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.

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:

• 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

Application Link