1,298 Pharmaceutical Quality jobs in India
Pharmaceutical Quality Control Analyst
201001 Ghaziabad, Uttar Pradesh
₹70000 Annually
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Posted 1 day ago
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Job Description
Our client is seeking a detail-oriented and highly motivated Pharmaceutical Quality Control Analyst to join their team in Ghaziabad, Uttar Pradesh, IN . This role is critical in ensuring that our pharmaceutical products meet stringent quality standards and regulatory requirements. The ideal candidate will have a strong background in analytical chemistry and extensive experience with various quality control techniques and instrumentation used in the pharmaceutical industry. You will be responsible for performing a wide range of tests on raw materials, in-process samples, and finished products to verify their identity, purity, potency, and quality. Key responsibilities include operating and maintaining analytical instruments such as HPLC, GC, UV-Vis spectrophotometers, and Karl Fischer titrators. You will meticulously document all testing procedures, results, and deviations according to Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP). Furthermore, you will be involved in method validation, stability studies, and the investigation of out-of-specification (OOS) results. The successful applicant will possess excellent analytical skills, a strong understanding of pharmaceutical regulations (e.g., FDA, ICH guidelines), and the ability to work effectively in a fast-paced laboratory environment. Strong organizational skills and meticulous attention to detail are paramount. You must be able to work collaboratively with other departments, including R&D, Production, and Regulatory Affairs. A proactive approach to identifying potential quality issues and contributing to continuous improvement initiatives is highly valued. This position requires a commitment to upholding the highest standards of quality and safety in pharmaceutical manufacturing.
Responsibilities:
Qualifications:
Responsibilities:
- Perform analytical testing on raw materials, intermediates, and finished pharmaceutical products.
- Operate and maintain laboratory instruments (HPLC, GC, UV-Vis, etc.).
- Document all test results and maintain accurate laboratory records.
- Ensure compliance with GLP, GMP, and relevant regulatory guidelines.
- Conduct method validation and stability studies.
- Investigate out-of-specification (OOS) results and deviations.
- Prepare Certificates of Analysis (CoA).
- Collaborate with R&D, Production, and Regulatory Affairs teams.
- Participate in internal and external audits.
- Contribute to process improvement initiatives within the QC department.
Qualifications:
- Bachelor's or Master's degree in Chemistry, Pharmaceutical Sciences, or a related field.
- Proven experience as a Quality Control Analyst in the pharmaceutical industry.
- Hands-on experience with analytical instrumentation (HPLC, GC, UV-Vis).
- Strong knowledge of pharmaceutical quality systems and regulations.
- Excellent analytical and problem-solving skills.
- Meticulous attention to detail and record-keeping.
- Ability to work effectively in a laboratory setting and meet deadlines.
- Good communication and teamwork skills.
- Familiarity with method validation principles.
- Experience with OOS investigations and CAPA.
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0
Pharmaceutical Quality Control Analyst
380001 Ahmedabad, Gujarat
₹400000 Annually
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Posted 4 days ago
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Job Description
Our client is seeking a meticulous and skilled Pharmaceutical Quality Control Analyst to join their team in Ahmedabad, Gujarat, IN . This role is crucial in ensuring the highest standards of quality and compliance for pharmaceutical products. The ideal candidate will have a strong understanding of analytical techniques, quality control procedures, and regulatory guidelines within the pharmaceutical industry. You will be responsible for performing a wide range of laboratory tests on raw materials, in-process samples, and finished pharmaceutical products using sophisticated analytical instrumentation. This includes utilizing techniques such as High-Performance Liquid Chromatography (HPLC), Gas Chromatography (GC), UV-Vis Spectrophotometry, and dissolution testing. Key responsibilities involve preparing reagents, maintaining laboratory equipment, and meticulously documenting all test results according to Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP). You will also be involved in method validation, stability studies, and investigating out-of-specification (OOS) results. Collaboration with the Quality Assurance department to ensure product release meets all regulatory requirements is essential. We are looking for a detail-oriented individual with excellent analytical and problem-solving skills, a commitment to accuracy, and the ability to work effectively both independently and as part of a team. A bachelor's or master's degree in Pharmacy, Chemistry, or a related life science field is required. Prior experience in a pharmaceutical QC laboratory setting is highly desirable. Familiarity with pharmacopoeial standards (e.g., USP, EP, IP) and regulatory submissions is a strong advantage. This position offers a significant opportunity to contribute to the safety and efficacy of pharmaceutical products in a well-established organization.
