Biotechnologist, MFG (CGT)

Lonza; Singapore; Presencial; SGD 42 000 - 64 000; Tempo integral

Vantagens oferecidas por esta oferta de emprego

Daily bus service to Tuas site

Fully paid medical insurance with some

Shift allowances

Learning and development opportunities

Resumo da oferta

Lonza in Singapore's Tuas site is seeking a hands-on manufacturing associate to contribute to cGMP operations and aseptic processing in a dynamic biopharmaceutical environment.

You will work across batch record review, environmental monitoring and routine production support, using DMS, LIMS and TrackWise to ensure data integrity and compliance. A rotating 12‑hour shift and continuous learning opportunities are offered.

Qualificações

• Degree or equivalent qualification in Biotechnology, Biochemistry, Life Sciences, Engineering or a related discipline.
• Knowledge of biopharmaceutical manufacturing, aseptic processing or cleanroom operations is an advantage.
• Basic understanding of cGMP principles, quality requirements and data integrity practices.
• Willingness to work in a cleanroom environment and perform rotating 12-hour shifts.

Responsabilidades

• Perform cGMP manufacturing activities in accordance with aseptic techniques, cleanroom practices and approved procedures.
• Complete and review Batch Records, logbooks and GMP documentation accurately and on time, ensuring data integrity.
• Perform environmental monitoring and routine production support activities, including equipment cleaning and housekeeping.
• Operate electronic systems such as DMS, LIMS and TrackWise to support manufacturing and quality activities.
• Identify and upscale deviations, equipment alarms and other non-routine events in accordance with site procedures.
• Maintain training compliance and support assigned quality activities, including CAPAs and documentation updates.
• Participate in continuous improvement initiatives to enhance safety, quality and manufacturing efficiency.

Conhecimentos

Strong communication

Teamwork

Shift flexibility

Electronic systems familiarity

Formação académica

Biotech/Life Sciences degree or equivalent

Ferramentas

DMS

LIMS

TrackWise

Descrição da oferta de emprego

Join Lonza's Cell & Gene Therapy team and contribute to manufacturing innovative therapies that make a meaningful difference to patients. Based at our Tuas site, you will gain hands‑on experience in cGMP manufacturing, aseptic processing and cleanroom operations while developing your technical capabilities in a dynamic biopharmaceutical environment.

What you will get

• An agile career and dynamic working culture.
• An inclusive and ethical workplace.
• Compensation programs that recognize high performance.
• Daily company bus services from designated MRT locations to and from our Tuas site.
• Fully paid medical insurance, with family coverage available at partially subsidized premiums.
• Shift allowances and ongoing learning and development opportunities.
• Perform cGMP manufacturing activities in accordance with aseptic techniques, cleanroom practices and approved procedures.
• Complete and review Batch Records, logbooks and GMP documentation accurately and on time, ensuring data integrity.
• Perform environmental monitoring and routine production support activities, including equipment cleaning and housekeeping.
• Operate electronic systems such as DMS, LIMS and TrackWise to support manufacturing and quality activities.
• Identify and upscale deviations, equipment alarms and other non-routine events in accordance with site procedures.
• Maintain training compliance and support assigned quality activities, including CAPAs and documentation updates.
• Participate in continuous improvement initiatives to enhance safety, quality and manufacturing efficiency.

What we are looking for

• Degree or equivalent qualification or experience in Biotechnology, Biochemistry, Life Sciences, Engineering or a related discipline.
• Candidates with relevant academic or technical training are encouraged to apply; prior industry experience is not essential.
• Knowledge of biopharmaceutical manufacturing, aseptic processing or cleanroom operations is an advantage.
• Basic understanding of cGMP principles, quality requirements and data integrity practices.
• Ability to learn and use electronic manufacturing, laboratory and quality systems.
• Strong communication and interpersonal skills with a collaborative, proactive and team-oriented approach.
• Willingness to work in a cleanroom environment and perform a rotating 12-hour shift pattern.

About Lonza

At Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together. Everyone's ideas, big or small, have the potential to improve millions of lives, and that's the kind of work we want you to be part of.

Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we value diversity and are committed to creating an inclusive environment for all employees. If you're ready to help turn our customers' breakthrough ideas into viable therapies, we look forward to welcoming you on board.

• Take ownership, step forward, and enjoy meaningful responsibility
• Love solving problems and thrive in a complex, fast-moving environment
• Are curious, always looking to learn and improve
• Work collaboratively, contributing to something bigger than yourself
• Are motivated to make a difference through work that impacts customers and their patients

Why Lonza:

We are a place of unique opportunity, where your ideas, expertise and ambition can make a real difference. Here, will have the freedom to grow, the support to succeed and the chance to contribute to work that matters.

We are the makers of the medicines of tomorrow.