Full-Time

Business Performance Manager

Multiple Teams

Posted on 7/4/2026

Amgen

Amgen

10,001+ employees

Biotech company creating biologic medicines

No salary listed

Hyderabad, Telangana, India

In Person

Bachelor's, Master's, PhD, Associate's

Category
Business & Strategy (1)
Required Skills
Data Governance

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Requirements
  • Demonstrated experience as a Planisware business owner, including responsibility for requirements definition, system enhancements, testing, and stakeholder engagement.
  • Strong understanding of enterprise systems governance, configuration management, and lifecycle management processes.
  • Proven ability to translate business needs into scalable technical solutions and drive system-enabled process improvements.
  • Ability to influence stakeholders at multiple levels of the organization.
  • Strong critical thinking and creative problem-solving skills, with a track record of leveraging technology to improve efficiency and effectiveness.
  • Experience leading cross-functional initiatives and managing competing priorities in a complex, matrixed environment.
  • Solid analytical skills, including experience with data quality oversight, reporting, and performance monitoring.
  • Strong understanding of the drug development process and key milestones.
  • Ability to build and maintain strong relationships within the organization to understand business objectives and priorities.
  • Doctorate degree and 2 years of relevant experience, or master's degree and 4 years of relevant experience, or bachelor's degree and 6 years of relevant experience, or associate's degree and 10 years of relevant experience, or high school diploma/GED and 12 years of relevant experience.
Responsibilities
  • Serve as the business owner for the Planisware platform and act as the primary liaison between the business and the platform or information technology team.
  • Define and document business requirements for system enhancements, new rules, and logic changes; support user acceptance testing and ensure successful implementation of new functionality.
  • Provide user support, guidance, and training to stakeholders on system capabilities and best practices.
  • Drive data governance and data quality monitoring, including reporting, issue resolution, and stakeholder communication.
  • Lead the governance forum for Commercialization technology assets.
  • Lead development and drive continuous improvement of commercialization-related business processes to streamline workflows and improve cross-functional planning.
  • Partner with stakeholders to design and implement scalable process solutions that leverage technology, automation, and best practices to improve transparency, efficiency, and execution.
  • Develop a deep understanding of Commercialization processes and the voice of the customer to inform process improvement strategies.
Desired Qualifications
  • Industry experience in biotechnology, pharmaceutical, or another healthcare-related field.
  • Drug development knowledge, including understanding of Research, Preclinical, Clinical, Manufacturing, Commercial, and Regulatory functions.
  • A consistent track record of implementing project portfolio management tools, methodologies, practices, and infrastructure in the biopharmaceutical industry.
  • Project management experience operationalizing central initiatives, including cross-functional strategic planning, development of integrated plans, and monitoring and driving execution to plan.
  • Emotional intelligence skills, including influencing without authority.

Amgen develops medicines that treat serious illnesses by using biologic therapies made from living cells. These therapies are designed to target specific disease processes, such as cancer, cardiovascular disease, and autoimmune conditions, and are produced through biotechnology methods that create proteins or antibodies. Amgen’s products are sold to patients and healthcare providers worldwide, with revenue funding ongoing research and development to discover new treatments. The company stands out by focusing on biologic medicines at a large scale and maintaining a steady pipeline of potential therapies across multiple disease areas, supported by global manufacturing and a commitment to bringing therapies to patients. Its goal is to improve patient outcomes by discovering and delivering new, effective treatments while reinvesting a significant portion of earnings into research and development.

Company Size

10,001+

Company Stage

IPO

Headquarters

Thousand Oaks, California

Founded

1980

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Simplify Jobs

Simplify's Take

What believers are saying

  • Q2 2026 revenue hit $10.05 billion, and guidance rose to $38.2-$39.4 billion.
  • Repatha sales jumped 37% in Q2 2026; Uplizna climbed 90%.
  • MariTide Phase 3 programs are enrolling now, with obesity readouts expected in 2027.

What critics are saying

  • FDA proposed Tavneos withdrawal on April 27, 2026 after data-integrity findings.
  • July 2026 Amgen settled a $74 million IRS-disclosure suit; tax litigation continues.
  • July 2026 layoffs hit Amgen again, signaling operating strain and portfolio pruning.

What makes Amgen unique

  • Repatha, Uplizna, and Imdelltra diversified Amgen beyond Enbrel and Prolia.
  • MariTide’s quarterly-or-sparser dosing targets obesity with lower treatment burden than weekly injectables.
  • Amgen’s 2025-2026 launches span cardiology, oncology, and rare disease globally.

