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8 Qa Head Jobs

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17.0 - 26.0 years

20 - 25 Lacs

Samba

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Overall responsibility of QA & Qc activities in the plant Managing Validation, Hygiene, Micro biologist teams in plant Responsible for Implementing & Reviewing the quality mgt system Waste water quality standards Handled Global audits GMP & GHP s Required Candidate profile Having worked in Pharma, FMCG and Aseptic is an advantage Process Statistical knowledge, EOSH and TCCQS systems knowledge Assertive and Ensure plant Compliances ONLY FROM BEVERAGES BACKGROUND

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15.0 - 20.0 years

20 - 30 Lacs

Ahmedabad

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ORGANISATIONAL OVERVIEW Lambda Therapeutic Research is a Global full-service Clinical Research Organization (CRO) with its headquarters in Ahmedabad, India. With facilities and operations strategically located in Mehsana (India), Las Vegas (USA), Toronto (Canada), Barcelona (Spain), London (UK) and Warsaw (Poland), we offer comprehensive end-to-end clinical research services to the global innovator, biotech, and generic pharmaceutical industries. JOB DETAILS Department: Late Phase QA Designation: Assistant General Manager Job Location: Ahmedabad (Gujarat) Education: M.Pharm/Ph.D. Experience: 15+ years CTC Range: 20 to 30 Lacs Job Description: Ensure data compilation for Quality Review Board Meeting for Late Phase trials and functions; Data compilation, meeting preparation and discussion, MOM preparation and further followup of action items. Review effectiveness of CAPA management (identification, reporting, impact assessment and CAPA implementation) and Review of various study documents. QA statement and Audit certificate issuance as per applicable regulatory guideline. To determine whether all trial related activities were conducted, data recorded, analyzed and reported accurately & in compliance to all applicable Regulatory requirements, Organizational requirements (Policy, Procedures and processes) and Client s requirements (protocol, contract etc.) by routinely conducting audits (In process, on-site and off-site) at various stages for allassigned projects. Conducting & reporting of system audits as per system audit annual calendar to ensure compliance w.r.to current ICH GCP, Lambda SOPs, Quality Systems, Protocol and applicable regulatory requirements. Participate in key internal project team meetings and facilitate quality discussions during these meetings, as appropriate.To Support Head- QA/Designee for preparation & review of QA sops and review of system sops of other department (Clinical Trial Management, Medical affairs, medical imaging) for correctness, adequacy and compliance. To provide audit and inspection support for assigned projects, including, where feasible, advising the project team during preparation and conduct of audits and inspections. To support Head-QA/Designee for handling regulatory inspections and sponsor system audit, arranging data for regulatory inspection and sponsor system audit, responding to regulatory or sponsor queries pertaining to clinical trial/medical imaging issues, co-ordinate for regulatory/sponsor inspections/audits. To perform retrospective audits of Study protocol and study related raw data, as required. Update Head-QA/Designee regularly on the level of compliance and compliance issues. COMPETENCIES Accountability Work Ethic Initiative Technical Knowledge Organizational Culture fit

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3.0 - 6.0 years

5 - 8 Lacs

Bharuch

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(Purpose/ objective of the job Department organogram to be enclosed) To check the Quality Assurance of the products and ensure compliance with the SOP s. Key Responsibilities (Performance Indicators) Quality professional of progressive experience with strong knowledge of Speciality Ingredient, Bulk Chemicals, Food additive/ Food supplement & API Manufacturing, Quality Management System (QMS), Qualification, Validation and other Manufacturing functions. Documentation & Handling i.e.: Integrated Management System (IMS) (ISO 9001:2015, ISO 14001:2015 & ISO 45001:2018), WHO-GMP, FSMS (ISO 22000), FAMI-QS, Energy Management System (EnMS), Halal, Kosher & Responsible Care & regulatory (FDCA, USFDA, MHRA). Expertise in change control, deviation, market complaint, non-conformance investigation, vendor audit, self-inspection, gap assessment, customer audit, training, vendor management, vendor questionnaire, validation, equipment & utility system qualification. Issuance and retrieval of Batch Manufacturing Records. Control and Issuance of formats. Ensure that retention of various documents, reports and records are as per documented procedures. Issue copy of Master Batch Production Instructions to production for batch manufacture & review critical control parameters before release of the batch. Qualification & Experience M.Sc Organic Chemistry with 3-6 yrs Key Competencies ( Technical, Functional & Behavioral) Integrated Management System (IMS) (ISO 9001:2015, ISO 14001:2015 & ISO 45001:2018), WHO-GMP, FSMS (ISO 22000), FAMI-QS, Energy Management System (EnMS), Halal, Kosher & Responsible Care & regulatory (FDCA, USFDA, MHRA). Knowledge of validation process. Practical experience in documentation as per various audits. Approval VP Mfg Unit HR

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9.0 - 15.0 years

11 - 13 Lacs

Dahej

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To take plant round and monitor production activities at shop floor. To prepare appropriate Quality related documents like SOP, BMR, BCR, BPR etc. To review BMR s, BCR s, and analysis records before release of API. To perform sampling of API s and maintain its records. To maintain control samples of API and its records. To perform and ensure the cleaning of sampling tools. To provide line clearance at the time of product changes over. To review dispatch of finished product and maintain record for the same. To Investigate the deviations identified in co-ordination with QA-Head/Designee. Product quality review of API Process and cleaning validation monitoring in plant

