Analytical Support Officer (18 months contract) | UK Pharma | West

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

Job summary

A leading pharmaceutical company in Singapore is seeking an Analytical Support Officer for an 18-month contract. You will ensure the timely calibration and maintenance of analytical equipment, lead investigations, and support laboratory compliance with regulatory requirements. A Science degree is required, but candidates without prior experience will also be considered. This position offers an opportunity to supervise and develop staff while ensuring a safe working environment.

Qualifications

• Min. Science degree holder with experience in the field of Chemical, Pharma or Manufacturing industry.
• Good knowledge of GMP and laboratory equipment/validation.
• Candidates with no prior experience will be considered.

Responsibilities

• Ensure analytical equipment is maintained and calibrated.
• Lead investigations from laboratory equipment events.
• Perform periodic validation review of systems/laboratory equipment.
• Ensure a safe working environment in the laboratory.

Skills

Good knowledge of GMP

Laboratory techniques

Regulatory expectations

Analytical equipment knowledge

Education

Science degree

Job description

Analytical Support Officer (18 months contract) | UK Pharma | West

Responsibilities

• 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 propose 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 documentations
• 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

Requirements

• 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.