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Dept: Account & Finance
Company: ALPS Global Holding Berhad
Location: Kuala Lumpur, Malaysia
Employment Type: Full-time
Salary: Competitive, based on experience
Position Overview:
We are seeking a detail-oriented and responsible Data Entry personnel to support the Accounts & Finance Department at ALPS Global Holding Berhad. The ideal candidate will handle the accurate entry of financial transactions, maintain proper records, and ensure data integrity in all accounting documentation. The candidate must possess an LCCI certification and demonstrate basic accounting knowledge.
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Preferred Skills:
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Benefits:
Dept: Globemedic – Business Development
Company: ALPS Globemedic Sdn Bhd (Subsidiary of ALPS Global Holding Berhad)
Location: Kuala Lumpur, Malaysia
Employment Type: Full-time
Salary: Competitive, based on experience
Position Overview:
We are looking for a reliable and detail-oriented Admin cum Account Executive to support the Business Development Department at ALPS Globemedic Sdn Bhd. This position will be responsible for handling administrative tasks and basic accounting functions such as inter-billing, purchase orders, invoicing, payment receipts, and monthly reporting. The ideal candidate should possess good organizational skills, financial accuracy, and a proactive working attitude.
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Dept: Human Resources & Admin
Company: ALPS Global Holding Berhad
Location: Kuala Lumpur, Malaysia
Employment Type: Full-time
Salary: Competitive, based on experience
Position Overview:
We are looking for a friendly, well-organized, and proactive Front Desk cum Admin Executive to serve as the first point of contact for guests and staff while providing essential administrative support to the office. The ideal candidate will ensure smooth day-to-day front desk operations while also assisting in documentation, coordination, and general office support.
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Company: Celestialab Sdn Bhd
Location: Kuala Lumpur, Malaysia
Employment Type: Full-time
Salary: Competitive, based on experience
Position Overview:
We are looking for a QA/QC Executive which is responsible for ensuring all products and processes meet established quality standards and regulatory requirements. This role will focus on maintaining quality assurance protocols, conducting inspections, and collaborating with cross-functional teams to implement corrective and preventive actions.
Key Responsibilities:
Quality Assurance (QA) – Documentation & Compliance:
• Support the development, implementation, and maintenance of the Quality Management
System (QMS) in accordance with CGTP and GMP guidelines.
• Assist in reviewing and controlling documents, SOPs, and quality records.
• Perform internal audits and support external audits and inspections.
• Participate in deviation, CAPA (Corrective and Preventive Action), and change control
processes.
• Conduct routine checks and quality-related activities in cleanrooms and controlled areas.
• Assist in batch record review and product release processes.
• Collaborate with production, QC, and regulatory teams to ensure product and process
compliance.
Quality Control (QC) – Sample Handling & Testing Coordination:
• Coordinate in-process and final product sample collection from the production team.
• Conduct or assist with basic laboratory tests such as cell characterisation, sampling, and
environmental monitoring.
• Maintain lab records and ensure proper labelling, handling, and storage of test samples.
• Calibrate and maintain QC instruments and assist in laboratory housekeeping.
• Work closely with external testing labs (if applicable) to send samples and receive test results.
• Participate in trend analysis and quality monitoring initiatives.
Qualification Requirements:
• Bachelor or Master degree in Biotechnology, Biomedical Sciences, or a related life sciences
field.
• 1–3 years of experience in QA, QC, or GMP-related roles in a pharmaceutical, biotech, or
CGTP environment.
• Familiarity with GMP principles, documentation standards, and regulatory expectations.
• Knowledge of quality standards and frameworks (e.g. GMP, ISO 9001, ISO 13485).
• Good understanding of laboratory practices and basic testing procedures.
• Strong attention to detail, critical thinking, and record-keeping skills.
• Able to work independently, manage tasks efficiently, and communicate effectively with
cross-functional teams.
Preferred Skills:
• Experience in a cell therapy, biologics, or regenerative medicine setting.
• Knowledge of CGTP, PIC/S, or ISO 13485 standards.
• Exposure to cell-based product testing
Why Join Us?
Benefits: