9,708 Quality Control Processes jobs in India

• Design, develop, and optimize manufacturing processes for new and existing products.
• Develop and refine tooling, fixtures, and machinery for production lines.
• Conduct root cause analysis for manufacturing defects and implement corrective actions.
• Collaborate with design engineers to ensure manufacturability of new product designs.
• Implement and monitor quality control procedures to ensure products meet specifications.
• Analyze production data to identify areas for improvement in efficiency, cost, and quality.
• Manage small to medium-sized engineering projects related to process improvements or new equipment installation.
• Ensure compliance with safety regulations and environmental standards in all manufacturing activities.
• Stay abreast of the latest advancements in manufacturing technologies and methodologies.
• Prepare technical documentation, including process flow diagrams, work instructions, and test procedures.

• Bachelor's degree in Mechanical Engineering or a related field.
• 3-5 years of experience in a manufacturing or production engineering role.
• Proficiency in CAD software (e.g., AutoCAD, SolidWorks, CATIA) for design and drafting.
• Experience with CNC machining, injection molding, or other relevant manufacturing processes is highly desirable.
• Strong understanding of lean manufacturing principles and Six Sigma methodologies.
• Excellent analytical, problem-solving, and troubleshooting skills.
• Good communication and teamwork abilities.
• Familiarity with quality management systems (e.g., ISO 9001).
• Ability to read and interpret technical drawings and specifications.

• Lead the design and development of complex mechanical systems and equipment for advanced manufacturing applications, including automation and robotics.
• Perform detailed engineering analysis, including Finite Element Analysis (FEA) and Computational Fluid Dynamics (CFD), to validate designs.
• Create comprehensive 3D models and detailed 2D manufacturing drawings using CAD software (e.g., SolidWorks, AutoCAD, Inventor).
• Develop and optimize process parameters for various manufacturing techniques such as additive manufacturing, CNC machining, and assembly lines.
• Collaborate with cross-functional teams, including electrical engineers, software developers, and production specialists, to ensure integrated system solutions.
• Oversee the fabrication, assembly, and testing of prototypes and new equipment.
• Troubleshoot and resolve complex mechanical issues encountered during development and production phases.
• Research and implement new manufacturing technologies and methodologies to improve product quality and reduce costs.
• Develop technical documentation, including operation manuals and maintenance procedures.
• Stay abreast of emerging trends and innovations in mechanical engineering and advanced manufacturing.

Company Description

MEDICUBE HEALTH CARE PRIVATE LIMITED is a ISO 13485 certified disposable medical device manufacturing company located in Medical Devices Park, Sultanpur, Hyderabad, Telangana, India. We are dedicated to enhancing healthcare products and ensuring the well-being of health care professionals and patients.

Role Description

This is a full-time on-site role for a Quality Assurance Quality Control professional, located in Medical Devices Park, Sultanpur, Hyderabad. The individual will be responsible for ensuring that all healthcare products meet the highest standards of quality. Daily tasks include implementing quality control measures, conducting quality audits, overseeing quality management systems, and ensuring compliance with Good Manufacturing Practices (GMP).

Qualifications

• Proficient in Quality Control, Quality Assurance, and Quality Management
• Knowledgeable in Good Manufacturing Practice (GMP) and Quality Auditing
• Strong attention to detail and analytical skills
• Excellent organizational and communication skills
• Ability to work independently and within a team
• Bachelor's degree in a related field is preferred
• Experience in the healthcare industry is a plus

Job Title: QA / QC Engineer

Location: Bhiwandi, Mumbai

Experience: 1+ Years

Salary: ₹30,000 – ₹5,000 per month

About the Role:

We are looking for a Quality Assurance / Quality Control professional with at least 1 year of experience in QA/QC functions. The ideal candidate should come from an engineering background or have prior experience in manufacturing / industrial setups.

Key Responsibilities:

Conduct quality checks on incoming materials, in-process production, and finished goods

Maintain QA/QC documentation and reports as per company standards

Ensure compliance with industry quality standards and internal processes

Identify defects and coordinate with production teams for corrective action

Support audits and inspections (internal and external)

Work closely with cross-functional teams to ensure continuous improvement in quality processes

Job Type: Full-time

Pay: , ,000.00 per month

Work Location: In person

Company Description

SREE EXPORTS PVT. LTD. is a textiles company located at 17A SURY 3RD LANE, CALCUTTA, West Bengal, India. We specialize in high-quality textiles and have a strong reputation in the industry. Our operations are based on a commitment to excellence and customer satisfaction. We aim to deliver superior products through consistent quality and innovative practices.

