Job Title: Quality Control Analyst
Type: Contract
Location: Onsite - CT
Experience: 0–2 Years
Job Summary:
We are seeking a detail-oriented and motivated Entry-Level Quality Control Analyst to support laboratory testing, sample analysis, documentation, and quality activities within a regulated pharmaceutical or life sciences environment. The role will help ensure raw materials, in-process materials, finished products, and laboratory operations meet established quality and regulatory requirements.
Key Responsibilities:
Laboratory Testing: Assist with routine testing and analysis of raw materials, in-process samples, finished products, and stability samples.
Sample Management: Support sample collection, preparation, labeling, tracking, and storage according to approved procedures.
Analytical Testing: Assist with techniques such as HPLC, GC, UV-Vis, FTIR, pH, titration, and dissolution, as applicable.
Documentation Management: Prepare and maintain laboratory worksheets, test records, notebooks, Certificates of Analysis, and other QC documentation.
Data Review: Record, review, and verify analytical data for accuracy, completeness, and compliance.
Instrument Support: Assist with calibration, maintenance, qualification, and troubleshooting of laboratory instruments.
Regulatory Compliance: Ensure QC activities comply with cGMP, FDA, GDP, and applicable laboratory procedures.
Investigation Support: Assist with OOS, OOT, deviations, root-cause analysis, and CAPA activities.
Cross-Functional Collaboration: Work with QA, Manufacturing, Validation, and other laboratory teams to support quality requirements.
Audit Readiness: Maintain accurate and complete laboratory records to support internal and external audits and regulatory inspections.
Required Skills:
Bachelor’s degree in Pharmacy, Chemistry, Biochemistry, Pharmaceutical Sciences, Biotechnology, Microbiology, Life Sciences, or a related field.
Basic understanding of pharmaceutical QC laboratory operations.
Familiarity with analytical testing techniques and laboratory equipment.
Basic knowledge of HPLC, GC, UV-Vis, FTIR, dissolution, pH, and titration is preferred.
Understanding of cGMP, GDP, SOPs, and good laboratory documentation practices.
Basic knowledge of OOS, OOT, deviations, CAPA, and quality investigations.
Strong analytical and problem-solving skills with excellent attention to detail.
Good written and verbal communication skills.
Fresh graduates and candidates with 0–2 years of relevant experience are encouraged to apply.

Quality Control Analyst

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