What Jobs are available for Quality Director in Mumbai?

Our client, a leading pharmaceutical company, is seeking a meticulous and experienced Senior Quality Control Analyst to join their dynamic team in Mumbai, Maharashtra, IN . This critical role ensures that all manufactured pharmaceutical products meet stringent quality standards and regulatory requirements before they reach the market. You will be responsible for conducting a wide range of laboratory tests and analyses on raw materials, in-process samples, and finished products using advanced analytical techniques and instrumentation. This includes performing physicochemical tests, microbiological assays, and stability studies to verify product identity, strength, quality, and purity. The Senior Quality Control Analyst will be proficient in operating and maintaining various laboratory equipment such as HPLC, GC, UV-Vis spectrophotometers, and dissolution testers. You will meticulously document all test results, maintain accurate laboratory records, and prepare comprehensive analytical reports. Ensuring compliance with Good Laboratory Practices (GLP), Good Manufacturing Practices (GMP), and relevant regulatory guidelines (e.g., FDA, WHO) is paramount. This role also involves troubleshooting analytical methods, investigating out-of-specification (OOS) results, and implementing corrective and preventive actions (CAPA). You will collaborate closely with R&D, Production, and Quality Assurance departments to resolve quality issues and support product development. The ideal candidate possesses strong analytical skills, a keen eye for detail, and a thorough understanding of pharmaceutical quality control principles. Excellent problem-solving abilities and a commitment to maintaining the highest standards of quality and safety are essential. This is an excellent opportunity for a seasoned QC professional to contribute to a reputable organization dedicated to improving global health.
Responsibilities:

• Perform routine and non-routine analytical tests on raw materials, intermediates, and finished products.
• Operate and maintain laboratory equipment such as HPLC, GC, FTIR, UV-Vis, and dissolution apparatus.
• Analyze samples using validated methods and ensure compliance with pharmacopoeial standards.
• Document all laboratory activities, results, and observations accurately and contemporaneously.
• Investigate out-of-specification (OOS) results and deviations, and implement corrective and preventive actions (CAPA).
• Prepare certificates of analysis (CoA) and other quality control reports.
• Ensure adherence to Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP).
• Participate in method validation and transfer activities.
• Maintain laboratory inventory and ensure proper storage of reagents and samples.
• Collaborate with Quality Assurance and Production teams on quality-related issues.
• Stay updated with the latest regulatory guidelines and scientific advancements in pharmaceutical quality control.
• Contribute to continuous improvement initiatives within the QC department.

Qualifications:

• Bachelor's or Master's degree in Pharmacy, Chemistry, Biotechnology, or a related life science field.
• Minimum of 4-6 years of experience in a pharmaceutical Quality Control laboratory setting.
• Hands-on experience with analytical instrumentation (HPLC, GC, etc.).
• Thorough understanding of GMP, GLP, and regulatory requirements.
• Proficiency in data analysis and interpretation.
• Strong attention to detail and accuracy.
• Excellent problem-solving and investigative skills.
• Good written and verbal communication skills.
• Ability to work effectively in a team environment.

Our client is seeking a highly experienced Senior Quality Control Analyst to oversee and enhance their pharmaceutical quality assurance processes. This role is pivotal in ensuring that all manufactured products meet stringent quality standards and regulatory compliance requirements before they reach the market. The ideal candidate will possess a deep understanding of pharmaceutical manufacturing, quality control methodologies, and relevant regulatory guidelines (e.g., GMP, ICH). You will be responsible for developing and implementing robust quality control plans, performing advanced analytical testing, interpreting complex data, and ensuring the accuracy and reliability of results. This is a fully remote position, requiring you to manage quality control operations and provide expert guidance from your home office. You will collaborate closely with manufacturing, R&D, and regulatory affairs teams to identify potential quality issues, conduct root cause analysis, and implement corrective and preventive actions (CAPA). Your responsibilities will include managing stability studies, validating analytical methods, and overseeing the release of raw materials, in-process samples, and finished products. The ability to interpret deviations, out-of-specification (OOS) results, and change controls effectively is essential. You will also contribute to the continuous improvement of quality systems and processes. This role demands meticulous attention to detail, strong problem-solving skills, and excellent written and verbal communication abilities for report generation and inter-departmental collaboration. Proficiency in various analytical techniques and instrumentation (e.g., HPLC, GC, UV-Vis, dissolution apparatus) is required. The Senior Quality Control Analyst will play a key role in safeguarding product quality and patient safety.

