Urwah Admin

Amgen

<div>
 
 HOW MIGHT YOU DEFY IMAGINATION?
 
 
 
 If you feel like you&rsquo;re part of something bigger, it&rsquo;s because you are. At Amgen our shared mission&mdash;to serve patients&mdash;drives all that we do. It is key to our becoming one of the world&rsquo;s leading biotechnology companies. We are global collaborators who achieve together&mdash;researching, manufacturing and delivering ever-better products that reach over 10 million patients worldwide. It&rsquo;s time for a career you can be proud of. Join us.
 
 
 
 SENIOR ASSOCIATE REGULATORY AFFAIRS
 
 
 
 
 What You Will Do
 
 
 
 In this vital role you will assist in the local coordination and execution of regulatory submissions in compliance with Amgen corporate standards and national regulatory requirements, and Regulatory Affairs processes and deliverables for the ELI markets Egypt, Jordan, Iraq and Lebanon.
 
 
 <ul>
 <li>
 Ensure regulatory submissions are made on time and meet Amgen&rsquo;s corporate and local regulatory requirements
 </li>
 <li>
 Responsible for completion of regulatory files for submission. (Prepare/Receive files and submit them to regulatory authorities within the defined and agreed submission/approval dates) and according to guidelines and requirements
 </li>
 <li>
 Manufacturing site registration and license maintenance
 </li>
 <li>
 Responsible for coordinating with the International regulatory team to ensure right first-time dossiers are provided
 </li>
 <li>
 Coordinate and respond to the requests by authorities during the evaluation process and check the correct handling of deficiency letter within a specific timeframe in order not to delay MOH approvals
 </li>
 <li>
 Establish effective communication and continuous follow-up with the external agencies &amp; distributors to ensure timely submissions and approvals of all company&rsquo;s applications
 </li>
 <li>
 Monitoring of emerging guidelines and changes affecting business and communication to relevant internal customers
 </li>
 <li>
 Providing guidance on the approval processes to internal stakeholders within the region and providing regulatory input for launch planning
 </li>
 <li>
 Maintenance of all lifecycle activities/ Product renewal license details by accurately preparing filling submissions and approval within the preset global timelines -accountable for overall accuracy and compliance
 </li>
 <li>
 Ensure alignment of regulatory objectives with regional / global regulatory objectives and commercial plans
 </li>
 <li>
 Accountable for solving all supply issues related to regulatory activities.
 </li>
 <li>
 To provide regulatory intelligence
 </li>
 <li>
 Ensure compliance with company's SOPs and working practices for Good Regulatory Practice
 </li>
 <li>
 Management of documentation archiving and record keeping according to SOP and local legislation
 </li>
 <li>
 Contact for agency interactions for portfolio of products and coordinating and reviewing briefing documents and/or other submissions for meetings with Regulatory agencies
 </li>
 <li>
 Collate, distribute, exchange and archive regulatory information with colleagues across the business
 </li>
 <li>
 Participate in regulatory and affiliate process improvements initiatives
 </li>
 <li>
 Review promotion and non-promotion materials to ensure compliance with local license, company procedures and Code of Practice
 
 
 </li>
 </ul>
 
 BE PART OF OUR TEAM
 
 
 
 Reporting to the Regulatory Affairs Manager for ELI, you would be joining a team of regulatory professionals passionate about delivering the best outcomes for our medicines to patients.
 
 
 
 What We Expect Of You
 
 
 
 We are all different, yet we all use our unique contributions to serve patients. What we seek in you as an experienced professional, are these qualifications and skills:
 
 
 <ul>
 <li>
 Pharmacy Bachelor&rsquo;s degree
 </li>
 <li>
 2-3 years of directly related experience in regulatory affairs (ELI markets)
 </li>
 <li>
 Knowledge and awareness of the relevant regulatory guidelines and legislation for ELI markets
 </li>
 <li>
 Strong communication skills both verbal and written
 </li>
 <li>
 Organizational skills &amp; developing regulatory project management skills
 
 
 </li>
 </ul>
 
 Thrive
 
 
 
 
 What You Can Expect Of Us
 
 
 
 As we work to develop treatments that take care of others, so we work to care for our teammates&rsquo; professional and personal growth and well-being.
 
 
 <ul>
 <li>
 Vast opportunities to learn and move up and across our global organization
 </li>
 <li>
 Diverse and inclusive community of belonging, where teammates are empowered to bring ideas to the table and act
 </li>
 <li>
 Generous Total Rewards Plan comprising health, finance and wealth, work/life balance, and career benefits
 
 
 </li>
 </ul>
 
 Apply now for a career that defies imagination
 
 
 
 In our quest to serve patients above all else, Amgen is the first to imagine, and the last to doubt. Join us.
 
