Intern

2 weeks ago

Tuas West Region, Singapore Lonza Full time $30,000 - $60,000 per year

Singapore, Tuas Singapore

Lonza is the pioneer and world leader in the CDMO industry operating across 5 continents, setting the pace with cutting-edge science, smart technology and lean manufacturing. We turn our customers' break-through innovations into viable therapies and manufacture the medicines of tomorrow. At the heart of every scientific breakthrough are talented individuals collaborating to develop solutions that empower businesses to improve lives. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that's the kind of work we want to be part of.

Join our best-in-class high performance Integrated Biologics team at our Tuas site in Singapore to gain unparalleled exposure to cutting-edge biotechnology and innovation, and make a difference from day one. Learn new skills and capabilities, and grow your career with us in manufacturing therapeutic proteins under cGMP conditions. Find out more about what a life at Lonza in Singapore could look like for you by watching this short video.

We are currently looking for an intern to join us at our location in Singapore Tuas. As an Intern you will have the opportunity to gain valuable hands-on experience in pharmaceutical manufacturing and supporting the team (Manufacturing/Quality Assurance/Quality Control/Development Services/ Manufacturing Science and Technology (MSAT)) in day-to-day operations.

Your Key Responsibilities

  • Process Learning:

  • Learn and understand the principles and processes involved in fill and finish operations for pharmaceutical products.

  • Quality Compliance:

  • Ensure strict adherence to cGMP (current Good Manufacturing Practices) and safety regulations in all activities.

  • Documentation:

  • Participate to the development of the standard working procedures of the related activities in compliance with company policies.

  • Problem-Solving:

  • Collaborate with team members to identify and troubleshoot process-related issues.

Supervision And Development

  • Receive daily supervision for routine work and step-by-step guidance on new tasks.
  • Provide support in task organization and documentation.
  • Receive coaching on process flow within a cGMP manufacturing environment.
  • Be encouraged to develop problem-solving and decision-making skills with appropriate guidance.

Requirements

  • Currently pursuing a degree in biomedical science, pharmaceutical science, biotechnology, chemical engineering or a related field.
  • Strong analytical and problem-solving skills.
  • Excellent communication and interpersonal skills.
  • Ability to work independently and as part of a team.
  • Proficient in Microsoft Office Suite and other relevant software.
  • A passion and desire to learn new things.

Every day, Lonza's products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically.

People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference.

Reference: R70855

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