Job Description

We are seeking a QC Chemist to join our growing team. The QC Chemist performs routine and non-routine chemical analyses of raw materials, in-process samples, and finished products to ensure product quality and regulatory compliance. This role supports production troubleshooting, laboratory operations, and continuous improvement activities within the Quality Control function.

Primary Responsibilities

• Perform qualitative and quantitative chemical analysis using techniques such as GC-MS, LC, FTIR, UV-Vis, Rheology, Particle Size Analysis, Spectrophotometry, titration, wet chemistry, and basic microbiological testing.
• Conduct method validations, verifications, and transfers as assigned.
• Execute testing of raw materials, intermediates, finished goods, and stability samples according to established methods, SOPs, and regulatory requirements.
• Review, interpret, and document analytical data clearly and accurately in laboratory notebooks and electronic data systems.
• Support investigations of OOS (Out-of-Specification) and OOT (Out-of-Trend) results, including root cause analysis and CAPA activities.
• Make material disposition decisions (Approve / Reject / Rework) based on analytical results.
• Calibrate and maintain laboratory equipment in alignment with internal procedures.
• Ensure testing activities adhere to cGMP, GLP, and applicable quality standards.
• Train and mentor junior laboratory staff as required.
• Assist in preparing for internal and external audits, providing data and documentation.
• Support preparation and revision of SOPs, test methods, and laboratory records.
• Maintain a safe, organized, and compliant laboratory environment.
• Perform additional related duties as needed.

Minimum Requirements

• 4–5+ years of experience in a Quality Control or Analytical Laboratory environment (required).
• Bachelor’s degree in Chemistry, Biochemistry, or related scientific field (required); Master’s degree preferred.
• Experience in cGMP-regulated manufacturing environments (cosmetics, pharmaceuticals, chemicals, food science, or nutraceuticals).
• Solid understanding of cGMP, GLP, and regulatory documentation standards.
• Experience with LIMS or other electronic laboratory data systems (preferred).

Knowledge, Skills, & Abilities

• Strong analytical, problem-solving, and troubleshooting skills.
• Excellent documentation accuracy and attention to detail.
• Clear written and verbal communication skills.
• Ability to prioritize and manage multiple tasks in a fast-paced environment.
• Collaborative work style with strong interpersonal skills.
• Proficiency in Microsoft Office (Excel, Word, Outlook, Teams) and general data analysis.

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