Quality Assurance Specialist (3 months Contract)

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 motivated and detail-oriented Junior Quality Assurance (QA) Specialist to support our manufacturing operations. This role ensures that products are manufactured in compliance with Good Manufacturing Practices (GMP), internal quality standards, and regulatory requirements. The successful candidate will collaborate closely with production, engineering, and quality teams to maintain a culture of quality and continuous improvement.

Key Responsibilities

• Review and approve batch records, standard operating procedures (SOPs), and deviations related to manufacturing operation.
• Support timely documentation and ensure adherence to GDP (Good Documentation Practices).
• Participate in internal audits and support regulatory inspection.
• Provide on-the-floor QA presence to oversee manufacturing activities and ensure compliance with GMP.
• Assist in the investigation of deviations, non-conformances, and complaints.

Required Qualifications

Why join us?

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.