Key Responsibilities:

• Conduct tests and analyze  pharmaceutical products/ Raw Materials/Packaging Materials
• Document and report test results and deviations.
• Collaborate with cross-functional teams to ensure quality assurance.
• Maintain compliance with quality standards and regulatory requirements.
• Help keep the QC laboratory organized and efficient.
• Overseeing processes, testing materials, and products, and maintaining records of quality assurance activities.
• Ensuring manufacturing processes follow standard operating procedures.
• Reviewing batch manufacturing and packing records to ensure products are properly packed and labeled.
• Inspecting, sampling, and testing starting materials, intermediate products, and finished products according to defined Standard Operating Procedures (SOPs).
• Involvement in the preparation of documents to meet in-house and regulatory requirements.
• Performing department activities as assigned by the immediate supervisor.

Qualifications:

• Bachelor's Degree in Pharmacy (Master's preferred).
• Minimum 1-2 years of experience in a relevant field.
• Proficiency in analytical techniques and laboratory equipment.
• Strong attention to detail and effective problem-solving skills.
• Familiarity with pharmaceutical quality standards (WHO-GMP, GLP, ISO etc.).
• Excellent communication and teamwork skills.
• NPC Registration.

Source: Merojob

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