9 Tata Steel jobs in Bhubaneshwar
Quality Control Chemist
751001 Bhubaneswar, Orissa
₹55000 Monthly
WhatJobs
Posted 6 days ago
Job Viewed
Job Description
Our client is seeking a meticulous and qualified Quality Control Chemist for their pharmaceutical manufacturing facility in Bhubaneswar, Odisha, IN . This role is critical in ensuring the quality and safety of our pharmaceutical products by conducting rigorous testing and analysis. You will be responsible for performing in-process and finished product testing, validating analytical methods, and maintaining detailed records of all quality control activities. The ideal candidate will have a strong understanding of analytical chemistry techniques, pharmacopeial standards, and regulatory requirements within the pharmaceutical industry. This position requires excellent laboratory skills, a keen eye for detail, and a commitment to upholding the highest standards of quality.
Key Responsibilities:
Key Responsibilities:
- Perform qualitative and quantitative analyses on raw materials, in-process samples, and finished products using various analytical techniques (e.g., HPLC, GC, UV-Vis spectroscopy, titrations).
- Ensure all testing is conducted in compliance with Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP).
- Validate analytical methods and instrumentation according to regulatory guidelines.
- Maintain accurate and detailed records of all laboratory tests, results, and observations.
- Prepare certificates of analysis (CoA) for raw materials and finished products.
- Calibrate and maintain laboratory equipment, ensuring optimal performance and accuracy.
- Investigate out-of-specification (OOS) results and deviations, identifying root causes and implementing corrective actions.
- Participate in internal and external audits of the quality control laboratory.
- Stay updated with the latest pharmacopeial standards (e.g., USP, BP, IP) and regulatory requirements.
- Assist in the development and improvement of quality control procedures and protocols.
- Collaborate with production, R&D, and regulatory affairs departments to address quality issues.
- Ensure proper handling and disposal of chemicals and hazardous materials.
- Contribute to a culture of continuous improvement within the quality department.
- Bachelor's or Master's degree in Chemistry, Pharmaceutical Chemistry, or a related field.
- Minimum of 3-5 years of experience in pharmaceutical quality control or analytical testing.
- Proficiency in using analytical instruments such as HPLC, GC, UV-Vis, FTIR, etc.
- Strong knowledge of pharmacopeial standards and regulatory guidelines (e.g., ICH, FDA, GMP).
- Excellent understanding of analytical chemistry principles.
- Meticulous attention to detail and accuracy in testing and record-keeping.
- Ability to work independently and as part of a team in a laboratory setting.
- Good problem-solving and critical-thinking skills.
- Strong written and verbal communication skills.
- Experience with laboratory information management systems (LIMS) is a plus.
This advertiser has chosen not to accept applicants from your region.
0
Pharmaceutical Quality Control Analyst
751001 Bhubaneswar, Orissa
₹55000 Annually
WhatJobs
Posted 6 days ago
Job Viewed
Job Description
Our client is seeking a diligent and meticulous Pharmaceutical Quality Control Analyst to join their established team in Bhubaneswar, Odisha, IN . This hybrid role requires a strong understanding of analytical testing methods and quality assurance principles within the pharmaceutical industry. You will be responsible for performing a variety of tests on raw materials, in-process samples, and finished products to ensure they meet stringent quality and regulatory standards. The role involves both hands-on laboratory work and collaborative efforts with various departments to uphold the highest levels of product quality and compliance.
Key Responsibilities:
Key Responsibilities:
- Perform analytical testing on raw materials, intermediates, and finished pharmaceutical products using techniques such as HPLC, GC, UV-Vis spectroscopy, and dissolution testing.
- Accurately document all testing procedures, results, and observations in compliance with Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP).
- Prepare reagents, solutions, and standards required for analytical testing.
- Calibrate and maintain laboratory equipment to ensure accuracy and reliability of test results.
- Review and interpret analytical data, identifying any deviations from specifications and escalating them to the Quality Control Supervisor.
- Participate in method validation and transfer activities for new analytical methods.
- Contribute to the investigation of out-of-specification (OOS) results and implementation of corrective and preventive actions (CAPAs).
- Ensure a safe working environment by adhering to all laboratory safety protocols and procedures.
