Posted:
9/13/2024, 4:55:39 AM
Location(s):
Mexico City, Mexico
Experience Level(s):
Senior
Field(s):
Legal & Compliance
If you feel like you’re part of something bigger, it’s because you are. At Amgen, our shared mission—to serve patients—drives all that we do. It is key to our becoming one of the world’s leading biotechnology companies. We are global collaborators who achieve together—researching, manufacturing, and delivering ever-better products that reach over 10 million patients worldwide. It’s time for a career you can be proud of. Join us.
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What you will do
Ensure regulatory submissions are made on time and meet Amgen’s corporate and local regulatory requirements.
Contribute, implement, and execute the filing plan for Mexico where applicable.
Prepare, review & approve of source text for Mexico country specific labeling.
Review & approve promotion and non-promotion materials
Communicate relevant information to team(s) in advance
Participate and give input in local regulatory process improvements initiatives.
Collate, distribute and exchange regulatory information with other regulatory colleagues and cross functional teams on an ongoing basis and provide advice on local regulatory considerations in a timely manner.
Update, maintain internal regulatory systems and tracking tools in accordance with internal policies and standard operating procedures.
Develop & execute the local strategy to obtain the new Marketing Authorizations of the assigned business unit, ensuring compliance with local and current regulations and procedures.
Analysis of technical, scientific, and legal information to prepare dossiers of innovative products, complying with all applicable requirements and guidelines, avoiding preventions by the health authority (New Marketing Authorizations, technical and administrative variations, and renewals).
Collate, review, and distribute Regulatory information & intelligence with other regulatory colleagues and cross functional teams on an ongoing basis.
Partner where required with International Regulatory Leads (IRLs), CMC and other functions to support the regulatory strategy, registration, timelines and lifecycle management of all Amgen molecules.
Ability to work with different cross functional teams to share, discuss and negotiate the strategy and planning of submissions.
What we expect of you
We are all different, yet we all use our unique contributions to serve patients. The professional we seek has these qualifications.
Master’s degree O
Bachelor’s degree and 2 years of experience in similar positions on a big pharmaceutical company Or
Associate’s degree and 6 years of experience in similar positions on a big pharmaceutical company Or
High school diploma / GED and 8 of experience in similar positions on a big pharmaceutical company.
Proficiency in English, both in oral and written communication.
Knowledge and experience in Mexican regulation relating to medicinal products and diverse portfolio of small molecules, innovative biotechs, biosimilars and orphan drugs.
Knowledge of drug development Scientific / Technical Excellence.
Experience in regulatory processes with Cofepris for a portfolio of innovative products: New Marketing Authorizations, variations & renewals.
THRIVE!
As we work to develop treatments that take care of others, we also work to care for our teammates’ professional and personal growth and well-being.
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, 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.
.Website: https://amgen.com/
Headquarter Location: Thousand Oaks, California, United States
Employee Count: 10001+
Year Founded: 1980
IPO Status: Public
Last Funding Type: Post-IPO Debt
Industries: Biotechnology ⋅ Health Care ⋅ Manufacturing ⋅ Pharmaceutical