8,261 Pharmaceutical Qa jobs in India
Pharmaceutical Quality Assurance Manager
160022 Chandigarh, Chandigarh
₹90000 Annually
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Our client, a leading pharmaceutical company, is seeking a meticulous and experienced Pharmaceutical Quality Assurance Manager to oversee quality systems and compliance at their facility in **Chandigarh, Chandigarh, IN**. This vital role ensures that all pharmaceutical products meet rigorous quality standards and comply with regulatory requirements set forth by bodies such as the FDA, EMA, and national health authorities. The QA Manager will be instrumental in maintaining and improving the company's overall quality management system (QMS).
Key responsibilities include developing, implementing, and maintaining quality assurance policies and procedures, managing internal and external audits, and ensuring Good Manufacturing Practices (GMP) are strictly adhered to. You will be responsible for batch record review, deviation investigations, change control management, and CAPA (Corrective and Preventive Actions) implementation. This hybrid role requires your presence in the **Chandigarh, Chandigarh, IN** office for critical quality oversight, batch release, and team leadership, with opportunities for remote work on documentation review and system analysis. The ideal candidate will possess strong leadership skills, a thorough understanding of pharmaceutical manufacturing processes, and excellent analytical and problem-solving abilities.
Responsibilities:
Key responsibilities include developing, implementing, and maintaining quality assurance policies and procedures, managing internal and external audits, and ensuring Good Manufacturing Practices (GMP) are strictly adhered to. You will be responsible for batch record review, deviation investigations, change control management, and CAPA (Corrective and Preventive Actions) implementation. This hybrid role requires your presence in the **Chandigarh, Chandigarh, IN** office for critical quality oversight, batch release, and team leadership, with opportunities for remote work on documentation review and system analysis. The ideal candidate will possess strong leadership skills, a thorough understanding of pharmaceutical manufacturing processes, and excellent analytical and problem-solving abilities.
Responsibilities:
- Develop and implement quality assurance strategies and systems.
- Ensure compliance with cGMP, ICH, and other regulatory guidelines.
- Manage and conduct internal and external audits.
- Review and approve batch records, validation protocols, and reports.
- Lead deviation investigations and implement CAPA plans.
- Manage change control processes for manufacturing and quality systems.
- Oversee the qualification and validation of equipment and processes.
- Train QA/QC personnel and other relevant staff on quality systems.
- Monitor and report on key quality performance indicators (KPIs).
- Stay up-to-date with evolving regulatory requirements.
- Bachelor's or Master's degree in Pharmacy, Chemistry, or a related life science field.
- Minimum 6 years of experience in Quality Assurance within the pharmaceutical industry.
- In-depth knowledge of cGMP and pharmaceutical regulatory requirements.
- Proven experience in audit management, deviation investigation, and CAPA implementation.
- Strong understanding of pharmaceutical manufacturing processes.
- Excellent leadership, communication, and interpersonal skills.
- Proficiency in quality management software and documentation practices.
- Strong analytical and problem-solving skills.
- Ability to work effectively in a fast-paced, regulated environment.
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Pharmaceutical Quality Assurance Specialist
800001 Patna, Bihar
₹60000 Annually
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Our client is seeking a meticulous and experienced Pharmaceutical Quality Assurance Specialist to join their team in Patna, Bihar, IN . This role is vital for ensuring that all pharmaceutical products meet stringent quality standards and regulatory requirements throughout the manufacturing process. You will be responsible for developing, implementing, and maintaining quality management systems, conducting internal audits, reviewing batch records, and investigating deviations and non-conformances. The ideal candidate will have a strong understanding of GMP (Good Manufacturing Practices), regulatory guidelines, and analytical techniques relevant to the pharmaceutical industry.
Key responsibilities include:
Key responsibilities include:
- Developing and implementing Quality Assurance (QA) policies and procedures.
- Ensuring compliance with GMP, ICH guidelines, and other relevant regulations.
- Reviewing and approving batch manufacturing records, validation protocols, and reports.
- Conducting internal audits and supplier audits to assess quality systems.
- Investigating deviations, out-of-specification (OOS) results, and customer complaints.
- Implementing Corrective and Preventive Actions (CAPA) to address quality issues.
- Participating in regulatory inspections and audits by health authorities.
- Managing change control processes and ensuring proper documentation.
- Training personnel on quality systems and GMP requirements.
- Collaborating with R&D, manufacturing, and regulatory affairs departments to ensure product quality.
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Pharmaceutical Quality Assurance Specialist
641002 Coimbatore, Tamil Nadu
₹60000 Annually
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Our client, a prominent pharmaceutical company, is seeking a detail-oriented and experienced Pharmaceutical Quality Assurance Specialist to join their regulatory compliance team. This role is primarily remote, allowing you to contribute to ensuring the highest standards of quality and compliance within our manufacturing and development processes from anywhere. You will be responsible for reviewing and approving manufacturing batch records, ensuring adherence to Good Manufacturing Practices (GMP), and participating in internal and external audits. The ideal candidate will possess a strong understanding of pharmaceutical regulations, quality control systems, and validation principles. Key responsibilities include developing, implementing, and maintaining quality management systems, investigating deviations and out-of-specification (OOS) results, and implementing corrective and preventive actions (CAPA). You will also be involved in the qualification and validation of equipment and processes, as well as ensuring the accuracy and completeness of all quality-related documentation. Collaboration with R&D, production, and regulatory affairs departments is crucial for maintaining compliance and driving continuous improvement. This position requires exceptional analytical skills, meticulous attention to detail, and the ability to work autonomously in a remote setting. Strong written and verbal communication skills are essential for documenting findings, reporting on quality metrics, and collaborating effectively with colleagues across different functions. We are looking for a proactive individual who is passionate about pharmaceutical quality and committed to upholding the integrity of our products. Your expertise will directly contribute to patient safety and product efficacy. Experience with electronic quality management systems (eQMS) and data analysis tools is highly valued. This role offers a significant opportunity to impact quality assurance strategies in a dynamic pharmaceutical environment, ensuring that our operations consistently meet stringent global standards.
Responsibilities:
Responsibilities:
- Review and approve pharmaceutical batch records and related documentation.
- Ensure compliance with Good Manufacturing Practices (GMP) and regulatory requirements.
- Participate in internal and external quality audits and inspections.
- Investigate deviations, out-of-specification (OOS) results, and customer complaints.
- Implement and manage Corrective and Preventive Actions (CAPA).
- Assist in the qualification and validation of equipment, processes, and systems.
- Develop, implement, and maintain quality management system procedures.
- Monitor and report on key quality metrics and performance indicators.
- Collaborate with R&D, manufacturing, and regulatory affairs teams.
- Contribute to the continuous improvement of quality processes.
- 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.
- In-depth knowledge of GMP regulations and pharmaceutical quality systems.
- Experience with batch record review, deviation investigation, and CAPA implementation.
- Familiarity with validation processes (IQ, OQ, PQ).
- Strong analytical, problem-solving, and documentation skills.
- Excellent written and verbal communication abilities.
- Ability to work independently and manage workload effectively in a remote environment.
- Proficiency in Microsoft Office Suite and quality management software.
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2
Pharmaceutical Quality Assurance Specialist
700001 Kolkata, West Bengal
₹70000 Annually
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Our client, a reputable pharmaceutical company, is seeking a detail-oriented and knowledgeable Pharmaceutical Quality Assurance Specialist to join their dynamic team in **Kolkata, West Bengal**. This role is crucial in ensuring that all pharmaceutical products meet stringent quality standards and comply with regulatory requirements. You will be responsible for developing, implementing, and maintaining quality management systems, conducting internal audits, and investigating deviations and non-conformances. Your expertise will be vital in ensuring product safety, efficacy, and quality throughout the manufacturing process. Key responsibilities include reviewing and approving batch records, SOPs, and validation protocols; conducting risk assessments; and participating in regulatory inspections. You will also work closely with manufacturing, R&D, and other departments to resolve quality issues and implement corrective and preventive actions (CAPA). The ideal candidate will possess a bachelor's or master's degree in Pharmacy, Chemistry, Biology, or a related scientific field, along with 3-5 years of experience in pharmaceutical quality assurance or quality control. A strong understanding of GMP (Good Manufacturing Practices), regulatory guidelines (e.g., FDA, EMA), and quality management principles is essential. Excellent analytical skills, meticulous attention to detail, and strong documentation abilities are a must. You should also have good communication and interpersonal skills to effectively collaborate with internal teams and external stakeholders. Experience with pharmaceutical manufacturing processes and quality systems is highly valued. This role offers a great opportunity to contribute to the development of life-saving medicines.
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3
Pharmaceutical Quality Assurance Officer
395004 Surat, Gujarat
₹70000 Annually
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Our client is seeking a meticulous and diligent Pharmaceutical Quality Assurance Officer to join their esteemed team in Surat, Gujarat, IN . This role is vital for ensuring that all pharmaceutical products manufactured by the company meet the highest standards of quality, safety, and efficacy, in compliance with regulatory requirements and Good Manufacturing Practices (GMP). The officer will be responsible for developing, implementing, and maintaining the Quality Management System (QMS) of the organization. Close collaboration with production, R&D, and regulatory affairs departments will be a key aspect of this position.
