Total 5 job vacancies by Pm Asia Project Services Pte. Ltd.

Due to current demand, PM Group is currently looking to expand the CQV team.

Your day to day role would involve the following activities:

• Planning, Performance, and Coordination of Computer System Validation, Equipment Qualification, Temperature Controlled Objects (Freezers, Incubator etc), Clean Utilities Validation and cleaning validation in accordance with internal procedures and industry standards.
• The qualification includes, FAT, SAT, IQ, OQ, PQ of any additional / modifications of existing manufacturing process equipment, package units (e.g. Ultrafiltration Unit, Chromatography Columns, autoclave, FIT testers), commercial off the shelves (COTS) analytical instruments, freezers,
• Experience to creates, reviews and approve equipment qualification and analytical instruments lifecycle documentations, e.g. FAT, SAT, IQ, OQ, PQ protocols and reports, risk assessments, technical specifications.
• Can lead investigation revolving around discrepancies identified during qualification activities.

We would like to hear from candidates who have:

• Experience in coordinating the commissioning and qualification activities (including the creation, pre-execution approval, execution, post-execution review, and post-execution approval of all validation lifecycle documents)
• Experience in leading daily validation meetings with cross functional in resolving validation issues.
• Experience in equipment qualification including analytical instrumentation and manufacturing equipment.
• Experience in ASTM2500 of process equipment commissioning and qualification (Ultrafiltration units and chromatography column is preferred)
• Relevant work experience in Pharmaceutical and/or Biopharmaceutical industries
• Hands on validation execution experience
• Review validation documents
• Write validation protocols and reports
• Able to execute activities in cGMP environment, including cleanrooms or technical areas.
• Attention to detail

As a MEP Engineer, your day to day role would involve, but would not be limited to the following activities:

• Ownership of equipment modules and packages through design and procurement phases
• Generation of Data Sheets, Material Requisitions & Enquiry Packages for procurement of equipment
• Generation of Technical Bid Tab Evaluation of vendors in compliance with Client specifications
• Developing Technical Specifications in compliance with Client requirements
• Development of each package through Kick-off meetings, Design Reviews, FAT’s etc.
• Project manage Suppliers to ensure packages are designed, manufactured and tested as per project requirements
• Interfacing with clients, vendors, client project management and other disciplines ensuring the highest level of service is provided
• Interfacing with client design team/end users
• Delivery of agreed design scope within budget hours and schedule
• Ensuring all systems meet local building codes, safety regulations, and energy efficiency standards.

Requirements

• Degree in Mechanical Engineering
• Min 5 years of relevant work experience in the pharmaceutical and/or biotech companies
• Excellent verbal and written communication skills
• Ability to work on own initiative and in a team environment
• Ability to produce accurate work to agreed time schedules

We have an immediate requirement for a Senior Project Engineer, who can support the Project Manager in fit-out projects.

Some of the key attributes that we are looking for:

• Handle all aspects of the Project Execution from URS Design review to commissioning and handover.
• Foresee potential challenges and address them before issues arise
• Unblock the routine obstacles that inevitably occur on fast-track projects.
• Participate in site walkdowns
• Ensure compliance with engineering, EHS and GMP work standards

Requirements

• Min 8 years of project management experience
• Strong technical knowledge coupled with hands-on working experience in a pharmaceutical / biotech facility/ food & beverage manufacturing sectors would be an advantage
• Vast knowledge of all local legal issues, permits, and building codes involved

Due to current demand, PM Group is currently looking to expand the CQV capabilities. This role will be supporting one of our many pharmaceutical clients in the field of commissioning, qualification and validation work.

Your day to day role would involve the following activities:

• Planning, Performance, and Coordination of Computer System Validation, Equipment Qualification, Temperature Controlled Objects (Freezers, Incubator etc), Clean Utilities Validation and cleaning validation in accordance with internal procedures and industry standards.
• The qualification includes, FAT, SAT, IQ, OQ, PQ of any additional / modifications of existing manufacturing process equipment, package units (e.g. Ultrafiltration Unit, Chromatography Columns, autoclave, FIT testers), commercial off the shelves (COTS) analytical instruments, freezers,
• Experience to creates, reviews and approve equipment qualification and analytical instruments lifecycle documentations, e.g. FAT, SAT, IQ, OQ, PQ protocols and reports, risk assessments, technical specifications.
• Can lead investigation revolving around discrepancies identified during qualification activities.

We would like to hear from candidates who have:

• Experience in coordinating the commissioning and qualification activities (including the creation, pre-execution approval, execution, post-execution review, and post-execution approval of all validation lifecycle documents)
• Experience in leading daily validation meetings with cross functional in resolving validation issues.
• Experience in equipment qualification including analytical instrumentation and manufacturing equipment.
• Experience in ASTM2500 of process equipment commissioning and qualification (Ultrafiltration units and chromatography column is preferred)
• Relevant work experience in Pharmaceutical, BioPharma or Food industries
• Hands on validation execution experience
• Review validation documents
• Write validation protocols and reports
• Able to execute activities in cGMP environment, including cleanrooms or technical areas.
• Attention to detail

We are currently looking for an Electrical Design Engineer who can provide support for multiple projects in Singapore.

Your day-to-day role would involve the following activities:

• Design / Engineering Electrical Systems including High, Medium and Low voltage system, IT system and Designing Fire Alarm, Access Control
• Perform electrical services design input including Lighting & Emergency lighting, Power Distribution, 11kV Medium Voltage, LV Panel, Fire Alarm, Earthing, Security, CCTV and Cable Containment design
• Provide comprehensive scope of works, specifications, calculations and basis of design documentation for projects
• Analysis and assessment of design work (including load flow analysis).
• Perform Feasibility, Concept, Basis Design, Detailed Design for Procurement and Construction
• Progress reporting and manhour control for the electrical and instrumentation scope.
• Participate in troubleshooting and root cause investigation

We would like to hear from candidates who have:

• Min Degree in Electrical Engineering or its equivalent
• At least 6 years of relevant working experience
• Good knowledge of electrical and instrumentation specifications & requirements
• Be able to work independently with minimum guidance and under pressure to meet tight deadlines
• Experience across a broad range of site electrical and instrumentation engineering projects
• Experience in industrial buildings (Pharmaceutical, Food or Mission Critical projects) would be an advantage