QC Sr. Executive

Asence Pharma is hiring experienced professionals for the role of QC Sr. Executive for its pharmaceutical quality control operations in Ranoli, Vadodara, Gujarat, India. This full-time opportunity is suitable for candidates with 5 to 8 years of experience in pharmaceutical quality control, analytical laboratory operations, GMP compliance, quality systems management, analytical testing, documentation control, laboratory coordination, compliance verification, operational quality workflows, and pharmaceutical manufacturing quality systems.

The selected candidate will support quality control and laboratory management activities related to pharmaceutical manufacturing operations. Responsibilities include conducting analytical testing and laboratory quality workflows, ensuring adherence to GMP and pharmaceutical compliance standards, maintaining laboratory documentation and operational records, coordinating with production and quality assurance teams, supporting quality audits and compliance verification activities, monitoring analytical instruments and laboratory process systems, participating in operational review meetings and quality coordination discussions, assisting in troubleshooting and corrective action implementation, supporting workflow management and quality reporting activities, and contributing to continuous improvement initiatives related to pharmaceutical quality systems. Candidates should possess strong understanding of pharmaceutical laboratory systems and analytical quality workflows.

This opportunity provides valuable exposure to pharmaceutical laboratory systems, analytical quality workflows, GMP operations, compliance management systems, laboratory coordination activities, and modern pharmaceutical manufacturing environments within a reputed pharmaceutical organization. Professionals interested in pharmaceutical quality control and laboratory operations can strengthen their technical and operational expertise through this opportunity.

Location

Ranoli, Vadodara, Gujarat, India

Employment Type

Full-time

Experience Required

5 to 8

About Asence Pharma

Asence Pharma operates in the pharmaceutical industry specializing in pharmaceutical manufacturing systems, analytical laboratory operations, healthcare product development, and quality-focused pharmaceutical solutions.

Key Responsibilities

• Conduct analytical testing and laboratory quality workflows.
• Ensure adherence to GMP and compliance standards.
• Maintain laboratory documentation and operational records.
• Coordinate with production and quality assurance teams.
• Support quality audits and compliance verification.
• Monitor analytical instruments and laboratory systems.
• Participate in quality review and coordination meetings.
• Assist in troubleshooting and corrective actions.
• Support workflow management and quality reporting.
• Contribute to continuous improvement in QC systems.

Required Skills

• Strong understanding of pharmaceutical QC systems.
• Knowledge of analytical laboratory workflows.
• Awareness of GMP and compliance procedures.
• Communication and coordination management expertise.
• Problem-solving and analytical thinking abilities.
• Documentation and laboratory reporting skills.
• Time management and workflow planning capabilities.
• Attention to operational accuracy and compliance.
• Team coordination and multitasking expertise.
• Adaptability to pharmaceutical manufacturing environments.

Educational Qualification

M.Sc Chemistry / Analytical Chemistry / B.Pharm / M.Pharm

Industry

Pharmaceutical

Why Join Asence Pharma?

Asence Pharma offers professionals opportunities to work in advanced pharmaceutical manufacturing environments with exposure to analytical laboratory systems and modern quality management practices.