Regulatory Affairs - Intern
Roche is hiring a Regulatory Affairs - Intern in Dhaka, Bangladesh. Level rates it ; you can apply on Roche.
Level's read on this job
- On Level's scale, this role is Little AI ●○○○: aI is not part of the work.
- Tools and skills the posting cites include Microsoft Office, regulatory affairs and compliance.
- Level classifies it as an internship.
- Level lists 1,200+ other open roles at Roche.
- The role was posted in the last few days.
AI in this role
Support regulatory operations and compliance for pharmaceutical products and medical devices as an intern.
At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.
The Position
We are excited to announce the Regulatory Affairs Internship Program, designed to give fresh graduates a comprehensive understanding of regulatory requirements within the pharmaceutical industry. This program offers hands-on experience, engagement in essential regulatory activities, and insights into regulatory frameworks that impact the sector.
As an intern, you will contribute to achieving operational excellence by providing support in the oversight and monitoring of regulatory activities, ensuring compliance with both local regulations and global standards through close collaboration with key stakeholders. You will assist in maintaining regulatory operations, ensuring compliance for Roche medicinal products and medical devices throughout their lifecycle, and enabling the company’s continued license to operate.
Duration: 6 Months
Key Responsibilities:
- Execute day-to-day regulatory operations to ensure regulatory compliance of Roche products and medical devices.
- Collaborate with local Health Authorities (HAs) and internal stakeholders to build trusted partnerships and effectively manage regulatory operations.
- Support the development and maintenance of local product information and country-specific packaging compliant with local and global regulatory standards.
- Maintain and oversee all Roche regulatory platforms/systems to ensure alignment with compliance matrices and continuously monitor and improve tracking/control systems.
- Participate in the monitoring, preparation, and negotiation of regulatory submissions and responses as part of regulatory lifecycle management.
Who You Are:
- A recent graduate with a degree in Pharmacy, Life Science or a related field.
- Passionate and genuinely interested in pursuing a career in Regulatory Affairs.
- Possess excellent written and verbal communication skills in English.
- Demonstrate strong analytical and problem-solving abilities.
- Detail-oriented with the ability to work independently and manage multiple tasks effectively.
- Proficient in Microsoft Office Suite (Word, Excel, PowerPoint).
Behavioral Competencies:
- Demonstrate high ethical standards and integrity in professional actions.
- Possess the ability to handle sensitive information with confidentiality.
- Strong interpersonal and teamwork skills, with the ability to collaborate effectively across teams.
- Eager to learn and adapt quickly in a dynamic and fast-paced work environment.
Why Join Us?
At Roche, we endeavor to provide a meaningful and enriching experience that ensures our interns gain valuable industry insights, hands-on knowledge, and the opportunity to build a foundation for their career in regulatory affairs.
What we offer
Roche offers rewarding growth opportunities, a competitive remuneration package and a collaborative culture where people are united in purpose and will stretch you to be brave, speak up and think differently. Feel empowered to deliver meaningful outcomes, supported by accessible and inspiring leaders.
Roche encourages a high-performance culture where you are empowered and trusted to make decisions. We strive for excellence and extraordinary results and take a genuine interest in our people and their well-being, and our patients.
Take pride in knowing you can make a difference to millions of patients worldwide in developing diagnostics and treatments for oncology, neuroscience, inflammation, immunology, ophthalmology, rare diseases, respiratory disease and diabetes.
We are committed to providing an inclusive, safe, secure and healthy workplace, and to minimise any such impacts to our employees, customers and the community. We welcome applications from all people and encourage you to advise of any individual circumstances that may require consideration.
Who we are
A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.
Let’s build a healthier future, together.
Roche is an Equal Opportunity Employer.
How we rate this
Regulatory Affairs - Intern at Roche rates 0 out of 100 for how much of the daily work is AI. That makes it Little AI (AI Level 1 of 4). The level is about AI in the job, not seniority.
Little AI. AI is not part of the work.
- ●●●● Builds AI80 to 100
- ●●●○ Works on AI60 to 79
- ●●○○ Uses AI40 to 59
- ●○○○ Little AI0 to 39
Levels come from how often the tools, models and workflows of the role are named in the posting itself. Read the description and count the AI tools, models and workflows it names.
Prepare for this job
Built from this posting and from similar jobs on Level.
Skills and AI tools this role asks for
Questions you could be asked
- Tell me about a project where regulatory affairs was part of your work. What did you do?
- Tell me about a project where compliance was part of your work. What did you do?
- Tell me about a project where pharmaceuticals was part of your work. What did you do?
- Tell me about a project where document management was part of your work. What did you do?
- Walk me through how you've used Microsoft Office in your day-to-day work.
Adapt your resume
- List these exact terms on your resume: Regulatory Affairs, Compliance, Pharmaceuticals, Document Management, and Microsoft Office. An applicant tracking system matches the wording, not the idea.
- Attach one line of real, concrete experience to at least one of them. A tool named with nothing behind it rarely survives a human read.
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