What Quality Control Specialists Jobs are in India?
Showing 245 Quality Control Specialists jobs in India
Quality Control Reviewer
500051 Hindustan Cables Ltd
SAIN MEDICAMENTS PVT. LTD
Posted today
Job Viewed
Job Description
JD FOR QC ANALYST – Sr. Executive – 5+ YEARS EXPERIENCE
Sain Medicaments Pvt Ltd, Uppal, Hyderabad.
1. To perform analysis i.e. Raw Materials, Packing Materials, In-Process Materials, Finished Products and Stability samples.
2. To handle the instruments like UV, HPLC, GC, Dissolution Apparatus and other analytical instruments.
3. To initiate the Deviations / Incidents / Laboratory Incidents and ensure the implementation.
4. To ensure the preventive maintenance and AMC (Annual Maintenance Contract) is followed as per the schedule, all the records are in place and the Preventive Maintenance labels are updated.
5. To perform the calibration of all the instruments and update the calibration labels.
6. To ensure the Good Laboratory Practices (GLP).
7. To execute the analysis of Analytical and Cleaning Method Validations.
8. Execution of worksheets of Raw Materials, Packing Materials, In-Process Materials, Finished Products and Stability.
9. Analysis of Stability, CDP, forced degradation study Protocols, Reports and Raw Data.
10. To update log books and ensure the compliance for the same.
11. To handle the working standards, reference standards and its documentation.
12. Preparation of Specifications and STP.
13. To initiate change controls.
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0
AP Quality Control Specialist I, Accounts Payable Quality Control
Hyderabad
Amazon
Posted 2 days ago
Job Viewed
Job Description
Description
We are seeking a detail-oriented and tech-curious FinOps Quality Analyst to join our Accounts Payable Quality Control team. In this role, you will ensure accuracy, compliance, and process health across AP operations - conducting quality audits, identifying defect patterns, performing root cause analysis, and reporting quality metrics in a clear, actionable manner.
Beyond traditional quality assurance, you will actively look for ways to use technology - including Python scripting, automation tools, and AI-assisted solutions - to make quality processes faster, more accurate, and less manual. You won't just flag problems; you'll help build solutions.
This role operates with guidance from your manager and senior team members while owning defined quality workstreams. You'll partner with operations teams to improve service quality and contribute to continuous improvement projects.
The ideal candidate has a solid grounding in AP processes, a sharp eye for data discrepancies, and the initiative to pick up a scripting tool or AI solution when they see a manual process that could work better. We need someone who is proactive, detail-oriented, customer-obsessed, and genuinely curious about how technology can transform quality assurance in finance operations.
Key job responsibilities
- Execute quality control checks across AP processes and report quality health metrics in a clear, insightful manner.
- Review financial transactions and data to identify discrepancies, defect trends, and compliance risks.
- Perform root cause analysis on defects and partner with operations teams on corrective actions.
- Maintain quality scorecards, dashboards, and periodic reports for leadership review.
- Identify repetitive manual steps in quality workflows and propose automation solutions using Python scripts, Excel macros, RPA, or AI-assisted tools.
- Use AI tools to accelerate data analysis, report generation, or defect pattern detection.
- Build or modify basic scripts (Python, VBA, SQL) for data extraction, reconciliation, or automated checks.
- Participate in continuous improvement projects (Kaizen, JDI) to reduce defects with measurable results.
- Collaborate with cross-functional teams to implement process enhancements.
- Create SOPs and process documentation to support knowledge transfer and onboarding.
- Stay updated on financial controls, compliance standards, and internal policies relevant to AP operations.
Basic Qualifications
- 5+ years of Accounts Receivable or Account Payable experience
- Knowledge of financial controls and procedures
- Experience using data to influence business decisions
- Experience that includes strong analytical skills, attention to detail, and effective communication abilities
- Experience leading process improvements
- Work flexible schedules/shifts/areas, including weekends, nights, and/or holidays
Preferred Qualifications
- 2+ years of participating in continuous improvement projects in your team to scale and improve controllership with measurable results experience
- Experience in data analysis, reporting, and forecasting to guide business decisions
- Experience with Excel, Access, PowerPoint, Essbase and Oracle Financial Applications
Our inclusive culture empowers Amazonians to deliver the best results for our customers. If you have a disability and need a workplace accommodation or adjustment during the application and hiring process, including support for the interview or onboarding process, please visit for more information. If the country/region you're applying in isn't listed, please contact your Recruiting Partner.
We are seeking a detail-oriented and tech-curious FinOps Quality Analyst to join our Accounts Payable Quality Control team. In this role, you will ensure accuracy, compliance, and process health across AP operations - conducting quality audits, identifying defect patterns, performing root cause analysis, and reporting quality metrics in a clear, actionable manner.
Beyond traditional quality assurance, you will actively look for ways to use technology - including Python scripting, automation tools, and AI-assisted solutions - to make quality processes faster, more accurate, and less manual. You won't just flag problems; you'll help build solutions.
This role operates with guidance from your manager and senior team members while owning defined quality workstreams. You'll partner with operations teams to improve service quality and contribute to continuous improvement projects.
