Jobs at Msd in Singapore, Singapore

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.

THE OPPORTUNITY

• To work in a culturally diverse and high-performance team who has built a lot of capabilities in Pharmaceutical Manufacturing.
• 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 (2020, 2021, 2022).
• Join the premier biopharmaceutical company that has been in Singapore for more than 25 years and in AP for over 60 years.

Job Purpose

• Plans, organizes, performs engineering and maintenance activities related to the installation, modifications, troubleshooting, repairs, calibrations and maintenance of equipment / system to ensure that they are safe, efficiently, reliable and meet GMP/ regulatory / production requirements.
• Other engineering activities include maintaining spares and parts storage, operation of utilities supplies and up-keeping of facilities.

Main Responsibilities:

• Assists team lead to complete work activities timely, efficiently and satisfactorily
• Follow up and continue with the previous shift or day incomplete work
• Collates and reports the team shift or day activities to the team lead
• Provides troubleshooting and diagnostic of equipment failure to determine the root cause and perform immediate corrective actions
• Standby for any emergency repair after office hours / weekends and public holidays
• Operates and maintains Utilities and Production support equipment efficiently and reliably to support production activities
• Performs and coordinates utilities shutdown, startup, swing over, and equipment servicing and inspection
• Identifies, executes and reports improvement to routine work activities
• Participates in the improvement to enhance equipment or system efficiency, reduce energy cost/usage and other cost saving/avoidance projects
• Performs jobs assigned by Supervisor pertaining to installation, modification, fabrication, testing, servicing and repairs of equipment, with adherence to site change control procedures or minor projects
• Performs testing, commissioning, qualification (IQ, OQ, PQ) activities
• Carries out Safety, Health, and Environment (SHE) improvement initiatives (i.e., audits, training, etc) and submit recommendation
• Performs job assignments by Supervisor pertaining to equipment or system or documentation or housekeeping
• Performs corrective and preventive maintenance for the MEI systems and facilities to ensure efficient running of equipment (e.g. checking line components, servicing of sensors, lubrication of bearings, servicing of dryer)
• Performs calibrations and preventive maintenance on all types of industrial instruments for temperature, pressure, level, flow, RH and analyzers (e.g. Sensors, indicators, recorders, transmitters, transducers, control valves, annunciators, pH and conductivity meters)
• Executes CMMS Work Instruction from process plants (e.g. Isolation and Reconnection of electrical supply, leakages, replace faulty part, troubleshoot/repair any E/I or mechanical faults)
• Performs basic troubleshooting of the PLC, BMS, EMS and FAS systems
• Ability to perform machining and fabrication activities
• Participate in SHE, Business Compliance, cGMP and all other compliance-related matters, where applicable
• Supervise and oversee Third Party Contractors, where applicable
• Any other tasks as and when assigned by Supervisors

cGMP Standards

• Understands and follows proper cGMP principles and Worldwide Quality Standards related to the execution of assigned work

Problem Solving

• Provides solutions to routine and simple problems
• Able to properly assess the situation and understand when to escalate to a higher level

Leading Self or Others, and Department

• Works with minimum direct supervision
• Seeks advice in personal and professional development

WHAT YOU MUST HAVE

To be successful in this role, you will have:

Qualification:

• Diploma / ITC/ NTC in Mechanical, Mechantronics, Electrical or Instrumentation & Control Engineering

Experience:

• 5 years experience in maintenance or related fields;
• Work experience in the pharmaceutical (preferred) or chemical or semiconductor industry
• PUB electrician license will be an advantage
• Fitting and welding skills will be an added advantage

Other Attributes:

• Demonstrates Ethics & Integrity
• Drive Results
• Focus on Customers & Patients
• Make Rapid Disciplined Decisions
• Act with Courage & Candor
• Build Talent
• Foster Collaboration
• Ability to prepare simple report
• Communicates in a clear and unambiguous manner

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

Chemical Technician (WDA) 2 Year Contract

• This is part of the WDA programme – the contract will be 2 years in duration
• 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 two consecutive years (2020, 2021).
• Join the premier biopharmaceutical company that has been in Singapore for more than 25 years and in AP for over 60 years.