Key Responsibilities:
Key Responsibilities:
- Conduct analytical testing on pharmaceutical raw materials, intermediates, and finished products.
- Utilize various analytical instruments like HPLC, GC, and spectrophotometers.
- Document all laboratory activities and results according to GMP and GLP.
- Participate in method validation and stability studies.
- Investigate and report out-of-specification (OOS) results.
- Maintain laboratory equipment and ensure proper calibration.
- Prepare reagents and samples for testing.
- Collaborate with Quality Assurance for product release.
- Adhere to all safety and environmental protocols in the laboratory.
- Contribute to continuous improvement initiatives in the QC department.
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1
Pharmaceutical Quality Control Analyst
440032 Nagpur, Maharashtra
₹45000 Monthly
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Posted 6 days ago
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Job Description
Our client, a prominent pharmaceutical company, is seeking a meticulous and experienced Pharmaceutical Quality Control Analyst to join their dedicated team. This position is based at our advanced manufacturing facility in Nagpur, Maharashtra, IN . The ideal candidate will possess a Bachelor's or Master's degree in Pharmacy, Chemistry, or a related life science discipline, with a solid understanding of pharmaceutical quality control principles and regulatory guidelines (e.g., GMP, ICH). 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 stringent quality specifications. Key duties include operating and maintaining analytical instruments such as HPLC, GC, UV-Vis spectrophotometers, and dissolution testers; preparing reagents and standard solutions; documenting all laboratory activities accurately; and investigating out-of-specification (OOS) results. You will also be involved in method validation, stability testing, and preparing quality control reports. A strong background in analytical chemistry, method development, and data interpretation is essential. The successful candidate must demonstrate excellent attention to detail, strong problem-solving skills, and the ability to work effectively both independently and as part of a collaborative team in a laboratory setting. Adherence to safety protocols and a commitment to maintaining the highest quality standards are paramount. This is an excellent opportunity to contribute to the development and production of safe and effective medicines within a reputable organization. We are looking for a highly motivated individual to ensure the integrity and quality of our pharmaceutical products.
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2
Pharmaceutical Quality Control Chemist
248001 Dehradun, Uttarakhand
₹75000 Monthly
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Posted 6 days ago
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Job Description
Our client, a prominent pharmaceutical company, is seeking a meticulous and qualified Pharmaceutical Quality Control Chemist. This hybrid role is crucial for ensuring the quality and safety of pharmaceutical products throughout the manufacturing process. You will be responsible for performing a variety of analytical tests on raw materials, in-process samples, and finished products to ensure they meet stringent regulatory and internal quality standards. Key responsibilities include operating and maintaining analytical instruments such as HPLC, GC, UV-Vis spectrophotometers, and dissolution testers. You will document all testing procedures, results, and deviations accurately in accordance with Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP). The ideal candidate possesses a strong understanding of pharmaceutical analysis, quality control principles, and regulatory guidelines. Excellent attention to detail, strong problem-solving skills, and proficiency in analytical techniques are essential. You will collaborate with the quality assurance team and production personnel to address any quality deviations or out-of-specification results. Responsibilities also include method validation, stability testing, and preparing test methods and specifications. We are looking for an individual who is organized, detail-oriented, and committed to maintaining the highest standards of quality. The ability to work effectively both independently and as part of a team in a hybrid work setting is important. A Bachelor's or Master's degree in Chemistry, Pharmaceutical Sciences, or a related field, with practical experience in a pharmaceutical QC laboratory, is required. This role is based in Dehradun, Uttarakhand, IN .
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3
Pharmaceutical Quality Control Analyst
122001 Gurgaon, Haryana
₹500000 Annually
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Posted 7 days ago
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Job Description
Our client is seeking a detail-oriented and highly motivated Pharmaceutical Quality Control Analyst to join their esteemed organization in Gurugram. The successful candidate will be responsible for performing various analytical tests on raw materials, in-process samples, and finished products to ensure they meet stringent quality standards and regulatory requirements. This role is critical to maintaining the integrity and safety of our pharmaceutical offerings.