Responsibilities:

• Develop, implement, and manage comprehensive quality control strategies.
• Perform advanced analytical testing on raw materials, in-process samples, and finished products.
• Interpret and analyze complex analytical data, ensuring accuracy and reliability.
• Validate analytical methods and instrumentation according to regulatory guidelines.
• Oversee and manage stability study programs.
• Investigate deviations, out-of-specification (OOS) results, and out-of-trend (OOT) data.
• Implement and track Corrective and Preventive Actions (CAPA).
• Collaborate with manufacturing and R&D teams to resolve quality issues.
• Ensure compliance with Good Manufacturing Practices (GMP) and other relevant regulations.
• Prepare and review quality control reports, specifications, and procedures.
• Contribute to the improvement of the overall Quality Management System (QMS).

Qualifications:

• Bachelor's or Master's degree in Pharmacy, Chemistry, Analytical Chemistry, or a related life science discipline.
• Minimum of 6 years of experience in pharmaceutical quality control or quality assurance.
• Extensive hands-on experience with analytical instrumentation (HPLC, GC, KF, UV-Vis, dissolution).
• Thorough understanding of GMP, ICH guidelines, and regulatory submission requirements.
• Proven experience in method validation, stability studies, and OOS investigations.
• Strong analytical, problem-solving, and critical thinking skills.
• Excellent written and verbal communication skills for technical reporting and collaboration.
• Ability to work independently and manage workload effectively in a remote setting.
• Detail-oriented with a strong commitment to quality and compliance.
• Experience with quality management software systems is a plus.

This role offers a challenging and rewarding opportunity for a dedicated QC professional to significantly contribute to ensuring the highest standards of pharmaceutical quality.

Our client is seeking a meticulous and skilled Pharmaceutical Quality Control Analyst to join their team in Mumbai, Maharashtra, IN . This critical role ensures that all pharmaceutical products meet stringent quality and safety standards before they reach the market. You will be responsible for conducting a wide range of laboratory tests on raw materials, in-process samples, and finished products using advanced analytical techniques and instrumentation. The ideal candidate will possess a strong background in analytical chemistry, excellent laboratory skills, and a thorough understanding of Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP). Key responsibilities include performing qualitative and quantitative analyses, validating analytical methods, troubleshooting instrumentation, and maintaining detailed records of all testing procedures and results. You will collaborate closely with the R&D and production departments to address any quality deviations and implement corrective actions. A proactive approach to identifying potential quality issues and contributing to continuous improvement initiatives is highly valued. We are looking for an individual with exceptional attention to detail, strong problem-solving abilities, and the capacity to work efficiently under pressure. This position offers a rewarding opportunity to contribute to the development and production of life-saving medicines. The ability to interpret complex data, generate comprehensive reports, and communicate findings clearly to relevant stakeholders is essential. A Bachelor's or Master's degree in Pharmacy, Chemistry, or a related science field is required. Familiarity with pharmacopoeial standards (e.g., IP, USP, BP) and experience with various analytical instruments such as HPLC, GC, UV-Vis spectrophotometers, and dissolution testers are preferred. Your dedication to quality will play a crucial role in upholding our client's commitment to patient safety and product efficacy.

**Make an impact with NTT DATA**
Join a company that is pushing the boundaries of what is possible. We are renowned for our technical excellence and leading innovations, and for making a difference to our clients and society. Our workplace embraces diversity and inclusion - it's a place where you can grow, belong and thrive.
**Your day at NTT DATA**
The Senior Manager, Quality is a senior management role, primarily responsible for leading and overseeing the relevant quality management efforts, thereby ensuring that the company's products or services consistently meet or exceed client expectations.
This role is responsible for developing and implementing quality strategies, managing quality control processes, and driving continuous improvement initiatives.
This role, through expertise in quality management methodologies, strong leadership skills, and attention to detail, is to promote a culture of quality excellence.
**Key responsibilities:**
+ Develops and implements a comprehensive quality management strategy, including policies, procedures, and standards, to ensure the delivery of high-quality products or services.
+ Defines quality objectives, metrics, and targets, and establishes mechanisms to monitor and measure performance against these targets.
+ Leads and manages a team of quality professionals, providing guidance, training, and performance feedback to ensure the effective execution of quality control activities.
+ Oversees the implementation and maintenance of quality control processes, including inspections, testing, and data analysis, to identify and address deviations, defects, or non-conformities in products or services.
+ Conducts regular audits and assessments of operational processes and procedures to identify areas for improvement and ensures compliance with quality standards and regulations.
+ Monitors customer feedback and complaints, facilitating timely investigations, root cause analysis, and corrective actions to address issues and prevent recurrence.
+ Drives continuous improvement initiatives to enhance quality performance, efficiency, and customer satisfaction, leveraging methodologies such as Lean Six Sigma and Kaizen.
+ Stays updated on industry trends, emerging technologies, and best practices in quality management, incorporating relevant advancements into the organization's quality practices.
+ Prepares and presents quality performance reports and insights to senior management, highlighting key metrics, trends, and recommendations for process improvements.
**To thrive in this role, you need to have:**
+ Extended knowledge of quality management methodologies, tools, and techniques, such as ISO 9001, Six Sigma, Lean, or similar frameworks.
+ Extended leadership and team management skills, with the ability to inspire and motivate teams to achieve quality objectives.
+ Extended analytical and problem-solving abilities, with a keen attention to detail and the ability to analyze complex data to drive data-driven decision-making.
+ Excellent communication and interpersonal skills, with the ability to effectively engage and collaborate with stakeholders at all levels of the organization.
+ Extended project management skills, with the ability to manage multiple priorities, meet deadlines, and deliver results within established timelines.
+ Extended familiarity with relevant regulations and industry standards related to the organization's products or services.
**Academic qualifications and certifications:**
+ Bachelor's degree in Business Management or Operations or a related field.
+ Six Sigma Green Belt/ Six Sigma Black belt certification is desirable.
+ ISO 9001 Lead auditor certification is desirable.
+ Certified Quality Manager certification is optional.
**Required experience:**
+ Extended experience in quality management or a related role, with a strong track record of developing and implementing effective quality management systems.
+ Extended experience in conducting audits and assessments to evaluate compliance with quality standards and regulations.
+ Extended experience managing and leading quality teams.
**Workplace type** **:**
Hybrid Working
**About NTT DATA**
NTT DATA is a $30+ billion business and technology services leader, serving 75% of the Fortune Global 100. We are committed to accelerating client success and positively impacting society through responsible innovation. We are one of the world's leading AI and digital infrastructure providers, with unmatched capabilities in enterprise-scale AI, cloud, security, connectivity, data centers and application services. Our consulting and industry solutions help organizations and society move confidently and sustainably into the digital future. As a Global Top Employer, we have experts in more than 50 countries. We also offer clients access to a robust ecosystem of innovation centers as well as established and start-up partners. NTT DATA is part of NTT Group, which invests over $3 billion each year in R&D.
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Our client is a highly respected manufacturing firm known for its commitment to quality and innovation. They are seeking an experienced Senior Quality Control Manager to oversee and elevate their quality assurance and control processes at their facility in Mumbai, Maharashtra, IN . This leadership position is critical for ensuring all manufactured products meet stringent quality standards, regulatory requirements, and customer expectations. The ideal candidate will possess a deep understanding of quality management systems and a proven ability to drive continuous improvement in quality performance.

Key Responsibilities:

• Develop, implement, and maintain comprehensive quality control policies, procedures, and standards across all manufacturing operations.
• Lead and manage the quality control team, providing direction, training, and performance evaluations.
• Oversee all quality assurance activities, including incoming material inspection, in-process quality checks, and final product testing.
• Establish and monitor key quality metrics (KPIs) such as defect rates, customer complaints, and first-pass yield, reporting findings to senior management.
• Conduct root cause analysis for quality deviations and implement effective corrective and preventive actions (CAPA).
• Ensure compliance with relevant industry standards (e.g., ISO 9001, industry-specific certifications) and regulatory requirements.
• Collaborate with production, engineering, and R&D teams to address quality issues and improve product design and manufacturability.
• Manage the calibration and maintenance of quality control equipment and instrumentation.
• Develop and deliver quality training programs for manufacturing personnel.
• Conduct internal audits and support external audits by customers or regulatory bodies.
• Drive continuous improvement initiatives to enhance product quality, reduce waste, and increase overall operational efficiency.
• Maintain accurate quality records and documentation.

Qualifications:

• Bachelor's degree in Engineering (Mechanical, Industrial, or related field) or a related scientific discipline.
• Minimum of 7 years of experience in quality control or quality assurance within a manufacturing environment, with at least 3 years in a leadership or management role.
• Strong knowledge of quality management systems (QMS), such as ISO 9001, and quality control methodologies (e.g., Six Sigma, SPC).
• Proven experience in root cause analysis and CAPA implementation.
• Excellent analytical, problem-solving, and decision-making skills.
• Strong leadership, team management, and communication skills.
• Proficiency in quality control tools and techniques, including statistical process control (SPC).
• Familiarity with relevant manufacturing processes and standards.

This is an excellent opportunity for a dedicated quality professional to take on a key leadership role and significantly contribute to maintaining and enhancing the company's reputation for excellence.

Our client is looking for a meticulous and experienced Senior Pharmaceutical Quality Control Analyst to join their esteemed team in Mumbai, Maharashtra, IN . This critical role ensures the quality and safety of pharmaceutical products through rigorous testing and analysis. You will be responsible for performing a wide range of laboratory tests on raw materials, in-process samples, and finished products, adhering to strict regulatory guidelines and company SOPs. Key responsibilities include operating and maintaining analytical instruments such as HPLC, GC, UV-Vis spectrophotometers, and other relevant equipment. You will analyze test results, interpret data, and document findings accurately in compliance with Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP). The Senior Analyst will also be involved in method development and validation, troubleshooting analytical issues, and contributing to the investigation of deviations and out-of-specification (OOS) results. This role requires a strong understanding of pharmaceutical quality systems and regulatory requirements (e.g., FDA, ICH). You will collaborate with various departments, including R&D, Production, and Regulatory Affairs, to ensure product quality throughout its lifecycle. The ability to train and mentor junior analysts is also a requirement. We are seeking a candidate with excellent analytical skills, a keen eye for detail, and a strong commitment to quality and compliance. A Bachelor's or Master's degree in Chemistry, Pharmacy, or a related science field, coupled with significant experience in pharmaceutical QC, is essential. This is a vital position for ensuring the integrity of our pharmaceutical products and maintaining our reputation for excellence.

Our client, a prominent manufacturing organization, is seeking an experienced Senior Quality Control Inspector to join their team in **Mumbai, Maharashtra, IN**. This role is critical in ensuring that all manufactured products meet stringent quality standards and specifications. The ideal candidate possesses a deep understanding of quality control methodologies, inspection techniques, and relevant industry standards. You will be responsible for performing detailed inspections of raw materials, in-process components, and finished goods, using various measurement tools and equipment. Your duties will include identifying defects, documenting non-conformities, analyzing quality data, recommending corrective actions, and collaborating with production and engineering teams to resolve quality issues. Strong attention to detail, precision, and a systematic approach are paramount. You will also be involved in developing and implementing quality control procedures, conducting internal audits, and ensuring compliance with regulatory requirements. The Senior Quality Control Inspector will play a key role in training and mentoring junior inspectors, promoting a culture of quality throughout the manufacturing process. Excellent communication skills are necessary for reporting findings and working effectively with cross-functional teams. We are looking for a proactive individual who can independently manage inspection processes, contribute to continuous improvement initiatives, and uphold the highest standards of product quality. This hands-on role requires diligence, accuracy, and a commitment to excellence in a fast-paced production environment.
Responsibilities:

• Perform comprehensive quality inspections on materials and products.
• Utilize measurement and testing equipment to verify specifications.
• Identify and document product defects and non-conformities.
• Analyze quality data and trends to identify root causes of issues.
• Collaborate with production and engineering to implement corrective actions.
• Ensure compliance with quality standards and regulatory requirements.
• Develop and update inspection procedures and work instructions.
• Conduct internal quality audits.
• Train and mentor junior quality control personnel.

Qualifications:

• High school diploma or equivalent; technical certification in Quality Assurance or a related field is preferred.
• Minimum of 4-6 years of experience in quality control inspection within a manufacturing setting.
• Proficiency with various measurement and testing instruments (calipers, micrometers, CMM, etc.).
• Strong understanding of quality control principles and methodologies (e.g., Six Sigma, Lean).
• Ability to read and interpret technical drawings and specifications.
• Excellent attention to detail and accuracy.
• Good analytical and problem-solving skills.
• Effective communication and interpersonal skills.
• Experience with documentation and reporting.

A prominent manufacturing and production company in the heart of Mumbai, Maharashtra, IN is seeking a highly experienced Senior Quality Control Inspector. This role is critical in ensuring that all manufactured products meet rigorous quality standards and specifications. You will be responsible for conducting detailed inspections, identifying defects, and implementing corrective actions to maintain product integrity and customer satisfaction. This position offers a hybrid work model, allowing for a balance between on-site operational oversight and off-site quality management tasks.

Key responsibilities include developing and executing comprehensive quality control plans and procedures. You will perform visual and dimensional inspections of raw materials, in-process materials, and finished goods using various measuring instruments and testing equipment. The Senior QC Inspector will also be tasked with documenting inspection results, analyzing quality data to identify trends and areas for improvement, and collaborating with production and engineering teams to resolve quality issues promptly.

Furthermore, this role involves training and mentoring junior quality inspectors, ensuring consistency and adherence to standards across the team. You will contribute to the continuous improvement of quality management systems and participate in internal audits. A thorough understanding of quality control methodologies, statistical process control (SPC), and relevant industry standards is essential. The ability to interpret technical drawings and specifications accurately is crucial.

Qualifications include a minimum of 5 years of experience in quality control or assurance within a manufacturing environment. A strong technical background, preferably with a diploma or degree in a related engineering field, is required. Excellent analytical, problem-solving, and communication skills are necessary for effective collaboration and reporting. Proficiency with measurement tools and quality management software is expected. This is an excellent opportunity for a detail-oriented professional to play a key role in maintaining the highest quality standards in a leading manufacturing operation.

Our client is seeking a highly skilled and detail-oriented Senior Pharmaceutical Quality Control Analyst to join their esteemed team in Mumbai, Maharashtra, IN . This critical role involves performing comprehensive quality control testing on raw materials, in-process samples, and finished pharmaceutical products to ensure they meet stringent regulatory and internal quality standards. The ideal candidate will have a strong background in analytical chemistry, pharmaceutical manufacturing processes, and quality assurance.

Responsibilities:

• Perform a variety of analytical tests on raw materials, intermediates, and finished products using techniques such as HPLC, GC, UV-Vis spectrophotometry, and titrations.
• Ensure all testing is conducted in accordance with Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), and relevant pharmacopoeial standards (e.g., USP, EP, BP).
• Prepare reagents, standards, and samples for analytical testing.
• Calibrate and maintain laboratory equipment, ensuring proper functioning and accuracy.
• Document all testing procedures, results, and observations meticulously in laboratory notebooks and reports.
• Investigate and troubleshoot out-of-specification (OOS) results, deviations, and laboratory investigations.
• Participate in method development and validation activities.
• Review and approve analytical data and reports generated by other QC analysts.
• Collaborate with production, R&D, and quality assurance departments to resolve quality issues.
• Maintain a safe and organized laboratory environment.
• Contribute to regulatory inspections and audits.
• Train and mentor junior QC analysts.

Qualifications:

• Bachelor's or Master's degree in Pharmacy, Chemistry, Analytical Chemistry, or a related life science field.
• Minimum of 5-7 years of hands-on experience in a pharmaceutical Quality Control laboratory.
• Proficiency in a wide range of analytical techniques, particularly HPLC and GC.
• Strong understanding of GMP, GLP, and regulatory requirements in the pharmaceutical industry.
• Excellent attention to detail and accuracy in data recording and reporting.
• Strong problem-solving skills and the ability to investigate OOS results effectively.
• Proficiency in using laboratory information management systems (LIMS) and data analysis software.
• Good written and verbal communication skills.
• Ability to work independently and as part of a team.
• Experience with method validation is a significant advantage.

This role offers a competitive salary and benefits package, along with opportunities for professional growth within a leading pharmaceutical company. The hybrid work model provides a balance between essential on-site laboratory work and remote administrative tasks.