
Executive QA
19 hours ago
Process Validation:
Plan and execute process validation activities for sterile injectable products as per cGMP and regulatory expectations.
Prepare and review validation protocols and reports, ensuring compliance with internal SOPs and global regulatory guidelines (e.g., USFDA, EU-GMP, WHO).
Cleaning Validation:
Develop and implement cleaning validation strategies for critical manufacturing equipment and facilities.
Review of cleaning validation protocols, analytical methods, and result interpretation to ensure carry-over limits are within acceptable criteria.
Hold Time Study:
Coordinate and conduct hold time studies for intermediates, bulk, and in-process materials to establish scientifically justified limits.
Review and trend hold-time data, identifying areas requiring optimization or revalidation.
Annual Product Quality Review (APQR):
Compile and review data for APQRs across product portfolios, analyze trends, and identify areas for continuous improvement.
Liaise with cross-functional teams (QA, QC, Production) to gather and verify relevant documentation and data.
New Product Introduction - Risk Assessment:
- Lead quality risk assessment activities for new injectable products, including impact analysis on facility, equipment, personnel, and processes.
- Participate in tech transfer meetings and review of validation and qualification documentation related to NPIs.
- Review and trend hold-time data, identifying areas requiring optimization or revalidation.
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Executive/Sr Executive- QA
22 hours ago
Pithampur, Madhya Pradesh, India Gufic Group Full time ₹ 20,00,000 - ₹ 25,00,000 per yearProcess Validation:Plan and execute process validation activities for sterile injectable products as per cGMP and regulatory expectations.Prepare and review validation protocols and reports, ensuring compliance with internal SOPs and global regulatory guidelines (e.g., USFDA, EU-GMP, WHO).Cleaning Validation:Develop and implement cleaning validation...
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Senior Executive- QA
20 hours ago
Pithampur, Madhya Pradesh, India Lupin Full time ₹ 20,00,000 - ₹ 25,00,000 per yearRoles and ResponsibilitiesReview and approval of Master Documents such as Batch manufacturing record /Batch packaging record, Specification, Standard test procedure, Standard operating procedure, Qualification/ Validation protocols and reports.Preparation and review of Site Master File.Review and approval of Quality System document such as Deviation, Change...
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QA (IPQA/QMS/Qualification Validation)
6 days ago
Pithampur, Madhya Pradesh, India Makin Laboratories Full time ₹ 8,00,000 - ₹ 10,00,000 per yearRole & responsibilitiesIn-Process Quality Assurance (IPQA):Perform line clearance and in-process checks during manufacturing and packing.Monitor critical process parameters and maintain real-time documentation.Ensure compliance with SOPs and cGMP during routine operations.Sampling of in-process and finished products as per defined procedures.Quality...
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l Manager/Quality
3 weeks ago
Pithampur, Madhya Pradesh, India Shakti Pumps Full timeJob DescriptionRole Overview:The Quality Manager is responsible for spearheading quality assurance and quality control (QA/QC) efforts to ensure that all products and processes meet internal and external quality standards. This role involves strategic planning, process validation, staff management, compliance monitoring, and continuous improvement.Key...
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Quality Chemist
3 weeks ago
Pithampur, Madhya Pradesh, India JIAAN BIOTECH Full timeJob Responsibilities - QC Chemist Analyst Perform sampling of raw materials packaging materials intermediates and finished products as per SOPs Carry out chemical physical and instrumental analysis UV IR KF etc as per pharmacopeia methods or validated in-house methods Conduct water stability and environmental monitoring sample analysis ...
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Quality Chemist
3 days ago
Pithampur, Madhya Pradesh, India JIAAN BIOTECH Full time ₹ 11,000 - ₹ 2,20,850 per yearJob Responsibilities – QC Chemist/ AnalystPerform sampling of raw materials, packaging materials, intermediates, and finished products as per SOPs.Carry out chemical, physical, and instrumental analysis (UV, IR, KF, etc) as per pharmacopeia methods or validated in-house methods.Conduct water, stability, and environmental monitoring sample analysis.Maintain...
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Executive/Sr Executive- QA
2 weeks ago
Pithampur, India Gufic Group Full timeProcess Validation: Plan and execute process validation activities for sterile injectable products as per cGMP and regulatory expectations. Prepare and review validation protocols and reports, ensuring compliance with internal SOPs and global regulatory guidelines (e.g., USFDA, EU-GMP, WHO). Cleaning Validation: Develop and implement cleaning validation...
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Quality Chemist
2 weeks ago
Pithampur, India JIAAN BIOTECH Full timeJob Responsibilities – QC Chemist/ Analyst Perform sampling of raw materials, packaging materials, intermediates, and finished products as per SOPs. Carry out chemical, physical, and instrumental analysis (UV, IR, KF, etc) as per pharmacopeia methods or validated in-house methods. Conduct water, stability, and environmental monitoring sample analysis....
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Production Officer/ Production Chemist
6 days ago
Dewas, Indore, Pithampur, India NMS Consultant Full time ₹ 9,00,000 - ₹ 12,00,000 per yearRole & responsibilitiesExecution of daily production activities as per production plan.Preparation and review of BMR/BPR.Supervision of manufacturing processes (granulation, compression, coating, filling, etc.).Ensuring adherence to SOPs, cGMP, and safety protocols.Coordination with QA for line clearance and in-process checks.Maintaining discipline and...