Total 5 job vacancies by Pharmeng Technology Pte. Ltd.

We are looking for a reliable and detail-oriented Manufacturing Technician to support pharmaceutical production operations. The role involves operating equipment, maintaining compliance with regulatory standards, and ensuring efficient manufacturing processes.

Key Responsibilities:

• Operate, monitor, and maintain manufacturing equipment in accordance with SOPs
• Assist in equipment setup, cleaning, and changeovers
• Accurately document production activities and batch records
• Follow Good Manufacturing Practices (GMP) and safety procedures
• Identify and report deviations, equipment malfunctions, and process issues
• Collaborate with cross-functional teams to meet production targets

Qualifications:

• ITE/Diploma graduates.
• 1–2 years of experience in pharmaceutical or manufacturing industry
• Basic knowledge of GMP and pharmaceutical production processes
• Strong attention to detail and organizational skills
• Willing to work in shifting schedules

Preferred Skills:

• Familiarity with production documentation and compliance requirements
• Problem-solving and analytical skills
• Good communication and teamwork abilities

We are seeking a detail-oriented and highly organized QC Sampler responsible for collecting and handling samples to ensure product quality and compliance with regulatory standards.

Key Responsibilities:

• Perform sampling of raw materials, in-process products, and finished goods
• Ensure sampling procedures comply with GMP and company standards
• Properly label, store, and transport samples
• Maintain accurate and complete sampling records
• Coordinate with QC laboratory and production teams
• Report any discrepancies or contamination risks

Qualifications:

• ITE/Diploma graduates.
• 1–2 years of experience in quality control, laboratory, or pharmaceutical environment
• Knowledge of Good Manufacturing Practices (GMP)
• Strong attention to detail and documentation skills
• Willing to work in a controlled/cleanroom environment and shifting schedules

Preferred Skills:

• Understanding of laboratory and sampling procedures
• Strong organizational and time management skills
• Good communication and teamwork abilities

We are seeking a skilled CSV Expert to support client projects in validating computerized systems within GMP-regulated environments.The role involves ensuring systems meet regulatory standards and industry best practices for compliance and data integrity.

Key Responsibilities

• Plan, execute, and document computer system validation activities
• Develop validation documentation
• Ensure compliance with regulatory requirements
• Support audits, data integrity reviews, and system qualification activities
• Collaborate with IT, QA, and business teams on system implementation and validation
• Identify risks and propose mitigation strategies for validated systems
• Provide technical guidance and mentorship where applicable

Qualifications

• Degree in Life Sciences, Engineering, IT, or related field
• Relevant experience in CSV within regulated industries
• Knowledge of GxP regulations, validation lifecycle, and data integrity principles
• Strong documentation, communication, and analytical skills

Only shortlisted candidates will be contacted. We appreciate your interest and look forward to reviewing your application.

We are looking for a Team Lead (Biomanufacturing) to support client projects and lead teams in GMP-regulated environments. This role combines technical expertise with team leadership and client interaction.

Key Responsibilities

• Lead and support biomanufacturing activities for client projects
• Provide technical guidance on bioprocessing and manufacturing operations
• Manage and mentor team members
• Ensure project deliverables meet quality and regulatory standards
• Collaborate with clients and internal teams
• Support documentation and compliance with GMP requirements

Qualifications

• Degree in Engineering, Life Sciences, or related field
• Experience in biomanufacturing or biopharmaceutical industry
• Basic leadership or team coordination experience
• Knowledge of GMP standards
• Good communication and organizational skills

Only shortlisted candidates will be contacted. We appreciate your interest and look forward to reviewing your application.

We are seeking a skilled Quality, Laboratory, or Operations Expert to support client projects in GMP-regulated environment. The role involves ensuring compliance, optimizing processes, and contributing technical expertise to client operations.

Key Responsibilities

• Support quality management systems, lab operations, or manufacturing processes
• Ensure compliance with GMP, GLP, and regulatory standards
• Prepare, review, and maintain SOPs, batch records, protocols, and reports
• Conduct audits, inspections, and risk assessments as needed
• Collaborate with cross-functional teams and client stakeholders
• Identify opportunities for process improvement and operational efficiency
• Provide technical guidance and mentorship where applicable

Qualifications

• Degree in Life Sciences, Pharmacy, Chemistry, or Engineering, depending on focus
• Relevant experience in quality assurance, laboratory, or manufacturing operations
• Knowledge of GMP, regulatory compliance, and industry best practices
• Strong communication, organizational, and analytical skills

Only shortlisted candidates will be contacted. We appreciate your interest and look forward to reviewing your application.