Production Engineer Intern jobs at Msd in Singapore, Singapore

• Based in Singapore , the regional hub for Asia Pacific (AP) and top-ranked biopharmaceutical company on the Straits Times and Statista’s list of Best Employers in Singapore for three consecutive years (2021, 2022, 2023).
• Join the premier biopharmaceutical company that has been in Singapore for more than 25 years and in AP for over 60 years.

Our Engineers support internal and external manufacturing operations remain operational, continuously improve and innovate. With our extensive range of facilities and environments, our Engineers have opportunities across many diverse areas including Biological, Chemical, Automation, Capital Projects, Maintenance, Safety, Process Development, Technical Services, Utilities and Validation.

WHAT YOU WILL DO

Responsibilities include, but are not limited to:

Routine work

• Provides engineering and troubleshooting support with the goal to increase operational efficiencies and minimize maintenance expenses.
• Coach technicians on troubleshooting technical problems.
• Provides engineering support to both corrective and preventive maintenance.
• Provide support on installation, modification, fabrication, testing, servicing and repairs of equipment instruments that comply to site change control procedures, good engineering practices and GMP.
• Collect and analyse data and follow up with recommendation to improve equipment’s reliability and reduce equipment failures.
• Develop/ improve maintenance programme to maintain plant assets. Guide, review and modify the PM to improve equipment reliability.
• Ensure smooth equipment operation by close monitoring of equipment condition. Carryout RCA to improve product quality and equipment reliability.
• Prepare Annual Trend Analysis Reports, documentation by collecting analysing and summarising information and trends. Manage the reliability equipment database.
• Perform maintenance activities and analyse reliability data to improve equipment health and performance.

Project work

• Manages maintenance related projects, CAPA Actions, schedule, costs and quality utilizing proper controls.
• Ensures that projects deliverables are met and all associated documentation is established
• Provides engineering support in the scoping, development, execution and documentation of upgrade projects.

Others

• Performs job assignments by Supervisor pertaining to equipment/ instrument or system or documentation or housekeeping.
• Development of technical procedures associated with areas of responsibilities
• Participate in HSE, Business Compliance, cGMP and all other compliance related matters, where applicable.
• Supervise and oversee Third Party Contractors, where applicable
• Able to influence stakeholders or business leaders and to build trust throughout the organisation.
• Any other duties as and when assigned by the Managers.

WHAT YOU MUST HAVE

To be successful in this role, you will have:

• Degree in Electrical/Electronics, Instrumentation and Control, Mechanical, Chemical Engineering
• 3 - 5 years of related experience in maintenance function, preferably in API manufacturing plant
• Good knowledge of cGMP and safety regulations of pharmaceutical industry.
• Demonstrates a knowledge of Engineering and Compliance standards
• Demonstrates excellent problem solving skills ie provides solutions which are practical for implementation.
• Able to properly assess the situation and understand when to escalate to a higher levels
• Knowledge in root cause analysis, able to analyse information from a variety of sources to make sound decisions
• Ability to work independently
• Working knowledge of Microsoft Office and SAP.
• Good knowledge on Failure Modes of Equipment Reliability Processes

This is a career conversion program under Workforce Singapore (WSG) and candidates must meet the following criteria and are open to the following conditions:

• Singaporeans/Singapore PRs only
• PMETs/Mid-Careerist with more than 2 years working experience
• Open to two years contract

WHAT YOU CAN EXPECT

• Limitless opportunities across various areas in Manufacturing; well-structured career path
• A state-of-the-art facility that delivers solution to its customers world-wide
• Highly engaging team that aims to innovate the future

This posting has been created to pipeline talent for prospective roles that we anticipate will be needed soon in our organization. By applying to this Pipeline Advertisement you will be submitting your interest to be contacted for roles similar to what is described in the Pipeline Advertisement.

Job Description

Production Engineering​ (PE) Intern

As part of the Production team in Singapore, the intern will be able to learn the different manufacturing process, operational systems and activities that support pharmaceutical manufacturing. He/she will be expose to the various process, systems and activities associated with cGMP manufacturing operations within IPT.

The PE intern key responsibilities are as follows:

• Assist in the management of cGMP documentation
• Assist in conducting daily tier meetings between operators, engineers and managers
• Collect and analyze operational data to drive productivity
• Work on continuous improvement activities that help to improve the current operation processes and systems
• Actively participate in group meeting discussions and continuous improvement. Collaborate with colleagues whenever possible to achieve both operational and project goals.

Job Requirements:

• Current pursuing a Diploma in a technical field, preferably in a science or engineering.
• Demonstrated capability in application of sound engineering and scientific principles, project management skills and structured / analytical problem-solving techniques
• An excellent team player who is able to readily take on responsibilities and work independently
• Strong interest in working in an engineering and operational environment
• Excellent communication and facilitation skills
• Have a positive, proactive, can-do attitude
• Keen to learn

What we look for

Current Contingent Workers apply

*A job posting is effective until 11:59:59PM on the dayBEFOREthe listed job posting end date. Please ensure you apply to a job posting no later than the dayBEFOREthe job posting end date.

Job Description

• Develop strategies that alignwith business imperatives

• Based in Singapore, the regional hub forAsia Pacific (AP)andtop-ranked biopharmaceutical company on the Straits TimesandStatista’s list of Best Employers in Singapore for two consecutive years (2020, 2021).

• Join thepremier biopharmaceutical companythat has beenin Singapore for more than 25 years and in AP for over 60 years.

Our Engineers support internal and external manufacturing operations remain operational, continuously improve and innovate. With our extensive range of facilities and environments, our Engineers have opportunities across many diverse areas including Biological, Chemical, Automation, Capital Projects, Maintenance, Safety, Process Development, Technical Services, Utilities and Validation.

Critical Responsibilities but not limited to:

• Supports or lead with guidance, new product introductions to the site by conducting process and equipment comparisons, new raw materials introduction, development studies, clinical supplies manufacturing, cleaning processes development/ validation and training of technicians as required. Authors protocols, reports and other associated documentation related to a new product introduction. Demonstrates strength in technical writing.

• Is involved in/supports the design and execution of small/ full scale experiments using appropriate methodology and/or simulations for products/ processes to evaluate the impact of proposed changes to validated equipment/ processes. Proactively identify solutions with support from seniors or direct supervisor to address issues that arose duringexperiment/evaluation.

• Provides technical guidance in support of site and divisional capital projects and new facility start-up activities. Ensures that the process design is well thought-out and robust for routine manufacturing.

• Provide technical input independently to the process design to ensure its fit for purpose for routine manufacturing. Responsible to transfer the knowledge of the project and facility to operations colleagues.

• Provides support to product, equipment andmanufacturing/cleaningprocesses in response to deviations/ product complaints/ adverse events to identify point of occurrence, root cause and corrective/ preventative actions.

• Provides support for compliance activities such as audit and regulatory support. Monitors and addresses potential regulatory risks during various phases of the lifecycle process as part of a team.

What you must have:

To be successful in this role, you will have:

Bachelors, Masters or Ph.D. degree in a technical field, including Chemical or Mechanical Engineering, Chemistry, Biological sciences or Pharmaceutical Sciences.

3 to 5 years technical experience in pharmaceutical, oil and gas or semiconductor industries.

WHAT YOU CAN EXPECT

• Limitless opportunities across various areas in Manufacturing; well-structured career path

• A state-of-the-art facility that delivers solution to its customers world-wide

• Highly engaging team that aims to innovate the future

What we look for…

Current Contingent Workers apply

*A job posting is effective until 11:59:59PM on the dayBEFOREthe listed job posting end date. Please ensure you apply to a job posting no later than the dayBEFOREthe job posting end date.

Job Description

Current Contingent Workers apply

*A job posting is effective until 11:59:59PM on the dayBEFOREthe listed job posting end date. Please ensure you apply to a job posting no later than the dayBEFOREthe job posting end date.

Job Description

The Opportunity

• Based in Hyderabad, join a global healthcare biopharma company and be part of a 130- year legacy of success backed by ethical integrity, forward momentum, and an inspiring mission to achieve new milestones in global healthcare.
• Be part of an organisation driven by digital technology and data-backed approaches that support a diversified portfolio of prescription medicines, vaccines, and animal health products.
• Drive innovation and execution excellence. Be a part of a team with passion for using data, analytics, and insights to drive decision-making, and which creates custom software, allowing us to tackle some of the world's greatest health threats.