The ideal candidate has a solid grounding in AP processes, a sharp eye for data discrepancies, and the initiative to pick up a scripting tool or AI solution when they see a manual process that could work better. We need someone who is proactive, detail-oriented, customer-obsessed, and genuinely curious about how technology can transform quality assurance in finance operations.
Key job responsibilities
- Execute quality control checks across AP processes and report quality health metrics in a clear, insightful manner.
- Review financial transactions and data to identify discrepancies, defect trends, and compliance risks.
- Perform root cause analysis on defects and partner with operations teams on corrective actions.
- Maintain quality scorecards, dashboards, and periodic reports for leadership review.
- Identify repetitive manual steps in quality workflows and propose automation solutions using Python scripts, Excel macros, RPA, or AI-assisted tools.
- Use AI tools to accelerate data analysis, report generation, or defect pattern detection.
- Build or modify basic scripts (Python, VBA, SQL) for data extraction, reconciliation, or automated checks.
- Participate in continuous improvement projects (Kaizen, JDI) to reduce defects with measurable results.
- Collaborate with cross-functional teams to implement process enhancements.
- Create SOPs and process documentation to support knowledge transfer and onboarding.
- Stay updated on financial controls, compliance standards, and internal policies relevant to AP operations.
Basic Qualifications
- 5+ years of Accounts Receivable or Account Payable experience
- Knowledge of financial controls and procedures
- Experience using data to influence business decisions
- Experience that includes strong analytical skills, attention to detail, and effective communication abilities
- Experience leading process improvements
- Work flexible schedules/shifts/areas, including weekends, nights, and/or holidays
Preferred Qualifications
- 2+ years of participating in continuous improvement projects in your team to scale and improve controllership with measurable results experience
- Experience in data analysis, reporting, and forecasting to guide business decisions
- Experience with Excel, Access, PowerPoint, Essbase and Oracle Financial Applications
Our inclusive culture empowers Amazonians to deliver the best results for our customers. If you have a disability and need a workplace accommodation or adjustment during the application and hiring process, including support for the interview or onboarding process, please visit for more information. If the country/region you're applying in isn't listed, please contact your Recruiting Partner.
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1
Job Description
**Job Description Summary**
To manage 12-member team of analysts, senior analysts in QC - microbiology laboratory.
To prepare plans, protocols, reports and to execute day to day operations in microbiology laboratory.
**Job Description**
To manage a team of analysts, senior analysts, trainees in QC - microbiology laboratory.
To prepare plans, protocols, reports and to execute day to day operations in microbiology laboratory.
**Commitment to Diversity, Equity, and Inclusion:**
At Endo, our diversity unites and empowers us as One Team, and we are committed to cultivating, and valuing, each person's unique perspective. We actively promote a culture of inclusion that draws strength from our broad spectrums of diversity, including race, ethnicity, religion, gender identity or expression, national origin, color, sexual orientation, disability status, age, and all our other unique characteristics, qualifications, demonstrated skills, achievements, and contributions, backgrounds, experiences, cultures, styles, and talents.
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.
To manage 12-member team of analysts, senior analysts in QC - microbiology laboratory.
To prepare plans, protocols, reports and to execute day to day operations in microbiology laboratory.
**Job Description**
To manage a team of analysts, senior analysts, trainees in QC - microbiology laboratory.
To prepare plans, protocols, reports and to execute day to day operations in microbiology laboratory.
**Commitment to Diversity, Equity, and Inclusion:**
At Endo, our diversity unites and empowers us as One Team, and we are committed to cultivating, and valuing, each person's unique perspective. We actively promote a culture of inclusion that draws strength from our broad spectrums of diversity, including race, ethnicity, religion, gender identity or expression, national origin, color, sexual orientation, disability status, age, and all our other unique characteristics, qualifications, demonstrated skills, achievements, and contributions, backgrounds, experiences, cultures, styles, and talents.
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.
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2
Job Description
**Job Description Summary**
Experienced Analytical/Quality Control Analyst with 3-5 years of hands-on experience in an FDA-regulated pharmaceutical environment. Proficient in performing analytical testing of drug products and raw materials using techniques such as HPLC, GC, UV, and dissolution. Skilled in handling stability samples, method execution, data integrity compliance, and troubleshooting laboratory instruments. Strong understanding of cGMP, GLP, and FDA regulatory requirements, with a proven ability to ensure accurate documentation and compliance during audits and inspections.
**Job Description**
+ Perform routine and stability sample analysis as per approved specifications and test methods
+ Operate and maintain analytical instruments (HPLC, GC, UV, Dissolution Apparatus, etc.)
+ Review and document analytical data in compliance with cGMP and data integrity principles
+ Investigate OOS/OOT results and support deviation and CAPA activities
+ Ensure compliance with FDA, cGMP, and GLP requirements
+ Prepare and review analytical reports, protocols, and SOPs
+ Participate in method transfer, verification, and validation activities
+ Support regulatory and internal audits
+ Strong knowledge of FDA regulations, cGMP, and data integrity
+ Analytical troubleshooting and problem-solving skills
+ Documentation and compliance expertise
+ Team collaboration and communication
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.
