About This Opportunity
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Full source description
- Looking for QA jobs and pharma jobs in quality systems? Join Pfizer in Vizag as an Associate – Quality Systems and grow your pharmaceutical careers in India
- About the Company Pfizer is a global biopharmaceutical leader committed to improving patient outcomes through innovative medicines and vaccines
- The company maintains a strong focus on scientific excellence, risk-based compliance, and quality culture across its operations worldwide
- With a flexible, innovative, and customer-oriented approach rooted in science, Pfizer ensures the delivery of safe and effective products
- Employees contribute directly to patient care while working in an environment that values continuous improvement, regulatory compliance, and meaningful impact on global health
- Job Details Company Name: Pfizer Experience: 1 to 4 years of relevant experience in the pharmaceutical industry Qualification: B.Pharma, M.Pharma or MSc Location: Vizag (Visakhapatnam), India Work Type: Full time (shift-based operations as required) Job Description Pfizer is hiring an Associate – Quality Systems for its operations in Vizag
- This full-time role supports GMP document and record management within the Quality Systems function
- It is ideal for professionals with pharmaceutical experience who want to contribute to document lifecycle processes, compliance, and operational efficiency in a regulated environment
- Associate – Quality Systems Department: Quality Assurance and Control / Quality Systems Market: India (Vizag) Role: Associate – Quality Systems Experience: 1 to 4 years in the pharmaceutical industry Education/Qualification: B.Pharma, M.Pharma or MSc Skills/Qualifications B.Pharma, M.Pharma or MSc degree 1 to 4 years of relevant pharmaceutical industry experience Knowledge of GMP Document and Record Management Familiarity with electronic document management systems (PDOCs, SDS, p-Log, Therefore, CICR) Understanding of Document Lifecycle Management processes Knowledge of Enterprise Records Retention Schedule (ERRS) requirements Experience with logbook management and secure document storage Understanding of change control and Quality Systems processes Strong written and verbal communication skills Willingness to work in shift-based operations Preferred: Experience using AI tools such as Microsoft Copilot or ChatGPT Key Responsibilities Manage GMP document issuance, retrieval, archival, and disposition Handle official print management and audit trail reviews Perform metadata verification, document scanning, and record tracking Support document creation, review, approval, and obsolescence processes Ensure compliance with records retention and storage requirements Administer logbook and secure bin management activities Support change control and impact assessment processes Maintain accurate documentation and quality system records Use digital applications and AI tools to enhance productivity Collaborate effectively across functions to meet quality standards Benefits/Perks Career growth within a leading global biopharmaceutical company Learning opportunities in quality systems and GMP compliance Competitive salary aligned with experience Collaborative and science-based work culture Exposure to advanced document management systems Opportunity to impact patient safety through quality processes Professional development in a regulated pharmaceutical environment Support for continuous improvement and operational excellence How to Apply Verified Post Verification: To confirm the legitimacy of this posting, you can view the original announcement on the Pfizer career page
- Click below to apply directly for this job APPLY FOR THIS JOB Apply directly through the official Pfizer careers portal
- You can also explore this and similar openings on trusted platforms such as Pharma Recruiter
- Highlight your pharmaceutical experience, document management knowledge, and relevant qualifications in your application
- Submit your resume today to join a team committed to delivering safe and effective products that improve patient outcomes
- Why You Should Join Pfizer offers a purpose-driven culture focused on quality, science, and patient care
- Employees work in an environment that values individual ownership, continuous learning, and risk-based compliance
- The role provides long-term career stability, exposure to modern quality systems, and the chance to contribute directly to high standards of product quality
- With a collaborative culture and opportunities to leverage digital tools, this Associate position is an excellent platform for professionals seeking growth in pharmaceutical quality systems
- FAQs Who is eligible for the Associate – Quality Systems role? Candidates with a B.Pharma, M.Pharma or MSc degree and 1 to 4 years of relevant pharmaceutical industry experience are eligible
- Knowledge of GMP document management is preferred
- How can I apply for this Pfizer position in Vizag? Submit your application via the official Pfizer careers website or check Pharma Recruiter for related opportunities
- Clearly showcase your quality systems experience
- Is a walk-in interview available? No walk-in interview details are provided
- Applications follow the standard online process
- Selected candidates will be contacted for further steps
- What growth opportunities does this role offer? Pfizer supports continuous learning, cross-functional collaboration, and career progression within Quality Assurance and Control
- High performers can advance while contributing to robust quality systems that support patient safety.
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