Commissioning & Qualification Planner (3 months/PHARMA MNC) - North/up to $6k #HAO

Recruit Express; Singapore; On-site; SGD 80,000 - 100,000; Full time

Job summary

A leading recruitment agency is seeking a candidate for a role focused on developing and maintaining C&Q schedules in a pharmaceutical environment. The ideal candidate should have a degree in Engineering and at least 3 years of experience in pharma manufacturing with familiarity in relevant validation documentation. This position is based in Kranji, Singapore, and offers a competitive salary up to $6000.

Qualifications

• Minimum 3 years of relevant experience in pharma manufacturing or engineering projects with GMP compliance.
• Experience with URS, DQ, IQ, OQ, PQ documentation.

Responsibilities

• Develop and maintain detailed C&Q schedules aligned with project timelines.
• Monitor progress and implement mitigation strategies for schedule risks.
• Support audits and inspections with schedule-related documentation.

Skills

Familiarity with validation documentation

Project planning tools (e.g., MS Project)

Collaboration with engineering and QA teams

Risk management

Education

Min Degree in Engineering or similar

Job description

Salary: up to $6000

Duration: 3 months

Working Days & Hours: Mon-Fri Office Hours

Location: Kranji

Job Description

• Develop and maintain detailed C&Q schedules using project planning tools (e.g., MS Project), aligned with overall project timelines.
• Collaborate with engineering, validation, QA, QC, and operations teams to plan and sequence commissioning and qualification activities.
• Monitor progress, identify schedule risks, and implement mitigation strategies to ensure timely delivery of C&Q milestones.
• Support the development and execution of C&Q strategies, including URS, DQ, IQ, OQ, and PQ documentation and activities.
• Ensure C&Q activities comply with GMP, FDA, EMA, and other applicable regulatory standards.
• Facilitate planning meetings, progress reviews, and reporting to project stakeholders.
• Coordinate resource planning and availability for C&Q tasks, including vendor and contractor support.
• Maintain accurate documentation and change control records related to C&Q scope.
• Support audits and inspections by providing schedule-related documentation and insights.

Job Requirements

Min Degree in Engineering or similar w min 3 yrs of relevant experience working in pharma manufacturing or engineering projects with GMP compliance.

• Familiarity with validation documentation like URS, DQ, IQ, OQ, PQ.

Interested candidates, please submit your resume to: [e-mail]

Ally Audrey Lok Xin Woon

Recruit Express Pte Ltd (Healthcare & Lifescience)

Company EA Licence number : 99C4599

Personnel EA License: R21102307

[e-mail]