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Amgen, a global leader in biotechnology, is hiring for the role of Associate QC – QC Systems Templating in Hyderabad, India. This is a full-time, on-site position where you will support Electronic Lab Notebook (ELN) infrastructure, consumable inventory systems, and Quality Control (QC) standardization across Amgen’s global network.
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If you’re passionate about quality control careers in pharma, this opportunity offers an excellent chance to build your expertise in a world-class biotech environment.
Key Responsibilities
As an Associate QC, you will:
- Create, revise, and qualify templates for analytical method executions in ELN.
- Develop and update consumable templates.
- Ensure deliverables meet established timelines, procedures, and service-level agreements.
- Collaborate with local and global QC teams across shifts and time zones.
- Maintain up-to-date training and compliance with GMP and GDP.
- Provide performance metrics and assist in QC process standardization.
Qualifications & Experience
- Master’s degree in Pharma, Biotech, or related sciences.
- 1–3 years of quality control experience in pharma or biotech (commercial or clinical manufacturing).
- Hands-on QC lab testing experience.
- Exposure to ELN (Electronic Lab Notebook) applications.
- Proficiency in Microsoft Office.
- Knowledge of Good Manufacturing Practices (GMP) and Good Documentation Practices (GDP).
Soft Skills
- Strong English verbal and written communication.
- Detail-oriented with quick learning ability.
- Team player with a “right first time” approach.
Why Join Amgen?
Working at Amgen means being part of an organization that:
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- Leads global biotech innovation.
- Provides opportunities to collaborate across diverse international teams.
- Values employee growth, inclusivity, and work-life balance.
- Offers competitive compensation packages.
How to Apply
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