Analytical Support Officer (1 year contract) | UK Pharma | West

GMP Technologies; Singapore; On-site; SGD 40,000 - 60,000; Full time

Job summary

A healthcare technology company in Singapore seeks an Analytical Support Officer for a 1-year contract. The role involves maintaining analytical equipment, conducting validations, leading investigations, and ensuring compliance with regulatory standards. Candidates with a Science degree and knowledge of GMP and laboratory techniques are preferred, while those without experience will also be considered. The position includes training laboratory staff and ensuring a safe work environment.

Qualifications

• Min. Science degree holder with experience in Chemical, Pharma or Manufacturing.
• Knowledge in GMP and laboratory equipment/validation.
• Familiar with regulatory expectations/CAP/ICH requirements.

Responsibilities

• Maintain and calibrate analytical equipment in accordance with site procedures.
• Lead investigations from laboratory equipment events and propose effective CAPA.
• Conduct training for laboratory staff on equipment and procedures.
• Ensure a safe working environment in the laboratory.

Skills

Knowledge of GMP

Laboratory techniques

Regulatory compliance

Analytical equipment knowledge

Education

Min. Science degree

Job description

Analytical Support Officer (1 year contract) | UK Pharma | West

• Ensure that analytical equipment are maintained and calibrated accurately and timely in accordance to site procedures, CAP and regulatory requirements.
• Lead and/or participate in investigations arising from laboratory equipment/computer systems events and effective CAPA to minimize reoccurrence.
• Perform periodic validation review of systems /laboratory equipment in a timely manner to ensure that the validation status is maintained, and make recommendations for re-validation as required.
• Lead or participate in laboratory equipment validation in accordance to site procedures and regulatory requirements, inclusive of writing, reviewing and approval of validation related documentation.
• Maintain and support computer systems and laboratory equipment according to site change control and access control procedures.
• Perform accurate and thorough impact assessment on laboratory equipment, systems change control to ensure all impacted areas are adequately assessed and impacted documentation are updated in a timely manner.
• Revise, review and maintain laboratory procedures, instructions, methods to ensure compliance with regulatory, QMS, CAP and pharmacopoeia.
• Ensure a safe working environment in the laboratory and perform 6S inspection.
• Supervise, develop and motivate team members and other assigned staff to help realize their maximum potential so as to contribute towards achieving the objectives of the department.
• Conduct effective training for laboratory staff on computer systems/equipment and relevant procedures.
• Ensure regulatory compliance, perform Level 1 audit and support L2 / L3 / L4 audits.
• Ensure timeliness and accuracy of Pharmacopoeia & CAP review.

Requirement

• Min. Science degree holder with experience in the field of Chemical, Pharma or Manufacturing industry
• Good knowledge of GMP and laboratory equipment/validation
• Good knowledge of quality, laboratory techniques and laboratory compliance
• Good knowledge of regulatory expectations /CAP/ICH requirements
• Good knowledge of analytical equipment capabilities and operational needs
• Candidates with no prior experience will be considered

To find out more about this opportunity, please contact Fiona Koh

We regret that only shortlisted candidates will be notified.