc.
• Trouble shooting equipment with a cross functional team
• Manage summary report writing wherever required
• Verification of Construction Contractor's Document deliverables (CTODs) and Vendor Document deliverables (VTODs)
• Support the review and revision of design document, wherever required
• Liaise with identified stake holders, including suppliers/contractors
• Provide SME input wherever required
• Manage the assigned system handover
• Support the management of project schedule
• Compliant to quality and safety requirements
• Complete trainings in a timely manner
• Support company operation and business as required
• Any other project responsibilities specified in the individual OAN and organizational responsibilities assigned by management

Required Qualifications

• Minimally a Bachelor of Science/ Bachelor of Engineering or related scientific degree
• At least 7 years of experience in Pharmaceutical industry
• 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
• A fast learner with "Can-do" attitude
• Good time management skill and great attention to detail
• Proficient presentation and facilitation skill is a plus

Why join us?

• Generous Leave Policy including 3 days to care 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.

Tell employers what skills you have

Pharmaceutical Industry
Report Writing
Construction
Transparency
Protocol
Compliance
Attention to Detail
Time Management
Regulatory Requirements
Facilitation
Laboratory
Turnover
Commissioning

---