Biotech Pharmacovigilance Job Grifols – Apply Now!
Would you like to join an international team working to improve the future of healthcare? Do you want to enhance the lives of millions of people? Grifols is a global healthcare company that, since 1909, has been working to improve the health and well-being of people around the world. We are leaders in plasma-derived medicines and transfusion medicine and develop, produce, and market innovative medicines, solutions, and services in more than 110 countries and regions. We believe that diversity adds value to our business, our teams and our culture. We are committed to equal employment opportunities that foster an inclusive environment.
About Grifols:
Grifols is a global healthcare company founded in 1909 with a mission to enhance health and well-being worldwide. As a pioneer in plasma-derived medicines and transfusion solutions, Grifols operates in over 110 countries. The company is committed to ethical innovation, equal opportunity employment, and continuous improvement of global healthcare systems through science and compassion.
Quality & Pharmacovigilance Specialist Job Details:
Job Title: Quality Specialist
Location: Gurgaon, IN
Contract Type: Regular Full-Time
Area: Quality
Req Id: 524202
Main Responsibilities
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Maintain and implement Quality Systems in compliance with ISO 9001 and local regulations
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Lead QA operations, SOP preparation, audits, risk assessments, and BCP planning
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Coordinate with Regulatory Affairs, SCM, Medical Affairs, and external agencies
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Ensure compliance with Good Distribution Practices and pharmacovigilance SOPs
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Manage 3PL quality activities, monthly audits, and partner engagements
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Submit safety reports (CIOMS), track regulatory updates, and support tender submissions
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Utilize QMS tools: SAP, Documentum, COSMOS, LSQM
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Act as local quality and PV contact for internal and external stakeholders
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Requirements for Quality & Pharmacovigilance Specialist Role
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Graduate in Biotechnology, Biology, or a related discipline
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Minimum 3 years of experience in quality and regulatory affairs
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Experience in ISO 9001 QMS implementation preferred
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Strong interpersonal, communication, and multitasking skills
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Comfortable working in cross-functional, multinational environments
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Willingness to travel occasionally within the region
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