Responsibilities:

• Operate and monitor the chemical processes assigned:

Each of these processes may comprise the following activities:

• Participate in an appropriate hand-over of the process(es) on which he / she is working.
• Obtain, follow and complete process related documentation. Check prior shifts' documentation for accuracy and thoroughness.
• Clean vessels and lines prior to and following batches as required.
• Conduct all required pre-batch checks.
• Charge vessels with solids or liquids as directed in procedures.
• Conduct post-charge verification checks and take any necessary corrective action.
• Adjust and monitor (using all information available, including automation input/outputs and personal inspection) process conditions as required.
• Carry out routine sampling, testing some samples as necessary.
• Transfer process streams to other units in coordination with other staff.
• Monitor process; both with Distributed Control System (DCS) and manually observing temperature, pressure, flow, PH, volume, colour, salt content, moisture content and adjusting the parameters accordingly.
• Perform Batch / Offloading operations.
• Operate general facility service equipment such as vacuum pumps, water systems, Volatile Organic Compound (VOC) scrubbers.
• Record all operational and analytical data on the appropriate documents and inform the Shift Production Lead of any process abnormalities.
• Put on appropriate clothing and personal protective equipment for the process and the processing area.
• Maintain material segregation and label appropriately and accurately all containers, bags and vessels.
• Carry out routine checks and scheduled cleaning procedures, for both process and facilities as required.
• Obtain and verify materials necessary for processing, monitor materials stock and notify Shift Production Lead as necessary in the event of a material or supply abnormality.
• Notify Shift Production Lead of requirement for maintenance. Prepare equipment before maintenance work e.g. depressurizing, cleaning of lines and equipment, de-energizing etc.
• Conduct on-the-job training of other Chemical Technicians.
• Perform material handling duties including forklift/reach-truck operation driving.
• Carry out assignments for alternate or simultaneous processes as directed.
• Meet eligibility requirements for the Emergency Response Team.
• Attend meetings and training events as required.
• Maintain all qualifications and development milestones as necessary for duties.

WHAT YOU MUST HAVE

To be successful in this role, you will have:

• Higher NITEC or Diploma in Engineering(Chemical, Mechanical, Electrical) or Science, or equivalent operations experience.

• Good stewardship awareness (including cGMP, regulatory inspection preparation, SHE)

• Good knowledge in applicable regulations and divisional policies/guidelines (especially cleaning/housekeeping/maintenance, environmental control, process/cleaning/equipment validation, change control and manufacturing practices).

• Demonstrate Ethics & Integrity & Result Driven

• Focus on Customers & Patients & Make Rapid Disciplined Decisions

• Act with Courage & Candor, Build Talent & Foster Collaboration

• Demonstrate Our Company's Inclusive Behaviors & Effective communication skills

This is a Career Conversion Programme (CCP) for Advanced Biopharmaceuticals Manufacturing Professionals (Place-and-Train) under Workforce Singapore (WSG) and candidates must meet the following criteria:

• PMETs/Mid-Careerist with no prior work experience in Biopharma industry are welcome to apply
• Singaporeans/PRs only

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

Organizational context

Reports to Director - Animal Health IT Manufacturing and Supply Contacts

Responsibilities

• Safeguards and drives the adoption of the Global SAP Template
• Reviews and approves changes before they are executed
• Build strong relationship with Local Business Process Owners (LBPO’s) and Key Users / SME’s
• Delivers input to the Global Business Process Owners (GBPO) and Team Manager for Projects and changes
• Manages medium complex projects
• Participate in workshops, support design, realization testing, training and go-live
• Support second line support team
• Connect with EPM colleagues to understand end-to-end processes and aim for improvements or impact of existing change requests

