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Job Summary:
We are seeking a motivated and detail-oriented Quality Control Analyst to join a fast-paced pharmaceutical manufacturing environment. In this role, you will be responsible for performing routine analytical testing on drug products to ensure quality and compliance with regulatory standards. This position is ideal for someone with a strong foundation in analytical chemistry who thrives in a collaborative and dynamic team setting.

Key Responsibilities:

• Perform qualitative and quantitative testing on raw materials, in-process, and finished products using analytical techniques such as HPLC, UV-Vis, and wet chemistry methods.

• Conduct stability testing to support shelf-life and regulatory requirements.

• Maintain accurate and detailed records of analytical data and observations in compliance with cGMP and internal SOPs.

• Evaluate test results and escalate discrepancies or deviations to supervisors as needed.

• Collaborate with cross-functional teams, including Manufacturing, Production, and R&D, to support continuous quality improvement.

• Assist in troubleshooting analytical instruments and investigating non-conformances.

• Ensure compliance with all safety protocols and quality standards.

Qualifications:

• Bachelor's degree in Chemistry, Biochemistry, Pharmaceutical Sciences, or a related field.

• Minimum of 1 year of laboratory experience beyond academic training, preferably in a pharmaceutical or GMP-regulated environment.

• Familiarity with laboratory instrumentation (HPLC, UV, IR, GC, etc.) and wet chemistry techniques.

• Strong attention to detail, organizational skills, and the ability to work independently or as part of a team.

• Effective written and verbal communication skills.

• Proficient in Microsoft Office and electronic data management systems.

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