Student Worker, Regulatory Affairs

Biopharma Careers; København; Hybrid; DKK 56,000 - 78,000; Part time

Benefits offered by this job

Competitive salary

Pension Scheme

Health Insurance

Hybrid working policy

Employee recognition scheme

Professional development

Job summary

Sandoz in Copenhagen is seeking a proactive Pharmaceutical Sciences student to join the Regulatory Affairs team and gain practical experience while studying. You will support proofreading and quality checks of critical documents and assist with administrative tasks to help ongoing projects stay on track.

You will work in a Nordic center, with a flexible hybrid setup, gaining exposure to company processes and cross-functional collaboration within a small, skilled RA group.

Qualifications

• Student enrolled in pharmaceutical sciences, ideally 2nd year.
• Solid basic pharmaceutical understanding and willingness to learn.
• Proficient with Windows Office and Excel.

Responsibilities

• Proofread and quality review SPC and PIL documents for accuracy and compliance.
• Collaborate with Lifecycle Management and Launch teams to support projects.
• Update and maintain trackers to keep information current for stakeholders.
• Provide administrative support across documentation and coordination tasks.
• Assist with day-to-day activities to support team delivery.

Skills

Danish language

English communication

Attention to detail

Organizational skills

Fast learner

Reliability

Education

Bachelor student in Pharmaceuticals (2nd year)

Tools

Microsoft Office

Excel

Job description

Job Description Summary

Join us, the future is ours to shape!

Job Description

Are you an ambitious, proactive, and self-driven individual with a passion to learn more about the pharmaceutical industry and use your theoretical knowledge from your education? If yes, join our teams in Sandoz and get a chance to work with essential pharmaceutical data simultaneously with your studies.

You will be part of the Regulatory Affairs Department of 21 motivated, knowledgeable, and highly skilled RA colleagues. The position is based in our Nordic affiliate located in Copenhagen in Ørestad.

Your Key Responsibilities:

Your responsibilities include, but not limited to:

• Excellent proofreading and quality review of SPC (Summary of Product Characteristics) and PIL (Patient Information Leaflet) documents, ensuring accuracy, consistency, and compliance with required standards.
• Close collaboration with Lifecycle Management (LCM) and Launch team members to support ongoing projects, coordinate activities, and facilitate smooth execution of initiatives.
• Regular updating and maintenance of various trackers, ensuring information is accurate, timely, and readily accessible for stakeholders.
• Providing administrative support through a range of ad hoc tasks, including documentation, coordination, and other operational activities as required to support the team's objectives.
• Assisting with additional day-to-day activities and responsibilities to ensure efficient team functioning and project delivery.

What you’ll bring to the role:

Essential Requirements:

• You are a Student at School of Pharmaceutical Sciences or similar (ideally currently studying 2nd year of bachelor´s degree)
• Basic pharmaceutical understanding and a great wish to learn more
• Have solid experience in working with the Windows Office package and in Excel
• Danish or another Nordic language as mother tongue and fluent communication skills in English
• You have a strong attention to details and are well organized
• You are comfortable challenging the status quo and enjoy going the extra mile to drive strong results
• You are highly reliable and committed with a strong personal drive
• You are a fast learner, hungry for new challenges, and embrace change with a positive attitude

You’ll receive:

• Competitive salary and Bonus based on personal and company results; Pension Scheme; Health Insurance; Flexible working conditions with hybrid working policy; Employee recognition scheme; Development both professionally and personally; Learning about company processes; This role is offered as a Fixed Term contract with a weekly working hour of 7.5 Hours.

Why Sandoz?

Sandoz is the global leader in Biosimilar and Generic medicines, a segment of the healthcare industry that delivers 80% of the world’s medicines at 30% of the cost, touching the lives of more than 1 billion people across 100+ countries! While we are proud of our achievements, we have an ambition to do more so that everyone can achieve the basic humanrightofgood health.

With investments in new development capabilities, production sites, new acquisitions, and partnerships, we have the opportunity to shape the future of Sandoz and help even more people gain access to low-cost, high-quality medicines, sustainably.

Our momentum is powered by an open, collaborative culture driven by our talented and ambitious colleagues, who, in return for applying their skills, experience an agile and collegiate environment with impactful careers, where diversity of thought is welcomed and where personal growth is supported!

Join us, help us make healthcare fairer and faster.

Commitment to Diversity & Inclusion:

We are committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.

#Sandoz

Skills Desired