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 looking for a QA Executive to support quality assurance activities within our biomedical/biotech manufacturing environment. The role involves ensuring compliance with quality standards, supporting deviation/CAPA processes, and maintaining robust documentation and inventory controls. This position is ideal for someone who is hands-on, detail-oriented, and experienced in biotech or pharmaceutical QA operations.
Key Responsibilities
- Support day-to-day QA activities within a biomedical/biotech manufacturing setup.
- Review batch records and ensure accuracy, completeness, and compliance with GMP expectations.
- Manage QMS activities, including deviations, CAPA, and change controls.
- Ensure proper documentation control and timely closure of quality records.
- Support warehouse and inventory-related QA processes, including material verification and release.
- Collaborate with cross-functional teams (Production, QC, Warehouse) to ensure quality standards are met.
- Participate in internal audits and assist in preparation for regulatory inspections.
- Provide QA oversight on operational activities to maintain compliance with internal and external requirements.
Required Qualifications
- Minimum 2 years of QA experience in a biomedical or biotech manufacturing environment.
- Strong familiarity with QMS processes, including deviations, CAPA, and change control.
- Experience in quality review of batch records.
- Working knowledge of warehouse and inventory management from a QA perspective.
- Good understanding of GMP and quality compliance requirements.
- Strong communication skills and attention to detail.
- Ability to work independently and meet deadlines in a fast-paced environment.
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.
