Job Description
Quality Control Officer – Quality Control Department | Neuland Laboratories Ltd. | Hyderabad, Telangana, India
Neuland Laboratories Ltd. is hiring professionals for the role of Quality Control Officer for its pharmaceutical quality control operations located in Hyderabad, Telangana, India. This full-time opportunity is ideal for candidates with 2 to 6 years of experience in QC operations, analytical testing workflows, laboratory coordination activities, GMP compliance systems, documentation management workflows, reporting systems, instrument handling operations, and regulated pharmaceutical environments.
The selected candidate will support quality control and laboratory coordination activities associated with pharmaceutical manufacturing systems and analytical workflows. Responsibilities include conducting analytical testing and laboratory activities, maintaining quality records and technical documentation, coordinating with QA and production teams for operational support activities, monitoring laboratory systems and analytical workflows, ensuring adherence to GMP procedures and quality standards, preparing test reports and operational documentation, assisting in troubleshooting and QC coordination workflows, participating in audit review and compliance activities, supporting laboratory management systems, and maintaining continuous improvement of quality operations and laboratory efficiency.
This role offers valuable exposure to pharmaceutical laboratory systems, analytical workflows, compliance coordination activities, technical documentation systems, testing operations, and regulated pharmaceutical environments within a reputed organization. Professionals interested in quality control careers can strengthen their technical and operational expertise through this opportunity.
Location
Hyderabad, Telangana, India
Employment Type
Full-time
Salary
Best in Industry
Experience Required
2 to 6 Years
About Neuland Laboratories Ltd.
Neuland Laboratories Ltd. operates in the pharmaceutical industry specializing in pharmaceutical manufacturing systems, laboratory testing workflows, analytical coordination activities, and healthcare product operations.
Key Responsibilities
Support QC and laboratory activities.
Conduct analytical testing and laboratory workflows.
Maintain quality records and technical documentation.
Coordinate with QA and production teams.
Monitor laboratory systems and testing activities.
Ensure adherence to GMP procedures and quality standards.
Prepare laboratory reports and operational documentation.
Support troubleshooting and QC coordination workflows.
Participate in audit review and compliance activities.
Assist in continuous improvement of laboratory systems.
Required Skills
Strong knowledge of QC and laboratory operations.
Understanding of analytical workflows and GMP systems.
Knowledge of HPLC, GC, and analytical testing activities.
Experience in laboratory documentation and reporting systems.
Good analytical and problem-solving abilities.
Strong communication and teamwork skills.
Knowledge of SOP procedures and pharmaceutical standards.
Ability to manage laboratory schedules and workflows.
Attention to analytical accuracy and compliance standards.
Adaptability to regulated pharmaceutical environments.
Educational Qualification
B.Pharm
Industry
Pharmaceutical
Why Join Neuland Laboratories Ltd.?
Neuland Laboratories Ltd. offers professionals opportunities to work in advanced pharmaceutical environments with exposure to laboratory systems, analytical workflows, operational coordination activities, and healthcare manufacturing operations.
How to Apply
Interested candidates can apply through ACKJOBS for this Quality Control Officer 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.
Neuland Laboratories Ltd. is hiring professionals for the role of Quality Control Officer for its pharmaceutical quality control operations located in Hyderabad, Telangana, India. This full-time opportunity is ideal for candidates with 2 to 6 years of experience in QC operations, analytical testing workflows, laboratory coordination activities, GMP compliance systems, documentation management workflows, reporting systems, instrument handling operations, and regulated pharmaceutical environments.
The selected candidate will support quality control and laboratory coordination activities associated with pharmaceutical manufacturing systems and analytical workflows. Responsibilities include conducting analytical testing and laboratory activities, maintaining quality records and technical documentation, coordinating with QA and production teams for operational support activities, monitoring laboratory systems and analytical workflows, ensuring adherence to GMP procedures and quality standards, preparing test reports and operational documentation, assisting in troubleshooting and QC coordination workflows, participating in audit review and compliance activities, supporting laboratory management systems, and maintaining continuous improvement of quality operations and laboratory efficiency.
This role offers valuable exposure to pharmaceutical laboratory systems, analytical workflows, compliance coordination activities, technical documentation systems, testing operations, and regulated pharmaceutical environments within a reputed organization. Professionals interested in quality control careers can strengthen their technical and operational expertise through this opportunity.
Location
Hyderabad, Telangana, India
Employment Type
Full-time
Salary
Best in Industry
Experience Required
2 to 6 Years
About Neuland Laboratories Ltd.
Neuland Laboratories Ltd. operates in the pharmaceutical industry specializing in pharmaceutical manufacturing systems, laboratory testing workflows, analytical coordination activities, and healthcare product operations.
Key Responsibilities
Support QC and laboratory activities.
Conduct analytical testing and laboratory workflows.
Maintain quality records and technical documentation.
Coordinate with QA and production teams.
Monitor laboratory systems and testing activities.
Ensure adherence to GMP procedures and quality standards.
Prepare laboratory reports and operational documentation.
Support troubleshooting and QC coordination workflows.
Participate in audit review and compliance activities.
Assist in continuous improvement of laboratory systems.
Required Skills
Strong knowledge of QC and laboratory operations.
Understanding of analytical workflows and GMP systems.
Knowledge of HPLC, GC, and analytical testing activities.
Experience in laboratory documentation and reporting systems.
Good analytical and problem-solving abilities.
Strong communication and teamwork skills.
Knowledge of SOP procedures and pharmaceutical standards.
Ability to manage laboratory schedules and workflows.
Attention to analytical accuracy and compliance standards.
Adaptability to regulated pharmaceutical environments.
Educational Qualification
B.Pharm
Industry
Pharmaceutical
Why Join Neuland Laboratories Ltd.?
Neuland Laboratories Ltd. offers professionals opportunities to work in advanced pharmaceutical environments with exposure to laboratory systems, analytical workflows, operational coordination activities, and healthcare manufacturing operations.
How to Apply
Interested candidates can apply through ACKJOBS for this Quality Control Officer 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.