Total 6 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.

PharmEng Technology has been providing quality services to leading manufacturers of healthcare and pharmaceutical products since 1997. Our specialists hold expertise in Commissioning & Qualification, Validation, Quality Systems, Regulatory Affairs, Engineering, and Training to ensure that our clients can keep on providing the world with their cost-effective and high-standard healthcare products. At PharmEng Technology, we strive to cultivate the best working environment where empowerment, passion and perseverance are nurtured while serving our clients to achieve their unique business goals. We are seeking an experienced Commissioning, Qualification and Validation (CQV) Engineer with experience in pharmaceutical company/Life Science industries for a role in Singapore.

Key Responsibilities:

Documentation & Execution

• Draft, review, and execute Commissioning and Qualification (C&Q) documentation, including Qualification Plans (PLAN/CVPR), Commissioning and Qualification Protocols (CQ), Data Integrity Assessments (DIA), Security Assessments (SA), and Qualification Summary/Completion Reports (QSR/CVSR).
• Ensure all documentation complies with Good Documentation Practices (GDP), GxP, and regulatory guidelines.
• Maintain accurate records of test execution and deviations.

Equipment & Systems Qualification

• Collaborate with Quality Control (QC) Subject Matter Experts (SMEs) to capture and align user requirements for the qualification of new laboratory and production equipment.
• Participate in risk assessments and define qualification strategies in alignment with project and regulatory requirements.

Vendor & Stakeholder Coordination

• Liaise with equipment vendors and service providers to review, assess, and approve vendor-supplied documentation such as Installation and Operational Qualification (IOQ) protocols.
• Coordinate execution of vendor IOQs and support resolution of technical or compliance issues.
• Ensure vendor activities align with site standards and project timelines.

Compliance & Continuous Improvement

• Support deviation management, change control, and CAPA activities related to qualification and commissioning projects.
• Contribute to continuous improvement initiatives to streamline CQV processes and enhance efficiency.
• Ensure adherence to data integrity principles and cybersecurity requirements during system qualification.

Qualifications & Skills:

• Bachelor’s degree in Engineering, Life Sciences, or related discipline.
• Experience in Commissioning, Qualification, and Validation (CQV) in a regulated (GMP) pharmaceutical/biopharma environment.
• Knowledge of regulatory guidelines (FDA, EMA, ICH, ISPE, GAMP 5).
• Strong technical writing, analytical, and problem-solving skills.
• Excellent coordination, communication, and stakeholder management abilities.

Why PharmEng Technology?

Our consultants come from different areas of the Pharmaceutical/Biotech/Medical Device industries and have extensive experiences obtained from world-class organizations in North America, Europe, and Asia. At PharmEng Technology, we value everyone’s unique talents and work together to support our clients. We offer continuous career growth, competitive wages, opportunities for travel and a team mentality that sets us apart from our competitors. It is the growth of our staff that continues to grow our company globally.

EEOC Statement

At PharmEng Technology, we don’t just accept difference — we celebrate it, we support it, and we thrive on it for the benefit of our employees, our clients, and our community. PharmEng Technology is proud to be an equal opportunity workplace.