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12.0 - 15.0 years

10 - 15 Lacs

Coimbatore

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Ensure the quality of incoming materials, in-process production, and finished products meets defined standards. Manage PPAP activities for new parts, engineering changes, and improvement projects to ensure compliance with design and industry requirements. Investigate root causes of internal defects, customer complaints, and rework using quality tools, and implement effective corrective and preventive actions (CAPA). Conduct regular internal and supplier audits to ensure compliance and drive quality improvements. Support continuous improvement initiatives to reduce defects and increase operational efficiency. Ensure all quality activities align with the requirements of the Integrated Management System (IMS). Qualification: B.E. in Mechanical Engineering Experience: 12 years of experience in the manufacturing industry Skills Required: Proficiency in relevant software and tools used in quality management, data analysis, and documentation In-depth knowledge in SAP QM module Knowledge in Microsoft Excel and PowerPoint are preferred

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20.0 - 28.0 years

30 - 45 Lacs

Chandigarh

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We are looking for a QA Manager with strong experience in cloud and on-premise product delivery. In this role, you will lead a QA team responsible for ensuring quality across the entire lifecycle from development and staging to customer implementation and deployment testing. This includes test planning, automation, and coordination with DevOps, implementation teams, and support. Key Responsibilities: Define and manage QA strategy for products deployed on both AWS and customer-managed environments. Collaborate with implementation and delivery teams to validate builds before deployment to on-premise customers. Oversee testing across development, staging, and UAT environments to ensure high-quality releases. Develop automated test frameworks for APIs, UI, and infrastructure validation (cloud and on-premise). Establish pre-deployment validation checklists for customer-specific builds and configurations. Ensure rigorous regression, performance, and security testing, especially for regulated industries. Coordinate with support and implementation teams to triage field issues and incorporate feedback into QA processes. Develop and track quality KPIs such as defect density, release stability, and field defect rates. Drive continuous improvement in QA practices across CI/CD pipelines, automation, and manual validation efforts. Requirements: Bachelors or Masters in Computer Science, Engineering, or a related field. 10+ years in QA, with 3+ in a leadership role managing both SaaS and on-premise product testing. Strong experience with cloud-native apps (AWS) and packaged software delivered to enterprise customers. Experience in installation and configuration testing for Linux/Windows environments. Expertise in automation tools (e.g., Selenium, Postman, PyTest) and CI/CD (e.g., Jenkins, GitLab). Familiarity with Docker, Kubernetes, and infrastructure as code (e.g., Terraform, CloudFormation). Excellent cross-functional communication, leadership, and problem-solving skills. Preferred Qualifications: AWS Certification (e.g., Solutions Architect, DevOps Engineer). Experience with configuration management tools (e.g., Ansible, Chef) for on-prem deployments. Exposure to compliance testing (e.g., SOC 2, HIPAA) in both cloud and on-premise contexts. Hands-on with monitoring/logging tools like CloudWatch, ELK, or Prometheus. Roles and Responsibilities Team mentoring, Risk Analysis, API Testing, Functional Testing, Cloud Server, Integration Testing, Agile, Database Testing, Complex Data queries

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15.0 - 20.0 years

8 - 13 Lacs

Sonipat

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Hiring for QA Head | Bahalgarh | Sonipat | Sheet Metal line Railway Industry Exp. - 15 - 20yrs Salary- 90k-1.10Lac Candidate must have knowledge of casting, steel melting Interested candidates contact on- 8222822052

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3.0 - 6.0 years

1 - 4 Lacs

Mumbai, Nagpur, Thane

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Quality check and Validation: Random cross-check of warehouse received fresh stock studded products diamonds quality and CVD screening against certification agency certified. 100% verification of warehouse received store return studded products diamonds quality and CVD screening. Verify diamond quality and mounting standards prior to dispatch or post-certification. Documentation & Validation: Maintain accurate records of all certified products and corresponding certificates. Certificate numbers, and matching SKU/product references. Vendor & Lab Communication: Liaise with vendors for sample correction if certification mismatches are found. Coordinate with labs for re-certification or rectification as needed. Reporting: Submit daily/weekly certification status reports to QA head or relevant stakeholders. Highlight discrepancies, rejections, or delays in certification processes. Key Skills & Competencies: Strong knowledge of diamond grading standards and certification norms. Familiarity with certification agencies like IGI, GIA, SGL, etc Attention to detail and accuracy in documentation and inspection. Good communication and coordination skills. Good Knowledge of jewe'llery manufacturing and quality parameters. Educational Qualification: Graduate in Gemology / Diamond Grading (from GIA, IGI, or similar reputed institution) Additional QA or Jewe'llery Management certification is a plus. Experience: 4 6 years of experience in quality assurance or diamond certification handling in the jewe'llery industry. Qualifications: Bachelor of Fine Arts

Posted 2 months ago

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