996 Pharmaceutical Qa jobs in India
Pharmaceutical Quality Assurance Manager
201001 Ghaziabad, Uttar Pradesh
₹1000000 Annually
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Posted 1 day ago
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Our client, a leading pharmaceutical company, is seeking a highly experienced and meticulous Pharmaceutical Quality Assurance Manager to oversee and enhance our quality management systems. This role is critical to ensuring that all products meet stringent regulatory standards and internal quality benchmarks. You will be responsible for developing, implementing, and maintaining comprehensive quality assurance programs, including SOPs, validation protocols, and batch record reviews. A key aspect of your role will involve conducting internal and external audits, investigating deviations and non-conformances, and implementing corrective and preventive actions (CAPA). You will also collaborate closely with regulatory affairs, manufacturing, and research and development departments to ensure compliance with GMP, ICH, and other relevant guidelines. The ideal candidate possesses a deep understanding of pharmaceutical manufacturing processes, regulatory requirements, and quality control principles. Excellent leadership, analytical, and problem-solving skills are essential. A Bachelor's or Master's degree in Pharmacy, Chemistry, Microbiology, or a related life science field is required. Extensive experience in quality assurance within the pharmaceutical industry, with a proven track record of managing quality systems and leading QA teams, is mandatory. Experience with regulatory submissions and inspections (e.g., FDA, EMA) is highly desirable. You must be proficient in quality management software and possess strong documentation and reporting skills. This is a vital role that directly impacts the safety and efficacy of our pharmaceutical products, offering a significant opportunity for professional growth and contribution to public health. The position is based at our state-of-the-art facility in Ghaziabad, Uttar Pradesh, IN , and requires full-time on-site commitment.
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Pharmaceutical Quality Assurance Specialist
440001 Nagpur, Maharashtra
₹900000 Annually
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Posted 1 day ago
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Our client is a dynamic pharmaceutical company seeking a diligent and meticulous Pharmaceutical Quality Assurance Specialist to ensure the highest standards of quality in our products and processes. This role is crucial for maintaining regulatory compliance and upholding our commitment to excellence. You will be involved in reviewing batch records, auditing manufacturing processes, and implementing quality control measures. The ideal candidate has a strong background in pharmaceutical quality systems, excellent analytical skills, and a keen eye for detail. This position involves a hybrid work model, requiring a balance between remote responsibilities and on-site engagement for critical operational tasks and collaboration.
Responsibilities:
Qualifications:
Responsibilities:
- Review and approve batch records, deviation reports, and change controls to ensure compliance with GMP regulations.
- Conduct internal audits of manufacturing processes, laboratories, and documentation systems.
- Participate in external audits by regulatory agencies and customers.
- Develop, implement, and maintain quality assurance policies and procedures.
- Monitor and ensure compliance with relevant regulatory guidelines (e.g., FDA, EMA, local regulations).
- Investigate quality deviations and implement corrective and preventive actions (CAPAs).
- Assist in the qualification and validation of equipment and processes.
- Prepare quality reports and metrics for management review.
- Provide training to personnel on GMP and quality system requirements.
- Collaborate with production, R&D, and other departments to resolve quality issues.
- Stay current with industry best practices and regulatory updates in pharmaceutical quality assurance.
- Contribute to the continuous improvement of the Quality Management System (QMS).
- Balance remote tasks, such as documentation review and report generation, with essential on-site activities for audits and process oversight.
Qualifications:
- Bachelor's degree in Pharmacy, Chemistry, Biology, or a related scientific field.
- Minimum of 3-5 years of experience in pharmaceutical Quality Assurance or Quality Control.
- Strong understanding of Good Manufacturing Practices (GMP) and relevant regulatory guidelines.
- Experience with auditing processes and documentation review.
- Excellent analytical, problem-solving, and critical thinking skills.
- Proficiency in quality management software and standard office applications.
- Strong written and verbal communication skills.
- Detail-oriented with a high degree of accuracy.
- Ability to work independently and as part of a team.
- Experience working in a hybrid environment is beneficial.
- Knowledge of validation principles is a plus.