- Collaborate with R&D, Production, and Quality Assurance departments to resolve quality-related issues.
- Stay up-to-date with current pharmacopoeial standards and regulatory guidelines.
- Bachelor's or Master's degree in Chemistry, Pharmaceutical Sciences, Biochemistry, or a related field.
- Minimum of 3 years of experience in a pharmaceutical quality control laboratory.
- Proficiency in common analytical techniques and instrumentation used in pharmaceutical testing.
- Familiarity with GMP and GLP requirements.
- Strong attention to detail and accuracy in data recording and reporting.
- Excellent problem-solving and critical thinking skills.
- Good written and verbal communication skills.
- Ability to work effectively both independently and as part of a team in a hybrid work environment.
This advertiser has chosen not to accept applicants from your region.
1
Production Quality Control Supervisor
751002 Bhubaneswar, Orissa
₹60000 Monthly
WhatJobs
Posted 6 days ago
Job Viewed
Job Description
Our client is seeking a vigilant and experienced Production Quality Control Supervisor to join their manufacturing team. This role is essential for ensuring that all manufactured products meet stringent quality standards and specifications. You will be responsible for implementing and overseeing quality control procedures, inspecting materials and finished goods, identifying defects, and working with production teams to implement corrective actions. The ideal candidate will have a strong understanding of quality management systems, excellent attention to detail, and the ability to lead a team of quality inspectors. A background in manufacturing is crucial for success in this position.
Responsibilities:
Qualifications:
This on-site role, located in Bhubaneswar, Odisha, IN , is critical for maintaining the high standards of our client's manufactured products.
Responsibilities:
- Develop, implement, and monitor quality control programs and procedures.
- Inspect raw materials, in-process materials, and finished products to ensure compliance with specifications.
- Identify and document product defects, non-conformities, and quality issues.
- Work closely with production teams to implement corrective and preventive actions.
- Train and supervise quality control inspectors and technicians.
- Maintain accurate quality control records and documentation.
- Conduct regular quality audits of production processes and finished goods.
- Analyze quality data to identify trends and areas for improvement.
- Ensure adherence to industry standards and regulatory requirements.
- Collaborate with engineering and production departments to resolve quality-related issues.
- Implement statistical process control (SPC) techniques.
- Develop and maintain quality control testing procedures.
- Champion a culture of quality throughout the manufacturing facility.
- Manage the return and rework process for defective products.
- Stay updated on best practices in quality assurance and control.
Qualifications:
- Bachelor's degree in Engineering, Quality Management, or a related technical field.
- Minimum of 4 years of experience in quality control or quality assurance in a manufacturing environment.
- Proven experience with quality management systems (e.g., ISO 9001).
- Strong understanding of inspection techniques and quality control tools.
- Excellent analytical and problem-solving skills.
- Proficiency in using measuring and testing equipment.
- Strong leadership and team management abilities.
- Excellent attention to detail and accuracy.
- Effective communication and interpersonal skills.
- Knowledge of statistical process control (SPC) is highly desirable.
- Ability to read and interpret technical drawings and specifications.
- Experience in troubleshooting manufacturing quality issues.
This on-site role, located in Bhubaneswar, Odisha, IN , is critical for maintaining the high standards of our client's manufactured products.
This advertiser has chosen not to accept applicants from your region.
2
Senior Quality Control Engineer
751001 Bhubaneswar, Orissa
₹85000 Annually
WhatJobs
Posted 6 days ago
Job Viewed
Job Description
Our client, a leader in advanced manufacturing solutions, is seeking a highly motivated and experienced Senior Quality Control Engineer to join their fully remote team. This is an exceptional opportunity for a proactive individual to contribute to the continuous improvement of our production processes and ensure the highest standards of product quality are met. You will be instrumental in developing and implementing robust quality assurance strategies, conducting rigorous inspections, and analyzing data to identify areas for enhancement. The role requires a deep understanding of manufacturing methodologies, statistical process control (SPC), and various quality management systems (QMS) like ISO 9001. You will collaborate closely with cross-functional teams, including R&D, production, and supply chain, to resolve quality issues, implement corrective and preventive actions (CAPA), and drive a culture of quality excellence across the organization. Your responsibilities will include managing quality documentation, performing root cause analysis for defects, and training junior team members on quality best practices. This position is based in Bhubaneswar, Odisha, IN , but operates entirely remotely, offering flexibility and work-life balance. We are looking for candidates who are meticulous, detail-oriented, and possess strong problem-solving and communication skills. If you are passionate about ensuring product integrity and have a proven track record in quality engineering within the manufacturing sector, we encourage you to apply.
