Careers

Experience: 6-8 Years

Qualification: B.Sc. / M.Sc.

Brief Job Description: 

• Supervising and coordinating all production activities during their shift to ensure targets are met, quality standards are maintained, and safety protocols are followed.
• Key duties include managing staff, troubleshooting operational issues, ensuring documentation is accurate, coordinating with other departments like maintenance and quality control, and maintaining a clean and compliant work environment.

Experience: 2 Years

Qualification: M.Sc. / M.Pharm

Brief Job Description: 

• Testing of in-process, RM, intermediate and finish product as per STP.
• To prepare laboratory reagent and volumetric solution.
• Preparation and maintaining working standard/reference standard.
• To perform calibration of All QC instruments.
• To perform critical analysis as per requirement.

Experience: 3-5 Years

Qualification: M.Sc. / M.Pharm

Brief Job Description: 

• Monitoring and Reviewing of QC activities related to Analysis, Validation and Qualification.
• To perform planning and review of HPLC & GC activities. Knowledge of Calibration and Qualification data of all QC Lab instruments.
• To be perform of stability sample and monitor Stability Chambers and its related documents.
• Updating the knowledge of control system and sharing with department personnel.

Experience: 5-8 Years

Qualification: M.Sc. / M.Pharm

Brief Job Description: 

• To plan, review and Monitor HPLC, GC and Stability activities related to Analysis, Validation, and Qualification.
• The responsibility of investigation (OOS/OOT) and closure of Change control, Incident, Liable for maintaining 21 CFR, GMP, GLP & Safety in QC Lab.
• Knowledge of Execute and review of annual calibration schedules of all QC instruments.

Experience: 2 Years

Qualification: B.Sc./ M.Sc.

Brief Job Description: 

• Developing, validating, and performing analytical methods using liquid chromatography-mass spectrometry (LC-MS) to test and characterize pharmaceutical or biological samples.
• Key responsibilities include method development and troubleshooting.

Experience: 5-8 Years

Qualification: B.Sc./ M.Sc.

Brief Job Description: 

• Developing, validating, and performing analytical methods using liquid chromatography-mass spectrometry (LC-MS) to test and characterize pharmaceutical or biological samples.
• Key responsibilities include method development and troubleshooting, data analysis and interpretation, preparing and reviewing technical reports, and collaborating with other departments to support product development and ensure regulatory compliance.

Experience: 0 to 5 Years

Qualification: B.Pharm/ M.pharm/ B.Sc/ M.Sc

Brief Job Description:

• Responsible for executing manufacturing operations as per batch manufacturing records and cGMP guidelines.
• Monitor equipment, processes, and ensure timely completion of production activities with quality compliance.
• Coordinate with QA, QC, and maintenance teams for smooth production flow and issue resolution.
• Maintain proper documentation and support regulatory inspections and audits.

Experience: 1 to 5 Years

Qualification: M.Sc (Analytical) / M.Pharm (QA)

Brief Job Description:

• Responsible for development, validation, and transfer of analytical methods for raw materials, intermediates, and finished products.
• Perform stability studies, impurity profiling, and dissolution testing as per regulatory guidelines.
• Prepare and review protocols, reports, and ensure compliance with cGMP and regulatory requirements.
• Support technology transfer, troubleshooting, and regulatory submissions with accurate analytical data.

Experience: 1 to 5 Years

Qualification: B.Sc/ M.Sc

Brief Job Description:

• Responsible for analysis and testing of raw materials, packaging materials, in-process, and finished products as per pharmacopeial standards.
• Ensure calibration, operation, and maintenance of laboratory instruments and equipment.
• Prepare and review analytical reports, COAs, and maintain proper documentation as per cGMP.
• Support regulatory audits and ensure compliance with quality standards and laboratory practices.

Experience: 1 to 5 Years

Qualification: B.Pharm/ M.pharm/ B.Sc./ M.Sc.

Brief Job Description:

• Responsible for vendor qualification, audits, and maintaining the Approved Vendor List (AVL) as per regulatory requirements.
• Coordinate with cross-functional teams for vendor assessments, risk evaluations, and audit CAPA closures.
• Prepare and review protocols/reports for equipment qualification, process validation, and cleaning validation.
• Ensure compliance with cGMP, regulatory guidelines, and maintain related documentation for inspections and audits.