Key Responsibilities:
Required Qualifications:
Key Responsibilities:
- Perform routine and non-routine analytical testing using a variety of laboratory techniques (e.g., HPLC, GC, UV-Vis Spectroscopy, Titration).
- Analyze samples of raw materials, intermediates, and finished pharmaceutical products.
- Document all laboratory activities, results, and observations accurately and in compliance with Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP).
- Prepare reagents, standards, and samples for testing.
- Calibrate and maintain laboratory equipment, ensuring proper functioning and calibration records.
- Investigate out-of-specification (OOS) results and deviations, participating in root cause analysis.
- Assist in the validation and qualification of analytical methods and equipment.
- Review and approve test results and associated documentation.
- Maintain a clean and organized laboratory environment.
- Stay updated on pharmacopoeial standards (e.g., IP, BP, USP) and regulatory guidelines.
- Contribute to the continuous improvement of quality control processes.
Required Qualifications:
- Bachelor's or Master's degree in Pharmacy, Chemistry, Microbiology, or a related life science discipline.
- Minimum of 3-5 years of experience in a pharmaceutical Quality Control laboratory.
- Proficiency in analytical techniques such as HPLC, GC, and wet chemistry.
- Thorough understanding of GLP, GMP, and relevant regulatory guidelines.
- Experience with laboratory information management systems (LIMS) is a plus.
- Strong attention to detail and accuracy in data recording and analysis.
- Excellent organizational and time management skills.
- Ability to work independently and as part of a team.
- Good written and verbal communication skills.
- Proficiency in Microsoft Office Suite.
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4
Pharmaceutical Quality Control Chemist
390001 Vadodara, Gujarat
₹80000 Annually
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Posted 7 days ago
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Job Description
Our client, a prominent pharmaceutical company, is seeking a meticulous and driven Pharmaceutical Quality Control Chemist to join their state-of-the-art facility. This role involves ensuring the quality and integrity of pharmaceutical products through rigorous testing and analysis. You will be responsible for performing a wide range of chemical tests, operating sophisticated analytical instrumentation, and meticulously documenting all findings. This position requires a strong understanding of pharmaceutical quality standards and regulatory compliance. A hybrid work model will allow for a blend of in-office lab work and remote data analysis and reporting.
Key Responsibilities:
The ideal candidate will possess a Bachelor's or Master's degree in Chemistry, Pharmaceutical Sciences, or a related field. Proven experience in a pharmaceutical quality control laboratory setting is essential. Strong knowledge of analytical chemistry principles and instrumentation is required. Excellent attention to detail, problem-solving skills, and the ability to work both independently and as part of a team are crucial. The candidate must be proficient in maintaining accurate records and have a thorough understanding of regulatory requirements within the pharmaceutical industry. This hybrid role requires strong organizational skills and the ability to manage workload effectively across both in-office and remote duties.
Key Responsibilities:
- Perform chemical and physical tests on raw materials, in-process samples, and finished pharmaceutical products using various analytical techniques (e.g., HPLC, GC, UV-Vis, Titration).
- Calibrate and maintain laboratory equipment to ensure accurate and reliable results.
- Analyze and interpret test data, comparing results against established specifications.
- Document all testing procedures, results, and observations in compliance with Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP).
- Prepare standard solutions and reagents.
- Investigate out-of-specification (OOS) results and deviations, collaborating with relevant departments to identify root causes and implement corrective actions.
- Participate in method validation and transfer activities.
- Maintain a clean and organized laboratory environment.
- Prepare reports summarizing test results and quality control status.
- Ensure compliance with all relevant regulatory guidelines (e.g., FDA, WHO).
The ideal candidate will possess a Bachelor's or Master's degree in Chemistry, Pharmaceutical Sciences, or a related field. Proven experience in a pharmaceutical quality control laboratory setting is essential. Strong knowledge of analytical chemistry principles and instrumentation is required. Excellent attention to detail, problem-solving skills, and the ability to work both independently and as part of a team are crucial. The candidate must be proficient in maintaining accurate records and have a thorough understanding of regulatory requirements within the pharmaceutical industry. This hybrid role requires strong organizational skills and the ability to manage workload effectively across both in-office and remote duties.