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Benefits

Professional Development Budget

Conference Attendance Budget

Company News

Yahoo Finance
Aug 9th, 2026
Amgen fair value rises to $372 after Q2 beat sparks analyst target hikes to $450

Amgen's modeled fair value has risen from $352.23 to $371.93 per share following strong Q2 results and updated analyst targets. Several firms, including Scotiabank, TD Cowen, BMO Capital, and Oppenheimer, lifted price targets to around $450, citing earnings revisions and a diversified product portfolio. Bernstein noted a 6.8% revenue beat and 12.5% non-GAAP EPS beat in Q2, with raised full-year guidance driven by portfolio-wide execution. Strength came from products including Repatha, Tezspire, Uplizna, Evenity, and Imdelltra. However, Wells Fargo and Citi maintain cautious stances with Equal Weight and Neutral ratings, suggesting current performance may already be priced in. BofA kept its Underperform rating, describing 2026 as focused on execution ahead of key 2027 readouts.

Yahoo Finance
Aug 5th, 2026
Amgen beats Q2 forecast with $10.05B revenue, raises 2026 outlook despite obesity drug setback

Amgen reported second-quarter revenue of $10.05 billion, up 9% year on year, beating Wall Street expectations. Adjusted earnings reached $6.29 per share, surpassing the $5.62 consensus estimate. The biotech firm raised its full-year 2026 outlook, increasing expected revenue to $38.2 billion-$39.4 billion from $37.0 billion-$38.4 billion. Adjusted earnings guidance rose to $22.30-$23.50 per share. Repatha sales surged 37% to $953 million, whilst Evenity jumped 38% to $714 million. Rare-disease therapy Uplizna saw roughly 90% growth. These gains offset a 32% decline in Prolia sales due to biosimilar competition. Amgen discontinued obesity candidate AMG 513 but continues developing MariTide, with Phase 3 data expected in 2027. The stock trades at $406.17, approximately 14.75% above its estimated fair value.

PR Newswire
Aug 4th, 2026
Amgen reports 10% revenue growth to $10.1B in Q2 2026, driven by 26% surge in six key growth products

Amgen reported second quarter 2026 revenues of $10.1 billion, a 10% increase year-over-year. Product sales grew 9%, driven by volume growth across 22 products that achieved double-digit sales growth. The company's six key growth drivers grew 26% year-over-year, generating nearly 70% of second quarter product sales. GAAP earnings per share increased 65% to $4.37, whilst non-GAAP EPS rose 4% to $6.29. Notable product performance included Repatha sales increasing 37% to $953 million and EVENITY growing 38% to $714 million. The company generated $3.5 billion in free cash flow, compared to $1.9 billion in the prior year period. For full year 2026, Amgen expects total revenues between $38.2 billion and $39.4 billion, with non-GAAP EPS guidance of $22.30 to $23.50.

Yahoo Finance
Jul 7th, 2026
Amgen wins Enbrel price cap reprieve as Class II recalls raise quality concerns

Amgen secured a preliminary injunction in early June 2026 blocking Colorado's proposed 70% price cap on Enbrel, its rheumatoid arthritis drug. The federal judge's decision preserves pricing flexibility for the legacy asset. However, the company initiated several voluntary Class II recalls of Corlanor and Sensipar batches in the US due to foreign substances and manufacturing deviations. While not yet financially material, the recalls highlight ongoing operational risks. Amgen's investment case depends on its diversified portfolio offsetting pricing pressure and biosimilar competition. The company projects revenue of $40.1 billion and earnings of $9.9 billion by 2029, requiring 2.5% annual revenue growth. Current 2026 guidance stands at $37.1–$38.5 billion in revenue. The combination of pricing relief and quality concerns presents investors with a rebalanced risk-reward profile for the biotech company.

Yahoo Finance
Jun 30th, 2026
NEJM retracts trial behind Amgen's $459M Tavneos as FDA probes data changes

The New England Journal of Medicine has retracted the 2021 clinical trial that supported approval of Amgen's Tavneos, a treatment for ANCA-associated vasculitis that generated $459 million in sales last year. The retraction followed an FDA investigation revealing that results from nine patients were altered after the study database was finalised, whilst some researchers had been unblinded. The FDA alleges the original data showed no statistically significant difference between Tavneos and existing treatments, but subsequent changes made the drug appear more effective. The agency proposed withdrawing Tavneos from the US market in April, whilst European regulators have also recommended removal. Amgen, which acquired ChemoCentryx for $3.7 billion in 2022, continues selling Tavneos and has requested an FDA hearing. The company says it is engaging independent researchers to reanalyse the data.

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