Bayer
In the ever-evolving world of pharmaceuticals and crop science, quality assurance is the invisible thread that weaves safety, efficacy, and trust into every product. At the heart of this process is a dedicated team of professionals who ensure that documentation, production, and compliance meet the highest standards. Bayer, a global leader in life sciences, is inviting aspiring QA professionals to join their team in Vapi, Gujarat for the role of GMP – QA Documentation.
Purpose that Matters
The role is designed to support end-to-end quality processes—from production verification to regulatory compliance—ensuring that every batch of product is reliable and safe. It’s a critical position that bridges technical documentation, real-time production oversight, and regulatory readiness.
Key Responsibilities That Define the Role
As a QA Documentation Associate, you’ll be part of the team that upholds Bayer’s legacy of quality and innovation. Your day-to-day responsibilities will include:
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Preparing and reviewing essential documentation such as SOPs, Specifications, Batch Manufacturing Records (BMRs), Batch Packaging Records (BPRs), and Master Formulas.
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Overseeing in-process quality checks and critical production operations.
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Maintaining audit readiness and supporting internal/external inspections.
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Managing Quality Management System (QMS) elements like Change Controls, Deviations, and CAPAs.
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Reviewing batch documentation for API release.
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Handling customer complaints, product recalls, and managing returned goods.
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Coordinating document lifecycle: issuance, archiving, and retrieval.
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Participating in qualification and validation review processes.
Collaborative Work Environment
The role interacts with various internal teams like Engineering, QC, HR, IT, Production, and Safety, as well as external stakeholders including vendors, housekeeping and pest control services, and validation/lab testing service providers.
This multi-departmental collaboration enriches your experience and provides a broader perspective on operational excellence in a regulated environment.
What Makes You a Good Fit?
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Education: B. Pharm, M. Pharm, or M.Sc.
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Experience: Freshers or professionals with up to 1 year of QA experience in the pharmaceutical industry.
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Background: A strong interest in pharmaceutical quality assurance, documentation, and regulatory standards.
Kickstart Your QA Career with Bayer
If you’re passionate about quality, eager to learn, and ready to contribute to a meaningful mission—this is your opportunity. Join Bayer’s Vapi team and begin a fulfilling career in GMP and QA documentation.
📍 Location: Vapi, Gujarat, India
🔎 Reference Code: 838661
📅 Division: Crop Science
To apply for this job please visit jobs.bayer.com.