Key responsibilities include conducting internal audits and quality checks on manufacturing processes, reviewing batch records and quality control data, investigating deviations and out-of-specification (OOS) results, implementing corrective and preventive actions (CAPA), and ensuring that all documentation is accurate and up-to-date. The QA Officer will also participate in external audits and regulatory inspections, and provide training to personnel on quality-related matters. A thorough understanding of pharmaceutical regulations and quality systems is essential. This role will involve hands-on involvement in the quality control processes and continuous improvement initiatives.
Qualifications required for this role include a Bachelor's or Master's degree in Pharmacy, Chemistry, Biotechnology, or a related life science field. A minimum of 3-5 years of experience in Quality Assurance or Quality Control within the pharmaceutical industry is necessary. Strong knowledge of GMP guidelines, regulatory requirements (e.g., FDA, EMA, Indian Pharmacopoeia), and quality management systems is essential. Excellent analytical skills, attention to detail, and proficiency in using laboratory equipment and documentation systems are mandatory. Strong communication and interpersonal skills are required to liaise effectively with different departments and regulatory bodies. This is a significant opportunity to contribute to the quality and compliance of life-saving medicines. You will play a crucial role in upholding the company's commitment to quality and patient safety. The successful candidate will be integral to maintaining our client's reputation for excellence in the pharmaceutical sector.
Key responsibilities include conducting internal audits and quality checks on manufacturing processes, reviewing batch records and quality control data, investigating deviations and out-of-specification (OOS) results, implementing corrective and preventive actions (CAPA), and ensuring that all documentation is accurate and up-to-date. The QA Officer will also participate in external audits and regulatory inspections, and provide training to personnel on quality-related matters. A thorough understanding of pharmaceutical regulations and quality systems is essential. This role will involve hands-on involvement in the quality control processes and continuous improvement initiatives.
Qualifications required for this role include a Bachelor's or Master's degree in Pharmacy, Chemistry, Biotechnology, or a related life science field. A minimum of 3-5 years of experience in Quality Assurance or Quality Control within the pharmaceutical industry is necessary. Strong knowledge of GMP guidelines, regulatory requirements (e.g., FDA, EMA, Indian Pharmacopoeia), and quality management systems is essential. Excellent analytical skills, attention to detail, and proficiency in using laboratory equipment and documentation systems are mandatory. Strong communication and interpersonal skills are required to liaise effectively with different departments and regulatory bodies. This is a significant opportunity to contribute to the quality and compliance of life-saving medicines. You will play a crucial role in upholding the company's commitment to quality and patient safety. The successful candidate will be integral to maintaining our client's reputation for excellence in the pharmaceutical sector.
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4
Pharmaceutical Quality Assurance Manager
751001 Bhubaneswar, Orissa
₹90000 Annually
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Our client is a leading pharmaceutical company seeking an experienced Pharmaceutical Quality Assurance Manager to oversee quality operations at their facility in Bhubaneswar, Odisha, IN . This critical role ensures that all pharmaceutical products meet stringent quality standards and regulatory requirements throughout their lifecycle. The Quality Assurance Manager will be responsible for developing, implementing, and maintaining the Quality Management System (QMS), ensuring compliance with Good Manufacturing Practices (GMP) and other relevant guidelines.
Key responsibilities include leading and managing the QA team, conducting internal audits and inspections, reviewing and approving batch records, validation protocols, and change controls. You will also manage external audits from regulatory agencies and customers, investigate deviations and out-of-specification (OOS) results, and implement corrective and preventive actions (CAPA). The role involves close collaboration with Production, QC, R&D, and Regulatory Affairs departments to ensure seamless integration of quality processes.
The ideal candidate will possess a Bachelor's or Master's degree in Pharmacy, Chemistry, or a related life science discipline. A minimum of 7-10 years of experience in pharmaceutical quality assurance is required, with at least 3 years in a managerial or supervisory capacity. A thorough understanding of GMP, ICH guidelines, and regulatory submission processes is essential. Strong leadership, communication, problem-solving, and decision-making skills are critical for success. Experience with quality risk management and data integrity principles is highly valued. This is a significant opportunity to make a substantial impact on product quality and patient safety within a reputable organization.
Key responsibilities include leading and managing the QA team, conducting internal audits and inspections, reviewing and approving batch records, validation protocols, and change controls. You will also manage external audits from regulatory agencies and customers, investigate deviations and out-of-specification (OOS) results, and implement corrective and preventive actions (CAPA). The role involves close collaboration with Production, QC, R&D, and Regulatory Affairs departments to ensure seamless integration of quality processes.
