• Assist in reviewing and updating standard operating procedures (SOPs)
• Support internal audits and documentation reviews.
• Help maintain quality management systems (QMS) and records.
• Participate in deviation, CAPA (Corrective and Preventive Action), and change control processes.
• Collaborate with cross-functional teams including R&D, Production, and Regulatory Affairs.
• Assist in data collection and report preparation for quality metrics.

What You’ll Gain:

• Insight into pharmaceutical quality systems and regulatory requirements.
• Real-world experience in a fast-paced QA environment.
• Mentorship from experienced quality professionals.
• Opportunity to contribute to meaningful projects that impact patient health.

This is your chance to gain valuable experience while contributing to a team that ensures the highest standards of product quality and safety.

Requirements:

• Qualification in;-
  • Pharmacy,
  • Life Sciences,
  • Chemistry,
  • Or related field.
• Strong attention to detail and organisational skills.
• Basic understanding of GMP, GLP, or other regulatory standards (preferred).
• Proficient in Microsoft Office (Word, Excel, PowerPoint).
• Excellent written and verbal communication skills.
• Ability to work independently and as part of a team.