Job Description
SNJ Lifecare Private Limited is inviting applications for the position of Officer Quality Assurance at its pharmaceutical operations in Rajkot, Gujarat, India. This full-time opportunity is suitable for freshers and professionals with 0 to 1 years of experience in pharmaceutical quality assurance, documentation management, compliance monitoring, batch record review, GMP coordination, process verification, quality systems management, and QA operational support within regulated pharmaceutical manufacturing environments. This opening is specifically for the QA department and candidates interested in pharmaceutical quality systems are encouraged to apply. The selected candidate will support quality assurance operations, maintain QA documentation, assist in compliance monitoring activities, coordinate batch review processes, support GMP implementation activities, participate in internal quality procedures, monitor workflow adherence, and coordinate with production and quality teams to ensure operational and regulatory compliance. Candidates having knowledge of pharmaceutical quality systems, documentation practices, and GMP standards will be preferred. This role offers valuable exposure to pharmaceutical QA systems, compliance operations, documentation workflows, and quality-focused manufacturing environments aimed at maintaining product quality, regulatory adherence, operational efficiency, and professional growth.
Location
Rajkot, Gujarat, India
Employment Type
Full-time
Experience Required
0 to 1
Compensation & Benefits
Competitive salary package with exposure to pharmaceutical quality assurance systems, GMP compliance workflows, and long-term professional development opportunities.
About SNJ Lifecare Private Limited
SNJ Lifecare Private Limited operates in the pharmaceutical industry specializing in healthcare manufacturing, regulated pharmaceutical operations, and quality-driven production systems.
Position Overview
The Officer Quality Assurance will support QA documentation, compliance monitoring activities, and pharmaceutical quality system operations.
Key Responsibilities
Support pharmaceutical quality assurance and compliance activities.
Maintain QA records, batch documentation, and operational reports.
Assist in GMP monitoring and quality system implementation.
Coordinate batch review and documentation verification activities.
Ensure adherence to pharmaceutical quality standards and procedures.
Support internal audits and quality monitoring initiatives.
Participate in quality reviews and compliance discussions.
Monitor workflow timelines and documentation accuracy.
Coordinate with production and QC teams for operational support.
Maintain discipline and efficiency within QA systems.
Required Skills & Competencies
Strong understanding of pharmaceutical quality assurance systems.
Knowledge of GMP standards and compliance workflows.
Documentation and reporting management capabilities.
Communication and coordination management skills.
Attention to operational accuracy and quality standards.
Time management and multitasking capabilities.
Problem-solving and analytical thinking abilities.
Awareness of pharmaceutical manufacturing processes.
Quality monitoring and documentation coordination skills.
Adaptability to regulated pharmaceutical environments.
Educational Qualification
BPharm
About the Industry
The pharmaceutical quality assurance industry depends on strict compliance systems, documentation accuracy, and quality-focused operational workflows to maintain healthcare manufacturing standards and regulatory excellence.
Why Join SNJ Lifecare Private Limited?
SNJ Lifecare Private Limited offers professionals opportunities to work in regulated pharmaceutical environments with exposure to quality assurance systems and GMP operations.
How to Apply
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