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

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

Job summary

UK Pharma in the West region is seeking an Analytical Support Officer for an 18-month contract. The role focuses on maintaining calibrated analytical equipment, leading investigations, and ensuring regulatory compliance in a GMP environment.

You will lead validation activities, manage change controls, train staff, and support internal audits while upholding quality and safety standards in a lab setting.

Qualifications

• Min. Science degree holder with experience in 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.

Responsibilities

• Ensure analytical equipment are maintained and calibrated per site procedures and regulatory requirements.
• Lead/participate in investigations from laboratory equipment/system events and propose CAPA.
• Perform periodic validation review of systems/lab equipment and recommend re-validation.
• Lead/participate in equipment validation and approve related documents.
• Maintain and support computer systems and equipment per change control procedures.
• Assess impact of changes on laboratory equipment and documentation.
• Revise and maintain laboratory procedures to ensure compliance.
• Ensure a safe lab environment and perform 6S inspections.
• Supervise, develop and motivate staff; conduct training on systems/equipment.
• Ensure regulatory compliance, perform audits.

Skills

GMP knowledge

Lab equipment validation

Quality systems

Education

Science degree

Job description

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

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

About the job Analytical Support Officer (18 months 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 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

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.

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