Experienced Analytical/Quality Control Analyst with 3-5 years of hands-on experience in an FDA-regulated pharmaceutical environment. Proficient in performing analytical testing of drug products and raw materials using techniques such as HPLC, GC, UV, and dissolution. Skilled in handling stability samples, method execution, data integrity compliance, and troubleshooting laboratory instruments. Strong understanding of cGMP, GLP, and FDA regulatory requirements, with a proven ability to ensure accurate documentation and compliance during audits and inspections.
**Job Description**
+ Perform routine and stability sample analysis as per approved specifications and test methods
+ Operate and maintain analytical instruments (HPLC, GC, UV, Dissolution Apparatus, etc.)
+ Review and document analytical data in compliance with cGMP and data integrity principles
+ Investigate OOS/OOT results and support deviation and CAPA activities
+ Ensure compliance with FDA, cGMP, and GLP requirements
+ Prepare and review analytical reports, protocols, and SOPs
+ Participate in method transfer, verification, and validation activities
+ Support regulatory and internal audits
+ Strong knowledge of FDA regulations, cGMP, and data integrity
+ Analytical troubleshooting and problem-solving skills
+ Documentation and compliance expertise
+ Team collaboration and communication
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.
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3
Job Description
The Associate Vice President – Quality Control will provide strategic leadership and operational oversight for the Quality Control function across sterile injectable manufacturing facilities. The incumbent will be responsible for ensuring that all analytical, microbiological, and stability testing activities comply with global regulatory requirements, current Good Manufacturing Practices (cGMP), and internal quality standards.
The role involves leading a high-performing QC organization, driving operational excellence, strengthening compliance systems, supporting regulatory inspections, and fostering a culture of quality and continuous improvement.
Key Responsibilities
Strategic Leadership
- Develop and execute the Quality Control strategy in alignment with the organization's business objectives.
- Provide leadership for Chemical, Instrumentation, Microbiology, Stability, Environmental Monitoring, and Incoming Material laboratories.
- Establish long-term quality objectives and performance metrics for the QC function.
- Drive a culture of quality, accountability, innovation, and operational excellence.
- Build and mentor future leaders within the Quality Control organization.
Quality Control Operations
- Oversee testing of raw materials, packaging materials, in-process samples, finished products, water systems, gases, and environmental monitoring samples.
- Ensure timely batch release through efficient laboratory operations and optimal resource utilization.
- Review and approve analytical methods, specifications, SOPs, protocols, reports, and laboratory documentation.
- Ensure compliance with approved testing procedures and validated analytical methods.
- Monitor laboratory productivity and implement initiatives to improve turnaround time without compromising quality.
Regulatory Compliance
- Ensure full compliance with cGMP, GLP, Data Integrity requirements, and applicable global regulatory guidelines.
- Maintain inspection readiness for global regulatory agencies including USFDA, MHRA, EMA, TGA, ANVISA, WHO-GMP, and other international authorities.
- Lead and represent the Quality Control function during customer audits, regulatory inspections, and corporate audits.
- Ensure timely closure of audit observations, CAPAs, deviations, and quality investigations.
Laboratory Management
- Provide oversight for all QC laboratories, ensuring proper qualification, calibration, and maintenance of analytical instruments.
- Ensure compliance with laboratory data integrity principles and computerized system requirements.
- Oversee qualification and validation of laboratory equipment and analytical methods.
- Optimize laboratory workflows through digitalization, automation, and continuous improvement initiatives.
Quality Systems
- Lead investigations related to OOS, OOT, deviations, laboratory incidents, and customer complaints.
- Ensure robust root cause analysis and implementation of effective CAPA.
- Review and approve change controls, risk assessments, and laboratory investigations.
- Monitor quality trends and implement preventive actions to minimize quality risks.
Stability Program
- Provide strategic oversight for ICH stability studies and stability chamber management.
- Review stability data and ensure timely reporting to Regulatory Affairs and Quality Assurance.
- Ensure compliance with global stability guidelines and product lifecycle management requirements.
Continuous Improvement
- Drive Lean Laboratory, Six Sigma, Kaizen, and Operational Excellence initiatives.
- Establish departmental KPIs and monitor performance through regular reviews.
- Improve laboratory efficiency, cost optimization, and resource utilization while maintaining compliance.
- Promote innovation through adoption of modern analytical technologies and digital solutions.
Cross-Functional Collaboration
- Collaborate closely with Manufacturing, Quality Assurance, Regulatory Affairs, Engineering, Supply Chain, R&D, and Technical Services.
- Support new product introductions, technology transfers, validation activities, and commercial launches.
- Participate in management reviews and provide strategic recommendations related to quality performance.
People Leadership
- Lead, mentor, and develop managers and senior scientists within the Quality Control function.
- Identify training needs and establish competency development programs.
- Conduct performance reviews, succession planning, and talent development initiatives.
