QC Analytical Chemist (Pharmaceutical)

Job Overview We are seeking a highly motivated and detail-oriented QC Analytical Chemist to join CMIC's quality control team. In this role, you will perform analytical testing of raw materials and finished pharmaceutical products to ensure compliance with internal specifications and global regulatory requirements. This position plays a critical role in maintaining product quality, supporting regulatory compliance, and contributing to continuous improvement initiatives within a cGMP environment. You will work in a collaborative, fast-paced pharmaceutical manufacturing setting focused on delivering safe and effective medicines.

Key Responsibilities:

Analytical Testing Perform analytical testing of raw materials, in-process samples, and finished products (tablets, capsules, and other dosage forms). Utilize a range of analytical techniques including HPLC, UPLC, GC, UV-Vis, FT-IR, dissolution testing, and particle size analysis . Data Analysis & Documentation Independently process, interpret, and report analytical data with a high degree of accuracy. Prepare detailed laboratory reports and maintain complete, compliant documentation in accordance with approved methods and laboratory systems. Ensure data integrity and adherence to ALCOA+ principles. Quality & Compliance Ensure all testing activities comply with cGMP, GLP, FDA, and EMA regulations . Partner with Quality Assurance to ensure product quality and regulatory readiness. Method Support & Troubleshooting Troubleshoot analytical methods and instrumentation issues. Support method validation, transfer, and continuous improvement initiatives as needed. Instrumentation & Laboratory Operations Operate, calibrate, and maintain laboratory equipment to ensure optimal performance. Perform routine maintenance and ensure proper functionality of analytical instruments. Collaboration & Support Collaborate cross-functionally with R&D, Manufacturing, and QA to support product development and production. Provide technical support and guidance to junior team members when required. Qualifications Education Bachelor's degree in Chemistry, Analytical Chemistry, Biochemistry, Biology, or related scientific discipline (required) Experience This role is designed for a mid-level chemist with 3-7 years of hands-on experience in a pharmaceutical quality control laboratory Strong experience with HPLC/UPLC, GC, dissolution, UV-Vis, and FT-IR Technical Skills Solid understanding of cGMP, GLP, and regulatory requirements (FDA/EMA) Experience with analytical data interpretation and laboratory documentation systems (LIMS preferred) Strong troubleshooting skills for analytical methods and instrumentation Core Competencies High attention to detail and strong problem-solving skills Ability to clearly interpret and communicate complex data Strong written and verbal communication skills Ability to work independently and in a team-oriented environment Working Conditions Laboratory-based environment with exposure to chemicals and specialized equipment Ability to stand for extended periods and lift up to 25 lbs. Flexibility to work overtime as needed to meet production and project timelines This job description is not intended to be all-inclusive. Employees may be required to perform other duties as assigned by management.

Pay:

$36.00 - $40.00 per hour

Benefits:

401(k) 401(k) matching Dental insurance Disability insurance Employee assistance program Flexible spending account Health insurance Health savings account Life insurance Paid time off Referral program Vision insurance Application Question(s): Do you have 3-7 years working as a bench Chemist?

Work Location:

In person