Key Responsibilities:
Qualifications:
Key Responsibilities:
- Develop, implement, and maintain quality control procedures and standards.
- Conduct comprehensive inspections and testing of raw materials, in-process products, and finished goods.
- Analyze quality data, identify trends, and prepare detailed reports for management.
- Lead root cause analysis for quality deviations and implement effective corrective and preventive actions.
- Ensure compliance with relevant industry standards and certifications.
- Collaborate with engineering and production teams to resolve quality-related issues.
- Manage and update quality documentation, including SOPs and work instructions.
- Oversee calibration and maintenance of quality control equipment.
- Mentor and guide junior quality control personnel.
- Contribute to the continuous improvement of manufacturing processes and product quality.
Qualifications:
- Bachelor's degree in Engineering (Mechanical, Industrial, or related field).
- Minimum of 5 years of experience in quality control or quality assurance within a manufacturing environment.
- Strong knowledge of quality management systems (ISO 9001) and statistical process control (SPC).
- Proficiency in data analysis and problem-solving techniques.
- Excellent communication, interpersonal, and teamwork skills.
- Experience with lean manufacturing principles is a plus.
This advertiser has chosen not to accept applicants from your region.
3
Senior Pharmaceutical Quality Control Analyst
751001 Bhubaneswar, Orissa
₹750000 Annually
WhatJobs
Posted 6 days ago
Job Viewed
Job Description
Our client, a prominent pharmaceutical company, is seeking a highly skilled Senior Pharmaceutical Quality Control Analyst to join their team in Bhubaneswar, Odisha . This is a hybrid role, offering a combination of on-site laboratory work and remote data analysis/reporting. As a Senior QC Analyst, you will be responsible for performing a wide range of analytical tests on raw materials, in-process samples, and finished pharmaceutical products to ensure they meet strict quality standards and regulatory requirements. Your duties will include operating and maintaining sophisticated analytical instruments such as HPLC, GC, UV-Vis spectrophotometers, and dissolution apparatus. You will meticulously document all testing procedures, results, and deviations, ensuring data integrity and compliance with Good Manufacturing Practices (GMP). The ideal candidate will possess a strong understanding of pharmaceutical quality control principles, analytical chemistry, and regulatory guidelines (e.g., ICH, FDA). Experience in method development and validation is highly desirable. You will also be involved in the investigation of out-of-specification (OOS) results, root cause analysis, and the implementation of corrective and preventive actions (CAPAs). Excellent attention to detail, problem-solving abilities, and strong communication skills are essential for collaborating with cross-functional teams, including R&D, production, and regulatory affairs. A Bachelor's or Master's degree in Pharmacy, Chemistry, or a related scientific discipline, along with at least 5 years of relevant experience in pharmaceutical QC, is required. This hybrid role provides flexibility while ensuring essential laboratory operations are maintained, fostering a productive and compliant work environment. The position is located in Bhubaneswar, Odisha .
This advertiser has chosen not to accept applicants from your region.
