8.0 - 10.0 years

10 - 15 Lacs

vapi

Work from Office

Responsibilities: Prepare Monthly and weekly production plan basis on sales plan/ sales requirement. Monitor daily production and work centres based on sales priorities and material availability. Resource Management Plan and coordinate manpower with the HRA team. Qualify workstations and standardize processes to account for production costs. Control cost of production CoP Establish and maintain quality standards for all products. strickly adhere the product and in process quality standards on shop floor. Responsible for production achivement Vs Production plan and installed capacity Vs utilisation Ensure compliance with cGMP guidelines to maintain production and quality standards. Documentat...

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Shift Engineer - Maintenance Quality HR Services

2.0 - 3.0 years

3 - 3 Lacs

vapi

Work from Office

Responsibilities: Execution of routine maintenance activities. Check utility daily Log sheet. Carry out all the maintenance activities as per given plan and record it. Carry out preventive maintenance of all the equipment and record it. Ensure smooth operation of utility equipments. Check the calibration of instruments as per the plan and test certificate it. Routine shift work. Good engineering practice to be follow. Carry out the proper maintenance work of equipment. Provide specific job trainings operation and preventive maintenance to the concerned personnel within the factory Maintain cGMP in the department and its related documentation. Ensure All type of work with proper safety. Ensur...

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Sr. Officer / Executive - QC Quality HR Services

3.0 - 5.0 years

4 - 4 Lacs

vapi

Work from Office

Responsibilities: Individually handling department & manpower. Strong leadership skills to guide, supervise work activities, and help team members develop their skills. Work allocation / Planning and Review of documents. Preparation of SOP, Specification, Standard Test Procedures (STP), Raw Data Sheet (Protocol), Excel worksheet validation etc. Preparation and review of Analytical Method Validation protocol & Report. Preparation and review of equipment qualification documents. Handling of QMS documents like Change control, Deviation, Incidents, OOS, OOT etc. To investigate, identify the root cause and troubleshoot. To maintain GLP and discipline in the QC department. Required Skills Change C...

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Manufacturing Executive Quality HR Services

3.0 - 5.0 years

5 - 6 Lacs

vapi

Work from Office

Responsibilities: Schedule daily production and Manufacturing work centres based on sales priorities and material availability. Resource Management To assist production head to qualify manufacturing work stations and resources. Establish and maintain quality standards for all products. strickly adhere the product and in process quality standards on shop floor Ensure compliance with cGMP guidelines to maintain production and quality standards. Documentation ( all statutory and internals) are upto date on day to day basis Supervise. Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), and plant housekeeping on a daily basis while ensuring proper record maintenance. Required Ski...

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Executive Lupin

5.0 - 10.0 years

5 - 9 Lacs

pune

Work from Office

Job Description 1 Knowledge of operation & maintenance of Utility equipments like Chiller, Air Compressor, DG set, Boiler, Water pretreatment plant, UPS & ETP. 2 Should have adequate knowledge of Electrical maintenance of HT & LT Electrical Panels, Breaker and Transformer. 3 Hands on experience of qualification/validation of equipments, SOP preparation, PM, calibration of equipments, 21-CFR compliances. Should have knowledge of regulatory guidelines related to Engineering i.e. Water system, HVAC & compressed air. 4 Work Experience in USFDA / MHRA approved plants is must. 5 SAP Knowledge, Auto cad, Exposure to online documentation like SAP PM, eLog Books, QAMS. Work Experience 8-15 Years Educ...

Posted Date not available

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Quality Assurance/Pharma Manufacturing / Kolkata SSP Solutions

5.0 - 8.0 years

6 Lacs

kolkata

Work from Office

Ensure compliance with cGMP guidelines Batch Manufacturing Record preparation Packaging Material Specification Preparation APQR New drug application Batch card preparation Endorse documents preparation Required Candidate profile Experience in Quality Assurance of 5 years Gender Male

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Senior Executive-Documentation Analyst MSN Group

5.0 - 6.0 years

4 - 6 Lacs

sangareddy, patancheru, hyderabad

Work from Office

Role & responsibilities Strong knowledge of SOP preparation, documentation structure, and revision cycles Experience in handling QMS documentation (e.g., change control, impact assessments, etc.) Good understanding of regulatory requirements Excellent written communication and organizational skills High attention to detail with the ability to manage multiple documentation tasks Hands-on experience with Caliber LIMS Preferred candidate profile The incumbent should have adequate knowledge in QMS documentation, Caliber LIMS & SOP preparation

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