- Foster employee engagement and a culture of ownership and continuous learning.
Educational Qualifications
- M.Sc. (Chemistry), M.Pharm., or equivalent qualification in Pharmaceutical Sciences.
- Ph.D. in Analytical Chemistry or Pharmaceutical Sciences will be an added advantage.
Experience
- 20–25 years of progressive experience in Pharmaceutical Quality Control.
- Minimum 10 years of leadership experience in sterile injectable manufacturing.
- Proven experience in leading multidisciplinary QC teams within regulated pharmaceutical environments.
- Hands-on experience in handling global regulatory inspections.
Technical Competencies
- Extensive knowledge of injectable manufacturing and Quality Control systems.
- Strong expertise in analytical chemistry, microbiology, environmental monitoring, and stability studies.
- Thorough understanding of cGMP, GLP, ICH guidelines, pharmacopeial requirements (USP, EP, BP, IP), and data integrity.
- Experience with laboratory systems such as LIMS, CDS (Empower, Chromeleon), SAP, TrackWise, and electronic quality management systems.
- Expertise in laboratory investigations, risk management, CAPA, change control, and analytical method validation.
Leadership Competencies
- Strategic thinking and business acumen.
- Excellent people leadership and mentoring skills.
- Strong decision-making and problem-solving abilities.
- Effective stakeholder management and cross-functional collaboration.
- Excellent communication and presentation skills.
- Change management and organizational development capabilities.
- High level of integrity, accountability, and quality mindset.
Key Performance Indicators (KPIs)
- Laboratory turnaround time (TAT)
- Batch release adherence
- Regulatory inspection outcomes
- Audit observation closure timelines
- OOS/OOT investigation effectiveness
- CAPA implementation effectiveness
- Laboratory productivity
- Data Integrity compliance
- Stability program compliance
- Employee engagement and team development
- Cost optimization and laboratory efficiency
Preferred Candidate Profile
- Proven leadership experience in injectable pharmaceutical manufacturing.
- Strong exposure to global regulated markets including the US, Europe, UK, Australia, Canada, and other international markets.
- Demonstrated success in leading regulatory inspections and driving quality excellence.
- Strong analytical, strategic, and people management capabilities with a commitment to continuous improvement and operational excellence.
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4
Job Description
Purpose of Job
The candidate will lead and coordinate all QC activities related to All glass decoration Processes to control product quality. He will be responsible for In process checks as Proactive quality detection, as well as Sorting/ inspection of all production and ensuring QA audit passed. The candidate will also provide support in the analysis, review, and trending of release data, SOPs.
The individual should have demonstrated ability to work effectively in analytical development, quality control, and manufacturing environment is also a requirement for the position.
Essential Qualifications
BE Mechanical Engineering
Essential Experience
- Min 18 to 20 Years of experience in Quality domain and at least 4 to 5 years experience in glass/ decoration in Quality Control related activities.
- Min 5 to 8 years should have worked as function HOD handling a team
- Should be well versed with Quality measurement, cost and Process driven
Location - At Ansa Decoglass Pvt. Limited,Kosamba, Gujarat
Reporting to: Plant head
Key Roles/Responsibilities: –
- Ensuring QC resources training and development.
- Developing and implementation of SOPs leading to Quality of production process.
- Having complete clarity on Quality definitions/ requirement and able to transfer the same to both Production team as well as his own team.
- Coordinate and lead QC shop floor related activities
- Ensuring inspection quality and data maintained and review analytical data and submit input to management.
- Time to time discuss quality expectations with Production team and also resolve cross function issues related the quality observations.
- Analyze and review quality control release.
- Prepare and review manufacturing process development studies for internal reports.
- Work collaboratively with manufacturing/supply chain, quality assurance, to ensure timely delivery of final goods as per schedule.
- Participate in authoring and review of Analytical Development, Quality Control, Manufacturing control documents such as: standard operation procedures (SOPs), validation/verification protocols, reports and technical reports, manufacturing process development reports, investigation (OOS/ deviations, change control and INCs) reports.
- Preparing glass defects observations and coordinating with Glass plant for bringing improvement at input level.
- Prepare and arrange QC meeting minutes, Sample/critical and other routine QC documentations as needed.
- Ensuring sorting efficiency tracking and monitoring.
- Sorting capacity utilization, proactively resource planning and expansion proposal to management.
- Searching for new technological advanced solution for inspection, and helping team to find actions on defects at generation level, so slippages can be minimised
- Additional responsibilities maybe assigned, as required, or in consideration of candidate’s expertise and skills.
- Shall have knowledge of ISO certification like ISO 9001/ ISO 15378 GMP and Reconcile audit results from multiple sources and maintain records of completed audits.
- Responsible for identifying and implementing system improvements to optimize performance and uptime in a manner consistent with organizational goals, best practices requirements.
Desired Behavioral Competencies:
- Good communication skills
- Excellent leadership qualities
- Quality and cost approach
- Excellent decision making
- 7QC tools
- Data and result oriented.
