4

Quality Manager Job Vacancies in Ankleshwar

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Quality Manager - Full Time

AICS Consultancy Service Pvt. Ltd

  • 2 - 6 yrs
  • 4.0 Lac/Yr
  • Ankleshwar
Quality Control QMS Implementation Quality Audit Quality Procedures
Quality Manager - HospitalExperience : 2 - 5 yearsLocation : Ankleshwar , bharuch (Gujarat)Key ResponsibilitiesLead the hospital's quality and NABH accreditation activities.Develop, implement and periodically review SOPs, policies, protocols and quality manuals.Conduct internal audits of clinical and non-clinical departments.Identify gaps/non-conformities and coordinate CAPA closure.Conduct Root Cause Analysis (RCA) for incidents, adverse events and recurring problems.Monitor and analyse quality indicators and hospital KPIs.Prepare monthly/quarterly quality dashboards and management reports.Coordinate with Infection Control, Pharmacy, Nursing, OT, Medical Records, HR and other hospital committees.Monitor patient complaints, feedback and satisfaction.Organize Quality/NABH Committee meetings and maintain minutes and action plans.Ensure timely implementation of corrective actions identified during audits.Coordinate NABH assessments, surveillance assessments and accreditation activities.Maintain NABH documentation and supporting evidence.Conduct NABH and quality training/awareness programs for hospital staff.Develop and monitor Quality Improvement Projects (QIPs/CQI).QualificationBachelor's degree in Hospital Administration, Healthcare Management, Nursing, Pharmacy, Life Sciences or a related field.MHA/MBA Healthcare/Hospital Administration is preferred.Interested candidates share your resume 9319808242
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  • 0 - 2 yrs
  • 3.0 Lac/Yr
  • Ankleshwar
Material Management Microsoft Office Quality Monitoring Construction Planning Autocad Site Supervision Site Execution Construction Civil 3D Problem Solving Building Construction Civil Construction
Job description:Key ResponsibilitiesDesign & PlanningPrepare structural designs for offshore and onshore facilities.Develop layouts, drawings, and specifications for civil works.Project ExecutionSupervise construction activities at project sites (pipelines, platforms, buildings).Ensure compliance with ONGCs safety and quality standards.Structural AnalysisPerform load calculations and stability checks for offshore platforms.Use engineering software for modeling and simulation.CoordinationWork with multidisciplinary teams (mechanical, electrical, petroleum engineers).Liaise with contractors and vendors to ensure timely project delivery.ComplianceAdhere to environmental and regulatory norms.Maintain documentation for audits and inspections.Qualifications & SkillsEducation: B.E./B.Tech in Civil Engineering (M.Tech preferred for structural roles).Experience: 0.5 - 1.5 yearTechnical Skills:Knowledge of STAAD Pro, AutoCAD, and other civil design tools.Familiarity with offshore construction standards (API, IS codes).Soft Skills:Strong project management and communication abilities.Ability to work in remote and challenging environments.Typical Work EnvironmentLocation: Gujarat (Ankleshwar, Ahmedabad, offshore sites).Nature of Work: Combination of office-based design and field/site supervision.Working in offshore environments can be physically demanding.Strict adherence to safety protocols is mandatory.Projects often involve tight deadlines and coordination with multiple stakeholders.Job Type: Full-timeBenefits:Health insuranceProvident FundAbility to commute/relocate:Ankleshwar, Gujarat: Reliably commute or planning to relocate before starting work (Preferred)Work Location: In person
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  • 5 - 8 yrs
  • 7.0 Lac/Yr
  • Ankleshwar
QA Quality Assurance Head API Chemical Company
Urgent OpeningQuality Assurance-Head(API Chemical Company)Location: Ankleshwar, Gujrat Qualifications: Graduate in a science-related field, such as chemistry or pharmacy Experience: Minimum 5 years experience in pharma from QA Department.Essential Duties and Responsibilities: Knowledge of all regulated Guideline & Pharmacopoeia. Preparation & implementation of SOPs related to the concerned department & Justification of Specification. Nitrosamine Impurity, Elemental Impurity, Genotoxic Impurity & their role related DMF Filing. Collaborates with the Quality control (QC) team to ensure that laboratory testing is conducted appropriately and meets the required specifications. The conducts regular internal audits of the manufacturing facility to ensure that the facility meets the required quality standards. handles the Regulatory and Customer audit and its compliance. Responsible for ensuring that all necessary documentation is completed accurately, in a timely manner, and in compliance with regulatory requirements Responsible for reviewing and approving deviation reports and ensuring that corrective and preventive actions (CAPA) are implemented. Responsible for reviewing and investigating product complaints to ensure implementation of corrective and preventive actions (CAPA). Preparation & review of process validation, cleaning validation, equipment qualification To prepare/review the Validation Master Plan, Site Master File, Drug Master File, Annual Product Quality Review, Plant Layout and other documents related to QA
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  • 3 - 7 yrs
  • Ankleshwar
Proficient With Metal Drum Barrel Process Quality Control Officer
We are looking for Quality Control Officer for METAL DRUM / BARREL MFG. Company at Ankleshwar. Candidate should have knowledge of QC , ISO 9001-2015, System,
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  • 5 - 8 yrs
  • 7.0 Lac/Yr
  • Ankleshwar
QA Quality Assurance Head API Chemical Manufacturing Company
Location: Ankleshwar, Gujrat Qualifications: Graduate in a science-related field, such as chemistry or pharmacy Experience: Minimum 5 years experience in pharma from QA Department.Essential Duties and Responsibilities: Knowledge of all regulated Guideline & Pharmacopoeia. Preparation & implementation of SOPs related to the concerned department & Justification of Specification. Nitrosamine Impurity, Elemental Impurity, Genotoxic Impurity & their role related DMF Filing. Collaborates with the Quality control (QC) team to ensure that laboratory testing is conducted appropriately and meets the required specifications. The conducts regular internal audits of the manufacturing facility to ensure that the facility meets the required quality standards. handles the Regulatory and Customer audit and its compliance. Responsible for ensuring that all necessary documentation is completed accurately, in a timely manner, and in compliance with regulatory requirements Responsible for reviewing and approving deviation reports and ensuring that corrective and preventive actions (CAPA) are implemented. Responsible for reviewing and investigating product complaints to ensure implementation of corrective and preventive actions (CAPA). Preparation & review of process validation, cleaning validation, equipment qualification To prepare/review the Validation Master Plan, Site Master File, Drug Master File, Annual Product Quality Review, Plant Layout and other documents related to QA.
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