QA-Quality Assurance Job Vacancies in Navi Mumbai

As a Data Consultant, you will play a crucial role in helping businesses make informed decisions based on data analysis. You will work remotely from Navi Mumbai and collaborate with various teams to enhance data strategies.**Key Responsibilities:**- **Data Collection:** Gather data from different sources to ensure a comprehensive understanding of the subject matter. This might include surveys, databases, or online resources.- **Data Cleaning:** Review and refine the collected data to remove any errors or inconsistencies. Accurate data is vital for reliable analysis.- **Data Analysis:** Analyze the cleaned data to identify trends and patterns that can help businesses in decision-making. You will be using various tools and methods to interpret data effectively.- **Report Creation:** Prepare clear and concise reports summarizing the findings from the data analysis. These reports will be used to present insights to stakeholders.- **Client Communication:** Interact with clients to understand their data needs and provide updates on project progress. Communication skills are essential for effective client relationships.**Required Skills and Expectations:**- Familiarity with data analysis tools such as Excel, Tableau, or similar software is preferred. Basic knowledge in statistics or data visualization will be helpful.- Strong analytical skills to interpret data and draw meaningful conclusions.- Excellent communication skills, both verbal and written, for effective reporting and client interaction.- A proactive attitude towards learning and adapting to new technologies in the data domain.- Ability to work independently while remaining organized and meeting deadlines.

Monitor and ensure quality of construction work as per approved drawings and specificationsConduct site inspections, tests, and audits to ensure compliance with standardsPrepare and maintain quality documentation, reports, and checklistsCoordinate with site engineers, contractors, and consultants for quality-related mattersEnsure materials used at site meet required quality standardsIdentify defects and suggest corrective and preventive actionsEnsure compliance with BMC and other regulatory guidelinesMaintain records of tests (concrete, soil, materials, etc.)Participate in client/authority inspections

Quality Oversight & ApprovalApprove analytical results, reports, protocols, methods, specifications, and other quality-related documents.Ensure the integrity, accuracy, and regulatory compliance of analytical and laboratory data.Provide final quality approval for services and deliverables provided to clients.2. Quality Management System (QMS)Establish, maintain, and continuously improve the Quality Management System (QMS) in compliance with GMP, GLP, and applicable regulatory guidelines.Ensure effective management of SOPs, deviations, CAPAs, change controls, OOS/OOT investigations, complaints, and risk management activities.Ensure data integrity compliance in line with ALCOA+ principles across all systems and documentation.3. Regulatory ComplianceEnsure compliance with applicable global regulations and guidelines, including FDA, EMA, ICH, WHO, and ISO standards.Lead, support, and manage regulatory inspections, client audits, and third-party audits.Act as the primary quality point of contact for regulatory authorities, auditors, and customers.4. Systems & ValidationReview and approve validation activities including analytical method validation, equipment qualification (IQ/OQ/PQ), computer system validation (CSV), and process validation.Ensure laboratory instruments, electronic systems, and software meet regulatory and data integrity requirements.5. Training & Quality CultureEnsure appropriate training of personnel on GMP, GLP, SOPs, and quality best practices.Promote and sustain a strong quality culture and compliance mindset across the organization.6. Risk Management & Continuous ImprovementIdentify potential quality and compliance risks and implement effective mitigation strategies.Drive continuous improvement initiatives to enhance regulatory compliance, operational efficiency, and service quality.

QC MANAGER

Develop comprehensive project plans outlining the scope, timeline, budget and resources required. Collaborate with clients, architects, and interior designers to understand project requirements and expectations. Ensure effective communication and coordination among various stakeholders involved in the project. Develop a detailed site plan based on the approved design, considering factors like space utilization, safety, and workflow efficiency. Work with project team to address any design or logical challenges during planning phase.

Urgent job opening for QA Officer. required fresher and experience candidate.job location - Navi Mumbai / Taloja / mahape / kopar khairne / Dombivali / Ambernath / Mumbai.experience - 0 to 5 years.salary - 15000 to 65000.interested candidate call on - 8850696229. or WhatsApp resume..

