International Regulatory Affairs Intern
vor 3 Wochen
**MISSION**:
**Job Summary**:
As an Intern in Regulatory Affairs International team, you will work closely with the regulatory affairs team to ensure compliance with applicable regulations, standards, and guidelines governing the development, manufacturing, and marketing of pharmaceutical products. This entry-level position provides an excellent opportunity to gain practical experience and knowledge in the field of regulatory affairs while contributing to the overall success of the organization.
**This will be a 6 month assignment, 40 hours/week, paid internship**
**Responsibilities and main tasks**:
- Support the preparation of regulatory documents to ensure compliance with local, regional, and international regulations.
- Liaise with RA CMC, RA Labelling, Regulatory Operations & other supportive functions to collect all the information required for preparation of regulatory activities.
- Ensure timely execution of regulatory activities as per the plan set up with the line manager.
- Support the RA International team to maintain tracking tools and regulatory databases up to date.
- Organize and maintain regulatory files and databases, ensuring accuracy, completeness, and confidentiality of information.
- Assist in the preparation and maintenance of working instructions, and other relevant documents related to regulatory affairs.
- Conduct research on regulatory requirements and stay updated with changes in regulations and guidelines.
- Provide appropriate support to the RA team.
- Attends and actively participate to RA department meetings.
**Minimum requirements**:
- Bachelor's degree in a scientific discipline.
- Good command in English (written and spoken), any other language
- advantage.
- Basic understanding of pharmaceutical regulations (e.g. FDA, EMA) is an advantage.
**Required skills**:
- Excellent organizational skills with keen attention to detail.
- Excellent communication and interpersonal skills
- Ability to work effectively both independently and within a team.
- Demonstrated ability to prioritize tasks and meet deadlines.
**Benefits for you**:
- Gain meaningful professional experience in the field of Regulatory Affairs
- Gain cross-functional insight learning how to work in a global company
- Working in a friendly and international environment with a collaborative spirit
- Given an opportunity to improve personal growth and development
**Application need to include a CV and a motivation letter answering these questions**:
- Why do you want to do an internship in Regulatory Affairs?
- What relevant skills and experience can you bring to this position?
LI-HYBRID
Mirum Pharmaceuticals is committed to Equal Employment Opportunity (EEO) and to compliance with all Federal, State and Local laws that prohibit employment discrimination on the basis of race, age, national origin, ethnicity, religion, gender, gender identity, pregnancy, marital status, sexual orientation, citizenship, genetic disposition or characteristics, disability, veteran’s status or any other classification protected by applicable State/Federal/Local laws.
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