Job Description
Quality Manager – Quality Assurance | Biorad Medisys | Vemgal Industrial Area, Kolar, Karnataka, India
Biorad Medisys is hiring experienced professionals for the role of Quality Manager for its pharmaceutical quality assurance operations in Vemgal Industrial Area, Kolar, Karnataka, India. This full-time opportunity is suitable for candidates with 15 years of experience in pharmaceutical quality assurance, quality systems management, GMP compliance, quality audits, documentation control, compliance verification, quality process monitoring, team coordination, operational quality management, and pharmaceutical manufacturing quality systems.
The selected candidate will support quality assurance and compliance management activities related to pharmaceutical manufacturing operations. Responsibilities include managing quality assurance systems and operational workflows, monitoring compliance with GMP and pharmaceutical quality standards, maintaining quality documentation and operational records, coordinating with production and laboratory departments, supporting quality audits and compliance verification activities, monitoring quality management systems and operational performance workflows, participating in management review meetings and quality coordination discussions, assisting in issue resolution and corrective action implementation, supporting workflow management and quality reporting activities, and contributing to continuous improvement initiatives related to pharmaceutical quality assurance systems. Candidates should possess strong understanding of pharmaceutical quality workflows and compliance management operations.
This opportunity provides valuable exposure to pharmaceutical quality systems, GMP workflows, compliance management operations, quality reporting activities, operational quality coordination systems, and large-scale pharmaceutical manufacturing environments within a reputed pharmaceutical organization. Professionals interested in pharmaceutical quality assurance and operational management can strengthen their technical and operational expertise through this opportunity.
Location
Vemgal Industrial Area, Kolar, Karnataka, India
Employment Type
Full-time
Experience Required
15
About Biorad Medisys
Biorad Medisys operates in the pharmaceutical industry specializing in healthcare product development, pharmaceutical manufacturing systems, quality management operations, and compliance management activities.
Key Responsibilities
Manage quality assurance systems and operational workflows.
Monitor compliance with GMP and pharmaceutical standards.
Maintain quality documentation and operational records.
Coordinate with production and laboratory departments.
Support quality audits and compliance verification activities.
Monitor quality systems and operational workflows.
Participate in quality review and coordination meetings.
Assist in issue resolution and corrective actions.
Support workflow management and quality reporting.
Contribute to continuous improvement in QA systems.
Required Skills
Strong understanding of pharmaceutical QA systems.
Knowledge of GMP and compliance management workflows.
Awareness of quality audits and documentation procedures.
Communication and coordination management expertise.
Problem-solving and analytical thinking abilities.
Documentation and quality 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
BE / MSc
Industry
Pharmaceutical
Why Join Biorad Medisys?
Biorad Medisys offers professionals opportunities to work in advanced pharmaceutical manufacturing environments with exposure to modern quality management systems and operational excellence practices.
How to Apply
Candidates need to register on our portal to apply for this opportunity. Already registered candidates can directly login and apply.
Check our website — www.ackjobs.com — regularly for the latest updates in the job market. Join our WhatsApp and social media groups from the website.
Biorad Medisys is hiring experienced professionals for the role of Quality Manager for its pharmaceutical quality assurance operations in Vemgal Industrial Area, Kolar, Karnataka, India. This full-time opportunity is suitable for candidates with 15 years of experience in pharmaceutical quality assurance, quality systems management, GMP compliance, quality audits, documentation control, compliance verification, quality process monitoring, team coordination, operational quality management, and pharmaceutical manufacturing quality systems.
The selected candidate will support quality assurance and compliance management activities related to pharmaceutical manufacturing operations. Responsibilities include managing quality assurance systems and operational workflows, monitoring compliance with GMP and pharmaceutical quality standards, maintaining quality documentation and operational records, coordinating with production and laboratory departments, supporting quality audits and compliance verification activities, monitoring quality management systems and operational performance workflows, participating in management review meetings and quality coordination discussions, assisting in issue resolution and corrective action implementation, supporting workflow management and quality reporting activities, and contributing to continuous improvement initiatives related to pharmaceutical quality assurance systems. Candidates should possess strong understanding of pharmaceutical quality workflows and compliance management operations.
This opportunity provides valuable exposure to pharmaceutical quality systems, GMP workflows, compliance management operations, quality reporting activities, operational quality coordination systems, and large-scale pharmaceutical manufacturing environments within a reputed pharmaceutical organization. Professionals interested in pharmaceutical quality assurance and operational management can strengthen their technical and operational expertise through this opportunity.
Location
Vemgal Industrial Area, Kolar, Karnataka, India
Employment Type
Full-time
Experience Required
15
About Biorad Medisys
Biorad Medisys operates in the pharmaceutical industry specializing in healthcare product development, pharmaceutical manufacturing systems, quality management operations, and compliance management activities.
Key Responsibilities
Manage quality assurance systems and operational workflows.
Monitor compliance with GMP and pharmaceutical standards.
Maintain quality documentation and operational records.
Coordinate with production and laboratory departments.
Support quality audits and compliance verification activities.
Monitor quality systems and operational workflows.
Participate in quality review and coordination meetings.
Assist in issue resolution and corrective actions.
Support workflow management and quality reporting.
Contribute to continuous improvement in QA systems.
Required Skills
Strong understanding of pharmaceutical QA systems.
Knowledge of GMP and compliance management workflows.
Awareness of quality audits and documentation procedures.
Communication and coordination management expertise.
Problem-solving and analytical thinking abilities.
Documentation and quality 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
BE / MSc
Industry
Pharmaceutical
Why Join Biorad Medisys?
Biorad Medisys offers professionals opportunities to work in advanced pharmaceutical manufacturing environments with exposure to modern quality management systems and operational excellence practices.
How to Apply
Candidates need to register on our portal to apply for this opportunity. Already registered candidates can directly login and apply.
Check our website — www.ackjobs.com — regularly for the latest updates in the job market. Join our WhatsApp and social media groups from the website.