QA-Quality Assurance Job Vacancies in Nashik

Key ResponsibilitiesIn-Process & Final Inspection: Establish and monitor inspection protocols for incoming raw materials, in-process production lines, and final pre-dispatch items using precise measuring instruments (e.g., Vernier calipers, micrometers, gauges).Root Cause Analysis (RCA): Lead investigations into internal non-conformances and external customer complaints. Implement corrective and preventive actions (CAPA) using quality tools like 8D, 5-Why Analysis, and Fishbone diagrams.Process Documentation: Maintain comprehensive quality management systems (QMS) documentation, including Quality Manuals, Standard Operating Procedures (SOPs), Control Plans, and Failure Mode and Effects Analysis (FMEA).Statistical Process Control (SPC): Collect and analyze production data using statistical methods to monitor machine capabilities ($C_p, C_pk$), identify process variations, and implement continuous improvements.Audit Compliance: Conduct regular internal quality audits and prepare the production facility for external compliance and certifications (e.g., ISO 9001, IATF 16949).Vendor Quality Management: Collaborate with the procurement team to evaluate supplier performance, conduct vendor audits, and resolve component quality issues.

1. Quality team management2. Overall inspection verification3. Proto Type parts inspection and reporting4. Customer Supports & Communication. (8D, CAPA, PPT)5. Supplier Handling and audit6. QA department documentation for QMS certification 7. Monthly PPAP as per customer requirement8. In-house MSA9. New Customer PSA10. Daily Work Management.11. SOP and QA documents monitoring for all stages and every live parts12. Horizontal Deployment13. Die fixture and machine audit14. Rejection and rework control (Supplier, In-house, Customer), Scrap data, COPQ monitoring15. Product and Process auditREQUIRED COMPETENCIES, SKILLS FOR THE JOB1. Knowledge of 5 core tools (APQP, FMEA, MSA, SPC, PPAP)2. Knowledge of QMS 3. Knowledge of action plan (8D, CAPA, PPT)4. New customer assessment5. New supplier development6. Supplier audit7. Customer satisfaction8. Die and fixture audit9. Knowledge of DWM10. Knowledge of product and process audit

We are Looking for 1 Qms Documentation Post in Shinde Gaon, Chakan Pune,Chakan Pune, Maharashtra, Quality Assurance Engineer,Quality Assurance Incharge, with Deep Knowledge in Quality Assurance Engineer,Quality Assurance Incharge and Required Educational Qualification is : Diploma, other Bachelor Degree, B.a

In process Part Inspection, Final Product Inspection , Pdir and all System Documentation.

Electronics Testing Equipment' Quality Testing Inspection production

Job description will be discussed during interviews.3 years bond will be compulsory, 1 year will be training period, After 1 year, salary will be increased depending upon performance.

Designation: Quality Control ExecutiveQualification: Diploma/Degree in printing and Packaging.Reporting To: QC Team lead.Experience: Minimum 3-4 years. (Preferably in quality and production department)CTC Cost : 4 to 5.5 LacsSkills Needed:Computer literateOn site job approvalsKnowledge of colour ManagementExperience in offset/ Flexo paper base printing.

Education : BE or Diploma in Mechanical/ ProductionExperience: 4 to 7 yearsHaving relevant experience in CNC/ VMC Machine shop in Production Process EngineeringHaving knowledge of Design, Lay out design & inspection, new product development , 4 M change, IATF 16949 auditing, VDA audit, ISO 14001: 2015, machine planning, KANBAN, Process audit, Product Audit etc.

Quality Control: To look quality of goodsMicrobiologist and Pharmacist as there professional jobs

We have vacant of 1 Quality Control Engineer Job in shindegaon chakan pune,Chakan Pune, Maharashtra, Experience Required : 2 Years Educational Qualification : Diploma, Other Bachelor Degree, B.A Skill QA-Quality Assurance etc.

Key Responsibilities1. Quality Strategy & Systems ManagementEstablish & Maintain QMS: Develop, implement, and upgrade the Quality Management System (QMS) in alignment with international standards (such as ISO 9001, IATF 16949 for automotive, or ISO 13485 for medical devices, depending on the industry).Audit Readiness: Lead internal and external quality audits, serve as the primary point of contact for regulatory bodies, and ensure swift closure of any non-compliance findings.Standard Operating Procedures (SOPs): Review, approve, and enforce SOPs across the receiving, in-process, and final inspection stages.2. Operations & ControlDefect Prevention: Implement advanced quality tools like FMEA (Failure Mode and Effects Analysis), SPC (Statistical Process Control), and MSA (Measurement Systems Analysis) to predict and prevent defects.Root Cause Analysis: Lead complex investigations into product failures or customer complaints using 8D, 5-Why, and Fishbone (Ishikawa) methodologies to implement permanent corrective actions (CAPA).Vendor Quality Management: Collaborate with the procurement team to evaluate supplier quality, establish incoming material standards, and conduct supplier audits.3. Continuous Improvement & MetricsKPI Tracking: Monitor and report on key quality metrics, including COPQ (Cost of Poor Quality), PPM (Parts Per Million) defect rates, FTR (First Time Right), and customer return rates.Lean Practices: Drive continuous improvement initiatives using Lean Six Sigma methodologies to eliminate waste and optimize process efficiency.4. Leadership & Team ManagementTeam Development: Lead, mentor, and build the capability of the quality engineering and inspection teams (QA/QC Engineers, Programmers, Inspectors).Culture Shift: Foster a plant-wide Quality First mindset by training production operators and floor staff on quality standards.

