Assist in reviewing and updating standard operating procedures (SOPs)oSupport internal audits and documentation reviews.oHelp maintain quality management systems (QMS) and records.oParticipate in deviation, CAPA (Corrective and Preventive Action), and change control processes.oCollaborate with cross-functional teams including R&D, Production, and Regulatory Affairs.oAssist in data collection and report preparation for quality metrics.
What You'll Gain:
Insight into pharmaceutical quality systems and regulatory requirements.oReal-world experience in a fast-paced QA environment.oMentorship from experienced quality professionals.oOpportunity 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. Qualifications:
Qualification in Pharmacy, Life Sciences, Chemistry, or related field.oStrong attention to detail and organizational skills.oBasic understanding of GMP, GLP, or other regulatory standards (preferred).oProficient in Microsoft Office (Word, Excel, PowerPoint).oExcellent written and verbal communication skills.Ability to work independently and as part of a team