Experience / knowledge

• Broad general IT knowledge and experience
• In depth knowledge of SAP Warehouse Management (WM) solutions in an Manufacturing Environment and SAP Manufacturing (PP/MM)
• Five years or more hands on experience with SAP customizing in WM, PP and MM and preferably other Manufacturing Modules and management of medium complex projects.
• Demonstrated track record as an ERP Specialist in a batch managed industry. Pharmaceutical or Life Science is preferred.
• Knowledge and experience in computer system validation is preferred.
• Knowledge of methods and techniques for the adjustments and implementation standard software.

Education

• Higher educational or academic level
• SAP R/3 relevant modules at customizing level
• Project management certification (eg PMI) and Lean Six Sigma green belt certification is preferred

Skills

• Strongly developed analytical skills
• Excellent communication skills
• Shows drive to deliver quality work
• Customer-oriented way of working
• Can maintain contacts with people from a wide variety of backgrounds
• Mature business partner
• Fluency in English (speaking and writing)
• Creative problem solver

Other requirements

• Travel: 20-25%

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.

THE OPPORTUNITY

• Based in Singapore, the regional hub for Asia Pacific (AP) and named one of the Best Companies to Work for in 2019 by HR Asia
• Join the premier biopharmaceutical company that has been in Singapore for more than 25 years and in AP for over 60 years.

As a Pharmacovigilance (PV) Senior Specialist, you will be responsible for adverse event management including aggregate and individual case safety report (ICSR) health authority submissions and compliance monitoring. You will be responsible for day-to-day case management activities for your assigned product portfolio as applicable. You will collaborate with colleagues to ensure compliance with local laws and regulations, as well as adjusting schedules to support your colleagues to ensure there is no gap in adverse event reporting and drug safety oversight.

WHAT YOU WILL DO

• Serves as the back-up Qualified Person for PV (QPPV) / Local Responsible PV person as required per local PV legislation.
• Serves as the point of contact for the local Health Authority for PV related questions from the Health Authorities (when assigned).
• Oversees all daily PV processes and activities within the countries covered by the country operation as required.
• Establishes and coordinates reconciliation activities for PV cases received from local operating units (e.g., Designated Point of Contact, Medical Information, etc.) and contractual partners (as applicable) and processes the reports in accordance to local procedures/ PV legislations
• Files, stores and archives safety-related and regulatory data and documentation in accordance with department and company policies and local requirements.
• Acts in full compliance with global and local SOPs and reports any deviations or compliance concerns immediately and assists in preparing necessary corrective actions and preventative actions (CAPAs) locally for non-compliance issues.
• Serves as SME and supports local PV audits and inspections including readiness activities and supports other audits/inspections including the development of CAPAs in response to findings/observations.
• Participates in and supports audits of contractual partners/vendors as necessary.
• Develops and maintains local PV-controlled documents (i.e., SOPs, CCPDs, training materials, etc. as applicable) ensuring that they are kept current.
• Assists in developing local procedures (in compliance with regional and standards) for the department, to ensure global quality PV data and evaluates processes for potential improvement in efficiency and effectiveness.

WHAT YOU MUST HAVE

• Degree in Life Science, medical science or health-related degree
• Demonstrated solid pharmaceutical industry experience in Pharmacovigilance/Drug Safety
• Good knowledge of PV regulations, processes and activities
• Demonstrated supervisory experience in managing people/teams/contractors
• Ability to be self-motivated and able to work with processes
• Fluent (written & oral) English communication skills with a collaborative mindset
• Ability to develop good working relationships
• Strong organisational and project management skills to handle multiple tasks under time pressure
• Proficient User of Microsoft Suite (Word, Excel)
• Experience working with safety databases such as ARGUS

WHAT YOU CAN EXPECT

• Opportunity to have a career of purpose
• Work with a passionate Pharmacovigilance and Regulatory Affairs Team
• Work within a company that believes in making a significant impact on the health and lives of people around the world.