4
Remote Pharmaceutical Quality Control Analyst
751001 Bhubaneswar, Orissa
₹75000 Annually
WhatJobs
Posted 6 days ago
Job Viewed
Job Description
Our client is seeking a meticulous and highly qualified Remote Pharmaceutical Quality Control Analyst to join their esteemed research and development team. This is a fully remote position that allows you to contribute significantly to ensuring the quality and safety of pharmaceutical products from your home office. You will be responsible for performing a wide range of analytical tests on raw materials, in-process samples, and finished pharmaceutical products. This involves using various analytical techniques and instrumentation, such as HPLC, GC, UV-Vis spectrophotometry, and dissolution testing, to ensure products meet stringent quality specifications and regulatory standards. The ideal candidate will have a strong understanding of Good Manufacturing Practices (GMP) and regulatory guidelines pertinent to the pharmaceutical industry (e.g., FDA, ICH). Responsibilities include developing, validating, and troubleshooting analytical methods; meticulously documenting all experimental procedures and results; and preparing comprehensive reports for review. You will collaborate closely with R&D scientists, production teams, and regulatory affairs personnel to address any quality-related issues and support product development lifecycles. This role requires exceptional attention to detail, strong analytical reasoning, and the ability to work independently with minimal supervision. Maintaining a well-organized laboratory environment (even in a remote setting) and ensuring the proper calibration and maintenance of analytical equipment are critical. Our client is dedicated to upholding the highest standards of pharmaceutical quality and safety and seeks a diligent professional who can ensure the integrity and reliability of their product portfolio. This is a significant opportunity to contribute to the development and release of life-saving medications while enjoying the flexibility of remote work. The ability to interpret complex data, identify deviations, and propose corrective actions will be key.
Qualifications:
Qualifications:
- Bachelor's or Master's degree in Pharmacy, Chemistry, or a related life science discipline.
- Minimum of 5 years of experience in pharmaceutical quality control or quality assurance.
- Extensive hands-on experience with analytical instrumentation (HPLC, GC, spectrophotometry, dissolution testers).
- In-depth knowledge of GMP, USP, and ICH guidelines.
- Proficiency in method development, validation, and transfer.
- Strong understanding of statistical analysis for quality control data.
- Excellent documentation and technical writing skills.
- Ability to work independently and manage time effectively in a remote setting.
- Meticulous attention to detail and commitment to accuracy.
- Experience with LIMS (Laboratory Information Management Systems) is a plus.
This advertiser has chosen not to accept applicants from your region.
5
Senior Pharmaceutical Quality Control Scientist
751001 Bhubaneswar, Orissa
₹70000 Annually
WhatJobs
Posted 6 days ago
Job Viewed
Job Description
Our client is seeking a highly skilled and detail-oriented Senior Pharmaceutical Quality Control Scientist to join our team in Bhubaneswar, Odisha, IN . This critical role will be responsible for ensuring the quality and safety of our pharmaceutical products through rigorous testing and analysis. You will perform a wide range of laboratory tests, interpret results, troubleshoot analytical issues, and contribute to the continuous improvement of our quality control processes. The ideal candidate will have a strong background in pharmaceutical analysis, excellent laboratory skills, and a thorough understanding of Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP).
Key Responsibilities:
Key Responsibilities:
- Perform analytical testing of raw materials, in-process samples, and finished pharmaceutical products using various analytical techniques (e.g., HPLC, GC, UV-Vis, FTIR).
- Develop, validate, and transfer analytical methods according to regulatory guidelines.
- Analyze and interpret test data, prepare reports, and document all laboratory activities accurately.
- Troubleshoot and resolve analytical issues encountered during testing.
- Ensure compliance with all relevant regulatory requirements, including GMP, GLP, and pharmacopeial standards (e.g., IP, USP, BP, EP).
- Maintain laboratory equipment, including calibration, qualification, and preventative maintenance.
- Participate in internal and external audits as a subject matter expert.
- Contribute to the investigation of deviations, Out-of-Specification (OOS) results, and CAPA implementation.
- Train and mentor junior QC analysts on laboratory procedures and techniques.
- Stay updated on the latest advancements in pharmaceutical quality control and analytical methodologies.
- Assist in the review and approval of batch records and quality control documentation.
- Ensure a safe and organized laboratory environment.
- Master's degree in Pharmacy, Pharmaceutical Sciences, Chemistry, or a related field.
- Minimum of 5 years of experience in pharmaceutical quality control, with a strong focus on analytical testing.
- Proven experience with analytical instruments such as HPLC, GC, and spectroscopy.
- In-depth knowledge of GMP, GLP, and relevant regulatory guidelines.
- Excellent understanding of pharmacopeial standards.
- Strong analytical, problem-solving, and critical-thinking skills.
- Meticulous attention to detail and accuracy in data recording and reporting.
- Effective communication and interpersonal skills.
