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Material Compliance Associate

Career Category

Regulatory

Job Description

Join Amgen’s Mission of Serving Patients

At Amgen, if you feel like you’re part of something bigger, it’s because you are. Our shared mission—to serve patients living with serious illnesses—drives all that we do.

Since 1980, we’ve helped pioneer the world of biotech in our fight against the world’s toughest diseases. With our focus on four therapeutic areas –Oncology, Inflammation, General Medicine, and Rare Disease– we reach millions of patients each year. As a member of the Amgen team, you’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’ll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.

Material Compliance Associate

What you will do

Let’s do this. Let’s change the world. In this vital role you will be responsible for assisting the Brand Marketers build and monitor their projects through the Material Approval and Compliance (MAC) review process. The MCA will quality check files submitted for review, collect “live” edits during compliance review and approval meetings, and edit submission documents within the electronic review system, Veeva. They will ensure all materials submitted adhere to Amgen MAC Standards and FDA requirements throughout the process.

Responsibilities

  • Supports one Material Approval and Compliance (MAC) Team.

  • Supports Global Initiative/Other Project.

  • Quality check submissions for review to ensure alignment with internal standards throughout the process.

  • Work with agencies and internal staff, including training on next steps and advising on process standards.

  • Collaborates with MRL to identify Reference QC issues and Match Text Harvesting

  • Provide administrative support during review meetings, including gathering “live” edits on submission documents.

  • Assist with Label updates.

  • Periodically assist on a variety of MAC-related projects

  • Run Veeva reports and communicate outputs to cross-functional partners.

  • Proofreading commercial and training materials produced by the Marketing teams.

  • Revise documents electronically.

  • Actively listen to and capture comments from meeting stakeholders.

  • Anticipate edits and work proactively to suggest solutions.

  • Ability to foster collaboration, work effectively on cross-functional teams, and consistently deliver on-time.

  • Strong oral and written communication skills; strong interpersonal skills; demonstrated time management and decision-making skills.

What we expect of you

We are all different, yet we all use our unique contributions to serve patients. The detail oriented professional we seek is an associate with these qualifications.

Basic Qualifications:

  • Bachelor’s degree OR

  • Associate’s degree and 4 years of Marketing Communications Project Management / Copy-Editing experience OR

  • High school diploma, or GED, and 6 years of Marketing Communications Project Management / Copy-Editing experience

Preferred Qualifications:

  • An understanding of the pharmaceutical commercialization process and knowledge of the legal and regulatory guidelines affecting promotion of prescription products

  • Project management experience in the Pharmaceutical, Biotechnology, Healthcare-related field, or other regulated industries

  • Experience with Microsoft Office 365 (e.g. Word, Excel, Outlook, and PowerPoint), Adobe products (e.g. Adobe Photoshop, Illustrator, and Acrobat Pro), and Veeva PromoMats

  • Experience in leading the creation of marketing materials from concept to commercialization.

  • Experience managing the approval process of marketing materials that are produced at high volumes.

  • Copy-Editing experience including excellent typing and spelling skills.

  • Able to proofread materials using Adobe Acrobat Professional

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’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:

  • 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

  • A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan

  • Stock-based long-term incentives

  • Award-winning time-off plans

  • Flexible work models, including remote and hybrid work arrangements, where possible

Apply now for a career that defies imagination

Objects in your future are closer than they appear. Join us.

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.

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.

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Salary Range

70,403.00 USD - 87,441.00 USD
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Average salary estimate

$78922 / YEARLY (est.)
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$70403K
$87441K

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What You Should Know About Material Compliance Associate, Amgen

At Amgen, we're on an exciting journey to innovate healthcare and make a lasting impact on the lives of patients worldwide. We're currently looking for a Material Compliance Associate to join our dynamic team. In this role, you'll be at the heart of our mission, helping Brand Marketers navigate the Material Approval and Compliance (MAC) review process. Your keen eye for detail will be essential as you assist in quality checking project submissions, facilitating compliance discussions, and managing document edits within our electronic review system, Veeva. Your understanding of regulatory requirements will ensure that all materials adhere to Amgen's high standards and FDA guidelines. You'll collaborate with various stakeholders, from marketing teams to external agencies, fostering a teamwork-driven atmosphere. Your responsibilities will also include troubleshooting and suggesting proactive solutions while ensuring timely delivery of project materials. With a focus on communication, you’ll actively gather feedback during review meetings and play a supportive role in label updates and ongoing MAC-related projects. If you're detail-oriented and passionate about making a difference in the biotech field, then the Material Compliance Associate position at Amgen could be a perfect fit for you. Join us as we change the world for patients and advance your career in an environment that values innovation and collaboration.