 
 
 careers.amgen.com
 
 
 
 Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, gender, sexual orientation, gender identity, national origin, protected veteran status, or disability status.
</div>

Senior Associate Regulatory Affairs

<div><div>United States - Remote
<div>JOB ID: R-251561 LOCATION: United States - Remote WORK LOCATION TYPE: Remote DATE POSTED: Jul. 30, 2026 CATEGORY: Strategy and Innovation SALARY RANGE: 190,140.75USD -257,249.25 USD
</div></div><div><div><h2 class="jobSectionHeader">Join Amgen&rsquo;s Mission of Serving Patients</h2>
At Amgen, if you feel like you&rsquo;re part of something bigger, it&rsquo;s because you are. Our shared mission&mdash;to serve patients living with serious illnesses&mdash;drives all that we do.
Since 1980, we&rsquo;ve helped pioneer the world of biotech in our fight against the world&rsquo;s toughest diseases. With our focus on four therapeutic areas &ndash;Oncology, Inflammation, General Medicine, and Rare Disease&ndash; we reach millions of patients each year. Amgen is advancing a broad and deep pipeline of medicines to treat cancer, heart disease, inflammatory conditions, rare diseases, and obesity and obesity-related conditions. As a member of the Amgen team, you&rsquo;ll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives.
Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you&rsquo;ll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.
ONCOLOGY STRATEGY DIRECTOR<h2 class="jobSectionHeader">
What you will do</h2>
Let&rsquo;s do this. Let&rsquo;s change the world. In this vital role, you will lead strategic initiatives that shape Amgen&rsquo;s Oncology Therapeutic Area future, with a focus on topics in the R&amp;D space. While the role can be located remotely there is an expectation that availability at times of high activity may need to accommodate some Pacific Time Zone working hours.<ul><li>
Lead and manage strategic, cross-functional projects commissioned by Development leadership.</li><li>
Independently drive project execution and influence stakeholders across multiple functions and levels.</li><li>
Develop and support annual therapeutic area strategies, including oncology portfolio planning.</li><li>
Conduct technology assessments, deep-dive analyses, and landscape evaluations.</li><li>
Perform cross-portfolio analytics, risk assessments, and strategic decision-support activities.</li><li>
Support scientific collaborations with external academic partners through the Amgen Partners of Choice program.</li><li>
Facilitate scientific exchange and coordinate partnership-related projects.</li><li>
Manage global external communications and represent the organization with key external stakeholders.</li><li>
Serve as a trusted advisor and representative for Development leadership.</li><li>
Navigate ambiguity and lead ad hoc strategic initiatives and special projects as business needs arise.</li></ul><h2 class="jobSectionHeader">
What we expect of you</h2>
We are all different, yet we all use our unique contributions to serve patients. The dynamic professional we seek is a leader with these qualifications.
Basic Qualifications:
Doctorate degree and 4 years of healthcare business experience
Or
Master&rsquo;s degree and 7 years of healthcare business experience
Or
Bachelor&rsquo;s degree and 9 years of healthcare business experience
Preferred Qualifications:<ul><li>
MD, MBA, MS, Ph.D. or equivalent</li><li>
Eight (8) or more years of strategy experience within management consulting, finance, or corporate strategy functions</li><li>
Robust knowledge of biopharma industry (i.e., pharma development, translational sciences, R&amp;D processes)</li><li>
Understanding of interplay among various stakeholders in the industry, awareness of trends and recent developments, and ability to research / learn/ synthesize findings on new topics</li><li>
Oncology R&amp;D experience in the biopharmaceutical industry (biotech, pharmaceutical company)</li><li>
Excellent cross-functional communication skills and a decisive yet affiliative leadership style to drive results while maintaining relationships</li><li>
Strong presence with Senior Executives including ability to communicate effectively on a prepared and ad-hoc basis</li><li>
Proven experience as a member and leader of a high performing team</li></ul><h2 class="jobSectionHeader">
What you can expect of us</h2>
As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we&rsquo;ll support your journey every step of the way.
The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is posted. Actual salary will vary based on several factors including but not limited to, relevant skills, experience, and qualifications.
In addition to the base salary, Amgen offers a Total Rewards Plan, based on eligibility, comprising of health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities that may include:<ul><li>
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, and flexible spending accounts</li><li>
A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan</li><li>
Stock-based long-term incentives</li><li>
Award-winning time-off plans</li><li>
Flexible work models where possible. Refer to the Work Location Type in the job posting to see if this applies.</li></ul><h2 class="jobSectionHeader">
 and make a lasting impact with the Amgen team.</h2><h2 class="jobSectionHeader">
careers.amgen.com</h2>
In any materials you submit, you may redact or remove age-identifying information such as age, date of birth, or dates of school attendance or graduation. You will not be penalized for redacting or removing this information.<h2 class="jobSectionHeader">
Application deadline</h2>
Amgen does not have an application deadline for this position; we will continue accepting applications until we receive a sufficient number or select a candidate for the position.<h2 class="jobSectionHeader">
Sponsorship</h2>
Sponsorship for this role is not guaranteed.
As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease.
Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law.
We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.</div></div></div>