The ideal candidate will possess a Bachelor's or Master's degree in Pharmacy, Chemistry, or a related life science discipline. A minimum of 7-10 years of experience in pharmaceutical quality assurance is required, with at least 3 years in a managerial or supervisory capacity. A thorough understanding of GMP, ICH guidelines, and regulatory submission processes is essential. Strong leadership, communication, problem-solving, and decision-making skills are critical for success. Experience with quality risk management and data integrity principles is highly valued. This is a significant opportunity to make a substantial impact on product quality and patient safety within a reputable organization.
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5
Pharmaceutical Quality Assurance Manager
400601 Thane, Maharashtra
₹1000000 Annually
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Our client is seeking a highly meticulous and experienced Pharmaceutical Quality Assurance Manager to lead their QA department in Thane . This role is critical for ensuring that all pharmaceutical products meet the highest standards of quality, safety, and efficacy, adhering strictly to regulatory guidelines. You will be responsible for developing, implementing, and maintaining the company's Quality Management System (QMS), overseeing compliance activities, and managing audits. The ideal candidate will possess a deep understanding of Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), and other relevant pharmaceutical quality standards. Exceptional leadership, analytical skills, and a keen eye for detail are essential. You will lead a team of QA professionals, drive continuous improvement initiatives, and ensure robust quality control processes throughout the manufacturing and development lifecycle. This is an outstanding opportunity to make a significant impact on product quality and regulatory compliance within a leading pharmaceutical organization. Key responsibilities include:
- Developing, implementing, and maintaining the company's Quality Management System (QMS).
- Ensuring compliance with all applicable regulatory requirements, including GMP, ICH guidelines, and local regulations.
- Overseeing all quality assurance activities, including batch record review, deviation management, and CAPA implementation.
- Conducting internal audits and facilitating external regulatory audits.
- Managing the validation of equipment, processes, and analytical methods.
- Leading and mentoring the Quality Assurance team.
- Reviewing and approving specifications, test methods, and validation protocols.
- Monitoring and analyzing quality metrics to identify trends and implement corrective actions.
- Collaborating with R&D, manufacturing, and regulatory affairs departments to ensure product quality.
- Managing product release processes.
- Developing and delivering quality training programs for employees.
- Staying current with pharmaceutical industry regulations and best practices.
- Bachelor's or Master's degree in Pharmacy, Chemistry, Biology, or a related scientific field.
- Minimum of 6-8 years of experience in Quality Assurance within the pharmaceutical industry.
- Extensive knowledge of GMP, GLP, and other relevant quality standards.
- Proven experience in managing QA teams and QMS.
- Strong understanding of pharmaceutical manufacturing processes.
- Excellent analytical, problem-solving, and decision-making skills.
- Exceptional attention to detail and commitment to quality.
- Strong communication, leadership, and interpersonal skills.
- Experience with regulatory inspections and submissions.
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Pharmaceutical Quality Assurance Specialist
380001 Ahmedabad, Gujarat
₹750000 Annually
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Our client, a reputable pharmaceutical company, is seeking a diligent and detail-oriented Pharmaceutical Quality Assurance Specialist to join their team in Ahmedabad, Gujarat . This role is vital in ensuring that all products meet stringent quality standards and comply with regulatory requirements. The ideal candidate will have a strong background in pharmaceutical manufacturing, quality control, and regulatory affairs.
Responsibilities:
Qualifications:
Responsibilities:
- Develop, implement, and maintain quality assurance systems and procedures for pharmaceutical products.
- Conduct internal audits and inspections to ensure compliance with GMP (Good Manufacturing Practices) and other regulatory guidelines.
- Review and approve batch manufacturing records, analytical data, and validation reports.
- Investigate deviations, customer complaints, and out-of-specification (OOS) results, implementing corrective and preventive actions (CAPA).
- Participate in regulatory inspections and provide necessary documentation and support.
- Collaborate with production, R&D, and QC departments to resolve quality-related issues.
- Monitor and analyze quality metrics, identifying trends and areas for improvement.
- Ensure all quality-related documentation is accurate, complete, and maintained in accordance with company SOPs and regulatory requirements.
- Stay updated on current pharmaceutical regulations and industry best practices.
- Train personnel on quality assurance procedures and GMP principles.
Qualifications:
- Bachelor's or Master's degree in Pharmacy, Chemistry, Biology, or a related life science field.
- Minimum of 3 years of experience in quality assurance or quality control within the pharmaceutical industry.
- In-depth knowledge of GMP, FDA regulations, and other relevant pharmaceutical quality standards.
- Experience with auditing, documentation review, and deviation management.
- Strong analytical skills and attention to detail.
- Excellent written and verbal communication skills.
- Ability to work independently and as part of a team.
- Proficiency in MS Office and experience with Quality Management Systems (QMS) software.
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