Job Description
QC Executive – Quality Control Department | Ajanta Pharma Ltd. | Pithampur, Madhya Pradesh, India
Ajanta Pharma Ltd. is hiring professionals for the role of QC Executive for its pharmaceutical quality control operations located in Pithampur, Madhya Pradesh, India. This full-time opportunity is ideal for candidates with 7 to 9 years of experience in pharmaceutical QC operations, analytical testing workflows, laboratory instrumentation systems, GMP compliance activities, quality documentation, stability testing operations, validation coordination workflows, analytical reporting systems, and regulated pharmaceutical industry environments.
The selected candidate will support quality control and analytical laboratory activities associated with pharmaceutical manufacturing and GMP systems. Responsibilities include performing analytical testing and laboratory operations, maintaining QC records and GMP documentation, operating analytical instruments such as HPLC, GC, UV, and dissolution systems, coordinating with QA and production teams for operational support activities, monitoring testing parameters and laboratory workflows, ensuring adherence to SOP procedures and regulatory standards, preparing laboratory reports and operational documentation, assisting in troubleshooting and QC coordination workflows, participating in stability studies and validation activities, and supporting continuous improvement initiatives related to pharmaceutical quality systems and laboratory operations.
This role offers valuable exposure to pharmaceutical laboratory systems, analytical testing workflows, GMP-regulated operations, quality coordination activities, validation systems, and industrial pharmaceutical environments within a reputed organization. Professionals interested in pharmaceutical quality control careers can strengthen their technical and operational expertise through this opportunity.
Location
Pithampur, Madhya Pradesh, India
Employment Type
Full-time
Salary
Best in Industry
Experience Required
7 to 9 Years
About Ajanta Pharma Ltd.
Ajanta Pharma Ltd. operates in the pharmaceutical industry specializing in pharmaceutical manufacturing systems, analytical laboratory operations, GMP workflows, healthcare product manufacturing, and regulated pharmaceutical services.
Key Responsibilities
Perform analytical testing and quality control activities.
Operate laboratory instruments including HPLC and GC systems.
Maintain QC records and GMP documentation.
Coordinate with QA and production teams.
Monitor testing parameters and laboratory workflows.
Ensure adherence to SOP procedures and regulatory standards.
Prepare laboratory reports and operational documentation.
Support troubleshooting and QC coordination workflows.
Participate in stability studies and validation activities.
Assist in continuous improvement of quality systems.
Required Skills
Strong knowledge of pharmaceutical QC operations.
Understanding of analytical instrumentation and laboratory systems.
Knowledge of GMP and regulatory compliance workflows.
Experience in HPLC, GC, UV, and dissolution testing.
Good analytical and problem-solving abilities.
Strong communication and teamwork skills.
Knowledge of SOP procedures and QC documentation.
Ability to manage laboratory schedules and workflows.
Attention to testing accuracy and compliance standards.
Adaptability to regulated pharmaceutical environments.
Educational Qualification
B.Sc / M.Sc
Industry
Pharmaceutical
Why Join Ajanta Pharma Ltd.?
Ajanta Pharma Ltd. offers professionals opportunities to work in advanced pharmaceutical laboratory environments with exposure to analytical systems, GMP workflows, quality operations, and regulated pharmaceutical manufacturing activities.
How to Apply
Interested candidates can apply through ACKJOBS for this QC Executive opportunity by submitting their updated resume and relevant documents.
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.
Ajanta Pharma Ltd. is hiring professionals for the role of QC Executive for its pharmaceutical quality control operations located in Pithampur, Madhya Pradesh, India. This full-time opportunity is ideal for candidates with 7 to 9 years of experience in pharmaceutical QC operations, analytical testing workflows, laboratory instrumentation systems, GMP compliance activities, quality documentation, stability testing operations, validation coordination workflows, analytical reporting systems, and regulated pharmaceutical industry environments.
The selected candidate will support quality control and analytical laboratory activities associated with pharmaceutical manufacturing and GMP systems. Responsibilities include performing analytical testing and laboratory operations, maintaining QC records and GMP documentation, operating analytical instruments such as HPLC, GC, UV, and dissolution systems, coordinating with QA and production teams for operational support activities, monitoring testing parameters and laboratory workflows, ensuring adherence to SOP procedures and regulatory standards, preparing laboratory reports and operational documentation, assisting in troubleshooting and QC coordination workflows, participating in stability studies and validation activities, and supporting continuous improvement initiatives related to pharmaceutical quality systems and laboratory operations.
This role offers valuable exposure to pharmaceutical laboratory systems, analytical testing workflows, GMP-regulated operations, quality coordination activities, validation systems, and industrial pharmaceutical environments within a reputed organization. Professionals interested in pharmaceutical quality control careers can strengthen their technical and operational expertise through this opportunity.
Location
Pithampur, Madhya Pradesh, India
Employment Type
Full-time
Salary
Best in Industry
Experience Required
7 to 9 Years
About Ajanta Pharma Ltd.
Ajanta Pharma Ltd. operates in the pharmaceutical industry specializing in pharmaceutical manufacturing systems, analytical laboratory operations, GMP workflows, healthcare product manufacturing, and regulated pharmaceutical services.
Key Responsibilities
Perform analytical testing and quality control activities.
Operate laboratory instruments including HPLC and GC systems.
Maintain QC records and GMP documentation.
Coordinate with QA and production teams.
Monitor testing parameters and laboratory workflows.
Ensure adherence to SOP procedures and regulatory standards.
Prepare laboratory reports and operational documentation.
Support troubleshooting and QC coordination workflows.
Participate in stability studies and validation activities.
Assist in continuous improvement of quality systems.
Required Skills
Strong knowledge of pharmaceutical QC operations.
Understanding of analytical instrumentation and laboratory systems.
Knowledge of GMP and regulatory compliance workflows.
Experience in HPLC, GC, UV, and dissolution testing.
Good analytical and problem-solving abilities.
Strong communication and teamwork skills.
Knowledge of SOP procedures and QC documentation.
Ability to manage laboratory schedules and workflows.
Attention to testing accuracy and compliance standards.
Adaptability to regulated pharmaceutical environments.
Educational Qualification
B.Sc / M.Sc
Industry
Pharmaceutical
Why Join Ajanta Pharma Ltd.?
Ajanta Pharma Ltd. offers professionals opportunities to work in advanced pharmaceutical laboratory environments with exposure to analytical systems, GMP workflows, quality operations, and regulated pharmaceutical manufacturing activities.
How to Apply
Interested candidates can apply through ACKJOBS for this QC Executive opportunity by submitting their updated resume and relevant documents.
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.