Job Description
Intern, Regulatory CMC APAC
Our company starts your journey on the career path within the pharmaceutical industry. Not only will you learn skills both technical and professional but work on projects that will contribute towards enhancing people’s lives across the world.
You will be part of a diverse and inclusive, and multi-skilled team of highly motivated individuals. We keep patients at the very heart of all that we do and strive to find solutions and treatments for some of the world’s most challenging healthcare needs.
As a company, we are committed to ‘Inventing for Life’ in all that we do and want you to join us to find new innovative ways to create new solutions, products and strategies we haven’t invented yet.
So, what will you be responsible for?
The Intern, Regulatory CMC APAC will be involved in and responsible for the execution and management of the APAC region submissions including new product registrations and life-cycle submissions to keep our products compliant and available for patients.

In this role you will be working to:

• Generate regulatory strategies
• Assess changes to dossiers in the APAC region
• Liaise with colleagues globally
• Review submission packages

Additionally, you will:

• Work alongside our team to deliver on operational excellence projects
• Work alongside our team in developing best practises for regulatory science
• Learn and apply regulatory policy and advocacy
• Provide ad-hoc support as needed

This internship will be completed in a hybrid model (virtual and/or on-site).
You will be looking to complete a 6 or 12-month placement in your third or penultimate year of study, returning to your course at the end of the placement.

The ideal person will have:

• A minimum of Diploma or BSc in a scientific discipline such as chemistry, biological sciences, engineering, or a related field. Fields of study include (but are not limited to) Pharmacy, Chemical Engineering, Biology, Microbiology, Virology, Molecular Biology, or Biochemistry (or equivalent qualification)
• Fluency in an additional language commonly used in the APAC region is a plus
• Demonstrated analytical skills and detail-oriented

So, if you are ready to:
Invent solutions to meet unmet healthcare needs, Impact the future by driving one of the world’s leading healthcare companies, and inspire your team to reach their full potential and push the boundaries of science and technology, please apply today.
Qualities we look for…

Someone who:

• Communicates, participates and collaborates as one team; winning and losing together
• Focuses on what matters the most to create the greatest value for patients
• Acts with urgency, rigor and determination to enable us to continue to deliver our medicines and vaccines around the world
• Is intellectually curious, adapts and has a commitment to never give up, whether we succeed or fail

Proprietary

• Aligns with and fosters a culture of diversity and inclusion; being part of an inclusive environment where everyone is able to contribute their best ideas
• Encourages curiosity, voices their opinions and engages in healthy debate to improve ideas and decisions to achieve better outcomes

Current Employees apply HERE
Current Contingent Workers apply HERE

REQUIRED SKILLS:

Analytical Problem Solving, Analytical Problem Solving, Applied Engineering, Audits Compliance, Biochemistry, Biological Sciences, Biomedical Sciences, Compliance Investigations, Data Quality Assurance, Detail-Oriented, Diversity and Inclusion (D&I), Documentation Standards, Document Control Systems, Electronic Common Technical Document (eCTD), Immunoassays, Immunochemistry, Immunology, Life Science, Management Process, Mentorship, Microbiology, Operational Excellence, Policy Implementation, Records Retention Management, Regulatory Affairs Compliance {+ 5 more}

• Generate regulatory strategies
• Assess changes to dossiers in the APAC region
• Liaise with colleagues globally
• Review submission package