Quality Control Analytical Chemist

2 weeks ago


Rahway, New Jersey, United States Astrix Inc Full time

Astrix Inc. is a prominent player in the pharmaceutical sector, focused on pioneering drug solutions that enhance patient care. Our commitment to scientific integrity and stringent quality protocols is evident in every facet of our operations.

Position Overview: We are in search of a dedicated Analytical Chemist to become an integral part of our team. The ideal candidate will engage in analytical evaluations to bolster drug product development initiatives. This position encompasses method formulation and verification, analytical assessments for process enhancement, data interpretation, and presenting results to management.

Key Responsibilities:

  • Formulate and verify analytical testing methodologies for novel drug products utilizing techniques such as HPLC, UPLC, UV, IR, Karl Fischer titration, and dissolution assessments.
  • Execute analytical evaluations to support process advancement and guarantee product integrity.
  • Conduct routine examinations of raw materials, intermediates, and finished drug products.
  • Employ Empower software for data management, analysis, and instrument oversight.
  • Resolve issues related to analytical methods and instruments as necessary.
  • Draft precise and comprehensive analytical reports summarizing experimental outcomes.
  • Adhere to GMP and GLP standards throughout all analytical procedures.
  • Collaborate effectively with interdisciplinary teams, including Research & Development, Quality Assurance, and Regulatory Affairs.

Qualifications:

  • Bachelor's degree in chemistry or a related scientific discipline.
  • 2-5 years of experience in analytical chemistry, ideally within the pharmaceutical field.
  • Expertise in a range of analytical techniques including HPLC, UPLC, UV, IR, Karl Fischer titration, and dissolution assessments.
  • Experience in method formulation, verification, and troubleshooting of analytical techniques.
  • Familiarity with Empower software for data management and instrument oversight is advantageous.
  • Strong collaborative and interpersonal abilities.
  • Exceptional written and verbal communication skills.
  • Detail-oriented with a commitment to precision and quality in analytical tasks.
  • Experience in a GMP/GLP environment is beneficial.

This job description outlines the desired qualifications, though not all are mandatory. We encourage candidates with relevant skills to consider this opportunity.



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