GC Analyst

Rhydburg Pharmaceuticals Ltd. is hiring professionals for the role of GC Analyst for its pharmaceutical quality control and laboratory operations located in Selaqui, Uttarakhand, India. This full-time opportunity is ideal for candidates with 3 to 5 years of experience in gas chromatography analysis, laboratory operations, analytical testing workflows, GMP compliance systems, documentation management workflows, reporting systems, and regulated pharmaceutical environments.

The selected candidate will support laboratory and analytical coordination activities associated with pharmaceutical manufacturing systems and quality workflows. Responsibilities include conducting GC analysis and laboratory testing activities, maintaining analytical records and technical documentation, coordinating with QA and production teams for operational support activities, monitoring laboratory systems and analytical workflows, ensuring adherence to GMP procedures and quality standards, preparing analytical reports and operational documentation, assisting in troubleshooting and laboratory coordination workflows, participating in audit review and compliance activities, supporting laboratory management systems, and maintaining continuous improvement of laboratory operations and analytical efficiency.

This role offers valuable exposure to pharmaceutical laboratory systems, analytical workflows, compliance coordination activities, technical documentation systems, testing operations, and regulated pharmaceutical environments within a reputed organization. Professionals interested in analytical quality control careers can strengthen their technical and operational expertise through this opportunity.

Location

Selaqui, Uttarakhand, India

Employment Type

Full-time

Salary

Best in Industry

Experience Required

3 to 5 Years

About Rhydburg Pharmaceuticals Ltd.

Rhydburg Pharmaceuticals Ltd. operates in the pharmaceutical industry specializing in pharmaceutical manufacturing systems, analytical workflows, compliance coordination activities, and healthcare product operations.

Key Responsibilities

• Conduct GC analysis and laboratory testing activities.
• Monitor analytical workflows and laboratory systems.
• Maintain analytical records and technical documentation.
• Coordinate with QA and production teams.
• Ensure adherence to GMP procedures and quality standards.
• Prepare analytical reports and operational documentation.
• Support troubleshooting and laboratory coordination workflows.
• Participate in audit review and compliance activities.
• Assist in instrument calibration and analytical activities.
• Support continuous improvement of laboratory systems.

Required Skills

• Strong knowledge of GC analysis and laboratory operations.
• Understanding of analytical workflows and GMP systems.
• Knowledge of analytical testing and compliance activities.
• Experience in laboratory documentation and reporting systems.
• Good analytical and problem-solving abilities.
• Strong communication and teamwork skills.
• Knowledge of SOP procedures and pharmaceutical standards.
• Ability to manage laboratory schedules and workflows.
• Attention to analytical accuracy and compliance standards.
• Adaptability to regulated pharmaceutical environments.

Educational Qualification

B.Pharma

Industry

Pharmaceutical

Why Join Rhydburg Pharmaceuticals Ltd.?

Rhydburg Pharmaceuticals Ltd. offers professionals opportunities to work in advanced pharmaceutical environments with exposure to laboratory systems, analytical workflows, operational coordination activities, and healthcare manufacturing operations.