Student Worker, Regulatory Affairs

DK07 (FCRS = DK007) Sandoz; København; Hybrid; DKK 54,000 - 90,000; Part time

Benefits offered by this job

Health Insurance

Pension Scheme

Hybrid work policy

Employee recognition

Development opportunities

Job summary

Sandoz is seeking a proactive student to join the Regulatory Affairs team in Copenhagen (Ørestad) for a fixed-term internship with a 7.5-hour week. You will proofread SPCs and PILs, support Lifecycle Management and Launch activities, and help maintain trackers and docs.

Strong Windows Office and Excel skills, plus Danish as mother tongue and fluent English, are required. We offer a competitive salary with bonus potential, pension, health insurance, and a hybrid working policy.

Qualifications

• Proactive student currently studying in a pharmaceutical sciences program.
• Basic pharmaceutical understanding with eagerness to learn more.
• Strong attention to detail and organized approach.
• Comfortable with Windows Office and Excel.

Responsibilities

• Proofread and quality review SPCs and PILs for accuracy and compliance.
• Collaborate with Lifecycle Management and Launch teams to support projects.
• Maintain trackers and ensure information is up-to-date and accessible.
• Provide administrative support and assist with day-to-day operations of the RA team.
• Support other team tasks to help project delivery.

Skills

Proofreading

Excel

MS Office

Danish & English

Education

Pharma Sciences student (2nd year)

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

• 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’re highly reliable and committed with a strong personal drive
• You’re 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;

Contract Details

• 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 human right of good 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!

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 Our Purpose here at Sandoz is pioneering access for patients. As the global leader in 'off-patent' high quality medicines, we are able to make medicine more affordable and accessible. Our broad global portfolio comprises of approximately 1,300 quality biosimilar and generic medicines, enabling us to provide more than 900 million patient treatments across 100+ countries per year, and while we are proud of this achievement, we have an ambition to do more! Powered by our talented and ambitious colleagues, who, in return for dedication and skills, experience a flexible, collaborative & inclusive culture where diversity of thought is welcomed and where personal growth is nurtured!