Manager (Quality Control)
- Piramal Pharma Limited
- 13 - 17 years
- Hyderabad
- 2 days ago
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Job Description
- Actively involve during LIMS deployment, act as LIMS admin, aware about CSV
- LIMS data management, Mater data creator and static maintainer for LIMS.
- Shall perform assessment, and supporting to investigations, deviations and implementing CAPA effectively.
- Overall responsible for Internal & External vendor follow ups and completions within the timelines.
- Responsible to procure and maintain the minimum stock for working standards, reference standards, impurity standards, chemicals, reagents, glass wares and solvents required for analysis and ordering as and when required
- Responsible to complete the work assigned and ensure the training on the activity which are assigned by supervisor/ HOD-QC prior execution.
- Responsible for completing assigned tasks and ensuring training on activities as assigned by the supervisor/HOD-QC prior to execution.
- Review of packing materials, raw materials, stability samples, in-process data, and finished product data.
- Review qualification, validation, calibration data, procedures, and audit trails in a timely manner.
- Identify unsafe conditions or acts in the laboratory, report them to the supervisor/HOD-QC, and ensure appropriate action is taken to address them.
- Receive and inward analysis samples, including packing materials, raw materials, in-process samples, intermediates, APIs, finished products, and stability samples, and log entries in the respective AR number logs.
- Allocate tasks for chemical and instrumentation areas, ensuring timely completion. Ensure assigned tasks align with analyst qualification reports.
- Review QC logs, incident reports, and other records, ensuring proper document archiving after the release of samples.
- Oversee control sample inspection and ensure the proper disposal of leftover samples after analysis.
- Ensure instrument calibration and AMC are completed as per the schedule.
- Prepare and revise SOPs, specifications, and procedures in line with regulatory requirements.
- Conduct training on SOPs, trending, and other relevant procedures.
- Prepare stability schedules, stability protocols, and reports, as well as validation/qualification and trending reports.
- Participate in investigations and ensure the effectiveness of CAPAs.
- Perform SAP activities and ensure QMS closure before batch releases in SAP.
- Actively participate during LIMS deployment, act as LIMS admin, and manage LIMS data. This includes master data creation and static maintenance.
- Conduct assessments, support investigations and deviations, and implement CAPAs effectively.
Job Classification
Industry: Pharmaceutical & Life SciencesFunctional Area / Department: Quality AssuranceRole Category: Quality Assurance - OtherRole: Quality Assurance - OtherEmployement Type: Full timeContact Details:
Company: Piramal Pharma LimitedLocation(s): Hyderabad+ View Contact
Keyskills: QC Compliance CAPA LIMS Investigation Change Control GMP
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