Oncology Strategy Director

<div><div>Egypt - Cairo
<div>JOB ID: R-251623 LOCATION: Egypt - Cairo WORK LOCATION TYPE: Flex Commuter / Hybrid DATE POSTED: Jul. 29, 2026 CATEGORY: Regulatory
</div></div><div><div>HOW MIGHT YOU DEFY IMAGINATION?
If you feel like you&rsquo;re part of something bigger, it&rsquo;s because you are. At Amgen our shared mission&mdash;to serve patients&mdash;drives all that we do. It is key to our becoming one of the world&rsquo;s leading biotechnology companies. We are global collaborators who achieve together&mdash;researching, manufacturing and delivering ever-better products that reach over 10 million patients worldwide. It&rsquo;s time for a career you can be proud of. Join us.
SENIOR ASSOCIATE REGULATORY AFFAIRS
WHAT YOU WILL DO
In this vital role you will assist in the local coordination and execution of regulatory submissions in compliance with Amgen corporate standards and national regulatory requirements, and Regulatory Affairs processes and deliverables for the ELI markets Egypt, Jordan, Iraq and Lebanon.<ul><li>
Ensure regulatory submissions are made on time and meet Amgen&rsquo;s corporate and local regulatory requirements</li><li>
Responsible for completion of regulatory files for submission. (Prepare/Receive files and submit them to regulatory authorities within the defined and agreed submission/approval dates) and according to guidelines and requirements</li><li>
Manufacturing site registration and license maintenance</li><li>
Responsible for coordinating with the International regulatory team to ensure right first-time dossiers are provided</li><li>
Coordinate and respond to the requests by authorities during the evaluation process and check the correct handling of deficiency letter within a specific timeframe in order not to delay MOH approvals</li><li>
Establish effective communication and continuous follow-up with the external agencies &amp; distributors to ensure timely submissions and approvals of all company&rsquo;s applications</li><li>
Monitoring of emerging guidelines and changes affecting business and communication to relevant internal customers</li><li>
Providing guidance on the approval processes to internal stakeholders within the region and providing regulatory input for launch planning</li><li>
Maintenance of all lifecycle activities/ Product renewal license details by accurately preparing filling submissions and approval within the preset global timelines -accountable for overall accuracy and compliance</li><li>
Ensure alignment of regulatory objectives with regional / global regulatory objectives and commercial plans</li><li>
Accountable for solving all supply issues related to regulatory activities.</li><li>
To provide regulatory intelligence</li><li>
Ensure compliance with company's SOPs and working practices for Good Regulatory Practice</li><li>
Management of documentation archiving and record keeping according to SOP and local legislation</li><li>
Contact for agency interactions for portfolio of products and coordinating and reviewing briefing documents and/or other submissions for meetings with Regulatory agencies</li><li>
Collate, distribute, exchange and archive regulatory information with colleagues across the business</li><li>
Participate in regulatory and affiliate process improvements initiatives</li><li>
Review promotion and non-promotion materials to ensure compliance with local license, company procedures and Code of Practice</li></ul>
BE PART OF OUR TEAM
Reporting to the Regulatory Affairs Manager for ELI, you would be joining a team of regulatory professionals passionate about delivering the best outcomes for our medicines to patients.
WHAT WE EXPECT OF YOU
We are all different, yet we all use our unique contributions to serve patients. What we seek in you as an experienced professional, are these qualifications and skills:<ul><li>
Pharmacy Bachelor&rsquo;s degree</li><li>
2-3 years of directly related experience in regulatory affairs (ELI markets)</li><li>
Knowledge and awareness of the relevant regulatory guidelines and legislation for ELI markets</li><li>
Strong communication skills both verbal and written</li><li>
Organizational skills &amp; developing regulatory project management skills</li></ul>
Thrive
What you can expect of us
As we work to develop treatments that take care of others, so we work to care for our teammates&rsquo; professional and personal growth and well-being.<ul><li>
Vast opportunities to learn and move up and across our global organization</li><li>
Diverse and inclusive community of belonging, where teammates are empowered to bring ideas to the table and act</li><li>
Generous Total Rewards Plan comprising health, finance and wealth, work/life balance, and career benefits</li></ul>
 for a career that defies imagination
In our quest to serve patients above all else, Amgen is the first to imagine, and the last to doubt. Join us.
careers.amgen.com
Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, gender, sexual orientation, gender identity, national origin, protected veteran status, or disability status.</div></div></div>