WHAT WE LOOK FOR

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.

THE OPPORTUNITY

• Be part of the team that ensures sustainable products meets standard quality and committed to deliver to customers worldwide!
• 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 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

Reporting to Lab Manager, Quality Control, the Chemist is responsible for performing and reviewing laboratory testing of raw materials, in-process samples, intermediates, final drug substances and stability batches in Active Pharmaceutical Ingredients Laboratories.

WHAT YOU WILL DO:

Critical responsibilities but not limited to:

• Ensure tests and other tasks assigned are performed in a timely manner in compliance to Standard Operating procedures, requirements specified in our company Quality and Safety Standards, regulatory dossiers and pharmacopoeia.
• Manage and perform calibration, maintenance and qualification of laboratory equipment.
• Participate in laboratory efficiency improvement tasks, analytical method transfer, development, validation and equipment qualifications activities.
• Conduct and support Laboratory investigation on laboratory equipment failure, OOT and OOS and identify the root cause and its report writing.
• Review and revise Standard Operating Procedures and laboratory test methods.
• Perform and maintain good laboratory housekeeping, inventory and in-house stock control, reference standards, chemical reagents, and consumables.

After one year on the position, you will be competent to perform most of the laboratory testing following cGMP, data integrity and GLP requirement. You will have been trained to use various laboratory equipment ranging from such as particle size analyzer, FTIR, UV-Vis spectrometer, microscope, Empower CDS, HPLC, GC, etc.

WHAT YOU MUST HAVE

• Bachelor Degree in Chemistry / Biochemistry with prior working experience preferred
• 0 – 3 years’ experience in pharmaceutical analysis is preferred. Fresh graduates with relevant internship experience will be considered
• Experience in particle size analyser, GC, HPLC, FTIR, Karl Fischer Titrator, Potentiometric titrators with technical competency is preferred
• Demonstrated knowledge and understanding of cGMP, GLP, and associated regulatory expectations related to Pharmaceutical Analytical testing is preferred
• Position can be on regular hours or 12 hours rotating shift (night/day including Sat/Sun). If on shift, shift allowance will be provided

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

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.

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.

Chemical Technician (WDA) 2 Year Contract

• This is part of the WDA programme – the contract will be 2 years in duration
• 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 two consecutive years (2020, 2021).
• Join the premier biopharmaceutical company that has been in Singapore for more than 25 years and in AP for over 60 years.

Responsibilities:

• Operate and monitor the chemical processes assigned:

Each of these processes may comprise the following activities:

• Participate in an appropriate hand-over of the process(es) on which he / she is working.
• Obtain, follow and complete process related documentation. Check prior shifts' documentation for accuracy and thoroughness.
• Clean vessels and lines prior to and following batches as required.
• Conduct all required pre-batch checks.
• Charge vessels with solids or liquids as directed in procedures.
• Conduct post-charge verification checks and take any necessary corrective action.
• Adjust and monitor (using all information available, including automation input/outputs and personal inspection) process conditions as required.
• Carry out routine sampling, testing some samples as necessary.
• Transfer process streams to other units in coordination with other staff.
• Monitor process; both with Distributed Control System (DCS) and manually observing temperature, pressure, flow, PH, volume, colour, salt content, moisture content and adjusting the parameters accordingly.
• Perform Batch / Offloading operations.
• Operate general facility service equipment such as vacuum pumps, water systems, Volatile Organic Compound (VOC) scrubbers.
• Record all operational and analytical data on the appropriate documents and inform the Shift Production Lead of any process abnormalities.
• Put on appropriate clothing and personal protective equipment for the process and the processing area.
• Maintain material segregation and label appropriately and accurately all containers, bags and vessels.
• Carry out routine checks and scheduled cleaning procedures, for both process and facilities as required.
• Obtain and verify materials necessary for processing, monitor materials stock and notify Shift Production Lead as necessary in the event of a material or supply abnormality.
• Notify Shift Production Lead of requirement for maintenance. Prepare equipment before maintenance work e.g. depressurizing, cleaning of lines and equipment, de-energizing etc.
• Conduct on-the-job training of other Chemical Technicians.
• Perform material handling duties including forklift/reach-truck operation driving.
• Carry out assignments for alternate or simultaneous processes as directed.
• Meet eligibility requirements for the Emergency Response Team.
• Attend meetings and training events as required.
• Maintain all qualifications and development milestones as necessary for duties.

