Senior Manager – Quality e-Compliance
1 week ago
Ensuring that computer system validation deliverables like GXP, Software categorization, software qualifications, configuration specification, Risk assessment, negative challenging tests, backup & restore procedure, validation summary report, requirement traceability matrix and CFR part requirements are available for all the GxP systems To revisit the site specific SOP’s related to IT and ITC periodically to in line with the corporate IT guidelines/current regulatory standards and to maintain the work practices is in line with the current SOP’s. Preparation and Execution of the IT Roadmap for the site. Facing Regulatory and customer audits and presenting the IT compliance status with the support from the respective SME. Evaluating, reviewing the IT observations, internally, or during the audits, and supporting the respective department in identifying effective CAPA. To perform IT supplier assessment for GAMP, GAMP or GAMP, software before procuring. Perform adequate investigation and providing the root cause for the deviations identified during the failures/Deviations of computerized systems. To ensure that all the computerized systems are meeting the CFR part and electronic signatures/records requirements. To review and approve of all the validation/qualification documents related to computerized systems and ensuring the documents are in compliance. To ensure that all IT related Risk assessments are made and necessary Risk mitigations are executed Providing the sufficient training to the site team and ensuring that all the IT team members are become experts in their job role. Report any incident/accident/ near miss/ illness to the superiors Identify unsafe conditions and unsafe acts and report to superiors.
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Senior Manager – Quality e-Compliance
4 days ago
Medak, Telangana, India Piramal Pharma Ltd Full time ₹ 12,00,000 - ₹ 36,00,000 per yearJob DescriptionEnsuring that computer system validation deliverables like GXP, Software categorization, software qualifications, configuration specification, Risk assessment, negative challenging tests, backup & restore procedure, validation summary report, requirement traceability matrix and 21 CFR part 11 requirements are available for all the GxP...
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Senior Manager – Quality e-Compliance
1 week ago
Medak, India Piramal Enterprises Full timeJob Description Job Description : 1. Ensuring that computer system validation deliverables like GXP, Software categorization, software qualifications, configuration specification, Risk assessment, negative challenging tests, backup & restore procedure, validation summary report, requirement traceability matrix and 21 CFR part 11 requirements are available...
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Deputy Manager
1 week ago
Medak, India Piramal Group Full timePreparation, Review & approval of investigation reports, risk assessment, impact assessment reports and other documents as an when required. Handling of product quality complaint (Adverse Event) related to Pharmacovigilance and market complaint investigations in CHEX system as per procedure in co-ordination with Pharmacovigilance team for adverse events as...
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Quality Control Engineer
3 weeks ago
Medak, India AMEENJI RUBBER LIMITED Full timeCompany Overview AMEENJI RUBBER LIMITED is an ISO certified company manufacturing products in accordance with IRC codes and specifications. Recognized by the Ministry of Road Transport and Highways and registered under the Ministry of Railways, the company specializes in Elastomeric Bridge Bearings among others. Headquartered in Hyderabad, Telangana, the...
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Quality Control Engineer
3 days ago
Medak, Telangana, India Ameenji Rubber Limited Full time ₹ 2,00,000 - ₹ 8,00,000 per yearCompany OverviewAMEENJI RUBBER LIMITED is an ISO certified company manufacturing products in accordance with IRC codes and specifications. Recognized by the Ministry of Road Transport and Highways and registered under the Ministry of Railways, the company specializes in Elastomeric Bridge Bearings among others. Headquartered in Hyderabad, Telangana, the...
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Deputy Manager
5 days ago
medak, India Piramal Full timePreparation, Review & approval of investigation reports, risk assessment, impact assessment reports and other documents as an when required. Handling of product quality complaint (Adverse Event) related to Pharmacovigilance and market complaint investigations in CHEX system as per procedure in co-ordination with Pharmacovigilance team for adverse events as...
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Deputy Manager
5 days ago
Medak, Telangana, India Piramal Full time ₹ 9,00,000 - ₹ 12,00,000 per yearPreparation, Review & approval of investigation reports, risk assessment, impact assessment reports and other documents as an when required. Handling of product quality complaint (Adverse Event) related to Pharmacovigilance and market complaint investigations in CHEX system as per procedure in co-ordination with Pharmacovigilance team for adverse events as...
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Deputy Manager
4 days ago
Medak, Telangana, India Piramal Group Full time ₹ 8,00,000 - ₹ 15,00,000 per yearDescriptionPreparation, Review & approval of investigation reports, risk assessment, impact assessment reports and other documents as an when required.Handling of product quality complaint (Adverse Event) related to Pharmacovigilance and market complaint investigations in CHEX system as per procedure in co-ordination with Pharmacovigilance team for adverse...
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Deputy Manager
1 week ago
Medak, Telangana, India Piramal Pharma Ltd Full time ₹ 2,00,000 - ₹ 6,00,000 per yearJob DescriptionTo carryout filling and packing activities as per BFR, BPR & SOPs.To follow & maintain current GMP standards in production area/activities.To follow day-to-day production schedule and ensure to complete production activities (filling & packing) as per schedule.To take & follow operating instructions for the shift activities from...
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Senior Executive-QA
1 week ago
Medak, Telangana, India Piramal Full time ₹ 9,00,000 - ₹ 12,00,000 per yearThe Senior Executive – QA (Engineering Assurance) will be responsible for executing and reviewing qualification lifecycle documents for GMP equipment, utilities, and facilities. The role includes oversight of URS, DQ, IQ, OQ, and PQ protocols, engineering change controls, risk assessments (FMEA), and periodic requalification activities. This position works...