612 Quality Manager jobs in Mumbai

• Developing, implementing, and maintaining comprehensive quality management systems (e.g., ISO 9001).
• Establishing quality control procedures and standards for raw materials, in-process production, and finished goods.
• Leading and managing the Quality Control team, including hiring, training, and performance evaluation.
• Overseeing all quality control testing and inspection activities to ensure product conformity.
• Analyzing quality data, identifying trends, and implementing corrective and preventive actions (CAPA) to address non-conformities.
• Collaborating with production, engineering, and R&D departments to resolve quality issues and improve product design.
• Ensuring compliance with all applicable industry regulations, customer requirements, and internal policies.
• Conducting internal audits and supporting external audits by regulatory bodies and customers.
• Managing supplier quality programs and evaluating supplier performance.
• Driving continuous improvement initiatives to enhance product quality and reduce defects.
• Developing and delivering quality training programs for employees at all levels.
• Maintaining all quality-related documentation and records.

• Develop, implement, and maintain comprehensive quality control procedures and protocols.
• Oversee all quality control testing activities, including raw material, in-process, and finished product testing.
• Ensure compliance with Good Manufacturing Practices (GMP) and relevant regulatory guidelines.
• Manage and mentor a team of quality control analysts and technicians.
• Investigate and resolve deviations, out-of-specification (OOS) results, and customer complaints related to product quality.
• Approve or reject raw materials, intermediate, and finished products based on established specifications.
• Conduct internal audits and participate in external regulatory inspections.
• Maintain all quality-related documentation and records in accordance with regulatory requirements.
• Develop and deliver training programs on quality control procedures and GMP compliance.
• Collaborate with production, R&D, and regulatory affairs departments to ensure product quality throughout the lifecycle.

• Bachelor's or Master's degree in Pharmacy, Chemistry, Microbiology, or a related science field.
• Extensive experience (typically 7+ years) in quality control or quality assurance within the pharmaceutical industry.
• Proven experience in managing a quality control laboratory and leading a team.
• In-depth knowledge of GMP, ICH guidelines, and other relevant regulatory standards.
• Strong understanding of analytical methods and instrumentation used in pharmaceutical QC.
• Excellent problem-solving, decision-making, and documentation skills.
• Strong leadership, communication, and interpersonal abilities.
• Experience with validation processes (IQ, OQ, PQ) is highly desirable.
• Proficiency in using laboratory information management systems (LIMS) is a plus.

• Manage and direct all activities of the Quality Control department, including raw material testing, in-process testing, and finished product release.
• Develop, implement, and maintain robust quality control procedures and standard operating procedures (SOPs).
• Ensure compliance with all applicable regulatory guidelines, including GMP, ICH, and local regulations.
• Oversee method validation, instrument calibration, and equipment qualification programs.
• Lead and mentor a team of QC analysts and supervisors, fostering a culture of excellence and continuous improvement.
• Review and approve batch records, analytical test results, and deviation reports.
• Investigate out-of-specification (OOS) results and implement corrective and preventive actions (CAPA).
• Collaborate with other departments, including R&D, Manufacturing, and Regulatory Affairs, to resolve quality issues.
• Manage the budget for the QC department and ensure efficient resource allocation.
• Stay current with advancements in analytical techniques and quality control technologies.
• Prepare for and host regulatory inspections and audits.
• Develop and implement training programs for QC personnel.
• Participate in internal and external quality audits.
• Contribute to the overall quality strategy of the organization.
• Ensure data integrity and accuracy in all QC-related activities.

• Master's or Ph.D. in Pharmacy, Chemistry, Biochemistry, or a related scientific discipline.
• Minimum of 8-10 years of progressive experience in pharmaceutical quality control, with at least 3-5 years in a management role.
• In-depth knowledge of GMP regulations and pharmaceutical quality systems.
• Proven experience with various analytical techniques such as HPLC, GC, spectroscopy, and wet chemistry.
• Strong understanding of method validation, instrument qualification, and process validation.
• Excellent leadership, team management, and interpersonal skills.
• Demonstrated ability to problem-solve complex quality issues.
• Strong analytical and critical thinking skills.
• Excellent written and verbal communication skills.
• Experience with regulatory inspections and audits.
• Proficiency in data analysis and statistical software.
• Ability to manage multiple priorities and meet strict deadlines.
• Commitment to quality, safety, and regulatory compliance.