We are hiring for Quality Engineer- Chemical A) Qualification : To become a QA person in the pharmaceutical industry, one should have a degree in a science-related field, such as chemistry or pharmacy, to better understand pharmaceutical products.B) Experience : 0 to 2 years in R&D Pharmaceutical Industry from QA Department.C) Responsibility :1. Review of Manufacturing Processes.2. Knowledge of All regulated Guideline & Pharmacopoeia.3. Preparation & implementation of SOPs related to the concerned department & Justification of Specification.4. Nitrosamine Impurity, Elemental impurity, Genotoxic Impurity & their role related DMF Filing.5. QA person collaborates with the Quality Control (QC) team to ensure that laboratory testing is conducted appropriately and meets the required specifications.6. The QA person conducts regular internal audits of the manufacturing facility at R&D to ensure that the facility meets the required quality standards. Also handles the external audit cand its compliance.7. A QA person is responsible for ensuring that all necessary documentation is completed accurately, in a timely manner, and in compliance with regulatory requirements8. The QA person is responsible for reviewing and approving deviation reports and ensuring that corrective and preventive actions (CAPA) are implemented.9. The QA person is responsible for reviewing and investigating product complaints to ensure implementation of corrective and preventive actions (CAPA).10. A QA person is responsible for training of manufacturing and laboratory personnel on quality-related procedures and regulations.11. Handling of out of specification (OOS) and out of trend (OOT) laboratory incidents and their closing.12. Preparation & review the method of analysis (MOA), standard testing procedure (STP) and other documents related to QC.Qualification- Graduate in Chemical Contact Person- Deepak - 7757087059ID- deepak.vijayamgmt@gmail.com

Job title QA Mgr.Department name Quality AssuranceExperience 12 To 15yrsIndustry Engineering services Reporting To PartnerReporter All QA /QC in place TeamSalary Range 7L To 7.2L/-PABased at Taloja, Navi Mumbai.Goals 1. Quality Management System review within 60days.2. Establish successfully a system for CAPA within 60days.3. Implementation of 5s in 24 zonal areas within the company in 90days.4. Develop and plan for presentation to management and drive the TQM best practices within the organization.5. Establish and Set Quality Objective according to departments.6. Establish and set KPI, KRA to achieve 8 departments quality and productivity.7. Identifying bottlenecks in Blasting, Machining department and streamline procedures. 8. Collecting and analyzing data to identify trends, detect variations, and make data-driven decisions through SPC in minimum of 2 departments to maintain quality standards.Key responsibilities and accountabilities 1. Conduct Systems Audits every first week in a month.2. Daily QA morning meeting to discuss & guide problems faced by QA/QC team.3. Qualification and evaluation of Suppliers and Subcontractors.4. Analysing customer complaints and Internal rejection on weekly basis. Actively involved in Troubleshooting of process problems and monitor the non-conformities.5. Plan, conduct and face internal and external quality audits to verify compliance with quality standards and identify improvement areas.6. Plan and review the annual training calendar. Arrange three department-wise trainings monthly. Check and verify the effectiveness of the training and share feedback with management on a monthly basis.7. Implement Work management practice for planning, execution, and monitoring of all tasks and activities required to accomplish jobs on time.Knowledge, skills, and abilities Education and experience Diploma / BE Should be Technically Sound.Work Days Friday Weekly offSunday Working

Production Manager position. Looking after daily production of medical devices and following SOP and maintaining QMS as per required. Looking after waste management, production management, raw material management and quality assurance in production. Looking after production time frame for dispatch

Hiring for 1 Mechanical Engineer Job in midc taloja, AutoCAD Designer, Quality Assurance Incharge, Quality Assurance Inspector, with minimum 3 Years Experience, Required Educational Qualification is : B.Tech/B.E with Good knowledge in AutoCAD, Mechanical Maintenance, Mechanical Electrical Plumbing, Mechanical Testing, Mechanical Metallurgy, AutoCAD Designer, Quality Assurance Incharge, Quality Assurance Inspector etc.,

