Job Description
Deputy Manager QC – Quality Control | Dishman Carbogen Amcis | Ahmedabad, Gujarat, India
Dishman Carbogen Amcis is inviting applications for the role of Deputy Manager QC for its AMV Bavla quality control operations in Ahmedabad, Gujarat, India. This full-time opportunity is ideal for candidates with 3 to 12 years of experience in pharmaceutical quality control, laboratory management, analytical testing, GMP compliance, documentation systems, QC operations, laboratory coordination, operational reporting, analytical instrument handling, and pharmaceutical compliance workflows.
The selected candidate will support quality control and laboratory operations related to pharmaceutical manufacturing activities. Responsibilities include managing analytical testing workflows and laboratory coordination systems, maintaining QC documentation and operational reports, coordinating with production and quality assurance teams, ensuring adherence to GMP and laboratory procedures, monitoring analytical instrument operations and testing systems, supporting compliance reviews and audit preparation activities, participating in laboratory planning and operational meetings, supervising quality verification and documentation workflows, maintaining operational standards and laboratory efficiency systems, and contributing to continuous improvement initiatives related to quality control operations. Candidates should possess strong understanding of pharmaceutical QC systems and analytical workflows.
This role provides valuable exposure to pharmaceutical laboratory systems, quality control management workflows, analytical testing operations, GMP compliance activities, laboratory coordination systems, and regulated pharmaceutical environments within a reputed pharmaceutical organization. Professionals interested in laboratory operations and quality management can strengthen their technical and leadership expertise through this opportunity.
Location
Ahmedabad, Gujarat, India
Employment Type
Full-time
Experience Required
3 to 12
About Dishman Carbogen Amcis
Dishman Carbogen Amcis operates in the pharmaceutical industry specializing in manufacturing systems, quality management operations, laboratory workflows, and healthcare product development activities.
Key Responsibilities
Manage pharmaceutical quality control operations.
Coordinate analytical testing and laboratory workflows.
Maintain QC documentation and operational reports.
Ensure adherence to GMP and laboratory procedures.
Coordinate with production and QA departments.
Monitor analytical instrument and testing systems.
Participate in audit preparation and compliance activities.
Support laboratory planning and workflow coordination.
Maintain operational standards and laboratory efficiency.
Support continuous improvement in QC systems.
Required Skills
Strong understanding of pharmaceutical QC systems.
Knowledge of laboratory operations and analytical 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.
Leadership and team coordination expertise.
Adaptability to regulated pharmaceutical environments.
Educational Qualification
M.Pharm
Industry
Pharmaceutical
Why Join Dishman Carbogen Amcis?
Dishman Carbogen Amcis offers professionals opportunities to work on advanced pharmaceutical laboratory systems and quality management operations within a regulated manufacturing environment.
Walk-in Interview Details
Walk-in interviews are scheduled for 2026-05-24 for candidates interested in QC and laboratory management opportunities.
How to Apply
Interested candidates can apply through ACKJOBS and participate in the walk-in recruitment process for this quality control opportunity.
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.
Dishman Carbogen Amcis is inviting applications for the role of Deputy Manager QC for its AMV Bavla quality control operations in Ahmedabad, Gujarat, India. This full-time opportunity is ideal for candidates with 3 to 12 years of experience in pharmaceutical quality control, laboratory management, analytical testing, GMP compliance, documentation systems, QC operations, laboratory coordination, operational reporting, analytical instrument handling, and pharmaceutical compliance workflows.
The selected candidate will support quality control and laboratory operations related to pharmaceutical manufacturing activities. Responsibilities include managing analytical testing workflows and laboratory coordination systems, maintaining QC documentation and operational reports, coordinating with production and quality assurance teams, ensuring adherence to GMP and laboratory procedures, monitoring analytical instrument operations and testing systems, supporting compliance reviews and audit preparation activities, participating in laboratory planning and operational meetings, supervising quality verification and documentation workflows, maintaining operational standards and laboratory efficiency systems, and contributing to continuous improvement initiatives related to quality control operations. Candidates should possess strong understanding of pharmaceutical QC systems and analytical workflows.
This role provides valuable exposure to pharmaceutical laboratory systems, quality control management workflows, analytical testing operations, GMP compliance activities, laboratory coordination systems, and regulated pharmaceutical environments within a reputed pharmaceutical organization. Professionals interested in laboratory operations and quality management can strengthen their technical and leadership expertise through this opportunity.
Location
Ahmedabad, Gujarat, India
Employment Type
Full-time
Experience Required
3 to 12
About Dishman Carbogen Amcis
Dishman Carbogen Amcis operates in the pharmaceutical industry specializing in manufacturing systems, quality management operations, laboratory workflows, and healthcare product development activities.
Key Responsibilities
Manage pharmaceutical quality control operations.
Coordinate analytical testing and laboratory workflows.
Maintain QC documentation and operational reports.
Ensure adherence to GMP and laboratory procedures.
Coordinate with production and QA departments.
Monitor analytical instrument and testing systems.
Participate in audit preparation and compliance activities.
Support laboratory planning and workflow coordination.
Maintain operational standards and laboratory efficiency.
Support continuous improvement in QC systems.
Required Skills
Strong understanding of pharmaceutical QC systems.
Knowledge of laboratory operations and analytical 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.
Leadership and team coordination expertise.
Adaptability to regulated pharmaceutical environments.
Educational Qualification
M.Pharm
Industry
Pharmaceutical
Why Join Dishman Carbogen Amcis?
Dishman Carbogen Amcis offers professionals opportunities to work on advanced pharmaceutical laboratory systems and quality management operations within a regulated manufacturing environment.
Walk-in Interview Details
Walk-in interviews are scheduled for 2026-05-24 for candidates interested in QC and laboratory management opportunities.
How to Apply
Interested candidates can apply through ACKJOBS and participate in the walk-in recruitment process for this quality control opportunity.
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.