Live opening · Posted 1 day ago

Quality Specialist (QMS, Documentation)

Merck Limited
Successfactors
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At a glance

The key details from the original listing.

Posted 1 day ago
CompanyMerck Limited
SourceSuccessfactors
Listed1 day ago

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About the role

Description supplied by the original job listing.

Work Your Magic with us!
Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us.
Job Title: Quality Assurance – Specialist
Your Role:
The Quality Assurance (QA) – Specialist will oversee the quality assurance processes within the Life Science division in India. This role is critical in ensuring that all products and processes meet the required quality standards and comply with regulatory requirements.
Develop, implement, and maintain the quality management system (QMS) in accordance with regulatory requirements and industry standards.
Lead and manage quality assurance activities, including audits and investigations.
Collaborate with cross-functional teams to ensure product quality throughout the product lifecycle.
Monitor and analyze quality metrics to identify trends and areas for improvement.
Prepare and review quality documentation, including standard operating procedures (SOPs), validation protocols, and reports.
Provide training and guidance to staff on quality assurance practices and regulatory compliance.
Drive continuous improvement initiatives to enhance product quality and operational efficiency.
Who you are:
Exp: 7 Years to 9 Years
Location is in Jigani, Bangalore
Education: Master degree in Life Sciences, Chemistry, Engineering, or a related field.
Minimum of 7 years of experience in quality assurance within the pharmaceutical/ Chemical/life sciences or biotechnology industry.
Strong understanding of regulatory requirements (e.g., FDA, EMA, NABL, ANAB) and quality standards (e.g., ISO, GMP).
Excellent analytical, problem-solving, and communication skills.
Ability to work collaboratively in a fast-paced, team-oriented environment.
What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We believe that this variety drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress!
Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity

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