<div><div>United States - Remote
<div>JOB ID: R-250804 LOCATION: United States - Remote WORK LOCATION TYPE: Remote DATE POSTED: Jul. 29, 2026 CATEGORY: Information Systems SALARY RANGE: 129,654.75USD -175,415.25 USD
</div></div><div><div>Join Amgen&rsquo;s Mission of Serving Patients
At Amgen, if you feel like you&rsquo;re part of something bigger, it&rsquo;s because you are. Our shared mission&mdash;to serve patients living with serious illnesses&mdash;drives all that we do.
Since 1980, we&rsquo;ve helped pioneer the world of biotech in our fight against the world&rsquo;s toughest diseases. With our focus on four therapeutic areas &ndash;Oncology, Inflammation, General Medicine, and Rare Disease&ndash; we reach millions of patients each year. Amgen is advancing a broad and deep pipeline of medicines to treat cancer, heart disease, inflammatory conditions, rare diseases, and obesity and obesity-related conditions. As a member of the Amgen team, you&rsquo;ll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives.
Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you&rsquo;ll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.
Machine Learning Engineer
What you will do
Let&rsquo;s do this. Let&rsquo;s change the world. In this vital role, you will contribute to the development of scalable machine learning platforms and workflows that enable scientists and researchers across Amgen to build, deploy, and manage AI/ML models. You will work closely with experienced engineers, data scientists, and domain experts to productionize machine learning solutions primarily in support of drug discovery and development.
This is an ideal role for engineers early in their ML engineering careers who want to grow their expertise in MLOps, cloud platforms, and applied AI in life sciences.
This role will be eligible for remote in the US.
Roles &amp; Responsibilities:<ul><li>
Deliver AI and ML-enabled applications, with deployed models ranging from classical ML models to natural language processing, protein language models, and large language models.</li><li>
Contribute to the development and maintenance of ML platform capabilities, including:<ul><li>
Data pipelines and feature engineering workflows</li><li>
Model training, evaluation, and deployment pipelines</li><li>
Experiment tracking and model registry systems</li><li>
Model performance evaluations and monitoring</li></ul></li><li>
Partner in implementation of AI and ML Ops best practices, including CI/CD, infra as code, monitoring, traceability and reproducibility.</li><li>
Collaborate with cross-functional teams to transition standards and outcomes from experimentation to production-grade enterprise solutions.</li><li>
Build and maintain scalable and efficient, productionized MLOps solutions on cloud platforms.</li><li>
Develop and deliver training content and knowledge articles to educate resident scientists on model lifecycle management best practices.</li></ul>
What we expect of you
We are all different, yet we all use our unique contributions to serve patients. The professional we seek is an individual with these qualifications.
Basic Qualifications:
Master&rsquo;s degree
OR
Bachelor&rsquo;s degree and 2 years of experience in Computer Science, IT, or engineering field
OR
Associate&rsquo;s degree and 6 years in Computer Science, IT, or engineering field
OR
High school diploma / GED and 8 years in Computer Science, IT, or engineering field
Required Skills:<ul><li>
Software programming (Python, version control, test-driven development).</li><li>
Familiarity with cloud technologies (AWS preferred, Databricks).</li><li>
Hands-on experience with AI/ML model training and serving.</li></ul>
Preferred Qualifications:<ul><li>
Experience with deployment and maintenance of AI/ML models in production.</li><li>
Substantial experience with cloud technologies and platforms, such as Databricks, AWS (preferred), or Azure.</li><li>
Experience with AI and MLOps frameworks and tools (MLflow, Kubeflow, Weights &amp; Biases, Terraform, etc.).</li><li>
Experience with containerization (Docker, Kubernetes).</li><li>
Familiarity with distributed data processing (e.g., Spark).</li><li>
Familiarity with data science libraries (scikit-learn, TensorFlow, PyTorch, LangChain).</li></ul>
Soft Skills:<ul><li>
Excellent critical-thinking and problem-solving skills.</li><li>
Strong communication and collaboration skills.</li><li>
Demonstrated presentation skills.</li><li>
Self-motivated, with independent ownership and leadership skills.</li></ul>
What you can expect of us
As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we&rsquo;ll support your journey every step of the way.
The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is posted. Actual salary will vary based on several factors including but not limited to, relevant skills, experience, and qualifications.
In addition to the base salary, Amgen offers a Total Rewards Plan, based on eligibility, comprising of health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities that may include:<ul><li>
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, and flexible spending accounts</li><li>
A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan</li><li>
Stock-based long-term incentives</li><li>
Award-winning time-off plans</li><li>
Flexible work models where possible. Refer to the Work Location Type in the job posting to see if this applies</li></ul>
 and make a lasting impact with the Amgen team.
careers.amgen.com
In any materials you submit, you may redact or remove age-identifying information such as age, date of birth, or dates of school attendance or graduation. You will not be penalized for redacting or removing this information.
Application deadline
Amgen does not have an application deadline for this position; we will continue accepting applications until we receive a sufficient number or select a candidate for the position.
Sponsorship
Sponsorship for this role is not guaranteed.
As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease.
Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law.
We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.</div></div></div>

