This is part of the government initiative, Advanced PCP programme -
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.
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
Lead maintenance plan improvement in assigned area (utility and manufacturing equipment system) with the goal to increase operational efficiencies and minimize maintenance expenses
Lead in the support of assigned unit operations and/or running the facility
Standby for any emergency repair after office hours/ weekend and public holidays
Lead corrective and preventive maintenance (including investigation) for utility and manufacturing equipment systems
Completes all compliance related requirements timely
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
Leads in performance testing, commissioning, qualification (IQ, QQ) activities
Lead in maintenance related project schedule, cost and quality utilizing proper controls. This can be sub components of a larger project
Lead in the evaluation of design solutions and provides feedback for the project team
Lead in the scoping, development, execution and documentation of upgrade projects
Lead in the process control systems projects
As part of a project team or individually responsible for the scoping, development, execution and documentation of small projects within the allotted timeline, budget, design requirements, and established quality standards involved in the selection and evaluation of third-party contractors
Lead in the assessment or improvement studies to enhance equipment or system efficiency, reduce energy cost/usage and other cost saving/avoidance projects
Performs job assignments by Supervisor pertaining to equipment or system or documentation or housekeeping
Lead in monitoring performance and implementing Safety, Health and Environment (SHE improvement initiatives (i.e., audits, training, etc.)
Provides technical support to process control systems projects. Works under guidance to ensure compliance with corporate, industry, regulatory and computer validation standards
Lead in the selection, and installation of automation systems
Lead with software development, configuration, programming, and documentation for various automation platforms
Works under guidance of Senior engineer to perform system security, back-up & recovery, managing electronic records, performance monitoring duties
Helps with developing technical procedures and related change management documentation
Participate in SHE, Business Compliance, cGMP and all other compliance-related matters, where applicable
Supervise and oversee Third Party Contractors, where applicable
WHAT YOU MUST HAVE
To be successful in this role, you will have:
Bachelor of Engineering (Mechanical/Mechatronics/Electrical or Instrumentation & Control Engineering) or equivalent
1-7 years' of working experience in production facility - oil & gas chemical / semiconductor / aerospace industry
Shows basic knowledge of the principles and importance of cGMP regulations and Worldwide Quality Standards related to the execution of assigned work
WHAT YOU CAN EXPECT
Opportunities across various functional group within biopharmaceutical manufacturing
Diverse and dynamic team that focuses on development and success.
This is an Advanced Professional Conversion Programme under Workforce Singapore (WSG) and candidates must meet the following criteria and are open to the following conditions:
Singaporeans/Singapore PRs only
Fresh graduates with relevant internship are welcome to apply
PMETs/Mid-Careerist with no prior work experience in Biopharma industry are welcome to apply
Selected candidates will get a flat monthly training allowance (including transport and meal allowance) based on qualification and experience
Our Manufacturing & Supply Division is committed to be the most trusted supplier of bio-pharmaceuticals worldwide. Our facilities, along with our external contractors, suppliers, and partners, create an interdependent global manufacturing network that's committed to delivering a high quality, reliable supply to customers and patients on time, every time.
WHO WE ARE
We are known as Merck & Co., Inc., Kenilworth, New Jersey, USA in the United States and Canada and MSD everywhere else. For more than a century, we have been inventing for life, bringing forward medicines and vaccines for many of the world's most challenging diseases. Today, our company continues to be at the forefront of research to deliver innovative health solutions and advance the prevention and treatment of diseases that threaten people and animals around the world.
WHAT WE LOOK FOR
Imagine getting up in the morning for a job as important as helping to save and improve lives around the world. Here, you have that opportunity. You can put your empathy, creativity, digital mastery, or scientific genius to work in collaboration with a diverse group of colleagues who pursue and bring hope to countless people who are battling some of the most challenging diseases of our time. Our team is constantly evolving, so if you are among the intellectually curious, join us--and start making your impact today.
We are proud to be a company that embraces the value of bringing diverse, talented, and committed people together. The fastest way to breakthrough innovation is when diverse ideas come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another's thinking and approach problems collectively. We are an equal opportunity employer, committed to fostering an inclusive and diverse workplace.
Current Employees apply
Current Contingent Workers apply
Secondary Language(s) :
To be provided.
Search Firm Representatives Please Read Carefully Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.
Employee Status: Intern/Co-op (Fixed Term)
Relocation: No relocation
VISA Sponsorship:
Travel Requirements:
Flexible Work Arrangements:
Shift:
Valid Driving License:
Hazardous Material(s):
Number of Openings: 1
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