Job Description
Officer QA – Quality Assurance | Dishman Carbogen Amcis | Ahmedabad, Gujarat, India
Dishman Carbogen Amcis is hiring professionals for the role of Officer QA for its Bavla API plant operations located in Ahmedabad, Gujarat, India. This full-time opportunity is ideal for candidates with 2 to 10 years of experience in pharmaceutical quality assurance, GMP compliance, quality systems, batch documentation review, deviation management, audit preparation, operational compliance, quality investigation activities, CAPA management, and pharmaceutical manufacturing operations. This opening is part of the Bavla API plant walk-in recruitment drive conducted by the organization.
The selected candidate will support quality assurance operations associated with API manufacturing and pharmaceutical compliance systems. Responsibilities include reviewing batch manufacturing and packaging records, monitoring GMP compliance within manufacturing operations, supporting deviation investigations and CAPA implementation, maintaining quality documentation and operational records, coordinating with production and quality control departments for compliance activities, participating in internal audit preparation and inspection readiness, ensuring adherence to pharmaceutical quality standards and SOPs, assisting in quality risk management activities, supporting change control and documentation review systems, and contributing to continuous improvement initiatives related to pharmaceutical quality assurance operations. Candidates should possess strong understanding of GMP regulated pharmaceutical manufacturing environments and quality management systems.
This role offers valuable exposure to API manufacturing operations, pharmaceutical quality systems, compliance management activities, audit preparation workflows, deviation handling systems, and regulated pharmaceutical manufacturing environments within a reputed pharmaceutical organization. Professionals interested in pharmaceutical quality assurance and compliance careers can strengthen their operational and regulatory expertise through this opportunity.
Location
Ahmedabad, Gujarat, India
Employment Type
Full-time
Experience Required
2 to 10
Walk-in Interview Details
Walk-in Date: 2026-05-24
About Dishman Carbogen Amcis
Dishman Carbogen Amcis operates in the pharmaceutical industry specializing in API manufacturing, pharmaceutical quality systems, regulated healthcare products, and compliance-driven operations.
Key Responsibilities
Review batch manufacturing and packaging records.
Monitor GMP compliance and quality systems.
Support deviation investigations and CAPA activities.
Maintain quality assurance documentation and records.
Coordinate with production and QC departments.
Participate in audit preparation and inspection readiness.
Ensure adherence to SOPs and pharmaceutical standards.
Support change control and compliance systems.
Assist in quality risk management activities.
Support continuous improvement in QA operations.
Required Skills
Knowledge of pharmaceutical quality assurance systems.
Understanding of GMP and compliance procedures.
Awareness of API manufacturing operations.
Documentation and operational reporting expertise.
Problem-solving and analytical abilities.
Communication and coordination skills.
Time management and workflow planning.
Attention to compliance accuracy and operational quality.
Adaptability to regulated pharmaceutical environments.
Technical understanding of pharmaceutical quality systems.
Educational Qualification
M.Pharm
Industry
Pharmaceutical
Why Join Dishman Carbogen Amcis?
Dishman Carbogen Amcis offers professionals opportunities to work in regulated API manufacturing environments with exposure to advanced pharmaceutical quality systems and compliance operations.
How to Apply
Interested candidates can attend the walk-in interview and apply through ACKJOBS for this pharmaceutical quality assurance 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 hiring professionals for the role of Officer QA for its Bavla API plant operations located in Ahmedabad, Gujarat, India. This full-time opportunity is ideal for candidates with 2 to 10 years of experience in pharmaceutical quality assurance, GMP compliance, quality systems, batch documentation review, deviation management, audit preparation, operational compliance, quality investigation activities, CAPA management, and pharmaceutical manufacturing operations. This opening is part of the Bavla API plant walk-in recruitment drive conducted by the organization.
The selected candidate will support quality assurance operations associated with API manufacturing and pharmaceutical compliance systems. Responsibilities include reviewing batch manufacturing and packaging records, monitoring GMP compliance within manufacturing operations, supporting deviation investigations and CAPA implementation, maintaining quality documentation and operational records, coordinating with production and quality control departments for compliance activities, participating in internal audit preparation and inspection readiness, ensuring adherence to pharmaceutical quality standards and SOPs, assisting in quality risk management activities, supporting change control and documentation review systems, and contributing to continuous improvement initiatives related to pharmaceutical quality assurance operations. Candidates should possess strong understanding of GMP regulated pharmaceutical manufacturing environments and quality management systems.
This role offers valuable exposure to API manufacturing operations, pharmaceutical quality systems, compliance management activities, audit preparation workflows, deviation handling systems, and regulated pharmaceutical manufacturing environments within a reputed pharmaceutical organization. Professionals interested in pharmaceutical quality assurance and compliance careers can strengthen their operational and regulatory expertise through this opportunity.
Location
Ahmedabad, Gujarat, India
Employment Type
Full-time
Experience Required
2 to 10
Walk-in Interview Details
Walk-in Date: 2026-05-24
About Dishman Carbogen Amcis
Dishman Carbogen Amcis operates in the pharmaceutical industry specializing in API manufacturing, pharmaceutical quality systems, regulated healthcare products, and compliance-driven operations.
Key Responsibilities
Review batch manufacturing and packaging records.
Monitor GMP compliance and quality systems.
Support deviation investigations and CAPA activities.
Maintain quality assurance documentation and records.
Coordinate with production and QC departments.
Participate in audit preparation and inspection readiness.
Ensure adherence to SOPs and pharmaceutical standards.
Support change control and compliance systems.
Assist in quality risk management activities.
Support continuous improvement in QA operations.
Required Skills
Knowledge of pharmaceutical quality assurance systems.
Understanding of GMP and compliance procedures.
Awareness of API manufacturing operations.
Documentation and operational reporting expertise.
Problem-solving and analytical abilities.
Communication and coordination skills.
Time management and workflow planning.
Attention to compliance accuracy and operational quality.
Adaptability to regulated pharmaceutical environments.
Technical understanding of pharmaceutical quality systems.
Educational Qualification
M.Pharm
Industry
Pharmaceutical
Why Join Dishman Carbogen Amcis?
Dishman Carbogen Amcis offers professionals opportunities to work in regulated API manufacturing environments with exposure to advanced pharmaceutical quality systems and compliance operations.
How to Apply
Interested candidates can attend the walk-in interview and apply through ACKJOBS for this pharmaceutical quality assurance 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.