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 Cleaning Validation Engineer to support cleaning validation activities within a biologics manufacturing environment. The role involves developing validation documentation, coordinating with manufacturing teams for execution of cleaning validation protocols, and supporting investigations related to cleaning deviations to ensure compliance with GMP requirements.
Key Responsibilities
- Develop and author cleaning validation protocols and reports in accordance with GMP and site procedures
- Coordinate with Manufacturing and cross-functional teams for the execution of cleaning validation protocols
- Support the execution of cleaning validation studies, including sampling and documentation review
- Participate in troubleshooting and investigation of cleaning deviations, identifying root causes and implementing corrective actions
- Ensure cleaning validation activities are conducted in compliance with regulatory and quality requirements
- Work closely with QA, Manufacturing, and Engineering teams to ensure timely completion of validation deliverables
- Support documentation updates and change control activities related to cleaning validation
Required Qualifications
- 1–3 years of relevant experience in a pharmaceutical or biologics manufacturing environment
- Prior exposure to cleaning validation is preferred
- Familiarity with GMP regulations and validation documentation practices
- Experience working with manufacturing teams for protocol execution is an advantage
- Strong problem-solving and investigation skills for deviation handling and troubleshooting
- Good communication skills and ability to collaborate with cross-functional teams
Preferred Qualifications
- Experience in biologics manufacturing systems or processes
- Knowledge of cleaning validation concepts such as residue limits, sampling methods, and cleaning verification
- Exposure to deviation investigations and CAPA processes
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.