Software QA Tester Team LeadJob DescriptionWe are looking for a QA Tester to assess software quality throughmanual and automated testing. You will be responsible for creatingproject-specific test-cases, finding and reporting bugs and glitches.In this role, you should have a keen eye for detail and excellentcommunication skills..Ultimately, you will ensure that our products, applications and systemswork correctly.Responsibilities Review and analyze system specifications Collaborate withQA Engineersto develop effective strategies and testplans Execute test cases (manual or automated) and analyze results Evaluate product code according to specifications Create logs to document testing phases and defects Report bugs and errors to development teams Help troubleshoot issues Conduct post-release/ post-implementation testing Work with cross-functional teams to ensure quality throughout thesoftware development lifecycleRequirements and skills Proven experience as a Quality Assurance Tester or similar role Experience in project management and QA methodology Familiarity with Agile frameworks and regression testing is a plus Ability to document and troubleshoot errors Working knowledge of test management software (e.g. qTest, Zephyr)and SQL Excellent communication skills Attention to detail Analytical mind and problem-solving aptitude Strong organizational skills BSc/BA in Computer Science, Engineering or a related field

Key Responsibilities :Good Knowledge in (products)- (Management and Quality assurance work) as per ISO 17025:2017,Required experience in our material testing as per REQUIRED scope.To establish quality policy and objectives.Assist with laboratory administrative duties.Follow all quality assurance and quality system procedures(QSP).Issuance of all quality system documents.Monitoring to control of non-conforming work and initiate corrective & preventive actions to forestall the recurrence of non-conformities.To maintain training records for all laboratory staff.Implementing internal quality checks.Coordinate customer complaints and interacts with customers for giving feedback etc.To prepare internal audit plan & conduct ainternal audit.To prepare agenda for management review meetings.Officiate Management Review Meeting.Record the minutes of management review meeting for the outcome of the review meeting.Issuance of all quality system documents.Promote good relations with all customers.To maintain smooth laboratory work flow.Provision of resources.Responsible for the safe storage, supervision and use of equipment by suitably trained persons.To plan, schedule, conduct and record the findings of internal audit, conduct verification audit and present summary report to management about audit findings and corrective actions initiated for closure of audit non-conformities.Monitoring to control of non-conforming work and initiate corrective & preventive actions to forestall the recurrence of non-conformities.To control log book and maintenance of equipment.To supervise and perform the site testing activities.Reports to Lab Director/Technical Manager.To ensure safety and security of all office recordsEnsure proper maintenance of personal files, service registers etc., of all the staff.To deal with the matters relating to telephone, housekeeping, security, upkeep of the building etc.To initiate proposals for procurement of stores like computers, furn

Need a candidate who has good amount of production management knowledge with minimum 5 to 6 years of experience in the same field. He should have qualities like Production control, quality control, stock management waste management, error control, costing control, QMS, SOP, 5 P of production. production staff management. We looking for candidate for long term for at least 5 years.

Designation : QA ManagerLocation : MumbaiQualifications : Degree in a science-related field, chemistry or pharmacyExperience : 3+ years in R&D Pharmaceutical Industry from QA DepartmentResponsibility :* Review of Manufacturing Processes.* 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.* QA person collaborates with the Quality Control (QC) team to ensure that laboratory testing is conducted appropriately and meets the required specifications.* The QA person conducts regular internal audits of the manufacturing facility at R&D to ensure that the facility meets the required quality standards. Also handles the external audit cand its compliance.* QA person is responsible for ensuring that all necessary documentation is completed accurately, in a timely manner, and in compliance with regulatory requirements* The QA person is responsible for reviewing and approving deviation reports and ensuring that corrective and preventive actions (CAPA) are implemented.* The QA person is responsible for reviewing and investigating product complaints to ensure implementation of corrective and preventive actions (CAPA)* QA person is responsible for training of manufacturing and laboratory personnel on quality-related procedures and regulations.* Handling of out of specification (OOS) and out of trend (OOT) laboratory incidents and their closing.* Preparation & review the method of analysis (MOA), standard testing procedure (STP) and other documents related to QC.* Implementation & verification, in-process checks, online entries in BPR of product at Pilot plant manufacturing site.* Monitoring and ensuring the good manufacturing practice (GMP) at manufacturing site.Contact Person- Deepak - 7757087059ID- deepak.vijayamgmt@gmail.com