Job Description

SUMMARY

Seeking a skilled QC Chemist to support essential laboratory operations within a regulated environment. This role includes qualitative and quantitative chemical analyses, instrumentation calibration and maintenance, environmental monitoring, and technical documentation. The position offers hands-on experience with a wide range of analytical techniques and equipment, while maintaining strict adherence to GMP/GLP guidelines.

You’ll join a collaborative team where your contributions help maintain product quality and regulatory compliance. This is an excellent opportunity for candidates who want to deepen their technical expertise while supporting pharmaceutical quality initiatives in a growth-focused, science-driven organization.

RESPONSIBILITIES

• Perform chemical and physical testing on raw materials, intermediates, and finished products in accordance with regulatory and internal standards.
• Follow cGMP guidelines, compendial methods, and internal SOPs for all laboratory analyses.
• Prepare reagents, solutions, and standards for use in analytical procedures.
• Operate and troubleshoot lab instruments including HPLC, GC, UV-Vis, IR, Dissolution, Malvern particle size analyzers, Karl Fischer titrators, potentiometers, and auto titrators.
• Ensure proper documentation practices (ALCOA principles) and maintain comprehensive records of analytical activities.
• Carry out investigations under supervision to address lab deviations or non-conformances.
• Maintain lab instruments through routine calibration, qualification, and preventive maintenance activities.
• Prepare and review protocols, test methods, SOPs, and validation reports as assigned.
• Uphold safety and waste management standards; ensure compliance with regulatory and in-house procedures.
• Contribute to training and mentoring of support staff as needed.
• Continuously enhance knowledge through training to meet evolving regulatory and technical requirements.

QUALIFICATIONS

• Education: Bachelor’s or Master’s degree in Chemistry, Biology, Pharmaceuticals, or a closely related discipline.
• Experience: At least 5 years of experience as a QC Chemist in a GMP-compliant laboratory; total 5–6 years of relevant laboratory work.
• Technical Proficiency: Strong hands-on experience with a variety of analytical instruments and techniques.
• Soft Skills: Capable of working independently and in cross-functional teams; able to prioritize multiple projects under tight timelines.
• Workplace Readiness: Comfortable working in a fast-paced lab environment with exposure to chemicals and time-sensitive tasks.
• Analytical Thinking: Ability to perform calculations, maintain accuracy under pressure, and document findings clearly.

What’s in it for You:

Gain exposure to a dynamic quality control environment that emphasizes professional development, compliance, and technical excellence. You'll work with a diverse suite of laboratory technologies and contribute to high-impact pharmaceutical projects. The role also offers potential for cross-training, leadership development, and future career growth within quality assurance and analytical sciences.

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