Position Overview
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.
Key Responsibilities
Provide support for routine QA operations, including quality reviews of: Logbooks, Periodic reviews & SOPs.
Participate in and contribute to continuous improvement projects
Liaise with cross-functional stakeholders to ensure alignment and timely execution of QA tasks
Required Qualifications
1-2 years of Quality Assurance experience in a GMP environment
Strong attention to detail; meticulous in document review and record-keeping
Good communication skills; able to collaborate effectively with stakeholders
Fast learner who can pick up new systems and processes quickly
Able to work independently with minimal supervision
Benefits
Comprehensive Health & Wellness Coverage: Receive medical coverage to support your health needs.
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.
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