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Intern, GxP Quality System and Compliance

Revolution Medicines is a clinical-stage precision oncology company focused on developing novel targeted therapies to inhibit frontier targets in RAS-addicted cancers.  The company’s R&D pipeline comprises RAS(ON) Inhibitors designed to suppress diverse oncogenic variants of RAS proteins, and RAS Companion Inhibitors for use in combination treatment strategies. As a new member of the Revolution Medicines team, you will join other outstanding professionals in a tireless commitment to patients with cancers harboring mutations in the RAS signaling pathway.

The Opportunity:

We are seeking an enthusiastic and highly motivated intern to assist our Quality Assurance (QA) Compliance team. This role will engage with and support multiple areas of RevMed’s Quality Management System (QMS). Our goal is that this internship will provide broader perspective of the QA function in product development and oversight, as well as exposure to cross-functional teams and stakeholder engagement. This position will report to the Manager, Quality Compliance. This opportunity will include:

  • Supporting KPI (key performance indicator) and KQI (key quality indicator) metric development.

  • Running periodic reports to monitor metrics and sharing with QA and sub-functional teams.

  • Building reporting tools, such as meeting slide decks, pre-read materials, etc.

  • Assisting with organizing GxP supplier management related documentation.

  • Performing administrative activities in Veeva Quality Platforms (electronic Document Management System and electronic Learning Management System).

  • Other tasks as assigned by management.

Required Skills, Experience and Education:

  • Must be currently enrolled in a full-time undergraduate or graduate degree program at an accredited University, with interest an in Life Sciences, Pharmaceutical Sciences, Engineering, or a related field.

  • Excellent written and verbal communication and interpersonal skills.

  • Demonstrate ability to multi-task and prioritize tasks.

  • Disciplined time management and organizational skills.

Preferred Skills:

  • Have a basic understanding of pharmaceutical development and regulatory requirements.

  • Experience working in Microsoft Word, Excel, PowerPoint, and Outlook.

  • Creative-thinker open to learning across a range of topics.

  • Strong desire to learn from and work with various QA team members.

The base salary range for this intern position is $32.75 to $35.00 for candidates working onsite at our headquarters in Redwood City, CA. The range displayed on each job posting is intended to be the salary for an individual working onsite in Redwood City and will be adjusted for the local market a candidate is based in. Our salary ranges are determined by role, level, and location. Individual pay is determined by multiple factors, including job-related skills, experience, market dynamics, and relevant education or training.

Please note that base salary is one part of the overall total rewards program at RevMed, which includes competitive cash compensation, robust equity awards, strong benefits, and significant learning and development opportunities.

Revolution Medicines is an equal opportunity employer and prohibits unlawful discrimination based on race, color, religion, gender, sexual orientation, gender identity/expression, national origin/ancestry, age, disability, marital status, medical condition, and veteran status.

Revolution Medicines takes protection and security of personal data very seriously and respects your right to privacy while using our website and when contacting us by email or phone. We will only collect, process and use any personal data that you provide to us in accordance with our CCPA Notice and Privacy Policy. For additional information, please contact privacy@revmed.com.

#LI-Hybrid  #LI-AP1

Average salary estimate

$33875 / YEARLY (est.)
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$32750K
$35000K

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What You Should Know About Intern, GxP Quality System and Compliance, Revolution Medicines

Are you ready to dive into the world of quality assurance in pharmaceuticals? Revolution Medicines, a pioneering clinical-stage precision oncology company, is looking for an enthusiastic Intern, GxP Quality System and Compliance to join our dynamic team in Redwood City, California. You will play an essential role in assisting our Quality Assurance (QA) Compliance team, where you’ll gain invaluable hands-on experience in our Quality Management System (QMS). Whether you're supporting the development of key performance indicators or organizing GxP supplier management documents, every task will enhance your understanding of effective product development. At Revolution Medicines, we value collaboration and innovation, so you'll work closely with diverse, cross-functional teams that are just as passionate about fighting cancer as you are. Do you have a knack for writing slick reports or creating engaging presentations? Perfect! Your skills will come in handy while you help build reporting tools and run periodic reports that keep our teams informed and on track. With a commitment to providing broader perspectives on QA functions, your journey here will open doors to a multitude of learning opportunities. So, if you’re all about personal growth and helping patients with RAS signaling pathway-related cancers, we’d love to hear from you! Let’s transform cancer treatment together!