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5
Pharmaceutical Quality Control Manager
440001 Nagpur, Maharashtra
₹80000 Annually
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Posted 10 days ago
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Job Description
Our client is seeking a highly skilled and meticulous Pharmaceutical Quality Control Manager to oversee and implement robust quality control systems within their manufacturing facility in Nagpur, Maharashtra, IN . This critical role ensures that all pharmaceutical products meet stringent regulatory standards and internal quality benchmarks. The ideal candidate will possess extensive knowledge of pharmaceutical quality assurance, GMP guidelines, and analytical testing methodologies.
Responsibilities:
Responsibilities:
- Develop, implement, and maintain the company's Quality Management System (QMS) in accordance with GMP and regulatory requirements.
- Supervise and lead the Quality Control (QC) laboratory operations, including raw material testing, in-process control, and finished product analysis.
- Ensure all analytical testing is performed accurately and in compliance with established methods and protocols.
- Manage the calibration and maintenance of laboratory equipment.
- Review and approve batch records, validation protocols, and reports.
- Investigate deviations, out-of-specification (OOS) results, and customer complaints, implementing corrective and preventive actions (CAPA).
- Conduct internal audits and participate in external regulatory inspections.
- Train QC personnel on analytical techniques, GMP principles, and safety procedures.
- Stay current with evolving regulatory guidelines and industry best practices in pharmaceutical quality control.
- Collaborate with Production, R&D, and other departments to ensure product quality and compliance.
- Master's degree in Pharmacy, Chemistry, Pharmaceutical Sciences, or a related discipline.
- Minimum of 5-7 years of experience in pharmaceutical quality control and quality assurance.
- In-depth knowledge of Good Manufacturing Practices (GMP), ICH guidelines, and regulatory requirements (e.g., US FDA, EMA).
- Proven experience in analytical method validation and instrument qualification.
- Strong understanding of various analytical techniques (e.g., HPLC, GC, spectroscopy).
- Excellent leadership, team management, and communication skills.
- Proficiency in quality management software and MS Office Suite.
- Strong problem-solving and decision-making abilities.
- Meticulous attention to detail and a commitment to quality.
- Experience with regulatory audits and inspections.
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Pharmaceutical Quality Control Manager
695001 Thiruvananthapuram, Kerala
₹1000000 Annually
WhatJobs
Posted 10 days ago
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Job Description
Our client is seeking a highly motivated and experienced Pharmaceutical Quality Control Manager to oversee operations at their facility in **Thiruvananthapuram, Kerala, IN**. This role requires a strong understanding of pharmaceutical manufacturing processes, regulatory compliance, and quality assurance principles. You will be responsible for developing and implementing robust quality control strategies to ensure the safety, efficacy, and consistency of all manufactured products. Key duties include managing a team of quality control analysts, overseeing laboratory operations, conducting method validation and stability studies, and ensuring compliance with cGMP (current Good Manufacturing Practices) and other relevant regulatory standards. You will also be involved in deviation investigations, CAPA (Corrective and Preventive Actions) implementation, and continuous improvement initiatives within the quality department. The ideal candidate will possess a Bachelor's or Master's degree in Pharmacy, Chemistry, or a related life science discipline, with significant experience in pharmaceutical quality control or quality assurance roles. Proven leadership and team management skills are essential, as is a deep knowledge of analytical techniques and instrumentation commonly used in pharmaceutical QC. Experience with regulatory audits (e.g., FDA, EMA) and a strong commitment to quality excellence are critical. You will play a crucial role in maintaining our high standards of product quality and ensuring regulatory compliance in a dynamic and critical industry. This is an excellent opportunity for a seasoned professional to lead a vital function within a respected pharmaceutical company.
