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 QC CQV Engineer is responsible for the commissioning, qualification, and validation of QC laboratory equipment, with a strong focus on temperaturecontrolled units such as refrigerators and freezers. This role will support change control activities, develop qualification protocols, execute testing, and ensure compliance with GMP and data integrity requirements.
Key Responsibilities
Temperature Mapping & Equipment Qualification
- Perform temperature mapping of refrigerators, freezers, and other temperaturecontrolled equipment according to GMP requirements.
- Analyze mapping data and ensure equipment meets acceptance criteria for uniformity and stability.
- Support qualification activities including IQ/OQ/PQ for QC laboratory instruments.
- Document all qualification activities in compliance with internal procedures and regulatory standards.
Protocol Development & Execution
- Draft validation documents such as URS, Risk Assessments, IQ/OQ/PQ protocols, and summary reports.
- Execute qualification protocols in the QC laboratory environment.
- Ensure all deviations are documented, investigated, and resolved appropriately.
Change Control & Compliance
- Initiate and manage Change Controls related to equipment qualification, upgrades, repairs, or replacements.
- Ensure all activities align with GMP, ALCOA+, and regulatory expectations.
- Support internal and external audits by presenting qualification and validation documentation.
Cross-Functional Collaboration
- Work closely with QC, QA, Engineering, and vendors to coordinate qualification and maintenance activities.
- Provide technical support to the QC team on equipment performance and compliance.
- Participate in continuous improvement initiatives for laboratory equipment lifecycle management.
Required Qualifications
- Degree or Diploma in Engineering, Life Sciences, Biotechnology, or related field.
- Experience in CQV, equipment qualification, and temperature mapping in a GMP environment.
- Strong understanding of qualification principles, validation lifecycle, and regulatory requirements.
- Good documentation, analytical, and problemsolving skills.
- Strong attention to detail and compliance mindset
- Good communication and technical writing skills
- Ability to work independently and in crossfunctional teams
- Practical understanding of laboratory operations
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.
