Total 2 maintenance repair job vacancies in Quality Assurance / Control category in tuas south west

Job Description & Requirements

Our Quality group ensures every single material inside our products is manufactured, processed, tested, packaged, stored and distributed aligned with our incredibly high standards of quality and meets all regulatory requirements. Partnering across our internal manufacturing facilities, external contract manufacturers and suppliers we create an interdependent global manufacturing network committed to deliver a compliant, reliable supply to customers and patients on time, every time, across the globe.

What will you do

• Responsible for planning, scheduling and performing calibration, maintenance and qualification of laboratory equipment.
• Responsible for maintaining laboratory chemicals and consumables inventories and disposals.
• Responsible for archival/retrieval of retention samples.
• Ensure laboratory equipment calibration, maintenance and qualification within timely manner and in compliance to standard operating procedures with necessary laboratory safety precautions.
• Liaise and coordinate with external service providers in carrying out calibration, maintenance and qualification of laboratory equipment and tools.
• Liaise with external vendors to ensure chemicals and consumables supply continuity.
• Support laboratory investigation on laboratory equipment failure, Out of Tolerance and Out of Specification
• Be the subject matter expert of laboratory maintenance and participate as auditee in site internal audit/external audit.
• Coordinate with laboratory team to ensure equipment availability for calibration, maintenance and troubleshooting work.
• Manage archival/retrieval of record for laboratory calibration, maintenance and qualification related documents.
• Understand customer needs and identifies solutions to non-standard requests by interpreting existing procedures, processes and practices.
• Ensure work and behave in accordance with EHS procedures and guidelines.
• Maintains positive working relationships among employees and fosters an environment where employee engagement, empowerment, teamwork and accountability are the cultural norm.
• Participate in continuous improvement initiative as part of the production system culture in Singapore.
• Participate in EHS, Business Compliance, cGMP and all other compliance-related matters, where applicable.
• Uses formal data based analytical tools (such as Lean Six Sigma process) to identify and implement operating improvement opportunities to eliminate waste, improving accuracy, compliance and productivity.
• Any other duties as assigned by the Senior Manager/Director.

What you must have

To be successful in this role, you will have:

QUALIFICATION:

Bachelor Degree in Science/ Life Science, Pharmacy, Pharmaceutical Science or Engineering or proven relevant experience.

EXPERIENCE:

This is a career conversion programme under Workforce Singapore (WSG) and candidates must meet the following criteria:

• Singaporeans/Singapore PRs only
• PMETs/Mid-Careerist with no prior work experience in Biopharma industry are welcomed to apply
• Open to two years contract
• Minimum 2 years of relevant experience in GMP manufacturing environment, preferably laboratory operations.

QUALIFICATION:

Bachelor Degree in Science/ Life Science, Pharmacy, Pharmaceutical Science or Engineering or proven relevant experience.

Expertise, Professional and Functional Competencies

· A continued improvement mindset.

· Good knowledge and understanding of GMP

· To be familiar with simple statistic to apply statistical analysis and process control techniques.

· Experience in MS-office applications.

· Proficient in English.

Other Personal Attributes:

· Good organization and time management skills.

· Able to work independently.

· Meticulous with high integrity.

· Good interpersonal and communication skills, with ability to work in cross-functional teams.

· Continuous improvement mindset.

· Positive attitude and self-motivated.

The individual shall report to the Site Manager for the project.

You shall be responsible for the preparation, not limited to, of the Project Quality Plan, ITP, Quality Procedures, Inspection Dossiers, Test Certificates and carrying out stage-wise and final inspection activities.

Your key responsibility is to ensure professional quality control and assurance for the delivery of works in excellent quality in compliance with the client’s requirements.

You shall co-ordinate with project team for all the works requiring your QC expertise/technical support for the works to be carried out effectively and as per specifications.

You shall support the Site Manager in the clearance of certain vendors and NDT contractors (if sourced out).

You shall support in the supervision of works such as fabrication, construction, welding, mechanical, piping and structural installations

You shall randomly check the essential parameters as per the WPS requirements and Quality Procedures, witness PT, MPI, UT, Hardness testing and any other activities requiring your expertise

You shall prepare Stage Inspection Reports as per ITP.

You shall lead the team to co-ordinate Plan and execute NDE works as per requirements and monitor the backing system for welding consumables, pre-heating and inter-pass temperature of Welds

You shall carry out post-test requirements on, but limited to, Bolt, nut, Gaskets and Bolt tightening or torque as per approved procedures, check that the line is complete and ready for test and prepare a punch list of outstanding items.

Ensure final document preparation & review and sign off of all relevant project documents, coordinate with client for the submission of documents as per client requirements.

Customer service oriented mindset

Relevant experience in the Petrol-Chemical Industry

Possess a Bachelor’s degree in Engineering (Mechanical) and/or Sciences

Possess certifications in Non-destructive testing systems / various types of welding / QA/QC certifications, audit compliances and certificates

Relevant experience in welding, NDT methods, total quality management and process