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7
Pharmaceutical Quality Control Analyst
520001 Krishna, Andhra Pradesh
₹700000 Annually
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Posted 11 days ago
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Job Description
Our client, a rapidly growing pharmaceutical manufacturing company, is actively recruiting a dedicated Pharmaceutical Quality Control Analyst to be part of their state-of-the-art facility in Vijayawada, Andhra Pradesh, IN . This critical role ensures that all manufactured pharmaceutical products meet stringent quality and safety standards. The Quality Control Analyst will perform a variety of analytical tests on raw materials, in-process samples, and finished products using advanced laboratory equipment and techniques. Responsibilities include operating and maintaining analytical instruments such as HPLC, GC, UV-Vis spectrophotometers, and dissolution testers. You will meticulously document all testing procedures, results, and deviations according to Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP). The analyst will also be involved in method validation, stability studies, and the investigation of out-of-specification (OOS) results. The ideal candidate will possess a Bachelor's or Master's degree in Pharmacy, Chemistry, or a related life science discipline, with a minimum of 2-3 years of experience in a pharmaceutical QC laboratory setting. A strong understanding of pharmaceutical quality systems, regulatory guidelines (e.g., FDA, WHO), and analytical chemistry principles is essential. Proficiency in operating and troubleshooting common QC laboratory instrumentation is required. Excellent attention to detail, strong organizational skills, and the ability to work independently and as part of a team are crucial. You will contribute to maintaining the integrity and quality of our pharmaceutical products, ensuring patient safety and regulatory compliance. This is an excellent opportunity to join a dynamic organization committed to quality and innovation in the pharmaceutical industry.
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8
Pharmaceutical Quality Control Analyst
500001 Hyderabad, Andhra Pradesh
₹60000 Annually
WhatJobs
Posted 12 days ago
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Job Description
Our client, a leading pharmaceutical company, is seeking a meticulous and experienced Pharmaceutical Quality Control Analyst to join their team in Hyderabad, Telangana, IN . This critical role involves ensuring the highest standards of quality and compliance for our pharmaceutical products. The ideal candidate will possess a strong scientific background, hands-on experience with analytical techniques, and a thorough understanding of regulatory requirements within the pharmaceutical industry. You will be responsible for performing a wide range of tests, analyzing data, and documenting results to guarantee product safety and efficacy.
Responsibilities:
Qualifications:
Responsibilities:
- Perform routine and advanced analytical testing of raw materials, in-process samples, and finished products using various laboratory techniques (e.g., HPLC, GC, UV-Vis, FTIR).
- Develop, validate, and transfer analytical methods according to established protocols and regulatory guidelines.
- Analyze test results, interpret data, and prepare accurate and comprehensive reports.
- Investigate out-of-specification (OOS) results and deviations, documenting findings and recommending corrective and preventive actions (CAPA).
- Maintain laboratory equipment, ensuring calibration, qualification, and routine maintenance are performed.
- Ensure adherence to Good Laboratory Practices (GLP), Good Manufacturing Practices (GMP), and other relevant regulatory standards.
- Prepare and review standard operating procedures (SOPs) for analytical testing and laboratory operations.
- Collaborate with R&D, Manufacturing, and Regulatory Affairs departments to resolve quality issues and support product development.
- Manage laboratory inventory, including chemicals, reagents, and consumables.
- Participate in internal and external audits as required.
- Stay updated with the latest advancements in pharmaceutical analysis and quality control techniques.
- Contribute to continuous improvement initiatives within the Quality Control department.
Qualifications:
- Bachelor's or Master's degree in Pharmacy, Chemistry, Biotechnology, or a related life science field.
- Minimum of 3-5 years of experience in pharmaceutical quality control or analytical development.
- Extensive hands-on experience with analytical instrumentation such as HPLC, GC, dissolution testers, and spectrophotometers.
- Proficiency in wet chemistry techniques and compendial testing (USP/EP/BP/IP).
- Strong understanding of GMP, GLP, and ICH guidelines.
- Excellent analytical, problem-solving, and critical thinking skills.
- Meticulous attention to detail and accuracy in data recording and reporting.
- Ability to work independently and as part of a team in a fast-paced laboratory environment.
- Proficient in Microsoft Office Suite and LIMS (Laboratory Information Management System) software.
- Strong written and verbal communication skills.
- Experience with method validation and transfer is highly desirable.
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