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Dishman Carbogen Amcis

Ahmedabad, Gujarat

Department: Quality Control

Experience: 2-7 Years

Industry: Pharmaceutical

Education: M.Sc

Remarks: Bavla formulation QC

Job Description

Job Description

Officer QC – Quality Control | Dishman Carbogen Amcis | Ahmedabad, Gujarat, India

Dishman Carbogen Amcis is inviting applications for the role of Officer QC for its Bavla formulation quality control operations located in Ahmedabad, Gujarat, India. This full-time opportunity is suitable for candidates with 2 to 7 years of experience in pharmaceutical quality control, analytical testing, laboratory operations, GMP compliance, sample analysis, instrument handling, quality systems, documentation management, formulation testing, and regulated pharmaceutical environments. This opening is part of the Bavla formulation QC walk-in recruitment drive organized by the company.

The selected candidate will support analytical laboratory and quality control activities associated with formulation manufacturing and pharmaceutical compliance systems. Responsibilities include performing analytical testing of raw materials, in-process samples, finished formulations, and stability samples, maintaining laboratory documentation and analytical records, operating analytical instruments and testing systems, ensuring adherence to GMP and GLP procedures, coordinating with production and quality assurance departments for sample handling and investigation activities, participating in laboratory compliance and audit preparation processes, supporting troubleshooting and deviation handling activities, maintaining laboratory cleanliness and operational efficiency, assisting in method verification and analytical review systems, and contributing to continuous improvement initiatives related to laboratory quality systems and pharmaceutical compliance operations. Candidates should possess strong understanding of pharmaceutical analytical workflows and formulation quality control systems.

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

Location
Ahmedabad, Gujarat, India

Employment Type
Full-time

Experience Required
2 to 7

Walk-in Interview Details
Walk-in Date: 2026-05-24

About Dishman Carbogen Amcis
Dishman Carbogen Amcis operates in the pharmaceutical industry specializing in formulation manufacturing, pharmaceutical analytical systems, quality operations, and regulated healthcare products.

Key Responsibilities

Perform analytical testing of pharmaceutical samples.
Maintain laboratory records and analytical documentation.
Operate analytical instruments and testing systems.
Ensure adherence to GMP and GLP procedures.
Coordinate with production and QA departments.
Participate in laboratory compliance and audit activities.
Support troubleshooting and deviation handling operations.
Maintain laboratory cleanliness and operational efficiency.
Assist in analytical review and method verification.
Support continuous improvement in laboratory systems.


Required Skills

Knowledge of pharmaceutical quality control systems.
Understanding of analytical laboratory procedures.
Awareness of GMP and GLP compliance.
Documentation and analytical reporting expertise.
Problem-solving and analytical abilities.
Communication and teamwork skills.
Time management and workflow planning.
Attention to laboratory accuracy and compliance.
Adaptability to regulated pharmaceutical environments.
Technical understanding of analytical operations.


Educational Qualification
M.Sc

Industry
Pharmaceutical

Why Join Dishman Carbogen Amcis?
Dishman Carbogen Amcis offers professionals opportunities to work in advanced formulation quality control environments with exposure to modern pharmaceutical analytical systems and GMP operations.

How to Apply
Interested candidates can attend the walk-in interview and apply through ACKJOBS for this pharmaceutical quality control opportunity.

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