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Lonza

Trainee, Quality Systems

Posted 7 Days Ago
Be an Early Applicant
Singapore
Entry level
Singapore
Entry level
The QA Trainee will support Quality Assurance activities in a cGxP contract manufacturing facility, manage GMP documents, analyze data, and provide compliance support while demonstrating teamwork and problem-solving skills.
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Today, Lonza is a global leader in life sciences operating across five continents. While we work in science, there’s no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. 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. 

Did you know that we are the 1st biologics contract manufacturer in Singapore? We offer you exposure to upcoming biotech and established pharmaceutical companies and to the manufacturing technology needed to produce mammalian treatments and cell therapies of tomorrow. Our global manufacturing network is recognized for its reliable, high-quality services, regulatory track record, global footprint, innovative technology platforms and extensive experience – we, in Singapore are proud to be part of this global network. 

The QA Trainee will support day-to-day Quality Assurance activities in accordance to the respective Quality Areas. 

Job Scopes

  • Support day-to-day Quality Assurance activities in accordance with approved

SOPs / Policies for a multi-product, cGxP contract manufacturing facility

  • Display a good level of problem solving ability by analyzing and interpreting

data and puts forward new ideas based on scientific knowledge or field experience

  • Detect non-compliance with cGxP and cGDP requirements and provide guidance on GDP corrections
  • Generally provide basic compliance support to staff in all departments
  • Demonstrate appropriate interpersonal skills that encourage collaboration of

individuals or teams to meet objectives

  • Management of GMP document lifecycle in Documentation Management System including archiving and inactive records
  • Issuance of controlled documents (e.g Batch records and Logbooks)
  • Uphold data integrity principle in accordance to Lonza policies. Proactively

evaluate, identify and improve data integrity process.

  • Any other tasks as and when assigned by Supervisor

Requirements

  • Diploma/ Degree in relevant science discipline (Biotechnology, Pharmaceutical Sciences, Biomedical Engineering etc.)
  • Strong interpersonal skills
  • Effective verbal and written communication skills
  • Meticulous eye for detail
  • Systematic
  • Analytical Skills
  • Positive team player

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.

Top Skills

Documentation Management System

Lonza Singapore Office

35 Tuas South Ave 6, Singapore, 637377

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