The posting
📍 Location: Tuas 💰 Salary: Up to $3800 📅 Working Days: Monday – Friday 🕘 Working Hours: 8am- 5pm
Job Responsibilities:
- Perform assigned operational tasks in accordance with Good
- Manufacturing Practices (GMP) and standard operating procedures
- (SOPs).
- Identify and report any deviations, non-conformances, or safety
- concerns in a timely manner.
- Support documentation activities such as data entry, reviewing of
- documents, submission of forms and other documentation
- management activities
- Assist in routine housekeeping, cleaning, and 6S activities to
- maintain a compliant and safe work environment.
- Participate in training as required for the tasks assigned.
- Handle materials, components, or equipment as per procedures and
- safety guidelines.
- Uphold data integrity principle in accordance to Lonza policies.
- Communicate effectively with team members, supervisors, and
- cross-functional personnel.
- Maintain confidentiality and integrity of company data and
- operations.
- Any other tasks as and when assigned by supervisor
Requirements:
- Bachelor's Degree in Engineering, Chemistry, Pharmaceutical Science, Life Sciences or a related discipline.
- Relevant experience in Quality Assurance (QA), manufacturing operations or pharmaceutical/medical device environments preferred.
- Knowledge of GMP, quality systems and regulatory compliance will be an advantage.