Machine Learning Engineer

<div><div>United Arab Emirates - Dubai
<div>JOB ID: R-250830 LOCATION: United Arab Emirates - Dubai WORK LOCATION TYPE: Field Worker DATE POSTED: Jul. 24, 2026 CATEGORY: Sales
</div></div><div><div>HOW MIGHT YOU DEFY IMAGINATION?
If you feel like you&rsquo;re part of something bigger, it&rsquo;s because you are. At Amgen, our shared mission&mdash;to serve patients&mdash;drives all that we do. It is key to our becoming one of the world&rsquo;s leading biotechnology companies. We are global collaborators who achieve together&mdash;researching, manufacturing, and delivering ever-better products that reach over 10 million patients worldwide. It&rsquo;s time for a career you can be proud of. Join us.
CW District Promotion Manager Kuwait &amp; Qatar &ndash; Cardio Renal Business Unit<h2 class="jobSectionHeader">
Live</h2>
What you will do
Let&rsquo;s do this. Let&rsquo;s change the world. In this vital role you will be responsible for improving revenue and market share in the assigned district by driving sales activities and providing leadership to the field force.<ul><li>
Design &amp; Implement Sales force/Customer Engagement strategy</li><li>
Lead &amp; Coach sales team</li><li>
Efficiently work with the brand team and take leadership for customer centric strategies with relevant internal partners</li><li>
Translate Amgen affiliate and brand strategy into regional plans (to deliver successful treatments)</li><li>
Analyze the sales performance of the relevant brands in the district and identifies key levers for action</li><li>
Keep business unit team advised of any market changes / competitor activity relevant to strategy implementation and development</li><li>
Ensure implementation of the Marketing/Commercial tactics by development of territory plans with the team</li><li>
Supervise progress of marketing messages and programs</li><li>
Lead approved budgets to ensure appropriate allocation of resources to meet the plan and financial control</li><li>
Plan, allocate and supervise team expenses budget to ensure budgetary control.</li><li>
Supervise implementation of plan of actions throughout sales cycles and ensures budget spend within agreed time, costs, compliance, and quality parameters</li><li>
Monitor, evaluate and act on field force metrics and standards to improve sales force efficiency from a quantitative and qualitative perspective</li><li>
Build a strong sales team by recruiting and selecting candidates and efficiently on-boarding new hires</li><li>
Coach and motivate team members to achieve/exceed territory goals and optimize individual and team engagement</li><li>
Conduct annual and ongoing performance reviews and capability assessment within the framework of Amgen&rsquo;s performance management process</li><li>
Develop individual team members to continuously improve overall level of performance in their role and for future (talent) development</li><li>
Support the team on external key customer visits as needed</li><li>
Take leadership in customer engagement strategies &amp; personal external partner management.</li></ul><h2 class="jobSectionHeader">
Win</h2>
What we expect of you
We are all different, yet we all use our outstanding contributions to serve patients. The professional we seek is with these qualifications.
Minimum Requirements<ul><li>
At least 2 years of people management experience in the Gulf region</li><li>
Experience in managing sales teams is required</li></ul><ul><li>
A minimum of 5 years of proven success in pharmaceutical sales within the Gulf Market</li><li>
Demonstrated leadership skills</li><li>
Familiarity with computer systems, including CRM databases and MS Office</li><li>
Strong command of English, both spoken and written</li><li>
Possession of relevant local legal qualifications</li></ul>
Preferred Requirements<ul><li>
Related experience in Cardiovascular &amp; Endocrinology therapies</li><li>
Prior experience in sales and marketing positions</li><li>
Bachelor&rsquo;s degree in life science or (bio)medical sciences</li><li>
Proficiency in interacting across different fields and interpersonal levels</li><li>
Project management experience</li></ul><h2 class="jobSectionHeader">
Thrive</h2>
What you can expect of us
As we work to develop treatments that take care of others, we also work to care for our teammates&rsquo; professional and personal growth and well-being.<ul><li>
Vast opportunities to learn and move up and across our global organization</li><li>
Diverse and inclusive community of belonging, where teammates are empowered to bring ideas to the table and act</li><li>
Generous Total Rewards Plan comprising health, finance and wealth, work/life balance, and career benefits</li></ul> 
for a career that defies imagination
In our quest to serve patients above all else, Amgen is the first to imagine, and the last to doubt. Join us.<h2 class="jobSectionHeader">
careers.amgen.com</h2>
Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.
We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.
Amgen requires all staff in the United States and Puerto Rico to be vaccinated from COVID 19 as a condition of employment. In accordance with applicable law, Amgen will provide reasonable accommodations to staff members who qualify on the basis of a medical reason or a sincerely held religious belief, practice, or observance. Such accommodation may not pose an undue hardship to Amgen, its operations, or its staff.</div></div></div>