- Customer Focus
- Effective
- Efficient
- Collaborating
- Innovation
- Agility
- Enabling People for Performance
- Process orientation and Documentation
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5
Job Description
Head – Projects Quality, Business Excellence & Innovation
Function
- Projects / Business Excellence
Reporting To
- MD / CEO / Executive Director
Location
- Mumbai
Role Purpose
- Build and institutionalize a robust quality culture across the entire real estate project lifecycle.
- Drive excellence from design, approvals, construction, handover, and post-possession.
- Improve project quality, delivery predictability, and customer satisfaction.
- Promote innovation in construction methodologies, materials, and technology.
- Enhance brand differentiation through superior quality and operational excellence.
Key Responsibilities
1. Project Quality Management
- Establish quality standards for design, engineering, and construction.
- Review design coordination among Architectural, Structural, and MEP consultants.
- Standardize material specifications and quality benchmarks.
- Monitor execution quality across civil, finishing, MEP, and external development works.
- Implement stage-wise quality gates (Design Freeze, Mock-ups, Sample Flats, Pre-Handover Audits).
- Conduct periodic quality inspections and site audits.
- Ensure timely closure of Non-Conformance Reports (NCRs).
- Minimize rework, snag lists, seepage, water leakage, and maintenance defects.
- Drive continuous quality improvement across all ongoing projects.
2. Standardization & Process Excellence
- Develop and implement Project Execution SOPs.
- Establish standardized construction quality checklists.
- Implement snag management and quality tracking systems.
- Standardize consultant coordination protocols.
- Define uniform handover and possession standards.
- Develop standard BOQs, specifications, and material standards.
- Benchmark quality practices across luxury, premium, redevelopment, and affordable housing projects.
- Drive process standardization across all project sites.
3. Customer-Centric Quality
- Strengthen Voice of Customer (VOC) across the customer lifecycle.
- Monitor quality from booking through possession and Defect Liability Period (DLP).
- Analyze customer complaints and identify recurring quality issues.
- Reduce the gap between sample flat quality and delivered product.
- Improve customer handover experience.
- Ensure timely resolution of post-possession defects.
- Improve Customer Satisfaction (CSAT) and Net Promoter Score (NPS).
4. Innovation & Technology
- Identify and implement modern construction technologies.
- Evaluate Aluform, Precast, Prefabrication, Drywall Systems, and Modular Construction.
- Introduce sustainable materials and green building practices.
- Drive adoption of cost-effective and durable construction solutions.
- Implement BIM and digital project monitoring tools.
- Introduce quality inspection and snag management applications.
- Promote PropTech solutions across projects.
- Balance cost, speed, and quality through innovation.
5. Governance & Compliance
- Ensure compliance with RERA commitments and approved specifications.
- Monitor adherence to local authority regulations.
- Ensure compliance with contractual quality commitments.
- Support Legal and Customer Care teams in quality-related disputes.
- Identify quality risks during project planning and feasibility.
- Strengthen governance through regular compliance audits.
6. Capability Building & Leadership
- Train engineers, project teams, and contractors on quality standards.
- Promote best construction and finishing practices.
- Build customer-focused project delivery culture.
- Mentor Project Heads and QA/QC teams.
- Conduct quality awareness and technical training programs.
- Foster a culture of quality ownership and continuous improvement.
Key Success Metrics (KPIs)
- Reduction in customer complaints per unit.
- Reduction in project rework costs.
- Reduction in snag count during handover.
- Reduction in water leakage and seepage complaints.
- Improvement in First-Time-Right handovers.
- Improvement in project quality audit scores.
- Improvement in Customer Satisfaction (CSAT).
- Improvement in Net Promoter Score (NPS).
- Increased adoption of innovative construction technologies.
- Reduction in execution deviations from approved specifications.
- Higher compliance with quality standards and SOPs.
- Timely closure of NCRs and quality observations.
Ideal Candidate Profile
Education
- B.E. Civil Engineering or Bachelor of Architecture.
- MBA / M.Tech preferred.
Experience
- 18–25 years in Real Estate Development or Construction.
- Experience in large residential, commercial, or mixed-use developments.
- Strong exposure to project execution and construction quality.
- Experience in QA/QC systems and finishing quality.
- Expertise in customer handover and possession management.
- Experience managing multiple consultants and large project portfolios.
Critical Competencies
- Strong knowledge of construction quality management.
- Expertise in project execution and finishing excellence.
- Practical understanding of on-site construction challenges.
- Strong analytical and problem-solving skills.
- Ability to influence Project Heads, Consultants, and Contractors.
- Leadership and stakeholder management capabilities.
- Customer-centric approach to project delivery.
- Process improvement and operational excellence mindset.
- Strong governance and compliance orientation.
- Strategic thinking with execution focus.
- High attention to detail and finishing quality.
- Ability to drive innovation and digital transformation in construction.
- Excellent communication, negotiation, and decision-making skills.
