69 Quality Control Manager jobs in Bhubaneswar

• Develop, implement, and maintain a robust Quality Management System (QMS) in accordance with relevant industry standards (e.g., IATF 16949).
• Establish quality control procedures, inspection plans, and testing protocols for raw materials, in-process production, and finished goods.
• Lead and manage the quality control team, providing guidance, training, and performance evaluations.
• Conduct regular internal audits of manufacturing processes and systems to ensure compliance and identify areas for improvement.
• Analyze quality data, identify trends, and implement corrective and preventive actions (CAPA) to resolve issues and prevent recurrence.
• Collaborate closely with production, engineering, and supply chain teams to ensure product quality throughout the entire lifecycle.
• Oversee the calibration and maintenance of testing and measuring equipment.
• Manage customer complaints related to quality and ensure timely and effective resolution.
• Drive continuous improvement initiatives using methodologies such as Lean Manufacturing and Six Sigma.
• Prepare and present quality reports to senior management, highlighting key performance indicators (KPIs), risks, and improvement opportunities.
• Ensure compliance with all relevant national and international quality regulations and standards.
• Develop training programs for quality-related topics for all relevant personnel.
• Monitor supplier quality performance and work with procurement to address any quality issues.
• Champion a quality-first culture throughout the organization.

• Bachelor's degree in Engineering (Mechanical, Industrial, or related field) or equivalent practical experience.
• Minimum of 8 years of experience in quality management or quality assurance within a manufacturing environment, preferably in the automotive industry.
• In-depth knowledge of quality standards such as IATF 16949, ISO 9001.
• Proven experience with quality tools and methodologies (e.g., SPC, FMEA, APQP, PPAP, 8D).
• Strong leadership and team management skills.
• Excellent analytical, problem-solving, and decision-making abilities.
• Proficiency in data analysis and reporting.
• Exceptional communication and interpersonal skills, with the ability to influence stakeholders at all levels.
• Experience in conducting audits and implementing CAPA systems.
• Ability to work effectively in a remote setting, demonstrating strong self-discipline and time management.
• Certification as an internal auditor for relevant quality standards is a plus.

Roles and Responsibilities

• Conduct regular audits to identify areas for improvement and implement corrective actions to maintain high-quality products and services.
• Collaborate with cross-functional teams to develop process improvements, reduce defects, and enhance customer satisfaction.
• Analyze data from various sources to track key performance indicators (KPIs) such as first-time right rate, defect rate, and customer complaints.
• Provide training and coaching to team members on quality principles, procedures, and best practices.

Desired Candidate Profile

• 5-10 years of experience in Quality Assurance/Quality Management or related field.
• Effective communication skills with ability to present findings and recommendations to stakeholders.
• Excellent analytical skills with ability to interpret complex data sets.

Current designation should be as Manager Quality

E-commerce experience Mandatory

Work Location: Bhubaneswar

Need immediate joiners

Interested candidates can apply

Dy Manager - Solar Cell QA

* Collaborate with cross-functional teams on quality improvement initiatives

* Ensure compliance with industry standards & customer requirements

* Lead quality control processes for solar cells & modules

Office cab/shuttle

Provident fund

• Develop, implement, and maintain the Quality Management System (QMS).
• Ensure compliance with GMP, ISO, and other relevant regulatory standards.
• Lead and mentor the Quality Assurance team.
• Conduct internal and external audits of manufacturing facilities and suppliers.
• Manage deviations, investigations, and Corrective and Preventive Actions (CAPA).
• Review and approve batch records, specifications, and validation protocols.
• Oversee change control management processes.
• Prepare for and participate in regulatory inspections and audits.
• Manage product quality complaints and investigations.
• Drive continuous improvement initiatives within the quality department.

• Master's or Bachelor's degree in Pharmacy, Chemistry, Biology, or a related science field.
• Minimum 7-10 years of experience in Pharmaceutical Quality Assurance.
• Proven experience in implementing and managing QMS.
• In-depth knowledge of GMP, ICH guidelines, and other relevant regulations.
• Experience with regulatory inspections (e.g., FDA, EMA, CDSCO).
• Strong leadership, analytical, and problem-solving skills.
• Excellent written and verbal communication skills.
• Ability to manage multiple projects and prioritize effectively in a hybrid work environment.
• Proficiency with quality management software and tools.
• Detail-oriented with a strong commitment to quality and compliance.

• Develop and implement comprehensive quality assurance strategies and procedures.
• Establish and manage quality control processes throughout the product lifecycle.
• Conduct internal audits and assessments to ensure compliance with quality standards and regulations.
• Analyze quality data, identify trends, and implement corrective and preventive actions.
• Lead and mentor a remote team of quality assurance professionals.
• Collaborate with cross-functional teams to resolve quality issues and drive continuous improvement.
• Oversee the testing and validation of products and services.
• Develop and maintain quality documentation, including SOPs and test protocols.
• Manage customer feedback related to product quality and implement necessary improvements.
• Promote a strong quality culture throughout the organization.

• Bachelor's degree in Engineering, Science, Business Administration, or a related field.
• Minimum of 7 years of experience in Quality Assurance or Quality Management roles.
• Proven experience in developing and implementing Quality Management Systems (QMS), such as ISO 9001.
• Strong knowledge of quality control tools and methodologies (e.g., Six Sigma, Lean Manufacturing).
• Experience in leading and managing remote QA teams.
• Excellent analytical, problem-solving, and decision-making skills.
• Strong communication, interpersonal, and leadership abilities.
• Proficiency with quality management software and data analysis tools.

• Develop, implement, and maintain a robust Quality Management System (QMS) in line with Good Manufacturing Practices (GMP), ICH guidelines, and other relevant regulatory requirements for pharmaceutical operations in Bhubaneswar, Odisha, IN .
• Oversee all quality assurance activities, including batch record review, product release, deviation management, change control, and CAPA (Corrective and Preventive Actions).
• Conduct internal audits and host regulatory inspections (e.g., FDA, EMA, local authorities), ensuring successful outcomes.
• Manage and mentor the Quality Assurance team, providing training and professional development opportunities.
• Ensure that all manufacturing processes, equipment, and facilities comply with current Good Manufacturing Practices (cGMP).
• Review and approve validation protocols and reports for manufacturing processes, analytical methods, and equipment.
• Monitor and analyze quality data, identify trends, and implement continuous improvement initiatives to enhance product quality and process efficiency.
• Manage product complaints and recalls, conducting thorough investigations and implementing necessary corrective actions.
• Liaise with regulatory bodies, suppliers, and external partners on quality-related matters.
• Champion a quality-focused culture throughout the organization.

• Bachelor's or Master's degree in Pharmacy, Chemistry, Biotechnology, or a related life science field.
• Minimum of 7-10 years of progressive experience in Quality Assurance within the pharmaceutical industry.
• Extensive knowledge of GMP, GDP, ICH guidelines, and other relevant pharmaceutical regulations.
• Proven experience in managing regulatory inspections and audits.
• Strong understanding of pharmaceutical manufacturing, analytical testing, and validation principles.
• Excellent leadership, team management, and interpersonal skills.
• Proficiency in quality management software and tools.
• Exceptional analytical, problem-solving, and decision-making abilities.
• Strong documentation and report-writing skills.
• Detail-oriented with a commitment to accuracy and compliance.

• Develop and implement pharmaceutical quality assurance systems.
• Ensure compliance with GMP, GLP, and other relevant regulations.
• Manage SOPs, change control, deviation management, and CAPA processes.
• Conduct internal audits and host regulatory inspections.
• Oversee batch record review and product release.
• Manage supplier quality assurance programs.
• Lead and mentor the QA team.
• Investigate quality incidents and implement corrective actions.
• Contribute to continuous improvement initiatives in quality management.

• Bachelor's or Master's degree in Pharmacy, Chemistry, or Life Sciences.
• 7-10 years of experience in pharmaceutical QA.
• In-depth knowledge of GMP and regulatory requirements.
• Experience with audits and inspections.
• Strong leadership and team management skills.
• Excellent analytical and problem-solving abilities.

• Developing, implementing, and maintaining a comprehensive Quality Management System (QMS) in compliance with cGMP, ICH, and other relevant regulatory guidelines.
• Leading and managing the QA team, providing guidance, mentorship, and performance management.
• Overseeing all QA activities, including batch record review and release, deviation investigations, CAPA management, change control, and document control.
• Conducting internal audits and participating in external regulatory inspections (e.g., FDA, EMA, WHO) and customer audits.
• Ensuring that all manufacturing and laboratory operations comply with approved procedures and regulatory standards.
• Reviewing and approving validation protocols and reports for manufacturing processes, equipment, and analytical methods.
• Managing supplier qualification programs and conducting audits of key raw material and component suppliers.
• Developing and delivering quality training programs for personnel involved in pharmaceutical operations.
• Monitoring quality metrics and key performance indicators (KPIs), identifying trends, and implementing continuous improvement initiatives.
• Investigating product quality complaints and ensuring timely and effective resolution.
• Acting as a key point of contact for regulatory bodies regarding quality matters.
• Staying abreast of evolving regulatory landscapes and industry best practices in pharmaceutical quality assurance.
• Contributing to the strategic direction of the company's quality initiatives.

• Master's degree in Pharmacy, Chemistry, Biology, or a related life science field. A PhD is a plus.
• Minimum of 8-10 years of progressive experience in Quality Assurance within the pharmaceutical industry, with at least 3 years in a managerial or supervisory role.
• Extensive knowledge of current Good Manufacturing Practices (cGMP) and global pharmaceutical regulatory requirements.
• Proven experience with regulatory submissions, inspections, and successful interactions with health authorities.
• Demonstrated ability to lead and develop a high-performing QA team.
• Strong understanding of pharmaceutical manufacturing processes, quality control, and validation principles.
• Excellent analytical, problem-solving, and decision-making skills.
• Exceptional communication, interpersonal, and negotiation skills.
• Proficiency in quality management software and data analysis tools.
• Strong project management skills and the ability to manage multiple priorities effectively.
• Experience with sterile product manufacturing or biologics is highly desirable.