WHAT YOU MUST HAVE

To be successful in this role, you will have:

• Higher NITEC or Diploma in Engineering(Chemical, Mechanical, Electrical) or Science, or equivalent operations experience.

• Good stewardship awareness (including cGMP, regulatory inspection preparation, SHE)

• Good knowledge in applicable regulations and divisional policies/guidelines (especially cleaning/housekeeping/maintenance, environmental control, process/cleaning/equipment validation, change control and manufacturing practices).

• Demonstrate Ethics & Integrity & Result Driven

• Focus on Customers & Patients & Make Rapid Disciplined Decisions

• Act with Courage & Candor, Build Talent & Foster Collaboration

• Demonstrate Our Company's Inclusive Behaviors & Effective communication skills

This is a Career Conversion Programme (CCP) for Advanced Biopharmaceuticals Manufacturing Professionals (Place-and-Train) under Workforce Singapore (WSG) and candidates must meet the following criteria:

• PMETs/Mid-Careerist with no prior work experience in Biopharma industry are welcome to apply
• Singaporeans/PRs only

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.

Role Overview

As a Software Engineer you will design, develop, and maintain software systems. This role involves both creative and analytical skills to solve complex problems and create efficient, reliable software. You will use your expertise in requirements analysis, programming languages, software development methodologies, and tools to build and deliver software products that meet the needs of businesses, organizations, or end-users. You will work with other engineers, product managers and delivery leads, to design systems, determine functional and non-functional needs and implement solutions accordingly. You should be ready to work independently as well as in a team.

What will you do in this role

• With a wealth of knowledge and hands-on experience, regularly mentor peers, provide help, aid in defining standards, and identify reusable code or application modules.

• Create and document detailed designs for custom software applications or components.

• Design, code, verify, test, document, amend and refactor moderately complex applications and software configurations for deployment in collaboration with cross-disciplinary teams across various regions worldwide.

• Elicit requirements for systems and software life cycle working practices and automation. Prepare design options for the working environment of methods, procedures, techniques, tools, and people. Utilize systems and software life cycle working practices for software components and micro-services. Deploy automation to achieve well-engineered and secure outcome.

• Contribute to the development of solution architectures in specific business, infrastructure, or functional areas. Identify and evaluate alternative architectures and the trade-offs in cost, performance, and scalability.

• Work within a matrix organizational structure, reporting to both the functional manager and the Product manager.

• Participate in Product planning, execution, and delivery, ensuring alignment with both functional and Product goals.

What should you have

• Bachelor’s degree in information technology, Computer Science, or any Technology stream.

• 7+ years of hands-on experience working with technologies - HTML, CSS, REST API, HTTP, SQL, and databases, at least one programming language from our supported stack (TypeScript / Node / React, Python)

• Working with DevSecOps tools for deploying and versioning code.

• Familiarity with modern product development practices – Agile, Scrum, test driven development, UX, design thinking.

• Familiarity with DevOps practices (Git, Docker , infrastructure as code, observability, continuous integration/continuous deployment - CI/CD).

• Cloud-native, ideally AWS certified.

• Product and customer-centric approach.

• Experience with other programming languages (Python, Java, TypeScript, .NET) is a nice to have.

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.