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.

REQUIRED QUALIFICATIONS

• Diploma or Bachelors degree in Life Sciences, Pharmaceutical Science, Chemistry, Biotechnology, or a related discipline.
• 1 to 3 years of relevant experience in pharmaceutical/biotech manufacturing or quality assurance.
• Strong attention to detail and ability to follow procedures accurately
• Good communication and interpersonal skills to work effectively with cross-functional teams

• 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.