- Ability to work independently and as part of a team in a fast-paced laboratory environment.
- Experience with method validation and transfer is highly desirable.
This advertiser has chosen not to accept applicants from your region.
Be The First To Know
About the latest Tata steel Jobs in Bhubaneshwar !
6
Senior Pharmaceutical Quality Control Analyst
751001 Bhubaneswar, Orissa
₹55000 Monthly
WhatJobs
Posted 6 days ago
Job Viewed
Job Description
Our client is seeking a meticulous and experienced Senior Pharmaceutical Quality Control Analyst to join our state-of-the-art facility in Bhubaneswar, Odisha, IN . This role is critical to ensuring the safety, efficacy, and quality of our pharmaceutical products. You will perform a wide range of analytical tests on raw materials, in-process samples, and finished products using various laboratory techniques and instrumentation. Responsibilities include operating and maintaining analytical equipment such as HPLC, GC, UV-Vis spectrophotometers, and dissolution testers. You will be responsible for method validation, stability testing, and preparing detailed analytical reports and documentation in compliance with cGMP guidelines. The ideal candidate will possess a strong understanding of pharmaceutical manufacturing processes, regulatory requirements (e.g., ICH, FDA), and quality assurance principles. You will also be involved in troubleshooting analytical methods and equipment issues, as well as participating in internal and external audits. Contributing to continuous improvement initiatives within the QC department and mentoring junior analysts will be key aspects of this position. Excellent attention to detail, strong problem-solving skills, and the ability to work effectively both independently and as part of a team are essential. A Bachelor's or Master's degree in Pharmacy, Chemistry, or a related life science discipline, along with substantial experience in a pharmaceutical QC laboratory setting, is required. Join our dedicated team and contribute to delivering high-quality medicines to patients.
This advertiser has chosen not to accept applicants from your region.
7
Remote Pharmaceutical Quality Control Scientist
751001 Bhubaneswar, Orissa
₹80000 Annually
WhatJobs
Posted 6 days ago
Job Viewed
Job Description
Our client, a forward-thinking pharmaceutical research and development company, is looking for a highly analytical and meticulous Pharmaceutical Quality Control Scientist to join their innovative team. This fully remote position offers a unique opportunity for experienced scientists to contribute to the development and manufacturing of high-quality pharmaceuticals without the need for physical office presence. You will be responsible for ensuring that all products meet stringent quality standards through rigorous testing and analysis, adhering to global regulatory requirements.
Responsibilities:
Responsibilities:
- Perform a wide range of analytical tests on raw materials, in-process samples, and finished pharmaceutical products using various laboratory techniques (e.g., HPLC, GC, UV-Vis, IR spectroscopy, dissolution testing).
- Develop, validate, and implement analytical methods according to regulatory guidelines and internal procedures.
- Analyze and interpret test results, ensuring accuracy and completeness.
- Prepare detailed reports on testing activities, results, and deviations.
- Troubleshoot and resolve analytical method issues and laboratory instrument problems.
- Maintain laboratory equipment and ensure proper calibration and qualification.
- Ensure compliance with Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), and other relevant regulatory standards.
- Collaborate with R&D, manufacturing, and regulatory affairs departments to support product development and issue resolution.
- Participate in internal and external audits as required.
- Maintain accurate and up-to-date laboratory records and documentation.
- Stay current with scientific literature, industry trends, and advancements in pharmaceutical quality control.
- Master's or Ph.D. in Chemistry, Pharmaceutical Sciences, Analytical Chemistry, or a related field.
- Minimum of 5 years of experience in pharmaceutical quality control or analytical development.
- Extensive hands-on experience with analytical instrumentation (e.g., HPLC, GC-MS, LC-MS).
- Proficiency in method development, validation, and transfer.
- Thorough understanding of GMP/GLP guidelines and regulatory requirements (e.g., FDA, EMA).
- Excellent analytical, problem-solving, and critical thinking skills.
- Strong report writing and data interpretation abilities.
- Ability to work independently with minimal supervision and manage time effectively in a remote setting.
- Excellent organizational skills and attention to detail.
- Proficiency in laboratory information management systems (LIMS) and relevant software.
This advertiser has chosen not to accept applicants from your region.
8