Total 9 supply chain operator job vacancies in Quality Assurance / Control category in Islandwide

Monitoring flight timings and aircraft type on various information systems

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CCTV monitoring and noting down timings of various activities on the aircraft parking stand

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Keeping records of various activities that have taken place on MS docs (e.g. Excel, Word etc)

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Respond to system alerts and notify other stakeholders to provide follow ups

Qualification :

GCE N or O levels,

a) Ensure that only authorised staff displaying valid SP Group (“SP”) security

passes are permitted to enter the Company’s installation

b) Ensure that all items / materials taken out of the TCC are accounted and

recorded

c) Ensure that the company’s facilities, main and pedestrian gates are closed

and locked whenever they are left unattended

d) Ensure that photo taking and video filming are not permitted in the premises

unless with the approval of at least the relevant Head of Section

e) Record all incidents in the Occurrence Book and immediately report all

incidents/fire alarms/malfunctioning of CCTV, Fence Intrusion Detection

System and Vehicle Crash Barrier System to the company and the Security

Command Centre (“SCC”)

f) Attend to any incidents/matters/activation of fire alarms with Comms set and

execute company’s Standard of Procedure

g) Contact the relevant Contact Person/s during an emergency

h) To enforce any instructions/directives in connection with CRISIS management

such as Severe Acute Respiratory Syndrome, Flu Pandemic or any other

matter health related incident as required by the relevant authorities

i) Ensure all equipment and keys are accounted for when changing shift

j) Comply with all Standard Operation Procedures (SOP) issued by the

Company

k) Support any other duties as assigned includes tunnel exercise with external

parties such as SCDF, EMA, etc

l) Check that the entries made by contractors/visitors in the visitor’s logbooks

are correct and complete

m) Not allow any unauthorized person, including the Company staff to enter the

control room unless approved by the Company

n) Operate and monitor RFID system to track all personnel enter/exit tunnels

o) Monitor Tunnel SCADA system (similar to Building Monitoring System)

p) Perform emergency SOP to guide staff/workers to evacuation out of tunnels

q) Monitor and trending data of M&E systems

r) Ensure an emergency call-out service is available at all times

s) Any other systems and components, which are to monitor but not specifically

mentioned in the abovementioned sub-clauses but are within the Contract

Area, shall be included in this Contract.

Shift Hours :

• Day Shift - 7.00 AM to 3.00 PM
• Evening shift -3.00 PM to 11.00 PM
• Night Shift - 11.00 PM to 7.00 AM

SUMMARY OF ESSENTIAL FUNCTIONS

• To support the execution of effective Quality Management System. Ensure clinical storage, secondary assembly/ packaging and distribution activities comply with applicable Quality standards (Good Manufacturing Practices and Good Distribution Practices).
• Execute quality procedures and related inspection/ release activities.
• Manage and participate in new material qualifications, execution of inspection activities, preparation of inspection reports, as applicable.
• Oversee and ensure non-compliance materials are maintained in the appropriate lot status in the inventory system and proper storage locations.
• Ensure retention samples, blinding samples, and printed labels are accounted for.
• Review and approve the label print request, if applicable.
• Support and manage both the Product Incoming and In-process inspection activities conform to the requirements prior to release activities.
• Track incoming materials performance indicators and establish trend analysis (where necessary) for quality improvement initiatives.
• Support and participate in Quality Management Review when needed. Audit Activities
• Plan and execute internal audit/ self-inspection in accordance with written procedures. Ensure selfinspections are completed within the timeline.
• Co-host or participate in external audit activities, e.g. Regulatory, customers and supplier audits/ inspections. Quality Management System
• Escalate and report non-compliance practices and activities for corrective and preventive actions.
• Support review and approval of Change Control, Customer Complaints and Deviations, CAPA and Risk Assessments.
• Initiate Change Control, Customer Complaints and Deviations, CAPA and Risk Assessments associated with Quality Operations.
• Review and approve site procedures. Ensure written procedures comply with applicable regulations and guidelines.
• Author procedures related to site Quality Operations, as applicable.
• Ensure document retention and archival activities are executed in accordance with written procedures.
• Ensure site procedures are aligned with corporate policies. Validation
• Participate and support qualification/validation activities. Training
• Ensure timely completion of training activities assigned, both local and global SOPs.

