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Quality Control Jobs at Amgen Careers
Amgen, a global biotechnology pioneer, is hiring for the Associate Quality Compliance Role at its R&D Quality Department in Hyderabad, India. This Msc Life Science Job plays a key role in maintaining quality excellence, ensuring compliance with GCP standards, and managing controlled documentation workflows. If you have a strong eye for detail and passion for innovation in the life sciences, Amgen Careers offers a rewarding opporunity by offering the Quality Control Jobs to unleash your R&D Career.
Job Details:
- Position: Associate Quality Compliance
- Department: R&D Quality
- Category: Quality
- Job ID: R-224288
- Location: Hyderabad, India
- Work Type: On-site
- Date Posted: October 28, 2025
- Global Career Framework (GCF): 3
Associate Quality Compliance Role Description:
The Controlled Documentation Associate plays a critical role in supporting Amgen’s R&D Quality Management System through the execution and maintenance of controlled document workflows. This MSc Life Science Job ensures that R&D controlled documents, such as SOPs and work instructions, are developed, maintained, and retired in compliance with global standards and GCP regulations. The candidate getting hired for the Associate Quality Compliance Role will collaborate across functions to facilitate document approval processes, conduct quality checks, and support inspection readiness activities.
About the Company:
Amgen is one of the world’s largest independent biotechnology companies, harnessing biology and technology to fight the toughest diseases. Founded over 40 years ago, Amgen has been a key force in advancing biotechnology, discovering, developing, and delivering innovative medicines that improve millions of lives. The company’s mission is to unlock the potential of biology for patients suffering from serious illnesses and to transform the promise of science into therapeutic breakthroughs.
Responsibilities of the Associate Quality Compliance Role:
- Execute and track workflows for creation, revision, and obsoletion of documents with the controlled document management system (CDOCS).
- Perform controlled document impact analysis in support of business requests and initiatives.
- Maintain document metadata in CDOCS.
- Conduct quality checks, editing, and proofreading of documents for consistency and compliance.
- Monitor document workflows, notify stakeholders of pending tasks, and follow up to ensure timely completion.
- Support inspections and audits by retrieving and compiling requested documents.
Basic Qualifications and Experience for the Associate Quality Compliance Role:
- Masters Degree in Sciences or related field with 2-6 years exp in Pharmaceutical/Biotechnology/Clinical research
Functional Skills Required for Associate Quality Compliance Role:
Must-Have Skills for the Quality Control Jobs:
- Strong attention to detail with proven ability to perform quality reviews.
- Working knowledge of document control tools and best practices.
- Excellent verbal and written communication skills.
- Ability to manage document workflows and prioritize tasks.
Good-to-Have Skills for the Quality Control Jobs:
- Experience working in a multinational environment with global teams.
- Experience using CDOCS or equivalent electronic document management system.
Soft Skills:
- Strong problem-solving abilities and adaptability to changing priorities.
- Strong attention to detail and accuracy.
- Excellent organization and coordination skills.
- Clear and concise communication abilities.
- Team-oriented and proactive approach.
How to Apply for Quality Control Jobs?
Interested candidates can apply through the official Amgen Careers Portal. Stay updated with the latest biotechnology job openings and career alerts by visiting the official website regularly.
