QA Officer

JobItUs; Daman; On-site; INR 270,000 - 330,000; Full time

Job summary

JobItUs in Daman is seeking a QA Officer to ensure cGMP/GMP compliance, review quality records, and coordinate validations and audits on the pharma shop floor.

Ideal candidate will have 1–3 years in pharma QA, strong documentation skills, and knowledge of regulatory guidelines. The role involves data integrity, product release support, and QA record maintenance.

Qualifications

• Knowledge of GMP, GLP, ICH, WHO, and regulatory guidelines.
• Experience in documentation review and QMS activities.
• Good understanding of validation, qualification, and audit compliance.
• Strong analytical, communication, and problem-solving skills.

Responsibilities

• Ensure compliance with cGMP, GLP, and regulatory requirements.
• Review and approve BMR, BPR, and analytical reports.
• Handle deviations, change controls, CAPA, OOS, OOT, and risk assessments.
• Conduct line clearance, in-process checks, and shop floor monitoring.
• Review and maintain SOPs, specifications, protocols, and quality documents.
• Coordinate qualification and validation activities (IQ/OQ/PQ, Process Validation, Cleaning Validation).
• Perform internal audits and support regulatory/customer audits.
• Monitor compliance with data integrity and documentation practices.Ensure timely closure of quality-related observations and investigations.
• Support product release activities and maintain QA records.

Skills

GMP/GLP/ICH/WHO

Documentation review

QMS compliance

Validation & Audit

Analytical skills

Communication skills

Problem solving

Education

B.Pharm/M.Pharm/BSc/MSc Chemistry

Job description

Position: QA Officer.

Location: Daman

Experience: 1 - 3 Years

Industries: Pharma

Responsibilities:

• Ensure compliance with cGMP, GLP, and regulatory requirements.
• Review and approve Batch Manufacturing Records (BMR), Batch Packing Records (BPR), and analytical reports.
• Handle deviations, change controls, CAPA, OOS, OOT, and risk assessments.
• Conduct line clearance, in-process checks, and shop floor monitoring.
• Review and maintain SOPs, specifications, protocols, and quality documents.
• Coordinate qualification and validation activities (IQ/OQ/PQ, Process Validation, Cleaning Validation).
• Perform internal audits and support regulatory/customer audits.
• Monitor compliance with data integrity and documentation practices.Ensure timely closure of quality-related observations and investigations.
• Support product release activities and maintain QA records.

Required Skills

• Knowledge of GMP, GLP, ICH, WHO, and regulatory guidelines.
• Experience in documentation review and QMS activities.
• Good understanding of validation, qualification, and audit compliance.
• Strong analytical, communication, and problem-solving skills.

Required Qualification: -B. Pharm/M. Pharm/B.Sc/M.Sc - Chemistry

Salary :- Upto 3.00 LPA