REQUIREMENTS

• Min Degree / Diploma preferably in Pharmaceutical or Science disciplines.
• Min 5+ years’ experience in quality functions in Pharmaceutical/ Healthcare organization

Salary range: $5K to $6K

Pharma Supply Chain MNC

Interested candidates, please forward your resume to [email protected]

Consultant: Huang Jingsheng Kevyn (R1333338)

Recruit Express Pte Ltd (99C4599)

SUMMARY OF ESSENTIAL FUNCTIONS

• To support the execution of effective Quality Management System. Ensure clinical storage, secondary assembly/ packaging and distribution activities comply with applicable Quality standards (Good Manufacturing Practices and Good Distribution Practices).
• Execute quality procedures and related inspection/ release activities.
• Manage and participate in new material qualifications, execution of inspection activities, preparation of inspection reports, as applicable.
• Oversee and ensure non-compliance materials are maintained in the appropriate lot status in the inventory system and proper storage locations.
• Ensure retention samples, blinding samples, and printed labels are accounted for.
• Review and approve the label print request, if applicable.
• Support and manage both the Product Incoming and In-process inspection activities conform to the requirements prior to release activities.
• Track incoming materials performance indicators and establish trend analysis (where necessary) for quality improvement initiatives.
• Support and participate in Quality Management Review when needed. Audit Activities
• Plan and execute internal audit/ self-inspection in accordance with written procedures. Ensure selfinspections are completed within the timeline.
• Co-host or participate in external audit activities, e.g. Regulatory, customers and supplier audits/ inspections. Quality Management System
• Escalate and report non-compliance practices and activities for corrective and preventive actions.
• Support review and approval of Change Control, Customer Complaints and Deviations, CAPA and Risk Assessments.
• Initiate Change Control, Customer Complaints and Deviations, CAPA and Risk Assessments associated with Quality Operations.
• Review and approve site procedures. Ensure written procedures comply with applicable regulations and guidelines.
• Author procedures related to site Quality Operations, as applicable.
• Ensure document retention and archival activities are executed in accordance with written procedures.
• Ensure site procedures are aligned with corporate policies. Validation
• Participate and support qualification/validation activities. Training
• Ensure timely completion of training activities assigned, both local and global SOPs.

REQUIREMENTS

• Min Degree / Diploma preferably in Pharmaceutical or Science disciplines.
• Min 5+ years’ experience in quality functions in Pharmaceutical/ Healthcare organization

Salary range: $5K to $6K

Pharma Supply Chain MNC

Interested candidates, please forward your resume to [email protected]

Consultant: Huang Jingsheng Kevyn (R1333338)

Recruit Express Pte Ltd (99C4599)

The role is focused on ensuring compliance with Good Distribution Practices (GDP) and the Falsified Medicines Directive within the EU regional supply chain network. The objective is to maintain product quality and authenticity throughout the supply chain. The responsibilities and requirements outlined highlight the key aspects of this position.

Salary up to $8000

Location: Tuas (WFH and transport provided)

1 year Contract role

Responsibilities

• Embed the principles of good distribution practices guideline (2013/C 343/01) in the EU regional supply chain network, to ensure that product quality is maintained.
• Embed the principles of the falsified medicines directive (2011/62/EU) in the EU Regional supply chain network, to ensure that the authenticity of product is maintained
• Own and manage temperature assessment records(CTET)
• Own and manage minor and Major deviation records and lead root cause analysis
• Own and manage CAPA and CPA EV records, ensuring that they are implemented as intended
• Manage missing product notifications, including leading event review team meeting if applicable
• Support audits and inspections involving EU supply chain, including audits and inspections at the affiliate level
• Support activities for product recall or annual mock recall exercise
• Incidental travel might be required
• Ensure up t date Smartsheet for minor, major, CTETS and missing products
• SME for document management control

Requirement

• Bachelor’s degree or equivalent in Life Sciences + 2 year experience in GMP/GDP compliance OR 4 years' experience in GMP/GDP compliance
• Sound knowledge of quality assurance principles, good manufacturing practice and good distribution practice
• Strong word process, database and spreadsheet application skills and experience in QM software system (Trackwise, Veeva, etc.)

