Chemist - II

The Chemist II will perform analytical testing, method validation, and data documentation in support of pharmaceutical development and research activities. This role involves chromatographic analysis using UPLC and HPLC techniques, technical problem-solving, and collaboration with cross-functional teams. The ideal candidate will demonstrate strong analytical skills, attention to detail, and the ability to manage multiple projects in a dynamic environment.

Key Responsibilities

• Perform analytical testing (release and stability) of drug products following SOPs and cGMP guidelines.
• Execute and document chromatographic analyses using UPLC and HPLC techniques.
• Plan and perform validation of analytical methods and adapt or develop methods as needed.
• Solve complex analytical problems with guidance from senior scientists.
• Troubleshoot analytical instrumentation and investigate new analytical technologies as needed.
• Document experimental results in Electronic Laboratory Notebooks (ELN) and RLIMS systems; perform second chemist review of data.
• Author analytical reports, standard operating procedures (SOPs), and related technical documentation.
• Maintain compliance with company standards and regulatory requirements related to safety, accuracy, and data integrity.
• Provide analytical support to research and development projects within the Analytical Sciences department.

Skills & Qualifications
Required:

• Bachelor’s degree in Chemistry, Pharmaceutical Sciences, Life Sciences, or equivalent, with 4–8 years of relevant experience; or a Master’s degree with 1–2 years of experience.
• Experience in chromatographic analysis (UPLC/HPLC) and related analytical techniques.
• Demonstrated experience working with SOPs, cGMP analytical testing, and technical problem-solving.
• Strong oral and written communication skills with high attention to detail.
• Excellent organizational skills with the ability to manage multiple projects simultaneously.
• Ability to work independently and collaboratively within a team environment.
• Self-motivated, adaptable, and demonstrates a positive attitude toward learning and innovation.

Desired:

• Experience with Empower chromatographic data software and analysis of oral solid dosage forms.
• Familiarity with dissolution testing, water activity, and Karl Fischer titration.
• Previous experience authoring analytical reports and SOPs in a regulated environment.
• Strong understanding of analytical method validation principles.

Education:

• B.S. in Chemistry, Pharmaceutical Sciences, or related Life Science discipline with 4–8 years of relevant experience;
• or M.S. degree with 1–2 years of experience.