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6
Quality Assurance & Quality Control Manager
560001 Bangalore Bazaar
Moonrider.ai
Posted today
Job Viewed
Job Description
Job Title - Manager Quality Assurance & Quality Control (QA & QC)
Location - Moonrider Head Office, Bengaluru, Karnataka
Experience - 5–6 years (or more)
Department - Quality
Role Summary
We are seeking an experienced Quality Manager to lead quality assurance and quality control activities for our EV tractor manufacturing operations. The role will drive implementation of quality systems, supplier quality, in-process and final inspection processes, root-cause problem solving, and continuous improvement to ensure products meet safety, performance, and regulatory requirements.
Key Responsibilities
- Develop, implement, and maintain the quality management system (QMS) and ensure compliance with relevant automotive standards and statutory requirements.
- Lead incoming, in-process, and final inspection activities for electrical, battery, powertrain, drivetrain, and chassis assemblies.
- Define and enforce quality plans, inspection criteria, sampling procedures, and control plans for production and development stages.
- Manage supplier quality assurance: assess suppliers, approve incoming materials, perform supplier audits, and drive supplier corrective actions (SCAR).
- Coordinate with design, engineering, sourcing, production, and planning teams to align on specifications, design validation, and part readiness.
- Lead root-cause analysis (8D, RCA), corrective and preventive actions (CAPA), and verification of effectiveness for quality issues.
- Support prototype, pilot, and production quality requirements for new product introductions and design changes.
- Implement continuous improvement initiatives to reduce defects, rework, and warranty claims.
- Maintain and manage quality documentation, nonconformance records, inspection reports, and QMS records in ERP and quality management tools.
- Train and mentor shop-floor QC inspectors and quality engineers; promote quality culture across the organization.
- Respond to customer complaints and field issues, coordinate corrective actions, and provide technical input for root-cause and containment measures.
Required Qualifications
- Diploma / B.E. / B.Tech in Mechanical, Electrical, Electronics, Automotive, or related discipline.
- 5–6 years of experience in automotive QA/QC, preferably in tractors or other heavy equipment.
- Strong knowledge of quality methods and tools: 8D, FMEA, APQP, PPAP, MSA, SPC.
- Hands-on experience with incoming inspection, process audits, supplier audits, and shop-floor quality controls.
- Proven experience in root-cause analysis, CAPA management, and driving supplier and process improvements.
- Working knowledge of ERP systems (Odoo preferred) and MS Excel/Google Sheets.
Preferred Skills
- Familiarity with tractor or off-highway vehicle systems and components (electrical, battery packs, harnesses, motors, controllers, power electronics).
- Experience with automotive standards and certifications.
- Vendor quality development and supplier performance management experience.
- Strong analytical, communication, and stakeholder management skills.
- Ability to work in a fast-paced, cross-functional environment.
Desired Competencies
- Technical depth in automotive components and manufacturing processes.
- Ownership and accountability for quality outcomes.
- Problem-solving and data-driven decision making.
- Attention to detail and process-oriented mindset.
- Leadership and team development.
Key Performance Indicators
- Reduction in incoming and production defect rates.
- Supplier defect rate and on-time corrective action closure.
- Reduction in product rework and warranty incidents.
- Timeliness and effectiveness of CAPA and 8D closures.
- Accuracy and completeness of quality documentation and reporting.
Reporting To
Head of Manufacturing & Quality
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7
Garment Production - Quality Control Supervisor
West Bengal
Times Fiberfill Pvt Ltd
Posted 1 day ago
Job Viewed
Job Description
We are looking for a diligent and experienced Quality Control Supervisor with hands-on expertise across all stages of garment production—from fabric cutting to final packing. The ideal candidate will oversee quality control processes, ensure product consistency, and implement robust quality systems to meet buyers’ specifications and international compliance standards.
Key Responsibilities
- Supervise quality operations at all stages: cutting, sewing, finishing, and packing.
- Ensure adherence to buyers’ specifications, measurement standards, and approved samples.
- Conduct in-line and final inspections, identifying defects and initiating corrective actions.
- Develop and implement quality control plans, checklists, and SOPs.
- Monitor production processes to reduce rejection rates and improve overall quality performance.
- Coordinate between production, merchandising, and technical teams to resolve quality concerns promptly.
- Train operators and floor inspectors on quality parameters and manufacturing best practices.
- Maintain complete records of inspection reports, audits, and non-conformance reports.
- Support pre-production meetings and assist in factory audits by buyers or compliance teams.
- Drive continuous improvement initiatives to enhance product consistency and operational efficiency.
Key Competencies
- Strong understanding of garment construction, fabrics, measurements, and finishing standards.
- Ability to identify, analyze, and resolve quality issues proactively.
- Excellent leadership and team supervision skills.
- Sharp attention to detail with strong organizational abilities.
- Effective communication skills to interact with production teams and global buyers.
- Commitment to maintaining high safety, compliance, and ethical manufacturing standards.
Qualifications
- Bachelor’s or Diploma in Textile Technology, Apparel Production, or related field.
- 3–6 years of hands-on experience in Quality Assurance within the garment industry.
- In-depth knowledge of knit, woven, and woven-blend product categories is preferred.
- Familiarity with AQL standards, quality audit procedures, and buyer compliance requirements.
