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 role is responsible for supporting Quality Assurance operations within a multi-product cGxP contract manufacturing environment. This includes managing GMP documentation lifecycle activities, supporting documentation system migrations, overseeing training records, and providing day-to-day compliance support. The position requires strong attention to detail, sound judgment in identifying and addressing compliance gaps, and effective collaboration with cross-functional teams while upholding data integrity principles in accordance with company policies.

Key Responsibilities

• Manage the GMP document lifecycle within the Documentation Management System (DMS), including archiving and handling of inactive records
• Maintain and manage documents within the onsite archive room
• Support DMS migration activities
• Manage training records, including form processing and data entry
• Support day-to-day Quality Assurance activities in accordance with approved SOPs and policies
• Identify non-compliance with cGxP and cGDP requirements and provide guidance on corrective actions
• Provide general compliance support to staff across all departments
• Apply problem-solving skills to analyze data, interpret findings, and propose improvements based on scientific knowledge or field experience
• Uphold data integrity principles in accordance with company policies and proactively identify opportunities for process improvement
• Perform other duties as assigned by the Supervisor

Required Qualifications

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

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.