
10,000+ employees
Founded 1980
🏥 Healthcare
🧬 Biotechnology
💊 Pharmaceuticals
💰 $28.5G Post-IPO Debt on 2022-12
Healthcare • Biotechnology • Pharmaceuticals
Amgen is a global leader in biotechnology, focusing on the development and commercialization of innovative medicines made from living cells. The company aims to treat serious illnesses, often targeting diseases with limited therapeutic options. Amgen emphasizes scientific innovation and is committed to ethical research, patient safety, and environmental sustainability. It actively engages in clinical trials and is known for its contributions to the fields of cancer treatment and obesity management among others.
🔥 13 hours ago
🇺🇸 United States – Remote
⏰ Full Time
🟢 Junior
🟡 Mid-level
🚔 Compliance
🚫👨🎓 No degree required
🦅 H1B Visa Sponsor
👻 Ghost score 10%
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10,000+ employees
Founded 1980
🏥 Healthcare
🧬 Biotechnology
💊 Pharmaceuticals
💰 $28.5G Post-IPO Debt on 2022-12
Healthcare • Biotechnology • Pharmaceuticals
Amgen is a global leader in biotechnology, focusing on the development and commercialization of innovative medicines made from living cells. The company aims to treat serious illnesses, often targeting diseases with limited therapeutic options. Amgen emphasizes scientific innovation and is committed to ethical research, patient safety, and environmental sustainability. It actively engages in clinical trials and is known for its contributions to the fields of cancer treatment and obesity management among others.
• 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 • Support Amgen’s R&D Quality Management System through controlled document workflows • Collaborate across functions to facilitate document approval processes and support inspection readiness activities
• High school/GED + 2 years of directly related experience OR Associate’s + 6 months directly related experience OR Bachelor’s • Strong attention to detail with proven ability to perform quality control reviews • Working knowledge of document control tools and best practices • Excellent verbal and written communication skills • Ability to manage document workflows and prioritize tasks • Sponsorship for this role is not guaranteed
• A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions • Group medical, dental and vision coverage • Life and disability insurance • Flexible spending accounts • A discretionary annual bonus program • Stock-based long-term incentives • Award-winning time-off plans • Flexible work models where possible • Career development opportunities • Work/life balance programs • Financial plans with opportunities to save towards retirement or other goals
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