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SalaryAre you passionate about ensuring the safety and efficacy of pharmaceutical products? Do you thrive in a dynamic environment where precision and attention to detail are paramount? If so, we have an exciting opportunity for you!
Role Overview:
As a Quality Control Analyst, you will play a pivotal role in our commitment to quality assurance. You will be responsible for performing various analytical tests and assays on pharmaceutical products to ensure compliance with regulatory standards and internal specifications. Your meticulous analysis will contribute directly to the safety and efficacy of our products, impacting the health and well-being of countless individuals.
Key Responsibilities:
- Conducting analytical testing of raw materials, in-process samples, and finished products using a variety of techniques such as HPLC, GC, FTIR, UV-Vis spectroscopy, and dissolution testing.
- Executing method validation, verification, and transfer protocols to ensure accuracy and reliability of test results.
- Documenting test procedures, results, and observations accurately and in compliance with regulatory requirements.
- Investigating and resolving deviations, out-of-specification results, and other quality issues in a timely manner.
- Collaborating cross-functionally with other departments including Manufacturing, Quality Assurance, and Research & Development to support continuous improvement initiatives and resolve quality-related issues.
Qualifications and Skills:
- Bachelor’s degree in Chemistry, Biochemistry, Pharmaceutical Sciences, or related field.
- Previous experience in a pharmaceutical or biotechnology laboratory setting preferred.
- Proficiency in analytical techniques such as HPLC, GC, FTIR, and UV-Vis spectroscopy.
- Strong understanding of cGMP regulations and industry standards.
- Excellent attention to detail and organizational skills.
- Effective communication skills and ability to work both independently and collaboratively in a team environment.