What will you do in this role:

• Understand divisional and site business system requirements for CIAM services.
• Must have experience in defining CIAM platform requirements, designing technical solutions and executing on those designs into a highly available, fault tolerant environment.
• Understanding of security best practices, administration and governance of Identity and Access Management the products and services including identify and evaluate security gaps.
• Customize CIAM product features to fulfil requirements that cannot be met with standard out-of-box functionality
• Perform vendor and technology assessments.
• Assist in the application of system lifecycle practices during CIAM design and deployment
• Recommend improvements, corrections, remediation for projects or internal processes.
• Advocate secure computing practices and procedures and communicate Information Security and CIAM best practices throughout the company.
• Maintain active and direct interaction with key stakeholders.
• Working with various technical teams to ensure we maintain high availability and uninterrupted outage of our production environment.
• Demonstrate ability to stay current with all industry trends/best practices, as well as new product releases so that we can maintain a proactive 3-year systems management roadmap.
• Ensure all third-party monitoring solutions that are integrated into the Identity & Access Management products are properly documented and function as designed.
• Assist in the application of system lifecycle practices during CIAM design and deployment.

What should you have:

• Bachelors’ degree in Information Technology, Computer Science or any Technology stream.
• 7+ years of experience with implementation and troubleshooting with CIAM technologies like Ping Identity
• Experience in administration of user and role provisioning, connectors, workflow, certificate management, session management, and encryption technologies
• Strong analytical and problem-solving skills and demonstrable ability to work independently as well as in a team environment
• Well versed in SAML, OpenID, OAuth and other industry standard authentication / authorization solutions
  • Excellent communication skills and interpersonal skills are required.
  • A demonstrated track record of making a difference and adding value.
  • Strong organizational skills with the ability to multi-task.
  • Ability to work and adjust to changing deadlines.
    • Excellent interpersonal, written and oral communication skills with the ability to communicate effectively across all levels of an organization. Able to present technical ideas in business-friendly and user-friendly language
    • Proven analytical, evaluative, and problem-solving abilities

Desired skills:

• Experience working in a large healthcare environment
• Demonstrated understanding of Identity-related NIST standards (e.g. 800-63-3)
• Prior experience with our company’s enterprise environment and business applications
• Good working knowledge of the ITIL framework
• Working knowledge and understanding of Remedy for Change, Incident and Knowledge Management
• CISSP, Security+ or similar industry certification

What we look for:

Current Contingent Workers apply

*A job posting is effective until 11:59:59PM on the dayBEFOREthe listed job posting end date. Please ensure you apply to a job posting no later than the dayBEFOREthe job posting end date.

Job Description

Current Contingent Workers apply

*A job posting is effective until 11:59:59PM on the dayBEFOREthe listed job posting end date. Please ensure you apply to a job posting no later than the dayBEFOREthe job posting end date.

Job Description

In this role, you will be part of the site utilities, facilities, energy operations and maintenance team to support pharmaceutical manufacturing activities.

WHAT YOU WILL DO:

The UFM intern's key responsibilities and opportunities:

· Work under the guidance of UFM Manager and engineers

· Understand and able to work in pharmaceutical manufacturing environment

· Be integral part of utilities, facilities team to support daily operational activities

· Support the maintenance, calibration and reliability program for utilities and facilities

· Propose improvement ideas and execute projects related to utilities, facilities and energy savings

· Carry out real time problem solving and actions follow up

· Actively participate in group discussions and project team meetings

· Partner the team and provide fresh perspectives to improve the team’s operations and productivity

· Develop competencies in areas such as: Project management; pharmaceutical manufacturing; utilities & facilities management; maintenance and reliability, engineering; root cause analysis (RCA); Lean six sigma program; pharma and safety engineering design standards

WHAT YOU MUST HAVE

· Pursuing degree in engineering related field

· Have a positive, proactive, can-do attitude and readily takes on responsibilities

· Keen to learn

· Good team player

· Motivated and has initiative

· Technically inclined and good problem solving skills

What we look for

Current Contingent Workers apply

*A job posting is effective until 11:59:59PM on the dayBEFOREthe listed job posting end date. Please ensure you apply to a job posting no later than the dayBEFOREthe job posting end date.