• Lead and manage the daily operations of the Quality Control laboratory.
• Develop, validate, and implement analytical test methods for raw materials, in-process samples, and finished products.
• Oversee the execution of routine testing, stability studies, and method validation protocols.
• Review and approve analytical data, ensuring accuracy, completeness, and compliance with specifications.
• Investigate out-of-specification (OOS) results and deviations, implementing appropriate CAPAs.
• Ensure all QC activities comply with GMP, regulatory guidelines, and company policies.
• Manage laboratory instrumentation, calibration, and maintenance programs.
• Train and mentor QC personnel, fostering a culture of quality and continuous improvement.
• Collaborate with R&D, Manufacturing, and Regulatory Affairs departments to support product development and lifecycle management.
• Prepare and review QC-related sections of regulatory submissions.
• Manage vendor qualification and oversight for critical raw materials and services.
• Contribute to internal and external audits as a subject matter expert.
• Maintain accurate and organized laboratory records and documentation.
• Monitor industry trends and regulatory changes impacting quality control.

• Bachelor's or Master's degree in Pharmacy, Chemistry, Biotechnology, or a related scientific discipline.
• Minimum of 8 years of experience in pharmaceutical quality control, with at least 3 years in a supervisory or management role.
• Extensive knowledge of analytical techniques (HPLC, GC, UV-Vis, FTIR, dissolution testing).
• Strong understanding of GMP, ICH guidelines, and other relevant regulatory requirements.
• Proven experience in method development, validation, and OOS investigations.
• Excellent leadership, team management, and communication skills.
• Strong problem-solving and decision-making abilities.
• Proficiency in using laboratory information management systems (LIMS) and other QC software.
• Ability to work effectively under pressure and meet strict deadlines.
• Detail-oriented with a strong commitment to quality and compliance.

• Lead and manage the daily operations of the Quality Control laboratory, including staff supervision, workload management, and resource allocation.
• Develop, validate, and implement analytical methods for raw materials, in-process samples, and finished products.
• Ensure all QC testing is performed according to approved procedures and in compliance with GMP, ICH, and other regulatory guidelines.
• Review and approve analytical test results, certificates of analysis (CoA), and QC documentation.
• Oversee instrument calibration, qualification, and maintenance programs.
• Investigate out-of-specification (OOS) and out-of-trend (OOT) results, determine root causes, and implement corrective and preventive actions (CAPA).
• Manage stability study programs and analyze stability data.
• Contribute to the development and maintenance of the company's Quality Management System (QMS).
• Train and mentor QC analysts, fostering a culture of quality and continuous improvement.
• Liaise with regulatory agencies during inspections and audits.
• Ensure laboratory safety procedures are strictly followed.
• Support process validation and cleaning validation activities as required.

• Bachelor's or Master's degree in Pharmacy, Chemistry, Pharmaceutical Sciences, or a related field. A Ph.D. is a plus.
• Minimum of 8 years of experience in pharmaceutical Quality Control, with at least 3-5 years in a supervisory or managerial role.
• Extensive knowledge of GMP, regulatory requirements (e.g., FDA, EMA, CDSCO), and quality control principles.
• Proven experience in analytical method development, validation, and troubleshooting.
• Proficiency with various analytical instruments (e.g., HPLC, GC, UV-Vis, FTIR).
• Strong understanding of stability testing and data analysis.
• Excellent leadership, team management, problem-solving, and decision-making skills.
• Effective communication and interpersonal skills, with the ability to interact with regulatory bodies and senior management.
• Experience in sterile injectables or solid dosage forms manufacturing is highly desirable.

Job description

 Will be responsible for managing day to day quality control operations, ensuring compliances
with regulatory requirements and developing strategies for continuous development of quality
control
Review specifications for products and processes as per FSSAI & IS standards
trictly follow requirements for raw material and intermediate products from suppliers and
monitor their compliance
ssist in maintaining hygiene for the overall plant including personal and Equipment
oordinate with the Operations team to identify process correction to eliminate deviation from
quality standards
pprove the right products or reject defectives
aintaining documentation for Audit purposes
evelop, implement, and maintain quality control systems to ensure the consistent production
of high-quality food products
ood understanding of the domain of food safety, RCA and CAPA, quality standards
nowledge of GMP, GHPANDHACCP
nsuring that all company policies and procedures are followed by all employees
verseeing the implementation and maintenance of quality control plans and processes
orking with management to develop new quality control processes and procedures
nsures that quality inspectors are properly trained to carry out of inspections of incoming
materials
ake sure that all the quality documents are properly filled, timely checked, verified and
controlled in a manner to be retrieved
aintain quality levels of products
onducting Internal and 3rd party audits
onitoring the progress of projects to ensure that deadlines are met
nspecting the final output, comparing it to the requirements, and approving or rejecting the
final products
nsuring that quality requirements are met by entities placed under the control of the quality
department
roubleshooting of key quality concerns with online QC Executives and packaging checkers
nsuring best quality of product and minimum customer complaints through stringent on-line
quality control checks and finished product inspection