Job Description
AM QA / QC – QA/QC | Cadila Pharmaceuticals | Dahej, Gujarat, India
Cadila Pharmaceuticals is inviting experienced pharmaceutical professionals for the role of AM QA / QC at its Dahej, Gujarat manufacturing facility. This full-time walk-in opportunity is ideal for candidates with 7 to 10 years of experience in pharmaceutical quality assurance, quality control operations, laboratory compliance, analytical review systems, HPLC analysis, GC analysis, microbiology review, GMP documentation, regulatory compliance, quality management systems, and pharmaceutical manufacturing support activities. Professionals with expertise in HPLC, GC Reviewer, and Microbiology functions are encouraged to attend the walk-in interview.
The selected candidate will be responsible for managing pharmaceutical QA and QC activities while ensuring adherence to GMP standards, regulatory guidelines, and operational quality systems. Responsibilities include reviewing analytical reports generated through HPLC and GC systems, monitoring laboratory operations and testing activities, supervising microbiology review functions, ensuring proper documentation and compliance management, coordinating with production and regulatory teams, maintaining laboratory records and validation documentation, supporting audit preparation and inspection readiness, handling deviation investigations and CAPA implementation activities, monitoring analytical workflow systems, ensuring adherence to SOPs and quality standards, and contributing to continuous improvement initiatives related to laboratory operations and pharmaceutical quality systems. Candidates should possess strong technical knowledge of pharmaceutical QA/QC operations and laboratory compliance systems.
This position provides excellent exposure to advanced pharmaceutical quality systems, analytical laboratory operations, regulatory compliance procedures, GMP workflows, microbiology review activities, validation systems, and modern pharmaceutical manufacturing environments within one of India’s reputed pharmaceutical organizations.
Location
Dahej, Gujarat, India
Employment Type
Full-time
Experience Required
7 to 10
Walk-in Interview Details
Walk-in Date: 2026-05-23
About Cadila Pharmaceuticals
Cadila Pharmaceuticals operates in the pharmaceutical industry specializing in formulation manufacturing, quality systems, analytical laboratories, research-driven healthcare solutions, and regulated pharmaceutical operations.
Key Responsibilities
Manage pharmaceutical QA and QC activities.
Review HPLC and GC analytical reports.
Monitor microbiology and laboratory operations.
Maintain GMP and quality compliance documentation.
Coordinate with production and regulatory teams.
Support audits and inspection readiness activities.
Handle deviation investigations and CAPA processes.
Ensure adherence to SOPs and quality standards.
Maintain analytical workflow and validation systems.
Support continuous improvement in laboratory operations.
Required Skills
Knowledge of pharmaceutical QA/QC systems.
Experience with HPLC and GC analytical operations.
Understanding of microbiology review procedures.
Awareness of GMP and regulatory compliance.
Documentation and analytical reporting expertise.
Problem-solving and investigation handling abilities.
Communication and team coordination skills.
Time management and workflow planning.
Attention to quality accuracy and compliance.
Adaptability to pharmaceutical laboratory environments.
Educational Qualification
M.Sc
Industry
Pharmaceutical
Why Join Cadila Pharmaceuticals?
Cadila Pharmaceuticals offers professionals opportunities to work in advanced pharmaceutical manufacturing and analytical environments with exposure to modern quality systems and regulatory operations.
How to Apply
Interested candidates can attend the walk-in interview and apply through ACKJOBS for this pharmaceutical QA/QC 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.
Cadila Pharmaceuticals is inviting experienced pharmaceutical professionals for the role of AM QA / QC at its Dahej, Gujarat manufacturing facility. This full-time walk-in opportunity is ideal for candidates with 7 to 10 years of experience in pharmaceutical quality assurance, quality control operations, laboratory compliance, analytical review systems, HPLC analysis, GC analysis, microbiology review, GMP documentation, regulatory compliance, quality management systems, and pharmaceutical manufacturing support activities. Professionals with expertise in HPLC, GC Reviewer, and Microbiology functions are encouraged to attend the walk-in interview.
The selected candidate will be responsible for managing pharmaceutical QA and QC activities while ensuring adherence to GMP standards, regulatory guidelines, and operational quality systems. Responsibilities include reviewing analytical reports generated through HPLC and GC systems, monitoring laboratory operations and testing activities, supervising microbiology review functions, ensuring proper documentation and compliance management, coordinating with production and regulatory teams, maintaining laboratory records and validation documentation, supporting audit preparation and inspection readiness, handling deviation investigations and CAPA implementation activities, monitoring analytical workflow systems, ensuring adherence to SOPs and quality standards, and contributing to continuous improvement initiatives related to laboratory operations and pharmaceutical quality systems. Candidates should possess strong technical knowledge of pharmaceutical QA/QC operations and laboratory compliance systems.
This position provides excellent exposure to advanced pharmaceutical quality systems, analytical laboratory operations, regulatory compliance procedures, GMP workflows, microbiology review activities, validation systems, and modern pharmaceutical manufacturing environments within one of India’s reputed pharmaceutical organizations.
Location
Dahej, Gujarat, India
Employment Type
Full-time
Experience Required
7 to 10
Walk-in Interview Details
Walk-in Date: 2026-05-23
About Cadila Pharmaceuticals
Cadila Pharmaceuticals operates in the pharmaceutical industry specializing in formulation manufacturing, quality systems, analytical laboratories, research-driven healthcare solutions, and regulated pharmaceutical operations.
Key Responsibilities
Manage pharmaceutical QA and QC activities.
Review HPLC and GC analytical reports.
Monitor microbiology and laboratory operations.
Maintain GMP and quality compliance documentation.
Coordinate with production and regulatory teams.
Support audits and inspection readiness activities.
Handle deviation investigations and CAPA processes.
Ensure adherence to SOPs and quality standards.
Maintain analytical workflow and validation systems.
Support continuous improvement in laboratory operations.
Required Skills
Knowledge of pharmaceutical QA/QC systems.
Experience with HPLC and GC analytical operations.
Understanding of microbiology review procedures.
Awareness of GMP and regulatory compliance.
Documentation and analytical reporting expertise.
Problem-solving and investigation handling abilities.
Communication and team coordination skills.
Time management and workflow planning.
Attention to quality accuracy and compliance.
Adaptability to pharmaceutical laboratory environments.
Educational Qualification
M.Sc
Industry
Pharmaceutical
Why Join Cadila Pharmaceuticals?
Cadila Pharmaceuticals offers professionals opportunities to work in advanced pharmaceutical manufacturing and analytical environments with exposure to modern quality systems and regulatory operations.
How to Apply
Interested candidates can attend the walk-in interview and apply through ACKJOBS for this pharmaceutical QA/QC 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.