Quality System Support

No Deviation is a provider of patient-centric solutions for the pharmaceutical industry, and we are currently seeking individuals who are passionate about joining our team. Our areas of expertise include engineering consultancy, Commissioning Qualification Validation (CQV), as well as Quality, Compliance, and Regulatory services.

We strongly uphold our core values of Empathy, Integrity, and Transparency, and we strive to create a collaborative, innovative, and inclusive work environment that fosters personal growth and development.

By joining our team, you will have the opportunity to make a meaningful impact in the pharmaceutical industry while advancing your career.

Responsibilities

• Support day-to-day Quality Assurance activities in Quality System team such as Document and Training record management
• Display a good level of problem solving ability by analyzing and interpreting data and puts forward new ideas based on scientific knowledge or field experience
• Detect non-compliance with cGxP and GDP requirements and provide guidance on GDP corrections
• Generally provide basic compliance support to staff in all departments
• Demonstrate appropriate interpersonal skills that encourage collaboration of individuals or teams to meet objectives
• Any other tasks as and when assigned by supervisor

Key Requirements

• Diploma / Degree in a related Science or Engineering discipline such as Biotechnology, Biological Science, Chemistry, Biomedical Engineering, Chemical Engineering
• Positive team oriented attitude
• Good communication skills
• Good problem solving and analytical skills