Role Description

This is a full-time on-site role for Quality Assurance Quality Control at SREE EXPORTS PVT. LTD., located in Vishakhapatnam. The role involves daily tasks such as performing quality assurance and control checks, managing quality systems, ensuring compliance with Good Manufacturing Practices (GMP), and conducting regular quality audits. The individual will be responsible for maintaining high standards and consistency in product quality.

Qualifications

• Experience in Quality Control and Quality Assurance
• Proficiency in Quality Management and Good Manufacturing Practice (GMP)
• Skills in conducting and managing Quality Audits
• Strong attention to detail and analytical skills
• Excellent problem-solving and decision-making abilities
• Ability to work independently and as part of a team
• Bachelor's degree in Quality Management, Engineering, or related field

Company Description

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Role Description

This is a full-time on-site role for a Quality Assurance Quality Control professional at Sankar Sealing Systems Private Limited, located in the Greater Chennai Area. The QA/QC professional will be responsible for implementing quality control processes, ensuring adherence to quality assurance standards, and maintaining compliance with Good Manufacturing Practice (GMP). The role involves conducting quality audits and managing overall quality management systems to ensure product quality and regulatory compliance.

Qualifications

• Experience in Quality Control and Quality Assurance
• Knowledge of and adherence to Quality Management principles
• Understanding of Good Manufacturing Practice (GMP)
• Experience with Quality Auditing processes
• Strong attention to detail and analytical skills
• Excellent communication and documentation skills
• Ability to work in a team and manage multiple tasks
• Bachelor's degree in Engineering, Quality Management, or related field

Company Description

Shandong SHENGLONG Biological Engineering Co., Ltd. is a mechanical and industrial engineering company based in Jinan, Jiyang County, Shandong, China. Located at No.18 Fuyang Street in the Jibei Development Zone, the company specializes in advanced engineering solutions. Potential applicants have the opportunity to join a cutting-edge organization committed to innovation and excellence in the field.

Role Description

This is a full-time on-site role for a Quality Assurance Quality Control professional. The position is based in Chennai. The successful candidate will be responsible for overseeing quality management systems, conducting quality audits, ensuring adherence to Good Manufacturing Practices (GMP), and implementing quality assurance processes. Daily tasks include monitoring production processes, identifying areas for quality improvements, and coordinating with teams to maintain high standards.

Qualifications

• Quality Control and Quality Assurance skills
• Experience in Quality Management and Good Manufacturing Practice (GMP)
• Proficiency in conducting Quality Auditing
• Strong analytical and problem-solving skills
• Excellent attention to detail and meticulous approach
• Bachelor's degree in a relevant field or equivalent experience
• Strong communication and teamwork abilities

Company Description

InVitro Research Solutions Private Limited (iVRS) is a Contract Research Organization providing comprehensive In-Vitro solutions for Pharmaceutical and Nutraceutical Product Development. The company serves Pharmaceutical, Medical Device, and Biotechnology organizations globally, ensuring compliance with stringent regulatory standards. iVRS prides itself on its experienced team, adept at methodical research and development, regulatory submissions, and systematic training. The organization specializes in a range of pharmaceutical dosage forms and adheres to regulatory standards to ensure seamless regulatory agency reviews.

Role Description

This is a full-time on-site role for a Quality Assurance Quality Control professional located in Bengaluru North. The individual will be responsible for overseeing day-to-day quality management tasks, including conducting quality control and quality assurance activities, adhering to Good Manufacturing Practice (GMP) standards, and performing quality audits. The role entails ensuring all processes meet regulatory and compliance guidelines.

Qualifications

• Proficiency in Quality Control tasks and standards
• Experience in Quality Assurance processes and techniques
• Knowledge of Quality Management systems and frameworks
• Understanding and implementation of Good Manufacturing Practice (GMP) standards
• Skills in conducting Quality Audits and assessments
• Excellent analytical and problem-solving abilities
• Strong attention to detail and organizational skills
• Bachelor's degree in Pharmacy, Chemistry, or relevant field
• Experience in the pharmaceutical Analytical Development & documentation,preparation of manual policies, review & approval of study protocols, validation protocols qualification protocols & CSV protocol ,implementation of analytical policies & basic knowledge of instruments like HPLC,LC-MS,GC-MS,ICP-MS etc.