QC Validation Specialist (Equipment Qualification/ Pharma/ Contract)

MANPOWER STAFFING SERVICES (SINGAPORE) PTE LTD; Singapore; On-site; SGD 101,556 - 121,644; Full time

Job summary

MANPOWER STAFFING SERVICES (SINGAPORE) PTE LTD is looking for a QC Validation Specialist to manage laboratory equipment qualification in a leading global biopharmaceutical company. The position requires at least 5 years of experience in GMP environments and a relevant engineering degree.

You will be responsible for performing equipment qualification, providing expert guidance, and optimizing processes. A competitive salary of up to $10,000 is offered, depending on experience.

Qualifications

• At least 5 years of experience in qualification and lifecycle management of GMP Lab equipment.
• Experience in a GMP environment within pharmaceutical/chemical manufacturing.

Responsibilities

• Perform and review qualification and lifecycle management for laboratory equipment.
• Act as Subject-Matter-Expert for lab system lifecycle.
• Lead root cause analysis and implement corrective actions.

Skills

Qualification of laboratory equipment

Problem-solving

GMP compliance

Education

Diploma or bachelor’s degree in chemical engineering or relevant field

Tools

UV-Vis Spectrometer

TOC Analyzer

HPLC

Job description

Overview

QC Validation Specialist (Equipment Qualification/ Pharma/ Contract)

Duration: 6 months

Location: Tuas

Salary: Up to $10,000 depending on experience

Our client is a US healthcare and a leading global biopharmaceutical company. They have more than 69,000 employees across 140 countries with a heritage of more than 125 years. Their global supply strategy relies on manufacturing capabilities and expertise to achieve this mission.

Responsibilities

• Perform/review system qualification, requalification, relocation, decommissioning and retirement for laboratory equipment in accordance with approved procedures and standard lead time.
• Assume role of Subject-Matter-Expert of laboratory system lifecycle, collaborates closely with cross-functional teams and above-site functions. This includes initiating alignments proactively, sharing expertise, and providing input to ensure alignment and consistency across the organization.
• Author/review Quality Notifications and Test Exception Reports, lead root cause analysis and ensure effective implementation of related actions within the agreed timeframe.
• Conduct troubleshooting of laboratory system lifecycle, identifying and resolving any issues that may impact the business/work efficiency and compliance.
• Identify opportunities and propose solutions to improve efficiency and compliance in processes, standards, and best practices within the team.
• Provide leadership, expert guidance and support to team members, acting as a go-to resource for problem-solving and decision-making.
• Provide skills training to other team members, ensuring they have the necessary knowledge and competencies to perform their duties effectively.
• Any other duties as assigned by reporting manager.

Requirements

• Diploma or bachelor’s degree in chemical engineering or any other relevant engineering field
• At least 5 years of experience in qualification, requalification, relocation, decommissioning and retirement of Good Manufacturing Practice (GMP) Lab equipment (not limited to Ultraviolet–Visible (UV-Vis) Spectrometer, Total Organic Carbon (TOC) Analyzer, Microplate Reader, Liquid Particle Counter, Capillary Electrophoresis (CE), High-Performance Liquid Chromatography (HPLC), Analytical Balances, Incubators, Particle Counters)
• Experience in GMP environment within the pharmaceutical/chemical manufacturing.

Lim Pey Chyi – [e-mail]

Recruitment Consultant (R2090579)

Manpower Staffing Services (S) Pte Ltd

EA Licence: 02C3423