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 Validation Support role is responsible for supporting validation lifecycle activities across direct, indirect, and no-impact systems within a regulated pharmaceutical environment. The position ensures that equipment and systems remain in a qualified state through ongoing validation maintenance reviews, execution of qualification and requalification activities, and coordination with cross-functional stakeholders such as QA and QC. This role plays a key part in maintaining compliance with GMP requirements and ensuring validation documentation and processes are properly executed, reviewed, and approved.
Key Responsibilities
- Perform Validation Maintenance Reviews for direct, indirect, and no-impact systems
- Generate, review, and approve validation documentation (e.g. DQ, IQ, OQ, PQ) for new equipment qualification
- Plan and execute periodic requalification protocols for temperature chambers using data loggers/sensors
- Coordinate with cross-functional stakeholders (QA, QC, Engineering) to plan and align execution schedules
- Ensure validation activities are executed in compliance with GMP and internal quality standards
- Support audit readiness by maintaining accurate and complete validation documentation
Required Qualifications
- Diploma or Degree in Engineering, Life Sciences, Pharmacy, or related field
- Experience in validation or qualification activities within a GMP-regulated environment (pharma, biotech, medical devices)
- Familiarity with validation documentation (DQ, IQ, OQ, PQ)
- Understanding of temperature mapping, calibration, or equipment qualification processes
- Strong attention to detail and documentation accuracy
- Good communication skills for cross-functional coordination (QA/QC/Engineering)
- Ability to manage multiple tasks and meet project timelines
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.