CW - Mgr District Promotion

<div><div>US - Ohio - New Albany
<div>JOB ID: R-247804 LOCATION: US - Ohio - New Albany WORK LOCATION TYPE: On Site DATE POSTED: Jun. 23, 2026 CATEGORY: Engineering SALARY RANGE: 148,715.15USD -201,202.85 USD
</div></div><div><div>Join Amgen&rsquo;s Mission of Serving Patients
At Amgen, if you feel like you&rsquo;re part of something bigger, it&rsquo;s because you are. Our shared mission&mdash;to serve patients living with serious illnesses&mdash;drives all that we do.
Since 1980, we&rsquo;ve helped pioneer the world of biotech in our fight against the world&rsquo;s toughest diseases. With our focus on four therapeutic areas &ndash;Oncology, Inflammation, General Medicine, and Rare Disease&ndash; we reach millions of patients each year. Amgen is advancing a broad and deep pipeline of medicines to treat cancer, heart disease, inflammatory conditions, rare diseases, and obesity and obesity-related conditions. As a member of the Amgen team, you&rsquo;ll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives.
Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you&rsquo;ll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.
Senior Manager Engineering
What you will do
Let&rsquo;s do this. Let&rsquo;s change the world.
In this vital role, you will provide leadership for Facilities &amp; Engineering operations supporting Amgen Ohio (AOH), a state-of-the-art final drug product manufacturing facility. You will be responsible for the safe, reliable, compliant, and efficient operation of site utility, facility, and infrastructure systems that support commercial manufacturing operations.
Reporting to the Director of Facilities &amp; Engineering, the Senior Manager will lead a team of engineers and technical professionals responsible for utility systems, sustainability initiatives, asset lifecycle management, and engineering support activities. The role will work closely with Reliability Engineering, Maintenance, Manufacturing, Quality, EHS, and Capital Projects to ensure site operational readiness and long-term asset performance.
The Senior Manager will be a key leader in driving reliability, operational excellence, sustainability, inspection readiness, and continuous improvement across the AOH campus.
Responsibilities
Engineering and Utility Systems Leadership<ul><li>
Provide leadership, coaching, and technical direction to a team of Facilities &amp; Engineering professionals responsible for plant utilities, HVAC, building automation systems, electrical distribution, refrigeration systems and facility infrastructure.</li><li>
Ensure safe, reliable, and compliant operation of utility and facility systems supporting commercial packaging manufacturing.</li><li>
Develop and implement engineering strategies that improve asset reliability, operational performance, and lifecycle sustainability.</li><li>
Partner closely with Reliability Engineering to drive asset performance, condition-based monitoring, predictive maintenance strategies, and risk reduction initiatives.</li><li>
Serve as the engineering owner for critical utility and facility systems, ensuring robust lifecycle management and system performance.</li></ul>
Operational Excellence and Reliability<ul><li>
Lead initiatives to improve equipment reliability, system availability, and operational efficiency across site infrastructure.</li><li>
Utilize performance metrics and engineering data to identify opportunities for continuous improvement and risk mitigation.</li><li>
Drive root cause investigations and corrective actions for significant utility, facility, or infrastructure events.</li><li>
Support the development and implementation of reliability-centered maintenance and asset management strategies.</li><li>
Foster a culture of operational excellence through Lean, Continuous Improvement, and problem-solving methodologies.</li></ul>
Compliance and Inspection Readiness<ul><li>
Ensure utility systems operate in accordance with cGMP, regulatory, safety, and environmental requirements.</li><li>
Maintain a state of inspection readiness and support internal audits, regulatory inspections, and partner visits.</li><li>
Ensure engineering documentation, procedures, change controls, deviations, CAPAs, and maintenance practices remain compliant and effective.</li><li>
Collaborate with Quality and Validation organizations to support qualification, requalification, and ongoing compliance activities.</li></ul>
Capital Projects and Asset Lifecycle Management<ul><li>
Support site capital investment planning and execution related to utility, facility, and infrastructure systems.</li><li>
Provide engineering oversight for facility upgrades, expansions, equipment replacements, and infrastructure modernization initiatives.</li><li>
Drive long-range asset lifecycle planning and support Amgen&rsquo;s Global Lifecycle Asset Management programs.</li><li>
Collaborate with project teams to ensure successful startup, commissioning, qualification, and operational integration of new assets.</li></ul>
Sustainability and Business Operations<ul><li>
Lead sustainability initiatives supporting Amgen&rsquo;s environmental and energy reduction commitments.</li><li>
Support utility forecasting, operating budgets, capital planning, and resource allocation activities.</li><li>
Collaborate with internal and external partners to optimize utility consumption, operational efficiency, and infrastructure performance.</li><li>
Ensure business continuity through proactive infrastructure planning, risk management, and contingency preparedness.</li></ul>
People Leadership<ul><li>
Build, develop, and retain a high-performing engineering organization.</li><li>
Establish clear goals, performance expectations, and development plans for team members.</li><li>
Foster a collaborative culture focused on safety, accountability, innovation, and continuous learning.</li><li>
Drive engagement and technical capability development across the Facilities &amp; Engineering organization.</li></ul>
What we expect of you
We are all different, yet we all use our unique contributions to serve patients. The professional we seek is a collaborative leader with these qualifications.
Basic Qualifications
Doctorate degree and 2 years of Engineering experience
OR
Master&rsquo;s degree and 6 years of Engineering experience
OR
Bachelor&rsquo;s degree and 8 years of Engineering experience
OR
Associate&rsquo;s degree and 10 years of Engineering experience
OR
High school diploma / GED and 12 years of Engineering experience
In addition to meeting at least one of the above requirements, you must have a minimum of 2 years experience directly managing people and/or leadership experience leading teams, projects, programs, or directing the allocation or resources. Your managerial experience may run concurrently with the required technical experience referenced above
Preferred Qualifications<ul><li>
Bachelor&rsquo;s degree in Mechanical Engineering, Chemical Engineering, Electrical Engineering, or related technical discipline.</li><li>
8+ years of experience in Facilities, Utilities, Engineering, Reliability, or related technical functions.</li><li>
5+ years of leadership experience managing engineering or technical teams.</li><li>
Experience within pharmaceutical, biotechnology, medical device, or other highly regulated manufacturing environments.</li><li>
Strong knowledge of plant utilities, clean utilities, HVAC systems, facility infrastructure, and building management systems.</li><li>
Experience supporting GMP manufacturing operations and regulatory inspections.</li><li>
Knowledge of reliability engineering principles, asset management programs, and predictive maintenance technologies.</li><li>
Experience with computerized maintenance management systems (CMMS) and asset management tools.</li><li>
Demonstrated success leading continuous improvement, operational excellence, and sustainability initiatives.</li><li>
Strong project management, problem-solving, and decision-making capabilities.</li><li>
Excellent communication, collaboration, and stakeholder management skills.</li><li>
Ability to manage multiple priorities in a fast-paced manufacturing environment.</li><li>
Ability to provide occasional off-hours support for critical business and operational needs.</li></ul><h2 class="jobSectionHeader">
What you can expect of us</h2>
As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we&rsquo;ll support your journey every step of the way.
The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is posted. Actual salary will vary based on several factors including but not limited to, relevant skills, experience, and qualifications.
In addition to the base salary, Amgen offers a Total Rewards Plan, based on eligibility, comprising of health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities that may include:<ul><li>
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, and flexible spending accounts</li><li>
A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan</li><li>
Stock-based long-term incentives</li><li>
Award-winning time-off plans</li><li>
Flexible work models, including remote and hybrid work arrangements, where possible</li></ul><h2 class="jobSectionHeader">
 and make a lasting impact with the Amgen team.</h2><h2 class="jobSectionHeader">
careers.amgen.com</h2>
In any materials you submit, you may redact or remove age-identifying information such as age, date of birth, or dates of school attendance or graduation. You will not be penalized for redacting or removing this information.<h2 class="jobSectionHeader">
Sponsorship</h2>
Sponsorship for this role is not guaranteed.
As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease.
Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law.
We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.</div></div></div>

