Summer Intern 2022 – Manufacturing Operations Fill Finish
Seqirus is one of the largest influenza vaccine providers in the world. Seqirus is a major contributor to the prevention of influenza globally and a transcontinental partner in pandemic preparedness. As the only vaccine company with a singular global focus on influenza, we work tirelessly on cutting-edge research, transformative technologies and the latest methods of production and distribution. Together with our partners we’re on the front line every day, helping to protect communities from seasonal influenza and global pandemic threats. When you join Seqirus, you join a skilled and passionate team dedicated to protecting people and communities from influenza. It's the feeling of purpose and possibility that inspires us every day.
Program Experience
Seqirus’ Internship Program is a hands-on experience that showcases the daily innovation and operations of a leading biotechnology company. Our environment is collaborative, global, and purpose-driven. The 12-week intern experience will immerse students in meaningful, thought-provoking projects that contribute to CSL's promise to save lives and protect the health of people around the world. In addition to making an impact, students will be developed personally and professionally while cultivating meaningful relationships. As an intern, you will have the opportunity to participate in leadership & development seminars, a structured mentorship program, community service, and team-building activities designed specifically for you.
Main Responsibilities
Seeking an intern to assist with batch record review to support the Fill Finish area of the Holly Springs, North Carolina Manufacturing site. Intern would get exposure to work with GMP systems such as SAP and EDMS as part of this process. Exposure to the manufacturing process and people as well as interfacing with the Front-Line QA personnel will also be part of this role. By the end of the internship the intern will have a greater understanding of working in a GMP environment and utilizing Good Documentation Practices that will set a foundation for work in any GMP environment.
- Work with the Manufacturing and Quality teams to complete batch record review
- Utilize SAP and EDMS in completion of batch record review
- Observe and learn about different types of manufacturing production from the manufacturing team.
- Utilize quality learning system to maintain training.
Strategic impact and learning opportunities for the Intern:
- Gain experience and complete batch record reviews.
- Gain experience in utilizing GMP systems (EDMS, SAP, etc.)
- Gain experience in a GMP manufacturing environment.
- Gain experience in interfacing with MFG and QA personnel.
- Gain experience with good documentation practices.
- Gain experience with managing schedule adherence.
- Gain experience utilizing quality learning systems to train on processes and documentation.
Qualifications
- Enrolled in a 4-Year University with progression toward an Undergraduate degree
- Biomanufacturing focus preferred
- Graduation years: 2023, 2024
- Excellent communication and presentation skills
- Must have the ability to work well with all levels of the organization
- A self-starter able to manage multiple priorities
- Keen on knowing when to work independently and collaboratively