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Pharmaceutical Quality Assurance Specialist
462001 Bhopal, Madhya Pradesh
₹60000 Annually
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Posted 4 days ago
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Our client is looking for a meticulous and experienced Pharmaceutical Quality Assurance Specialist to join their esteemed team in **Bhopal, Madhya Pradesh, IN**. This role is crucial for maintaining the highest standards of quality and compliance within the pharmaceutical manufacturing process. The ideal candidate will have a strong understanding of Good Manufacturing Practices (GMP), regulatory requirements, and quality control principles specific to the pharmaceutical industry. You will be responsible for developing, implementing, and maintaining quality assurance systems and procedures to ensure that all products meet stringent regulatory and internal specifications. Key duties include conducting quality audits, reviewing batch records, investigating deviations and out-of-specification results, and implementing corrective and preventive actions (CAPA). You will also participate in process validation activities, ensuring that manufacturing processes are robust and consistently produce high-quality products. The ability to collaborate effectively with manufacturing, R&D, and regulatory affairs departments is essential for success in this position. You will contribute to the continuous improvement of quality systems and support regulatory inspections. This hybrid role offers a combination of in-office responsibilities, including laboratory work and audits, with potential for remote work on specific documentation and review tasks. We expect candidates to possess strong analytical and problem-solving skills, with excellent attention to detail. A background in pharmacy, chemistry, or a related life science discipline is required, along with proven experience in pharmaceutical quality assurance. Join our client and play a vital role in ensuring the safety and efficacy of pharmaceutical products.
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2
Pharmaceutical Quality Assurance Specialist
700001 Kolkata, West Bengal
₹55000 Annually
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Posted 4 days ago
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Our client, a respected pharmaceutical manufacturer, is seeking a meticulous and detail-oriented Pharmaceutical Quality Assurance Specialist for its facility in Kolkata, West Bengal, IN . This role is integral to ensuring that all pharmaceutical products manufactured meet stringent quality standards and comply with regulatory requirements set by agencies such as the FDA, EMA, and local authorities. The QA Specialist will be responsible for reviewing and approving batch records, deviations, change controls, and other quality-related documentation. You will participate in internal audits, support external audits and inspections, and contribute to the development and implementation of the Quality Management System (QMS). Key duties include conducting investigations into quality issues, identifying root causes, and implementing effective corrective and preventive actions (CAPAs). The ideal candidate will possess a strong understanding of Good Manufacturing Practices (GMP) and relevant pharmaceutical quality regulations. Excellent analytical and problem-solving skills are required to assess compliance and identify areas for improvement. You will collaborate with various departments, including Production, Quality Control, and Regulatory Affairs, to ensure a consistent approach to quality. This role demands exceptional organizational skills, meticulous attention to detail, and strong written and verbal communication abilities for clear documentation and reporting. A commitment to maintaining the highest standards of pharmaceutical quality is paramount.
Key Responsibilities:
Key Responsibilities:
- Review and approve batch production and control records.
- Manage deviations, change controls, and CAPA systems.
- Participate in internal and external audits and inspections.
- Ensure compliance with GMP and relevant regulatory guidelines.
- Investigate quality incidents and perform root cause analysis.
- Contribute to the maintenance and improvement of the Quality Management System.
- Collaborate with cross-functional teams on quality initiatives.
- Prepare and review quality-related documentation.
- Bachelor's degree in Pharmacy, Chemistry, Biology, or a related scientific field.
- Minimum of 3 years of experience in Pharmaceutical Quality Assurance or Quality Control.
- Thorough understanding of GMP and pharmaceutical quality regulations.
- Experience with QMS, batch record review, and deviation management.
- Strong analytical and problem-solving skills.
- Excellent documentation and communication skills.
- Ability to work independently and collaboratively in a team environment.
- Proficiency in relevant software applications.
