QC Analyst (Shift, 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

To execute assigned quality control laboratory testing activities in accordance with cGxP requirements. The QC Analyst will perform analytical testing, ensure proper sample management, and support laboratory equipment maintenance and qualification activities to maintain compliance and operational efficiency.

Key Responsibilities

• Perform laboratory testing of API, drug substance, drug product, and finished product samples.
• Execute analytical methods in accordance with approved procedures and GMP requirements. 
• Manage sample receipt, storage, and documentation in compliance with data integrity standards.
• Maintain proper documentation of all laboratory activities.
• Support maintenance, calibration, and qualification of analytical equipment.
• Ensure compliance with GMP, SOPs, and regulatory requirements
• Able to work 12 hours rotating day and night shift, including weekends and public holidays. 
• Support stability testing activities, including:
  • Testing and sample storage management
  • Documentation of analytical results according to cGxP requirements.  

Required Qualifications

• Diploma/Graduate in Biological Sciences, Chemistry or relevant fields. 
• Prior 1 to 2 years experience working in a laboratory environment
• Preferred: Experience in pharmaceutical or quality-controlled environments.
• Familiarity with GMP standards and laboratory documentation practices
• Administrative activities and GMP and HSE-compliant, efficient
  production and documentation of standardized tasks in the
  infrastructure

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.