PERSOLKELLY Singapore Pte Ltd • RCB No. 200007268E EA License No. 01C4394 • EA Registration No. R21103542 (Ling Kai Jin)

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WhatsApp: +65 90820021 (Kyler)

Email: [email protected]

Location: Lentor (Shindo Industrial)
Working Day: 5 day work week (include weekend &PH)
Working Hours: 7am to 9pm (9 hour Shift with 1 hours break )
Salary: $4,000-$4,500

Roles & Responsibility:

• Quality control of flowers on the all production and supply chain;
• Plan, execute, and oversee product inspection and testing for quality and conformance to specifications and deliverables.
• Assist operations by tracking, documenting, and reporting quality levels and KPIs.
• Investigate reports of product quality issues and ensure resolution in accordance with company guidelines and regulatory requirements.
• Develop or update procedures for capture, investigation, and documentation of product complaints.
• Monitor risk-management procedures, maintain problem logs, and report issues to managers and product developers.
• Maintain complaint and nonconformance processing through records and tracking systems, including root-cause analysis and corrective actions.
• Develop improved standards for production and design, and create testing protocols for implementation across all service lines
• Cool chain management and improvement;
• Testing new varieties, new packaging, new processes;
• Hygiene and safety in all working areas;
• Team supervision and ability to coordinate with Operations team to ensure daily deadlines;
• Preparation of accurate and timely reports;
• Identify training needs and take action to ensure companywide compliance
• Pursue continuing education in new solutions, technologies, and skills
• Staff training and evaluation of progress;

Requirement:

• 3 Years’ experience as a QC in a fresh produce industry preferably the food industry
• University Degree or equivalent.
• IT knowledge Access, Excel and various data base;

The Supreme HR Advisory Pte. Ltd | 14C7279

Gan Kai Le | R23112683

Job Summary
Work with Friends| Immediate | Fasthire
No Experience Needed

Quality Engineer | QMS & Management Representative (MR) | Marine Supply | Tuas

5 Days 8:30am -5:15pm

Tuas Crescent (Company Transport provided at Marsiling / Jurong East MRT)

$3600 to $4300

Job scope

Work closely with the Engineering & Production Team to develop incoming quality, in process Quality & Outgoing Quality requirements.

Responsible for all Quality plans of all products to mee customers specifications

Work with relevant agencies to adhere to certification requirements when required

Work with management to establish/maintain company’s QMS and is Management Representative (MR) of company

Work with Procurement / Purchasing to ensure that contractors / supplies quote / supply items that meet customer’s specification.

Working out costing of products when required by management.

Responsible for all equipment calibration / maintenance program within the company

Complete other tasks assigned by management.

The Supreme HR Advisory Pte Ltd | 14C7279

Ong Boon Kiet (Travys) | R22104769

Senior Recruitment Consultant

Job Highlights

• Permanent Position
• Vacancies X 20
• Location: Near Woodlands MRT
• AWS & VB
• Annual Leave
• Medical Benefit
• Attendance Allowance + Shift Allowance
• Training will be provided
• Working hours : Mon-Fri 3pm-11pm / Sat : 1pm-7pm

Our client is a global advanced precision engineering & manufacturing solutions provider. Due to fast expansion, they are actively seeking for production operators.

Responsibilities:

• Carry out productions works according to tasks assigned.
• Checking and sorting product produced as and when required to ensure quality products are produced.
• Report any quality problem to immediate superior immediately.
• Rework the product as required according to instruction when required.
• Practise GMP and ensure good housekeeping at the workstations.
• Ensure quality parts are produced and production target are met.
• Ensure correct product packaging and product identification and segregation.

Requirements:

• No experience is highly welcome
• Relevant working experience in manufacturing industry or equivalent will be added an advantage

Interested candidates, please e-mail resume in Word document (indicating your current salary and expected salary) to:

Ryan Tan (EA Reg. no.: R23116422)

Recruitment Manager

Right Recruit Pte. Ltd.

10 Anson Road, #33-03, International Plaza, Singapore 079903

EA Licence No: 23C1743

[email protected] I www.rightrecruit.com.sg