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3
Pharmaceutical Quality Assurance Specialist
462001 Bhopal, Madhya Pradesh
₹650000 Annually
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Posted 4 days ago
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Our client is actively recruiting for a detail-oriented and experienced Pharmaceutical Quality Assurance Specialist to join their fully remote team. This crucial role ensures that all pharmaceutical products meet the highest standards of quality, safety, and efficacy, in strict adherence to regulatory guidelines. You will be responsible for developing, implementing, and maintaining the Quality Management System (QMS), conducting internal audits and gap analyses, reviewing and approving batch records and documentation, managing deviations and CAPA (Corrective and Preventive Actions), ensuring compliance with cGMP (current Good Manufacturing Practices), and participating in regulatory inspections. The ideal candidate will possess a strong understanding of pharmaceutical manufacturing processes and quality control principles. Excellent knowledge of regulatory requirements (e.g., US FDA, EMA, CDSCO) is essential. You must have impeccable attention to detail, strong analytical and problem-solving skills, and the ability to interpret complex regulatory texts. Effective written and verbal communication skills are vital for documenting findings, reporting deviations, and collaborating with internal departments and external regulatory bodies. A Bachelor's or Master's degree in Pharmacy, Chemistry, or a related life science field is required, along with demonstrated experience in pharmaceutical quality assurance or quality control. Experience with electronic QMS software and familiarity with risk management principles are highly advantageous. As this position is fully remote, you must be highly self-motivated, organized, and capable of working independently while ensuring seamless collaboration with colleagues through virtual platforms. This role, although nominally tied to Bhopal, Madhya Pradesh, IN , offers the flexibility of remote work, allowing you to contribute from your chosen location. If you are dedicated to ensuring pharmaceutical quality and safety, we invite you to apply and be a part of our commitment to excellence.
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4
Pharmaceutical Quality Assurance Specialist
682001 Kochi, Kerala
₹65000 Annually
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Posted 7 days ago
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Job Description
Our client is looking for a detail-oriented and experienced Pharmaceutical Quality Assurance Specialist to ensure compliance with stringent regulatory standards. This role is pivotal in maintaining the quality and safety of pharmaceutical products throughout their lifecycle, from development to market. You will be responsible for developing, implementing, and maintaining quality management systems, conducting internal audits, reviewing batch records, and managing deviations and CAPAs (Corrective and Preventive Actions). A deep understanding of Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), and relevant regulatory guidelines (e.g., FDA, EMA) is essential. This is a hybrid position, offering a balance between remote work for documentation and analysis, and on-site presence for laboratory and manufacturing oversight, ensuring a comprehensive approach to quality assurance.
Responsibilities:
Responsibilities:
- Develop and maintain the company's Quality Management System (QMS).
- Conduct internal audits of manufacturing processes, laboratories, and documentation to ensure compliance.
- Review and approve batch manufacturing records (BMRs) and analytical test results.
- Investigate deviations, non-conformances, and customer complaints, implementing CAPAs as necessary.
- Ensure all activities comply with GMP, GLP, and other relevant regulatory requirements.
- Participate in external regulatory inspections and audits.
- Manage vendor qualification and audits.
- Develop and deliver quality training programs for staff.
- Monitor key quality indicators and prepare quality reports for management.
- Oversee the change control process for manufacturing and quality procedures.
- Stay updated on evolving regulatory requirements and industry best practices.
- Bachelor's degree in Pharmacy, Chemistry, Biology, or a related scientific field.
- Minimum of 4 years of experience in quality assurance or quality control within the pharmaceutical industry.
- Strong knowledge of GMP, GLP, and ICH guidelines.
- Experience with audit processes, deviation management, and CAPA systems.
- Excellent analytical and problem-solving skills.
- Proficiency in documentation and report writing.
- Strong communication and interpersonal skills.
- Ability to work effectively in both remote and on-site settings.
- Familiarity with regulatory submission processes is a plus.
- Attention to detail and a commitment to upholding quality standards.
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5
Pharmaceutical Quality Assurance Specialist
160001 Chandigarh, Chandigarh
₹60000 Annually
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Posted 8 days ago
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Job Description
Our client is seeking a meticulous and experienced Pharmaceutical Quality Assurance Specialist to join their esteemed team in Chandigarh, Chandigarh, IN . This role is integral to ensuring that all pharmaceutical products meet the highest standards of quality, safety, and efficacy, adhering strictly to regulatory requirements. The ideal candidate will have a comprehensive understanding of Good Manufacturing Practices (GMP), regulatory guidelines, and quality management systems within the pharmaceutical industry. Key responsibilities include developing and implementing quality assurance protocols, conducting internal audits, reviewing batch records and documentation, investigating deviations and out-of-specification results, and participating in regulatory inspections. You will work closely with production, R&D, and regulatory affairs departments to ensure compliance throughout the product lifecycle. We are looking for a candidate with a Bachelor's or Master's degree in Pharmacy, Chemistry, Biology, or a related life science field, coupled with at least 4 years of experience in pharmaceutical quality assurance. Strong knowledge of ICH guidelines and other relevant regulatory frameworks (e.g., FDA, EMA) is essential. Excellent analytical, problem-solving, and documentation skills are required. The ability to conduct thorough investigations and implement effective corrective and preventive actions (CAPAs) is crucial. Attention to detail and a commitment to maintaining the highest quality standards are paramount. This is an outstanding opportunity for a dedicated QA professional to contribute to the development and manufacturing of life-saving medicines in a reputable organization. Effective communication and interpersonal skills are necessary for collaborating with various internal teams and external regulatory bodies.