Key Responsibilities:Ensure implementation and compliance with cGMP, GLP, GDP, and regulatory guidelines (WHO, USFDA, EU-GMP, Schedule M).Review and approve Batch Manufacturing Records (BMR), Batch Packaging Records (BPR), SOPs, specifications, and protocols.Handle deviations, change controls, OOS/OOT investigations, CAPA, and risk assessments.Monitor in-process quality checks and finished product documentation.Participate in internal, external, and regulatory audits and ensure timely closure of audit observations.Perform and review validation activities including process validation, cleaning validation, and equipment qualification.Control and maintain QA documentation, logs, and quality records.Coordinate with Production, QC, Engineering, and Warehouse teams for quality-related activities.Support product release and market complaint handling.Ensure compliance with data integrity and documentation practices.Required Qualifications:B.Pharm / M.Pharm / B.Sc / M.Sc (Chemistry or related discipline)1-5 years of experience in Quality Assurance within a pharmaceutical manufacturing environmentStrong knowledge of GMP documentation and regulatory compliancePreferred Skills & Competencies:Hands-on experience with regulatory audits (WHO / USFDA / MHRA)Knowledge of pharmaceutical quality systems (QMS)Good understanding of validation and qualification proceduresStrong analytical, documentation, and problem-solving skillsProficiency in MS Office and quality management systemsGood communication and coordination abilitiesIndustry:Pharmaceuticals / API / Formulations

Job Title:HOD - Quality Assurance (QA) & Management Representative (MR)Job Summary:The Head of Department - Quality Assurance & Management Representative is responsible for establishing, implementing, maintaining, and continually improving the organisations Quality Management System (QMS) in line with applicable standards such as ISO 9001 / IATF / ISO 14001 / ISO 45001 (as applicable). The role ensures compliance with statutory, customer, and regulatory requirements while acting as the key liaison between top management, certification bodies, customers, and internal departments on quality matters.Key Responsibilities:Quality Assurance (HOD - QA):Lead and manage the Quality Assurance department and quality personnel.Develop, implement, and monitor quality policies, objectives, SOPs, and work instructions.Ensure compliance with customer specifications, statutory requirements, and industry standards.Review and approve quality plans, inspection procedures, and control plans.Monitor product quality, analyse nonconformities, and drive root cause analysis (RCA) and corrective & preventive actions (CAPA).Handle customer complaints, quality audits, and qualityrelated communications.Ensure effective calibration, inspection, testing, and quality records management.Drive continuous improvement initiatives such as Kaizen, 5S, Lean, Six Sigma (if applicable).Management Representative (MR):Act as the Management Representative as per applicable ISO standards.Ensure the QMS conforms to standard requirements and is effectively implemented.Report QMS performance, audit results, risks, and improvement opportunities to Top Management.Plan, conduct, and close internal audits and coordinate external / certification audits.Ensure timely management review meetings and followup of action points.Promote awareness of customer requirements and quality culture across the organisation.Coordinate with certification bodies, regulatory authorities, and customers for audits and inspections.Required Qualifications:Bachelors degree in Engineering / Science or relevant discipline.Formal training in ISO 9001 (Lead Auditor preferred).Strong knowledge of Quality Management Systems and documentation control.Experience:8-15 years of experience in Quality Assurance / Quality Management.Minimum 3-5 years in a leadership or HOD role.Handson experience in handling internal and external audits.Key Skills & Competencies:Strong leadership and people management skills.Excellent knowledge of QMS standards and compliance requirements.Analytical and problemsolving skills.Effective communication and coordination abilities.Documentation, reporting, and audit management expertise.Customerfocused and continuous improvement mindset.Preferred (Optional):Experience in manufacturing / pharma / engineering industry.Knowledge of additional standards such as ISO 14001, ISO 45001, IATF 16949, GMP.Six Sigma Green/Black Belt certification.Reporting To:Top Management / Plant Head / Director

The candidate should be from Rubber & Plastic background . should know Production , Planning QA , Plant Maint , Improvement ,activities , Budgeting , Finance , MIS, General Administration , Union Mgmt , Agreements etc