QC Chemist

Harba; Indianapolis (IN); On-site; USD 55,000 - 85,000; Full time

Job summary

Harba in Indianapolis is seeking a QC Chemist to perform routine analyses (HPLC, GC, UV-Vis, FTIR) and stability testing under cGMP.

You will prepare reagents, document results, review data, calibrate equipment, and support investigations into OOS/OOT, SOP development, and product release with R&D, Manufacturing, QA.

Qualifications include a BSc/MSc in Chemistry, 2–3 years in pharma QC, instrument experience, knowledge of USP/ICH, and strong attention to detail.

Qualifications

• Bachelor’s or Master’s degree in Chemistry, Biochemistry, or a related field.
• 2–3 years of relevant QC laboratory experience in the pharmaceutical industry.
• Hands-on experience with analytical instruments (HPLC, GC, UV-Vis, FTIR).
• Knowledge of USP/NF monographs and regulatory guidelines (FDA, cGMP, ICH).
• Strong analytical thinking and problem-solving skills; attention to detail.

Responsibilities

• Perform routine chemical analyses using HPLC, GC, UV-Vis, FTIR, titration and other methods.
• Conduct stability testing and method validation per ICH guidelines.
• Prepare and standardize laboratory reagents and solutions.
• Document test results per cGMP and GDP.
• Review and interpret analytical data for trends or deviations.

Skills

Analytical thinking

Attention to detail

Time management

Education

Bachelor’s degree in Chemistry, Biochemistry, or related field

Master’s degree (optional)

Tools

HPLC

GC

UV-Vis

FTIR

Titration

LIMS

Job description

Job Responsibilities:

• Perform routine chemical analyses using HPLC, GC, UV-Vis, FTIR, titration, and other analytical techniques.


• Conduct stability testing and method validations according to ICH guidelines.


• Prepare and standardize laboratory reagents and solutions.


• Accurately document test results in accordance with cGMP requirements and Good Documentation Practices (GDP).


• Review and interpret analytical data, identifying trends or deviations.


• Maintain, calibrate, and troubleshoot laboratory equipment as needed.


• Participate in investigations related to out-of-specification (OOS) or out-of-trend (OOT) results.


• Assist in the development and revision of SOPs, test methods, and validation protocols.


• Ensure compliance with all applicable regulatory and safety standards (FDA, USP, ICH, etc.).


• Collaborate with other departments such as R&D, Manufacturing, and Quality Assurance to support product release and continuous improvement initiatives.

Qualifications:

• Bachelor’s or Master’s degree in Chemistry, Biochemistry, or a related field.


• 2–3 years of relevant experience in a QC laboratory within the pharmaceutical industry.


• Hands-on experience with analytical instruments (e.g., HPLC, GC, UV-Vis, FTIR).


• Knowledge of USP/NF monographs and pharmaceutical regulatory guidelines (FDA, cGMP, ICH).


• Strong analytical thinking, problem-solving skills, and attention to detail.


• Excellent organizational and time-management abilities.


• Proficient in Microsoft Office and Laboratory Information Management Systems (LIMS) is a plus.