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6
Pharmaceutical Quality Assurance Specialist
122001 Gurgaon, Haryana
₹850000 Annually
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Posted 8 days ago
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Job Description
Our client is a leading pharmaceutical company seeking a meticulous and dedicated Pharmaceutical Quality Assurance Specialist to join their fully remote team. This role is vital in ensuring that all pharmaceutical products meet the highest standards of quality, safety, and efficacy in compliance with regulatory requirements. As a remote-first position, you will be responsible for developing, implementing, and maintaining robust quality systems, conducting audits, reviewing documentation, and ensuring adherence to Good Manufacturing Practices (GMP) and other relevant guidelines. You will play a critical role in maintaining the integrity of our product lifecycle, from development through to market release.
Responsibilities:
The successful candidate will be instrumental in upholding the stringent quality standards expected in the pharmaceutical industry, working remotely to ensure all processes and products align with regulatory mandates. This includes rigorous review of manufacturing batch records, validation documentation, and change controls, all performed within a digital, remote framework. The collaborative nature of the remote team ensures thorough review and discussion of quality issues, maintaining a high level of scrutiny. The company culture emphasizes a commitment to quality and continuous improvement, providing ample resources and training to support professionals in this field. Your expertise will be key in navigating the complexities of pharmaceutical regulations and ensuring that every product leaving our facilities is of the highest standard. The role demands a proactive approach to risk management and a commitment to implementing effective corrective and preventive actions. We are looking for individuals who are not only technically adept but also possess strong ethical principles and a dedication to patient well-being. This is a chance to make a significant impact in a vital industry from a flexible, remote setting.
Responsibilities:
- Develop, implement, and maintain quality assurance policies and procedures for pharmaceutical manufacturing.
- Ensure compliance with cGMP, ICH guidelines, and other relevant regulatory standards.
- Review and approve batch records, validation protocols, and other critical quality documentation.
- Conduct internal and external audits of manufacturing sites, suppliers, and service providers.
- Investigate deviations, out-of-specification (OOS) results, and customer complaints, implementing corrective and preventive actions (CAPAs).
- Participate in regulatory inspections and audits, acting as a key point of contact for quality-related inquiries.
- Manage and maintain the company's quality management system (QMS).
- Train personnel on quality systems, GMP, and other relevant quality principles.
- Monitor key quality indicators and report on the overall effectiveness of the quality system.
- Contribute to the continuous improvement of quality processes and product quality.
- Bachelor's or Master's degree in Pharmacy, Chemistry, Biology, Biotechnology, or a related life science field.
- Minimum of 4 years of experience in Quality Assurance within the pharmaceutical or biotechnology industry.
- In-depth knowledge of cGMP, FDA regulations, and pharmaceutical quality systems.
- Experience with document control, CAPA management, and change control processes.
- Strong understanding of pharmaceutical manufacturing processes and laboratory testing.
- Excellent analytical, problem-solving, and critical thinking skills.
- Exceptional attention to detail and organizational skills.
- Strong written and verbal communication skills, crucial for remote collaboration and reporting.
- Ability to work independently, manage priorities, and meet deadlines in a remote setting.
- Experience with internal and external audits is highly desirable.
The successful candidate will be instrumental in upholding the stringent quality standards expected in the pharmaceutical industry, working remotely to ensure all processes and products align with regulatory mandates. This includes rigorous review of manufacturing batch records, validation documentation, and change controls, all performed within a digital, remote framework. The collaborative nature of the remote team ensures thorough review and discussion of quality issues, maintaining a high level of scrutiny. The company culture emphasizes a commitment to quality and continuous improvement, providing ample resources and training to support professionals in this field. Your expertise will be key in navigating the complexities of pharmaceutical regulations and ensuring that every product leaving our facilities is of the highest standard. The role demands a proactive approach to risk management and a commitment to implementing effective corrective and preventive actions. We are looking for individuals who are not only technically adept but also possess strong ethical principles and a dedication to patient well-being. This is a chance to make a significant impact in a vital industry from a flexible, remote setting.