- Proficiency in MS Office and quality documentation tools.
Compensation and Benefits
- Salary: Industry Standard (depending on experience).
- Perks and Benefits:
- Paid Leave
- Sick Leave
- Travel Reimbursement
- Medical Insurance Coverage
What We Offer:
- Opportunity to work with reputed global fashion brands.
- Exposure to world-class manufacturing and compliance standards.
- Supportive environment encouraging continuous learning and process excellence.
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8
Job Description
**We Are Teva**
We're Teva, a leading innovative biopharmaceutical company, enabled by a world-class generics business. Whether it's innovating in the fields of neuroscience and immunology or delivering high-quality medicine worldwide, we're dedicated to addressing patients' needs now and in the future. Here, you will be part of a high-performing, inclusive culture that values fresh thinking and collaboration. You'll have the room to grow, the flexibility to balance life with work, and the opportunity to better health worldwide, together.
**How You'll Spend Your Day**
1. Quality Control Laboratory
+ Handling all the Quality Control Laboratory operations in compliance with Good Laboratory Practices and Safety policies.
+ Selection, upgradation, procurement, installation and qualification of laboratory instruments and equipment.
+ Preparing and monitoring of Capex and Revenue budget for laboratory.
+ Preparation and execution of cost improvement plans for the laboratory expenses.
+ To identify the needs and to provide resources, adequate facility required for effective and efficient functioning of the department for timely analysis of samples.
2. Quality Management
+ Oversees the implementation of Standard Operating Procedures relating to the laboratory activities and compliance with the requirements of Good Laboratory practices.
+ Upgradation of laboratory systems as per the regulatory requirements.
+ Oversees calibration and preventive maintenance of laboratory instruments and equipment as per schedule, in accordance with approved Standard Operating Procedures. To arrange vendor assistance for AMC and other Instrument/ equipment breakdown.
+ To ensure upkeep and maintenance of all laboratory standards as per written procedures and to arrange the Laboratory standards based on forecast and priorities.
+ Responsible for monitoring the activities pertaining to upkeep and maintenance of Narcotics and controlled substances.
3. Stability Study
+ To ensure identification, tracking and Co-ordination of all stability batches packed at Goa site and at other approved packing site.
+ Responsible for activities related to stability management.
+ To ensure planning, supervision and review activities of Commercial Stability Study Samples, Hold Time study Sample, Temperature Excursion, and Thermal Cycling.
4. Documentation
+ Responsible for review of Specifications, Test Methods, Analytical Worksheet, Analytical Method Transfer/Verification/validation Protocol and Reports and Standard Operating Procedure of the Quality Control department.
+ Ensures review and approval of departmental and site documents.
5. Budget and Inventory Management
+ Ensure timely submission and monitoring of QC laboratory Capex budget.
+ Initiation of Capital Expenditure Request as per agreed Quarter to match cash flow and procurement of budgeted items.
+ Ensure completion of Unbudgeted Capital Expenditure Request as per requirement.
+ Capex assets and inventory management in co-ordination with Finance department.
6. Inspections/Audits
+ Participates in the self-inspection program conducted by the Quality Assurance Department.
+ Ensures Audit readiness of Quality Control Laboratory and to face all regulatory and customer inspections and ensure compliance.
+ Active participation in regulatory Audits, customer audits and compliance.
7. Data Integrity
+ To ensure compliance to the requirements of policy and procedures on Data Integrity.
+ To ensure that the GxP data handling is secure and adopt measures to ensure data Integrity.
+ To make sure that the current systems and practices are challenged to guarantee that data integrity is maintained.
8. Operational Excellence
+ Preparation and execution of cost improvement plans in co-ordination with OpEx team to reduce laboratory expenses.
+ OpEx initiatives in the laboratory such as Implementation of 5S standards for laboratory consumables, chemicals and instrument spares for easy traceability and to reduce searching time, Process simplification and efficiency enhancement.
+ Identification and execution of efficiency enhancement projects
**Your Skills and Experience**
+ Bachelor or Master of Science / Pharmacy
+ 15 - 20 years of experience in the Pharmaceutical Industry handling QC operations
**How We'll Take Care of You**
At Teva India, care is at the heart of how we work. From your first day, you'll be welcomed into a people-first culture built on inclusion, respect, and belonging.
That support extends to you and your loved ones through benefits designed for real life. These include comprehensive medical insurance, OPD coverage, annual health checkups, term life and accident insurance, and confidential emotional wellbeing support through our Optum Employee Assistance Program. You'll also enjoy healthy meals at work, holistic wellbeing initiatives, and volunteering programs that help you give back to the community.
Your growth matters too. You'll have opportunities to build future-ready skills, collaborate on projects with global teams, explore internal career opportunities, and learn through programs such as our AI-enabled Teva Twist program, R&D Academy, continuing education, and mentorship.
Join our vibrant workplace, where we celebrate milestones, festivals, achievements, and community impact together.
