QA Specialist

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

The Quality Assurance Specialist supports daily QA operations within a multi-product cGxP contract manufacturing environment, ensuring compliance with regulatory standards and internal policies. This role is responsible for managing documentation systems, maintaining training and archival records, and providing frontline compliance support across departments. The individual plays a key role in upholding data integrity, identifying non-compliance, and contributing to continuous improvement initiatives through effective problem-solving and collaboration.

Key Responsibilities

• Manage training records, including processing and data entry of relevant forms
• Oversee GMP document lifecycle within the Documentation
• Management System, including archiving and inactive records
• Maintain and organize documents within the onsite archive room
• Support day-to-day QA activities in accordance with approved SOPs and policies
• Identify non-compliance with cGxP and cGDP requirements and provide guidance on corrections
• Provide basic compliance support to staff across all departments
• Analyze and interpret data to support problem-solving and propose improvements
• Uphold data integrity principles in line with company policies and proactively improve processes
• Collaborate effectively with cross-functional teams to meet operational objectives
• Perform additional tasks as assigned by the Supervisor

Required Qualifications

• Diploma or Degree in a relevant Science or Engineering discipline (e.g., Biotechnology, Biological Science, Chemistry, Biomedical Engineering, Chemical Engineering)
• Positive, team-oriented attitude
• Good communication and interpersonal skills
• Strong problem-solving and analytical abilities

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.