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7
Pharmaceutical Quality Assurance Manager
122001 Gurgaon, Haryana
₹100000 Annually
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Posted 8 days ago
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Job Description
Our client is seeking a highly experienced and meticulous Pharmaceutical Quality Assurance Manager to join their fully remote team, based operationally near Gurugram, Haryana, IN . In this crucial role, you will be responsible for upholding the highest standards of quality and compliance throughout the pharmaceutical product lifecycle. You will lead and manage the Quality Assurance department, ensuring adherence to Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), and other relevant regulatory requirements. Your duties will include developing, implementing, and maintaining quality management systems, conducting internal audits, overseeing deviation investigations, change control processes, and CAPA (Corrective and Preventive Actions) management. You will also be involved in validating manufacturing processes and equipment, reviewing batch records, and managing regulatory submissions. The ideal candidate will possess a deep understanding of pharmaceutical regulations (e.g., FDA, EMA, CDSCO), quality control methodologies, and risk management principles. Exceptional attention to detail, strong analytical and problem-solving skills, and outstanding leadership capabilities are essential. This role requires excellent communication and interpersonal skills to effectively collaborate with internal teams, external partners, and regulatory agencies. This is a remote position, offering the flexibility to work from any location. You will play a pivotal role in ensuring the safety, efficacy, and quality of our pharmaceutical products, contributing directly to patient well-being.
Responsibilities:
Responsibilities:
- Develop, implement, and maintain the Quality Management System (QMS).
- Ensure compliance with GMP, GLP, and other relevant regulatory standards.
- Oversee internal and external audits.
- Manage deviation investigations, change controls, and CAPA processes.
- Review and approve batch records and quality control data.
- Participate in regulatory inspections and submissions.
- Train staff on quality assurance principles and procedures.
- Conduct risk assessments and implement risk mitigation strategies.
- Validate manufacturing processes, equipment, and analytical methods.
- Monitor quality metrics and drive continuous improvement initiatives.
- Bachelor's or Master's degree in Pharmacy, Chemistry, Biology, or a related life science field.
- Minimum of 8 years of experience in pharmaceutical quality assurance and quality control.
- Extensive knowledge of GMP, GLP, and regulatory guidelines.
- Proven experience in managing quality systems and leading audit processes.
- Strong analytical, problem-solving, and decision-making skills.
- Excellent leadership, communication, and interpersonal abilities.
- Experience with validation protocols and regulatory submissions.
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8
Pharmaceutical Quality Assurance Specialist
751001 Bhubaneswar, Orissa
₹900000 Annually
WhatJobs
Posted 12 days ago
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Job Description
Our client is searching for a meticulous and experienced Pharmaceutical Quality Assurance Specialist to join their team. This hybrid role, based in Bhubaneswar, Odisha, IN, combines strategic oversight with operational involvement. The ideal candidate will possess a strong understanding of pharmaceutical manufacturing processes, regulatory guidelines (e.g., GMP, FDA), and quality management systems. You will be responsible for ensuring that all products meet stringent quality standards and comply with regulatory requirements throughout the development and manufacturing lifecycle. Key duties include developing and implementing QA protocols, conducting internal audits, reviewing batch records, and investigating deviations and CAPAs. You will collaborate closely with R&D, manufacturing, and regulatory affairs teams to ensure product quality and consistency. The ability to identify and resolve quality issues proactively is essential. Strong analytical skills, excellent attention to detail, and robust documentation capabilities are required. Experience with validation activities (process, cleaning, analytical) and change control procedures is highly desirable. This hybrid position allows for focused analytical and review work remotely, complemented by essential on-site presence for audits, inspections, and direct collaboration with manufacturing and laboratory personnel. Our client is committed to upholding the highest standards of pharmaceutical quality and safety, and this role is critical to that mission. We are seeking a dedicated professional who is passionate about ensuring patient safety and product efficacy through rigorous quality assurance practices. Your expertise will be vital in maintaining our client's compliance and reputation within the pharmaceutical industry. The role demands a proactive approach to continuous improvement and a thorough understanding of the pharmaceutical regulatory landscape.
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