Technical Supervisor

Cadila Pharmaceuticals Limited; Jammu district; On-site; INR 300,000 - 420,000; Full time

Job summary

Cadila Pharmaceuticals Limited is seeking a QC/Material planning professional responsible for planning, analyzing and releasing raw materials. The role includes reviewing LIMS/SAP data, handling QC instrument maintenance, and ensuring GLP conformity throughout testing processes.

Key duties include coordinating with external labs for timely test reports, preparing change controls, SOPs and specifications, and ensuring testing is completed within stipulated timelines.

Qualifications

• GLP compliance knowledge.
• Experience with QC instruments.
• Coordination with external testing labs.

Responsibilities

• Plan Raw Material/GLP
• Review analytical reports of all sections
• Coordinate with external testing labs for timely reports
• Troubleshoot QC instruments and perform maintenance
• Raise change controls and prepare SOPs/STPs/specifications
• Update methods as per GLP and regulatory requirements
• Read relevant specifications to organize timely testing
• Participate in audits
• Prepare indents for materials and AMC/CMC of lab instruments

Skills

Raw Material planning

LIMS/SAP knowledge

Job description

Job Description:

• Major Purpose of the Job
• To ensure planning, analysis and release of Raw Material.
• Analytical results review and release in LIMS & SAP.
• Usage decision in SAP.Principal Tasks:
• Planning of Raw Material/GLP.
• Review of Analytical reports of all section.
• Follow up timely preventive maintenance of QC instruments.
• Indent of QC requirements.
• Responsibilities:
• Work allocation of Raw Materials to concerned analysts.
• Review of LIMS results entry done by analysts.
• To review and approve raw material and finished goods reports.
• Coordination with external testing lab to get the outside tests done and to receive reports in timely manner.
• Troubleshooting of QC Instruments.
• Formal investigation of out-of-specification, incidents, out-of-trend test results and errors and documentation of investigation, including action taken.
• To raise the change control and preparation of SOPs, STPs and specifications.
• Updation of method as per current GLP guidelines and regulatory requirements.
• To read the relevant specification and organize the work in such a manner that testing can be completed in stipulated time.
• To participate in audits.
• To prepare indent of material and AMC/CMC of different instrument related to Quality Control Lab and it’s follow up.

Requirements: