442 Qa Manager jobs in Mumbai
QA Manager
Posted 1 day ago
Job Viewed
Job Description
1. Quality Assurance Leadership:
- Develop, implement, and manage the factorys quality management system (QMS) in accordance with industry standards (e.g., ISO 9001).
- Lead the quality team, including quality engineers, inspectors, and technicians, to ensure consistent application of quality procedures.
- Establish quality objectives and key performance indicators (KPIs), and regularly report on performance.
2. Process Improvement:
- Identify areas for improvement in the production process through data analysis and feedback from internal and external sources.
- Lead and facilitate continuous improvement initiatives using Lean, Six Sigma, or other methodologies.
- Implement corrective and preventive actions to address quality issues and ensure they do not recur.
3. Inspection and Testing:
- Oversee the inspection and testing of raw materials, in-process components, and finished products to ensure compliance with specifications.
- Develop and maintain standard operating procedures (SOPs) for quality control processes.
- Ensure proper calibration and maintenance of inspection and testing equipment.
QA Manager
Posted 1 day ago
Job Viewed
Job Description
Location: Thane, Maharashtra
Job Description:
We are hiring a QA Manager with 8–14 years of experience in industrial/structural projects.
Responsibilities:
- Lead QA/QC activities for civil and structural works
- Implement quality systems and ensure compliance with standards
- Conduct inspections, audits, and reporting
Requirements:
- B.Tech / Diploma in Civil or Mechanical Engineering
- 8–14 years of QA/QC experience in industrial/infra projects
- Strong knowledge of QA procedures, ITPs, and codes
Note: Only relevant candidates should apply.
Job Type: Full-time
Pay: ₹400, ₹680,000.00 per year
Work Location: In person
QA Manager
Posted today
Job Viewed
Job Description
Role Summary
Site Lead for all Quality Control activities and localisation support activities. Responsible to
oversee operations and products (Raw Materials, intermediates, and Final) are meeting customer and industry standards / requirements.
Internal contacts:
External contacts: -
RESPONSIBILITIES:
First point of contact / site champion accountable for customer QP (Quality Product) complaint investigation and communications. Responsible to engage anyone necessary at the site to resolve, correct, and to prevent reoccurrence of the Quality Product Complaint.
Drive department compliance with environmental, health and safety standards and performance.
Responsible for implementation of Corporate Quality Strategy and policies at the site through indirect reporting to Corporate QA.
Ensure that leading / lagging targets, objectives & KPI performance is achieved.
Ensure all QC activity/tasks are value-assessed, prioritized, in alignment with corporate, plant, and department objectives, deliverables.
Ensure resources are optimally staffed to ensure all priorities are addressed in an efficient and timely manner.
Lead with excellence in the oversight of Operation/capital Expenses for his/her department in an intentionally controlled and proficient manner with a continuous improvement mindset.
Testing capability development/upgradation based on business need.
Accountable for the NCM and Corrective Action Processes for the QC lab, and ensure they are prioritized and progressing without delays.
Support unit/plant operations and corporate initiatives with QC personnel, time, and resources.
Lead and develop self-directed work teams in all areas of influence by coaching, enabling, developing, and mentoring all direct reports.
Empower and encourage direct reports to make calculated and well-informed data-based decisions on a regular interval through one-on-one interactions.
Actively spend time in the lab observing, encouraging, and leading the use of CI tools/methodologies.
Accountable to conform and comply with all QA, HSES policies and procedures
REQUIREMENTS (education, experience, competencies and specific job requirements):
Required Expertise / Knowledge / Skills
QA Manager
Posted today
Job Viewed
Job Description
Role Summary
Site Lead for all Quality Control activities and localisation support activities. Responsible to
oversee operations and products (Raw Materials, intermediates, and Final) are meeting customer and industry standards / requirements.
Internal contacts:
- Communication: -Intercompany stakeholders, LZAI functions.
External contacts: -
- Analytical instruments OEM/service providers.
- The customer and raw material vendors.
- Laboratory utility vendors.
RESPONSIBILITIES:
First point of contact / site champion accountable for customer QP (Quality Product) complaint investigation and communications. Responsible to engage anyone necessary at the site to resolve, correct, and to prevent reoccurrence of the Quality Product Complaint.
Drive department compliance with environmental, health and safety standards and performance.
Responsible for implementation of Corporate Quality Strategy and policies at the site through indirect reporting to Corporate QA.
Ensure that leading / lagging targets, objectives & KPI performance is achieved.
Ensure all QC activity/tasks are value-assessed, prioritized, in alignment with corporate, plant, and department objectives, deliverables.
Ensure resources are optimally staffed to ensure all priorities are addressed in an efficient and timely manner.
Lead with excellence in the oversight of Operation/capital Expenses for his/her department in an intentionally controlled and proficient manner with a continuous improvement mindset.
Testing capability development/upgradation based on business need.
Accountable for the NCM and Corrective Action Processes for the QC lab, and ensure they are prioritized and progressing without delays.
Support unit/plant operations and corporate initiatives with QC personnel, time, and resources.
Lead and develop self-directed work teams in all areas of influence by coaching, enabling, developing, and mentoring all direct reports.
Empower and encourage direct reports to make calculated and well-informed data-based decisions on a regular interval through one-on-one interactions.
Actively spend time in the lab observing, encouraging, and leading the use of CI tools/methodologies.
Accountable to conform and comply with all QA, HSES policies and procedures
REQUIREMENTS (education, experience, competencies and specific job requirements):
Required Expertise / Knowledge / Skills
- Post graduate/PhD in Chemistry from a recognised university.
- Minimum 15 year of experience in testing of lubricants, additives, chemicals, preferably in MNC environment.
- Sound knowledge of analytical testing instruments, wet analysis. Experience in laboratory blending/synthesis.
- Strong analytical and problem-solving ability.
- Sound knowledge / certification of ISO systems and statistical analysis.
- English communication.
- Computer -Software skills: - Adequate fluency with MS Office, proficient in SAP QM module.
- Execution of other work in consultation with plant manager.
- Exposure to workplace management tools like 5S will be advantage.
Deputy QA Manager
Posted 1 day ago
Job Viewed
Job Description
Location: Navi Mumbai, Maharashtra
Job Description:
We are seeking a Deputy QA Manager with 6–10 years of experience in QA for industrial/structural projects.
Responsibilities:
- Assist QA Manager in implementing QA systems
- Conduct quality checks, audits, and documentation
- Coordinate with contractors and site teams
Requirements:
- B.Tech / Diploma in Civil or Mechanical Engineering
- 6–10 years of QA/QC experience in infra/industrial projects
Note: Only relevant candidates should apply.
Job Type: Full-time
Pay: ₹400, ₹650,000.00 per year
Work Location: In person
QA Specialist / QA Manager (Clinical Quality Assurance)
Posted 6 days ago
Job Viewed
Job Description
Commitment: Full-Time Contract (30–40 hours per week)
Location: Based in India, Remote – Eastern Time Zone (preferred) or Mountain Time Zone
Reports To: Clinical QA Lead / Director of Quality
Position Overview
We are seeking an experienced QA Specialist / Manager-level contractor to provide day-to-day clinical quality assurance (QA) support across ongoing clinical trials. This individual will play a key role in guiding study teams, maintaining compliance with Good Clinical Practice (GCP) , and ensuring quality oversight. The ideal candidate brings strong experience with Veeva QMS , is highly tech-savvy, and can support clinical operations teams in a fast-paced, remote environment.
Key Responsibilities
- Serve as the primary QA support resource for clinical study teams, ensuring compliance with GCP and internal quality standards.
- Provide QA expertise during study calls, including:
- Protocol deviation meetings
- Risk-based quality management discussions
- Study operations and trial oversight meetings
- Write, review, update, and format standard operating procedures (SOPs) and other quality documentation.
- Manage and track quality processes within Veeva QMS , including document control, training, and CAPA management.
- Address QA-related questions from study teams in real time, providing clear and actionable guidance.
- Support inspection readiness and contribute to continuous improvement of QA systems and processes.
- Partner with cross-functional stakeholders (Clinical Operations, Data Management, Regulatory, etc.) to align on quality expectations and risk mitigation.
Qualifications
- Education: Bachelor’s degree in life sciences, healthcare, or related discipline (advanced degree preferred).
- Experience:
- 5+ years of Clinical Quality Assurance experience with a strong foundation in GCP.
- Prior experience supporting clinical study teams in a QA capacity.
- Hands-on experience with Veeva QMS .
- Technical Skills:
- Proficient in MS Office (Excel, PowerPoint, Word).
- Skilled in technical writing, SOP drafting, and document formatting.
- Soft Skills:
- Excellent communication and interpersonal skills.
- Strong organizational skills with the ability to work independently.
- Availability: Must be available during Eastern or Mountain Time Zone working hours to attend study calls and provide timely QA support.
Contract Opportunity
This is a full-time contract role offering 30–40 hours per week of consistent work. The contractor will act as a core member of the QA function, providing essential support to ongoing clinical programs and ensuring regulatory compliance.
QA Specialist / QA Manager (Clinical Quality Assurance)
Posted 6 days ago
Job Viewed
Job Description
Commitment: Full-Time Contract (30–40 hours per week)
Location: Based in India, Remote – Eastern Time Zone (preferred) or Mountain Time Zone
Reports To: Clinical QA Lead / Director of Quality
Position Overview
We are seeking an experienced QA Specialist / Manager-level contractor to provide day-to-day clinical quality assurance (QA) support across ongoing clinical trials. This individual will play a key role in guiding study teams, maintaining compliance with Good Clinical Practice (GCP) , and ensuring quality oversight. The ideal candidate brings strong experience with Veeva QMS , is highly tech-savvy, and can support clinical operations teams in a fast-paced, remote environment.
Key Responsibilities
- Serve as the primary QA support resource for clinical study teams, ensuring compliance with GCP and internal quality standards.
- Provide QA expertise during study calls, including:
- Protocol deviation meetings
- Risk-based quality management discussions
- Study operations and trial oversight meetings
- Write, review, update, and format standard operating procedures (SOPs) and other quality documentation.
- Manage and track quality processes within Veeva QMS , including document control, training, and CAPA management.
- Address QA-related questions from study teams in real time, providing clear and actionable guidance.
- Support inspection readiness and contribute to continuous improvement of QA systems and processes.
- Partner with cross-functional stakeholders (Clinical Operations, Data Management, Regulatory, etc.) to align on quality expectations and risk mitigation.
Qualifications
- Education: Bachelor’s degree in life sciences, healthcare, or related discipline (advanced degree preferred).
- Experience:
- 5+ years of Clinical Quality Assurance experience with a strong foundation in GCP.
- Prior experience supporting clinical study teams in a QA capacity.
- Hands-on experience with Veeva QMS .
- Technical Skills:
- Proficient in MS Office (Excel, PowerPoint, Word).
- Skilled in technical writing, SOP drafting, and document formatting.
- Soft Skills:
- Excellent communication and interpersonal skills.
- Strong organizational skills with the ability to work independently.
- Availability: Must be available during Eastern or Mountain Time Zone working hours to attend study calls and provide timely QA support.
Contract Opportunity
This is a full-time contract role offering 30–40 hours per week of consistent work. The contractor will act as a core member of the QA function, providing essential support to ongoing clinical programs and ensuring regulatory compliance.
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QA Specialist / QA Manager (Clinical Quality Assurance)
Posted 6 days ago
Job Viewed
Job Description
Commitment: Full-Time Contract (30–40 hours per week)
Location: Based in India, Remote – Eastern Time Zone (preferred) or Mountain Time Zone
Reports To: Clinical QA Lead / Director of Quality
Position Overview
We are seeking an experienced QA Specialist / Manager-level contractor to provide day-to-day clinical quality assurance (QA) support across ongoing clinical trials. This individual will play a key role in guiding study teams, maintaining compliance with Good Clinical Practice (GCP) , and ensuring quality oversight. The ideal candidate brings strong experience with Veeva QMS , is highly tech-savvy, and can support clinical operations teams in a fast-paced, remote environment.
Key Responsibilities
- Serve as the primary QA support resource for clinical study teams, ensuring compliance with GCP and internal quality standards.
- Provide QA expertise during study calls, including:
- Protocol deviation meetings
- Risk-based quality management discussions
- Study operations and trial oversight meetings
- Write, review, update, and format standard operating procedures (SOPs) and other quality documentation.
- Manage and track quality processes within Veeva QMS , including document control, training, and CAPA management.
- Address QA-related questions from study teams in real time, providing clear and actionable guidance.
- Support inspection readiness and contribute to continuous improvement of QA systems and processes.
- Partner with cross-functional stakeholders (Clinical Operations, Data Management, Regulatory, etc.) to align on quality expectations and risk mitigation.
Qualifications
- Education: Bachelor’s degree in life sciences, healthcare, or related discipline (advanced degree preferred).
- Experience:
- 5+ years of Clinical Quality Assurance experience with a strong foundation in GCP.
- Prior experience supporting clinical study teams in a QA capacity.
- Hands-on experience with Veeva QMS .
- Technical Skills:
- Proficient in MS Office (Excel, PowerPoint, Word).
- Skilled in technical writing, SOP drafting, and document formatting.
- Soft Skills:
- Excellent communication and interpersonal skills.
- Strong organizational skills with the ability to work independently.
- Availability: Must be available during Eastern or Mountain Time Zone working hours to attend study calls and provide timely QA support.
Contract Opportunity
This is a full-time contract role offering 30–40 hours per week of consistent work. The contractor will act as a core member of the QA function, providing essential support to ongoing clinical programs and ensuring regulatory compliance.
