🔬 Ensure Quality & Compliance in Pharmaceutical Manufacturing
Job Description Summary
This role is responsible for establishing and ensuring the testing of drug substance release, stability testing, and in-process control samples in accordance with written SOPs and local/international regulations. You will maintain high standards of cGxP compliance and data integrity while supporting laboratory operations and sample management.
đź“‹ Job Description
Key Responsibilities:
- Sample storage and management for API, drug substance, drug product, finished products, complaints, stability, and packaging materials.
- Perform analytical testing and documentation following validated methods and SOPs.
- Ensure all activities comply with cGxP standards and data integrity requirements.
- Support stability testing programs, including sample storage, testing, and documentation.
- Detect and report potential accidents, risks, and propose solutions.
- Conduct administrative and documentation activities in a GMP and HSE-compliant manner.
- Operate and maintain laboratory equipment with accuracy and care.
👤 Essential Requirements:
- Preferred: Previous experience in a pharmaceutical laboratory environment (quality assurance, production) with knowledge of aseptic techniques.
- Ability to perform standardized tasks in compliance with GMP and HSE standards.
- Competencies in:Â Breakthrough Analysis, Being Resilient, Operational Excellence, Continuous Learning, Digital & Tech Savvy.
- Knowledge of laboratory equipment, QC testing, QC sampling, TQM, and GxP standards.
- Willingness to work in shifts.
🌟 Desirable Requirements:
- University degree in Pharmacy, Chemistry, or equivalent.
- 0–4 years of relevant working experience in a pharmaceutical or analytical laboratory.
🔧 Skills Desired:
- Continued Learning, Dealing With Ambiguity, Decision Making, GxP, Industry Standards, Laboratory Equipment, Laboratory Excellence, Quality Control Testing, Quality Control Sampling, Self-Awareness, Technological Expertise, Total Quality Management.
đź’Ľ Why Join This Role?
- Foundational Impact: Play a critical role in ensuring the quality and stability of life-saving pharmaceuticals.
- Structured Training: Gain hands-on experience in GMP, analytical methods, and quality systems.
- Career Growth: Pathway to Senior QC Analyst, Specialist, or Laboratory Supervisor roles.
- Dynamic Environment: Work in a state-of-the-art pharmaceutical laboratory with advanced instrumentation.
- Team Culture: Join a collaborative, compliance-focused team dedicated to quality and patient safety.
⚗️ Ready to Launch Your Career in Pharmaceutical Quality Control?
👉 Apply Now for the QC Analyst Position.
We are an equal opportunity employer committed to quality, safety, and diversity in the workplace.