Sr. Manager Engineering (Facilities)

<div><div>US - Puerto Rico - Juncos
<div>JOB ID: R-246486 LOCATION: US - Puerto Rico - Juncos WORK LOCATION TYPE: On Site DATE POSTED: Jun. 23, 2026 CATEGORY: Quality
</div></div><div><div><div><div>Join Amgen&rsquo;s Mission of Serving Patients
At Amgen, if you feel like you&rsquo;re part of something bigger, it&rsquo;s because you are. Our shared mission&mdash;to serve patients living with serious illnesses&mdash;drives all that we do.
Since 1980, we&rsquo;ve helped pioneer the world of biotech in our fight against the world&rsquo;s toughest diseases. With our focus on four therapeutic areas &ndash;Oncology, Inflammation, General Medicine, and Rare Disease&ndash; we reach millions of patients each year. Amgen is advancing a broad and deep pipeline of medicines to treat cancer, heart disease, inflammatory conditions, rare diseases, and obesity and obesity-related conditions. As a member of the Amgen team, you&rsquo;ll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives.
Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you&rsquo;ll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.<h2 class="jobSectionHeader">
Specialist Quality Assurance &ndash; AML 14
</h2>What you will do 
Let&rsquo;s do this. Let&rsquo;s change the world! In this vital role, you will serve as a Quality leader accountable for the investigation and resolution of minor deviations, safeguarding product quality and patient safety through sound judgment, strong ownership, cross‑functional collaboration, and effective risk management in a dynamic drug product manufacturing environment. 
Specific responsibilities include but are not limited to:<ul><li>
Serve as Quality investigation lead and decision-maker for complex deviations, maintaining accountability for designation, documentation quality, timeliness and closure.</li><li>
Actively participate in deviation meetings, managing multiple concurrent deviations and driving effective resolution.</li><li>
Provide Quality oversight to ensure thorough documentation of deviations, including floor presence, process observation, and personnel interviews across shifts, including nights when required.</li><li>
Review, approve, and track cGMP documentation, including Deviations, procedure updates and associated records.</li><li>
Demonstrate strong critical thinking skills, the ability to distinguish between a minor and mayor designation using evidence-based decision making.</li><li>
Ensure that deviations with potential impact to product quality are properly assessed and documented per established procedures.</li><li>
Verify that deviations from established procedures are investigated, documented, and resolved in accordance with Quality System requirements.</li><li>
Ensure production records, laboratory results, and investigation documentation to be used as evidence for deviations are complete, accurate, and compliant with cGMP standards.</li><li>
Collaborate cross‑functionally with Manufacturing, Engineering, Validation, and Quality to ensure information required for designation and/or closure of deviations is complete and accurate.</li><li>
Escalate and communicate quality, compliance, supply, and patient safety risks to senior management as appropriate.</li><li>
Defend deviations during internal audits, regulatory inspections, and leadership review forums. Maintain flexibility to support network interactions across time zones and operational needs requiring schedule adaptability.</li><li>
Support Continuous Improvement initiatives, leveraging deviation learnings to strengthen systems and prevent recurrence.</li><li>
Complete required training and perform additional duties as assigned by management.</li></ul> 
What we expect of you 
We are all different! Yet, we all use our unique contributions to serve patients. The Specialist QA professional we seek is a Quality-driven professional with these qualifications. 
Basic Qualifications: 
 
