GMP QC & Documentation Specialist

No-Deviation-Pte.-Ltd; Singapore; On-site; SGD 31,000 - 50,000; Full time

Benefits offered by this job

Generous leave

Health & wellness coverage

Professional development

Inclusive culture

Career growth

Job summary

No deviation is seeking a detail-oriented operations team member to perform GMP-compliant tasks and support documentation, housekeeping, and data integrity across the site. The role emphasizes meticulous adherence to SOPs to maintain a compliant and efficient work environment.

Applicants should have a Diploma or higher in a relevant science or engineering field, with GMP experience preferred, and be willing to work shifts if required.

Qualifications

• Diploma or higher in a relevant science, engineering, or related discipline.
• GMP-regulated manufacturing experience preferred.
• Familiarity with SOPs, documentation practices, and data integrity.
• Good communication and teamwork skills.
• Willingness to work shifts, if required.
• Meticulous, safety-conscious, and able to follow procedures accurately.

Responsibilities

• Perform GMP/SOP-compliant operational tasks.
• Identify deviations, non-conformances, or safety concerns promptly.
• Support data entry, review, and form submissions.
• Assist in housekeeping and 6S activities.
• Participate in required training.
• Handle materials and equipment per procedures and safety guidelines.
• Maintain data confidentiality and integrity.
• Communicate effectively with team and supervisors.
• Perform other tasks as assigned by supervisor.

Skills

GMP experience

Documentation practices

Data integrity

Communication

Teamwork

Shift work

Education

Diploma or higher in science/engineering

Job description

No deviation is seeking a detail-oriented operations team member to perform GMP-compliant tasks and support documentation, housekeeping, and data integrity across the site. The role emphasizes meticulous adherence to SOPs to maintain a compliant and efficient work environment.

Applicants should have a Diploma or higher in a relevant science or engineering field, with GMP experience preferred, and be willing to work shifts if required.