Nataraj Gj Email & Phone Number | Self-directed and driven Quality Assurance professional with comprehensive background of 12 years’ experience in pharmaceutical quality assurance and compliance department. Quality Management Professional GMP Investigations Change Control CAPA Risk Assessment Customer Complaints Vendor Management Regulatory Compliance Highly skilled Quality Management Professional with a track record of effectively leading critical elements of the Quality Management System, including GMP investigations, Change Control, CAPA, and Risk Assessment. Proficient in managing Customer Quality Complaints and Medical Device Vigilance systems, ensuring timely resolution and continuous improvement. In my role, I provide valuable support to Qualified Person(s) by facilitating and performing meticulous data review audits, encompassing Batch Production Records, Validation Documents, Development Documentation, and Quality Control Data. With a keen eye for detail and in-depth regulatory knowledge, I contribute to maintaining compliance and upholding product integrity. Collaborating closely with the Quality Manager, I assist in defining and maintaining the annual internal and external audit programs, Annual Product Reviews, and Quality Management Reviews. Through comprehensive planning and systematic execution. As a dedicated professional, I take charge of managing and maintaining the site Vendor Management System. By implementing robust procedures, I establish strong relationships with suppliers and service providers. Additionally, I review and approve their qualifications, including conducting audits of critical suppliers, to guarantee adherence to stringent quality standards. Driven by a commitment to meet the growing business needs, I leverage my technical expertise, skills, knowledge, and experience to proactively resolve challenges and share insights within the quality organization. My collaborative approach fosters a culture of continuous improvement, enabling the team to address problems efficiently and enhance overall performance. Furthermore, I actively support the Quality Manager in hosting external audits and regulatory inspections. By meticulously preparing for these assessments and ensuring compliance across all processes, I contribute to successful outcomes and maintain the company's positive standing. In my role, I maintain a focus on overall compliance with Market complaints and lead investigations into customer concerns. It’s been a great professional journey so far and eagerly looks forward for new experiences & challenges to exercise my expertise.

Nataraj Gj

Self-directed and driven Quality Assurance professional with comprehensive background of 12 years’ e...
Hyderabad, Telangana, India

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Nataraj Gj’s Email nataraj.gj@orbicular.co.in

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Nataraj Gj’s Location Hyderabad, Telangana, India

Nataraj Gj’s Current Industry Viatris

Nataraj Gj’s Prior Industry Orbicular Pharmaceutical Technologies | Alembic Pharmaceuticals | Micro Labs

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Work Experience

Viatris

Sr. Team Leader

2024-01-01 00:00:00 - Present

Orbicular Pharmaceutical Technologies

Quality Operations (Sr. Team Lead)

2021-11-01 00:00:00 - 2024-02-01 00:00:00

Alembic Pharmaceuticals

Quality Assurance Operations

2016-07-01 00:00:00 - 2021-10-01 00:00:00

Micro Labs

Executive In D-Qa

2011-05-01 00:00:00 - 2013-04-01 00:00:00

Skills

No Skills Available

Languages

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FAQ About Nataraj Gj

Nataraj Gj is located at
Hyderabad, Telangana, India

Nataraj Gj is a Self-directed and driven Quality Assurance professional with comprehensive background of 12 years’ experience in pharmaceutical quality assurance and compliance department. Quality Management Professional GMP Investigations Change Control CAPA Risk Assessment Customer Complaints Vendor Management Regulatory Compliance Highly skilled Quality Management Professional with a track record of effectively leading critical elements of the Quality Management System, including GMP investigations, Change Control, CAPA, and Risk Assessment. Proficient in managing Customer Quality Complaints and Medical Device Vigilance systems, ensuring timely resolution and continuous improvement. In my role, I provide valuable support to Qualified Person(s) by facilitating and performing meticulous data review audits, encompassing Batch Production Records, Validation Documents, Development Documentation, and Quality Control Data. With a keen eye for detail and in-depth regulatory knowledge, I contribute to maintaining compliance and upholding product integrity. Collaborating closely with the Quality Manager, I assist in defining and maintaining the annual internal and external audit programs, Annual Product Reviews, and Quality Management Reviews. Through comprehensive planning and systematic execution. As a dedicated professional, I take charge of managing and maintaining the site Vendor Management System. By implementing robust procedures, I establish strong relationships with suppliers and service providers. Additionally, I review and approve their qualifications, including conducting audits of critical suppliers, to guarantee adherence to stringent quality standards. Driven by a commitment to meet the growing business needs, I leverage my technical expertise, skills, knowledge, and experience to proactively resolve challenges and share insights within the quality organization. My collaborative approach fosters a culture of continuous improvement, enabling the team to address problems efficiently and enhance overall performance. Furthermore, I actively support the Quality Manager in hosting external audits and regulatory inspections. By meticulously preparing for these assessments and ensuring compliance across all processes, I contribute to successful outcomes and maintain the company's positive standing. In my role, I maintain a focus on overall compliance with Market complaints and lead investigations into customer concerns. It’s been a great professional journey so far and eagerly looks forward for new experiences & challenges to exercise my expertise.