**Already Working @TEVA?**
Make sure to apply through our internal career site on Twist-your one-stop shop for career development
**Teva's Equal Employment Opportunity Commitment**
Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws. We are committed to a diverse and inclusive workplace for all. If you are contacted for a job opportunity, please advise us of any accommodations needed to support you throughout the recruitment and selection process. All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience.
EOE including disability/veteran
We're Teva, a leading innovative biopharmaceutical company, enabled by a world-class generics business. Whether it's innovating in the fields of neuroscience and immunology or delivering high-quality medicine worldwide, we're dedicated to addressing patients' needs now and in the future. Here, you will be part of a high-performing, inclusive culture that values fresh thinking and collaboration. You'll have the room to grow, the flexibility to balance life with work, and the opportunity to better health worldwide, together.
**How You'll Spend Your Day**
1. Quality Control Laboratory
+ Handling all the Quality Control Laboratory operations in compliance with Good Laboratory Practices and Safety policies.
+ Selection, upgradation, procurement, installation and qualification of laboratory instruments and equipment.
+ Preparing and monitoring of Capex and Revenue budget for laboratory.
+ Preparation and execution of cost improvement plans for the laboratory expenses.
+ To identify the needs and to provide resources, adequate facility required for effective and efficient functioning of the department for timely analysis of samples.
2. Quality Management
+ Oversees the implementation of Standard Operating Procedures relating to the laboratory activities and compliance with the requirements of Good Laboratory practices.
+ Upgradation of laboratory systems as per the regulatory requirements.
+ Oversees calibration and preventive maintenance of laboratory instruments and equipment as per schedule, in accordance with approved Standard Operating Procedures. To arrange vendor assistance for AMC and other Instrument/ equipment breakdown.
+ To ensure upkeep and maintenance of all laboratory standards as per written procedures and to arrange the Laboratory standards based on forecast and priorities.
+ Responsible for monitoring the activities pertaining to upkeep and maintenance of Narcotics and controlled substances.
3. Stability Study
+ To ensure identification, tracking and Co-ordination of all stability batches packed at Goa site and at other approved packing site.
+ Responsible for activities related to stability management.
+ To ensure planning, supervision and review activities of Commercial Stability Study Samples, Hold Time study Sample, Temperature Excursion, and Thermal Cycling.
4. Documentation
+ Responsible for review of Specifications, Test Methods, Analytical Worksheet, Analytical Method Transfer/Verification/validation Protocol and Reports and Standard Operating Procedure of the Quality Control department.
+ Ensures review and approval of departmental and site documents.
5. Budget and Inventory Management
+ Ensure timely submission and monitoring of QC laboratory Capex budget.
+ Initiation of Capital Expenditure Request as per agreed Quarter to match cash flow and procurement of budgeted items.
+ Ensure completion of Unbudgeted Capital Expenditure Request as per requirement.
+ Capex assets and inventory management in co-ordination with Finance department.
6. Inspections/Audits
+ Participates in the self-inspection program conducted by the Quality Assurance Department.
+ Ensures Audit readiness of Quality Control Laboratory and to face all regulatory and customer inspections and ensure compliance.
+ Active participation in regulatory Audits, customer audits and compliance.
7. Data Integrity
+ To ensure compliance to the requirements of policy and procedures on Data Integrity.
+ To ensure that the GxP data handling is secure and adopt measures to ensure data Integrity.
+ To make sure that the current systems and practices are challenged to guarantee that data integrity is maintained.
8. Operational Excellence
+ Preparation and execution of cost improvement plans in co-ordination with OpEx team to reduce laboratory expenses.
+ OpEx initiatives in the laboratory such as Implementation of 5S standards for laboratory consumables, chemicals and instrument spares for easy traceability and to reduce searching time, Process simplification and efficiency enhancement.
+ Identification and execution of efficiency enhancement projects
**Your Skills and Experience**
+ Bachelor or Master of Science / Pharmacy
+ 15 - 20 years of experience in the Pharmaceutical Industry handling QC operations
**How We'll Take Care of You**
At Teva India, care is at the heart of how we work. From your first day, you'll be welcomed into a people-first culture built on inclusion, respect, and belonging.
That support extends to you and your loved ones through benefits designed for real life. These include comprehensive medical insurance, OPD coverage, annual health checkups, term life and accident insurance, and confidential emotional wellbeing support through our Optum Employee Assistance Program. You'll also enjoy healthy meals at work, holistic wellbeing initiatives, and volunteering programs that help you give back to the community.
Your growth matters too. You'll have opportunities to build future-ready skills, collaborate on projects with global teams, explore internal career opportunities, and learn through programs such as our AI-enabled Teva Twist program, R&D Academy, continuing education, and mentorship.
Join our vibrant workplace, where we celebrate milestones, festivals, achievements, and community impact together.
**Already Working @TEVA?**
Make sure to apply through our internal career site on Twist-your one-stop shop for career development
**Teva's Equal Employment Opportunity Commitment**
Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws. We are committed to a diverse and inclusive workplace for all. If you are contacted for a job opportunity, please advise us of any accommodations needed to support you throughout the recruitment and selection process. All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience.
EOE including disability/veteran
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