Key Responsibilities:

Perform routine and non-routine analysis of raw materials, in-process samples, and finished products using various analytical techniques (HPLC, GC, UV-Vis, etc.)
Conduct physical and chemical testing of samples to ensure compliance with specifications and regulations
Prepare and maintain accurate records of all testing results and communicate any deviations or issues to the appropriate departments
Troubleshoot and resolve any technical issues related to analytical methods or instrumentation
Conduct stability studies to evaluate the shelf-life of products and recommend appropriate storage conditions
Assist in method development and validation studies to ensure accuracy and precision of analytical methods
Participate in quality audits and inspections to ensure compliance with cGMP and other regulatory requirements
Collaborate with cross-functional teams to investigate and resolve quality issues and implement corrective and preventive actions
Continuously monitor and improve the quality control processes to enhance efficiency and effectiveness

Qualifications:

Bachelor's or Master's degree in Chemistry, Biochemistry, or related field
Minimum of 3 years of experience in a quality control role in the pharmaceutical, biotech, or related industry
Strong knowledge of analytical techniques such as HPLC, GC, UV-Vis, and wet chemistry
Experience with method development and validation is preferred
Working knowledge of cGMP regulations and guidelines
Excellent communication and interpersonal skills to effectively collaborate with cross-functional teams
Detail-oriented with strong organizational and problem-solving skills
Ability to work independently in a fast-paced environment and prioritize tasks effectively
Proficient in using Microsoft Office and other relevant software applications

We look forward to receiving your application and learning more about you.

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