Pharmaceutical Quality Control Analyst - Method Development & Validation Specialist

Position SummaryThis role is vital for conducting routine and complex testing of in-process samples and final products. You will work in alignment with SOPs and pertinent procedures related to method development, qualification, validation, method transfer, product release, stability, process validation, and investigations.ResponsibilitiesPerform laboratory assays to support method development, qualification, validation, method transfer, product release, stability, and process validation and investigations.Maintain complex laboratory equipment.Review data for adherence to procedures and specifications.Calculate and evaluate results.Make detailed observations in support of Alert, Action, and OOS result investigations.Participate in writing and revising SOPs.Assist in the qualification of new controls, standards, and reagents.Demonstrate an understanding of and work in compliance with CGMPs.Practice safe work habits while adhering to safety procedures and guidelines.Actively engage in problem-solving meetings with senior staff members to propose process improvements.Work independently under supervision and direction.Basic QualificationsBachelor's degree or equivalent and 2+ years of laboratory experience.Master's degree or equivalent with 0-1 year of experience.Basic knowledge (1-2 years experience) in relevant method platforms (e.g. Bioburden, TOC, Endotoxin, Water Chemistry, ELISA).Attention to detail with the ability to maintain accurate records and excellent proofreading skills.Effective communication skills.Ability to work independently and collaboratively as part of a team.Proficiency in Microsoft Office tools such as Word, Excel, and PowerPoint.Employment Type: Contractor