Lead Engineer, Validation

LONZA BIOLOGICS TUAS PTE. LTD.; Singapore; On-site; Confidential; Full time

Benefits offered by this job

Medical insurance

Family coverage options

Job summary

Lonza Singapore is seeking a skilled Validation Engineer to ensure that our manufacturing facilities, systems, and equipment meet the highest quality and compliance standards in a GMP biotech environment. You will contribute to the safe and reliable manufacture of life-changing medicines and collaborate across engineering, quality, and operations teams.

You will be responsible for supporting validation activities, developing protocols, reviewing documentation, and helping prepare for

Qualifications

• A bachelor’s degree in an engineering discipline or a related field.
• Experience or exposure to validation activities in a GMP manufacturing environment.
• Understanding of regulatory expectations and validation principles.
• Ability to collaborate effectively across engineering, quality, and operations teams.
• Clear written and verbal communication skills.
• A proactive mindset with attention to detail and quality.
• Willingness to learn, adapt, and grow in a regulated biotech environment.

Responsibilities

• Support validation activities for facilities, equipment, utilities, computer systems, cleaning, and sterilization.
• Develop and execute validation protocols and reports in line with approved procedures.
• Collaborate with engineering, quality, and end users to deliver validation activities as planned.
• Support commissioning activities and site change implementations when required.
• Review engineering documentation related to commissioning and validation activities.
• Participate in site validation maintenance programs and inspection readiness activities.
• Uphold data integrity principles and identify opportunities for continuous improvement.

Skills

GMP experience

Engineering degree

Regulatory knowledge

Cross-functional collaboration

Communication skills

Attention to detail

Willingness to learn

Education

Bachelor's degree in engineering

Job description

Job Description

At Lonza Singapore, you will play a key role in ensuring that our manufacturing facilities, systems, and equipment meet the highest standards of quality and compliance. This is an exciting opportunity to contribute to a GMP biotech environment where your work supports the safe and reliable manufacture of life-changing medicines.

What you will get:

• An agile career with opportunities to grow your validation and engineering expertise.

• An inclusive, ethical, and safety-first workplace.

• A dynamic site environment supporting advanced biotech manufacturing.

• Collaboration with experienced engineering, quality, and operations teams.

• Compensation programs that recognize performance and contribution.

• Fully paid medical insurance, with options to enroll family members at subsidized rates.
  

What you will do:

• Support validation activities for facilities, equipment, utilities, computer systems, cleaning, and sterilization.

• Develop and execute validation protocols and reports in line with approved procedures.

• Collaborate with engineering, quality, and end users to deliver validation activities as planned.

• Support commissioning activities and site change implementations when required.

• Review engineering documentation related to commissioning and validation activities.

• Participate in site validation maintenance programs and inspection readiness activities.

• Uphold data integrity principles and identify opportunities for continuous improvement.

What we are looking for:

• A bachelor’s degree in an engineering discipline or a related field.

• Experience or exposure to validation activities in a GMP manufacturing environment.

• Understanding of regulatory expectations and validation principles.

• Ability to collaborate effectively across engineering, quality, and operations teams.

• Clear written and verbal communication skills.

• A proactive mindset with attention to detail and quality.

• Willingness to learn, adapt, and grow in a regulated biotech environment.

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.