Frequently Asked Questions (FAQs) for Intern, GxP Quality System and Compliance Role at Revolution Medicines
What are the key responsibilities for the Intern, GxP Quality System and Compliance at Revolution Medicines?

As an Intern in GxP Quality System and Compliance at Revolution Medicines, your primary responsibilities will include supporting KPI and KQI metric development, running reports to monitor those metrics, and assisting in organizing GxP supplier management documentation. Additionally, you will engage in creating tools for effective reporting, which are essential for our Quality Assurance team to function efficiently.

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What qualifications are required for the Intern position at Revolution Medicines?

To qualify for the Intern, GxP Quality System and Compliance role at Revolution Medicines, candidates must be currently enrolled in a full-time undergraduate or graduate program in Life Sciences, Pharmaceutical Sciences, Engineering, or a closely related field. Strong communication skills, time management, and multitasking capabilities are necessary for succeeding in this role.

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What learning opportunities can I expect as an Intern at Revolution Medicines?

As an Intern, you will have the opportunity to learn about the Quality Management System and gain insights into various aspects of product development and regulatory practices at Revolution Medicines. You'll also work with experienced QA team members, which will enhance your understanding of industry standards and regulatory requirements in a real-world context.

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Is there a chance for future employment after the internship at Revolution Medicines?

While an internship at Revolution Medicines does not guarantee a full-time position, exceptional performance, along with an ongoing commitment to learning and contributing, may lead to future career opportunities within the organization. Many of our previous interns have transitioned into full-time roles based on their excellent contributions.

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What does the compensation package look like for the Intern position at Revolution Medicines?

The base salary range for the Intern, GxP Quality System and Compliance position at Revolution Medicines is $32.75 to $35.00 per hour for candidates working onsite in Redwood City, CA. This salary is part of a comprehensive rewards program that includes competitive cash compensation, equity awards, and various learning and development opportunities.

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Common Interview Questions for Intern, GxP Quality System and Compliance
What interests you about the Intern, GxP Quality System and Compliance position at Revolution Medicines?

When answering this question, focus on your passion for quality assurance and how it integrates with your interest in life sciences and pharmaceuticals. Discuss your enthusiasm for supporting roles in products that can significantly impact patient lives, highlighting how this internship aligns with your career goals.

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What skills do you bring to the Intern position?

Highlight specific skills you possess that match the job description, such as strong communication abilities, proficiency in Microsoft Office, time management, and organizational skills. Use examples from past experiences to demonstrate how you’ve successfully applied these skills.

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Can you give an example of how you handled a challenging situation in a team project?

Provide a concise anecdote that illustrates your problem-solving and teamwork skills. Focus on how you identified the challenge, collaborated with others to resolve it, and what the outcome was, emphasizing your ability to adapt and support team dynamics.

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What is your understanding of QA functions in the pharmaceutical industry?

Express your knowledge of quality assurance functions, emphasizing their importance in ensuring compliance with regulatory standards and maintaining product integrity. You might mention specific QA processes such as inspections, audits, and the role they play in product development.

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How do you prioritize tasks when there are multiple deadlines?

Share your approach to prioritization, such as using tools like task lists or digital planners. Explain how you assess urgency and importance and how you communicate with team members or supervisors to stay on track.

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What do you hope to learn from this internship?

Discuss your eagerness to acquire practical knowledge in quality assurance processes and expose yourself to cross-functional team dynamics. Mention specific areas of interest that pique your curiosity and how they relate to your career aspirations.

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How would you handle constructive criticism from supervisors or team members?

Demonstrate your openness to feedback by describing how you view constructive criticism as an opportunity for growth. Share an example of how you've utilized feedback in the past to improve your skills or complete a project more effectively.

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Why is collaboration important in the context of quality assurance?

Highlight the benefits of teamwork in quality assurance roles, such as the pooling of diverse expertise, enhanced problem-solving capabilities, and improved compliance with regulatory standards. Share your perspective on fostering a collaborative environment.

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What tools or software are you familiar with that may be relevant for this role?

Mention any experience you have with Microsoft Office tools, especially Excel for managing data, as well as any familiarity with electronic Document Management Systems or Learning Management Systems. If applicable, cite specific tools that are common in QA roles.

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How do you ensure accuracy and attention to detail in your work?

Describe specific techniques you use to maintain accuracy, such as double-checking your work, keeping clear documentation, and utilizing templates for consistency. Emphasize your understanding of the significance of accuracy in the quality assurance process.

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Internship, on-site
DATE POSTED
April 4, 2025

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