Frequently Asked Questions (FAQs) for Material Compliance Associate Role at Amgen
What are the main responsibilities of a Material Compliance Associate at Amgen?

As a Material Compliance Associate at Amgen, your primary responsibilities include supporting the Brand Marketers through the Material Approval and Compliance (MAC) review process, quality checking submissions, and managing compliance discussions. You'll collaborate with internal teams, assist with label updates, and ensure all project materials adhere to both Amgen's MAC Standards and FDA regulations throughout the review process.

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What qualifications are required for a Material Compliance Associate at Amgen?

To qualify for the Material Compliance Associate position at Amgen, candidates should possess a Bachelor's degree, or an Associate's degree with four years of Marketing Communications Project Management experience, or a high school diploma with six years of related experience. Preferred qualifications include knowledge of the pharmaceutical commercialization process and experience with project management in regulated industries.

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Is experience with Veeva required for the Material Compliance Associate position at Amgen?

While previous experience with Veeva is preferred for the Material Compliance Associate role at Amgen, it is not strictly required. What's essential is your familiarity with marketing project management and compliance processes. Amgen is willing to provide training on the tools and systems needed for success in this position.

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What is the working environment like for a Material Compliance Associate at Amgen?

The working environment at Amgen for a Material Compliance Associate is collaborative and innovative. You will be part of a dedicated team focused on delivering high-quality marketing materials to serve patients effectively. The company also provides flexible work models, including remote arrangements, ensuring a balanced work-life dynamic.

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What benefits can I expect as a Material Compliance Associate at Amgen?

As a Material Compliance Associate at Amgen, you can expect a competitive benefits package including health and welfare plans, a retirement and savings plan, flexible time-off policies, and professional development opportunities. Additionally, you will be working in a supportive environment that values employee growth and well-being.

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Common Interview Questions for Material Compliance Associate
Can you describe your experience with project management and compliance?

In response to this question, highlight specific examples from your past roles where you’ve successfully managed marketing communications projects and ensured compliance with relevant standards. Discuss your familiarity with regulatory guidelines, quality checking procedures, and how you’ve collaborated with cross-functional teams to achieve compliance goals.

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How do you ensure attention to detail in your work?

Demonstrate your attention to detail by sharing a particular example where this skill was vital in achieving project outcomes. You can mention techniques you use, such as checklists or structured review processes, and how you capture feedback effectively to incorporate edits on documents.

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What do you know about Amgen's mission and values?

Showcase your knowledge of Amgen's mission focused on serving patients with serious illnesses and their dedication to innovation in biotechnology. You can discuss how these values resonate with you and how they align with your personal commitment to quality and patient care.

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Describe a time you had to collaborate with a team to solve a problem.

Provide a specific example of a challenging project where you and your team faced obstacles. Highlight your role in facilitating communication, leading discussions, and arriving at a solution, emphasizing your teamwork and problem-solving abilities.

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What methods do you use to manage your time effectively?

In your answer, emphasize strategies such as priority setting, using project management tools, or breaking tasks into manageable steps. Mention how these methods have helped you meet deadlines consistently in previous roles, particularly in fast-paced environments.

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How do you handle constructive criticism?

Discuss your openness to feedback by sharing how you’ve utilized constructive criticism in past roles to improve your work. Emphasize your willingness to learn and adapt, which aligns well with the collaborative nature of the Material Compliance Associate role at Amgen.

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What experience do you have with regulatory guidelines in the pharmaceutical industry?

You should draw on any relevant experience regulating marketing materials, particularly focusing on how you ensured compliance with FDA regulations and internal standards. Provide specific examples that demonstrate your understanding of regulatory frameworks and adherence to guidelines.

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How do you approach quality assurance in your work?

Explain your quality assurance process, detailing steps like systematic checks and balances you implement to ensure that all materials meet the required standards. Give an example of a project where quality assurance played a key role in its success.

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What tools and software are you proficient in that relate to this position?

In this response, list relevant tools such as Microsoft Office 365 and Adobe products, as well as any experience with Veeva. Provide context on how you've used these tools to manage project workflows or enhance the quality of marketing materials.

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How would you describe your communication skills?

You should elucidate your communication style, emphasizing clarity and effectiveness in both verbal and written forms. Include examples of successful collaborations or presentations, showing how you can convey complex information to diverse stakeholders.

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To serve patients. Amgen strives to serve patients by transforming the promise of science and biotechnology into therapies that have the power to restore health or save lives. In everything we do, we aim to fulfill our mission to serve patients....

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DATE POSTED
March 27, 2025

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