QA Specialist / QA Manager (Clinical Quality Assurance)
Posted today
Job Viewed
Job Description
Commitment: Full-Time Contract (30–40 hours per week)
Location: Based in India, Remote – Eastern Time Zone (preferred) or Mountain Time Zone
Reports To: Clinical QA Lead / Director of Quality
Position Overview
We are seeking an experienced QA Specialist / Manager-level contractor to provide day-to-day clinical quality assurance (QA) support across ongoing clinical trials. This individual will play a key role in guiding study teams, maintaining compliance with Good Clinical Practice (GCP) , and ensuring quality oversight. The ideal candidate brings strong experience with Veeva QMS , is highly tech-savvy, and can support clinical operations teams in a fast-paced, remote environment.
Key Responsibilities
- Serve as the primary QA support resource for clinical study teams, ensuring compliance with GCP and internal quality standards.
- Provide QA expertise during study calls, including:
- Protocol deviation meetings
- Risk-based quality management discussions
- Study operations and trial oversight meetings
- Write, review, update, and format standard operating procedures (SOPs) and other quality documentation.
- Manage and track quality processes within Veeva QMS , including document control, training, and CAPA management.
- Address QA-related questions from study teams in real time, providing clear and actionable guidance.
- Support inspection readiness and contribute to continuous improvement of QA systems and processes.
- Partner with cross-functional stakeholders (Clinical Operations, Data Management, Regulatory, etc.) to align on quality expectations and risk mitigation.
Qualifications
- Education: Bachelor’s degree in life sciences, healthcare, or related discipline (advanced degree preferred).
- Experience:
- 5+ years of Clinical Quality Assurance experience with a strong foundation in GCP.
- Prior experience supporting clinical study teams in a QA capacity.
- Hands-on experience with Veeva QMS .
- Technical Skills:
- Proficient in MS Office (Excel, PowerPoint, Word).
- Skilled in technical writing, SOP drafting, and document formatting.
- Soft Skills:
- Excellent communication and interpersonal skills.
- Strong organizational skills with the ability to work independently.
- Availability: Must be available during Eastern or Mountain Time Zone working hours to attend study calls and provide timely QA support.
Contract Opportunity
This is a full-time contract role offering 30–40 hours per week of consistent work. The contractor will act as a core member of the QA function, providing essential support to ongoing clinical programs and ensuring regulatory compliance.
QA Specialist / QA Manager (Clinical Quality Assurance)
Posted today
Job Viewed
Job Description
Commitment: Full-Time Contract (30–40 hours per week)
Location: Based in India, Remote – Eastern Time Zone (preferred) or Mountain Time Zone
Reports To: Clinical QA Lead / Director of Quality
Position Overview
We are seeking an experienced QA Specialist / Manager-level contractor to provide day-to-day clinical quality assurance (QA) support across ongoing clinical trials. This individual will play a key role in guiding study teams, maintaining compliance with Good Clinical Practice (GCP) , and ensuring quality oversight. The ideal candidate brings strong experience with Veeva QMS , is highly tech-savvy, and can support clinical operations teams in a fast-paced, remote environment.
Key Responsibilities
- Serve as the primary QA support resource for clinical study teams, ensuring compliance with GCP and internal quality standards.
- Provide QA expertise during study calls, including:
- Protocol deviation meetings
- Risk-based quality management discussions
- Study operations and trial oversight meetings
- Write, review, update, and format standard operating procedures (SOPs) and other quality documentation.
- Manage and track quality processes within Veeva QMS , including document control, training, and CAPA management.
- Address QA-related questions from study teams in real time, providing clear and actionable guidance.
- Support inspection readiness and contribute to continuous improvement of QA systems and processes.
- Partner with cross-functional stakeholders (Clinical Operations, Data Management, Regulatory, etc.) to align on quality expectations and risk mitigation.
Qualifications
- Education: Bachelor’s degree in life sciences, healthcare, or related discipline (advanced degree preferred).
- Experience:
- 5+ years of Clinical Quality Assurance experience with a strong foundation in GCP.
- Prior experience supporting clinical study teams in a QA capacity.
- Hands-on experience with Veeva QMS .
- Technical Skills:
- Proficient in MS Office (Excel, PowerPoint, Word).
- Skilled in technical writing, SOP drafting, and document formatting.
- Soft Skills:
- Excellent communication and interpersonal skills.
- Strong organizational skills with the ability to work independently.
- Availability: Must be available during Eastern or Mountain Time Zone working hours to attend study calls and provide timely QA support.
Contract Opportunity
This is a full-time contract role offering 30–40 hours per week of consistent work. The contractor will act as a core member of the QA function, providing essential support to ongoing clinical programs and ensuring regulatory compliance.