Doctorate degree
 
OR 
Master&rsquo;s degree and 2 years of Quality Assurance experience 
OR 
Bachelor&rsquo;s degree and 4 years of Quality Assurance experience
 
OR 
Associate&rsquo;s degree and 8 years of Quality Assurance experience
 
OR
 
High school diploma / GED and 10 years of Quality Assurance experience
Preferred Qualifications:<ul><li>
Life Science and/or Engineering academic degree.</li><li>
Advanced experience in Quality Systems, with demonstrated expertise documenting Deviations, CAPA, and CAPA Effectiveness Verification (EV) within a regulated GxP environment.</li><li>
Strong independent decision-making skills with the ability to influence others and drive alignment across teams.</li><li>
Proven experience supporting regulatory inspections and audits, including demonstrated ability to interact with regulatory agencies and contributing to successful inspection outcomes.</li><li>
Proven ability to lead and own complex root cause investigations, including facilitating RCA discussions and driving cross‑functional alignment.</li></ul><ul><li>
Experience supporting drug product operations in a GMP-regulated environment.</li><li>
Proficient technical writing skills with the ability to produce concise, objective, evidence-based, inspection-ready documentation in compliance with ALCOA+ and Good Documentation Practices.
</li><li>Strong sense of accountability and ownership, with the ability to manage multiple high‑impact deviations simultaneously and deliver timely, compliant outcomes.</li><li>
Demonstrated ability to evaluate compliance issues, perform advanced data trending and analysis, and assess systemic quality risks.</li><li>
Ability to identify systemic quality signals, recurring failure modes, and cross-functional process vulnerabilities through trend analysis and prior occurrence assessment.</li><li>
Experience engaging directly with manufacturing operations, including floor support, process observation, and personnel interviews across multiple shifts.</li><li>
Technically savvy and adaptable, with openness to leveraging digital tools, automation, and emerging technologies (including AI‑enabled tools) to improve investigation effectiveness.</li><li>
Flexibility to support variable schedules and cross‑time‑zone interactions, while consistently demonstrating Amgen Values and Leadership Practices.</li></ul><h2 class="jobSectionHeader">
What you can expect of us</h2>
As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we&rsquo;ll support your journey every step of the way.
In addition to the base salary, Amgen offers a Total Rewards Plan, based on eligibility, comprising of health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities that may include:<ul><li>
A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental &amp; vision coverage, and life &amp; disability insurance</li><li>
A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan</li><li>
Stock-based long-term incentives</li><li>
Award-winning time-off plans</li><li>
Flexible work models where possible. Refer to the Work Location Type in the job posting to see if this applies.</li></ul><h2 class="jobSectionHeader">
 and make a lasting impact with the Amgen team.</h2><h2 class="jobSectionHeader">
careers.amgen.com</h2>
In any materials you submit, you may redact or remove age-identifying information such as age, date of birth, or dates of school attendance or graduation. You will not be penalized for redacting or removing this information.<h2 class="jobSectionHeader">
Sponsorship</h2>
Sponsorship for this role is not guaranteed.
As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease.
Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law.
We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.</div></div></div></div></div>

Specialist Quality Assurance - AML -14

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Sr. Manager Engineering (Facilities)

Specialist Quality Assurance - AML -14