Responsibilities:

• Design and develop mechanical components and systems for electronic products.
• Collaborate with cross-functional teams to ensure seamless integration of mechanical and electronic components.
• Create detailed engineering designs and drawings using CAD software.
• Perform design analysis and validation to ensure product reliability and performance.
• Review and analyze design specifications and requirements.
• Coordinate with suppliers and manufacturing teams to ensure smooth production processes.
• Participate in product testing and troubleshoot any mechanical issues.
• Stay updated with the latest industry trends and technologies in electronics and manufacturing.
• Ensure compliance with regulatory standards and quality control processes.

Requirements:

• Degree or diploma in Mechanical Engineering or equivalent.
• Prior experience in mechanical design for electronics products.
• Proficiency in CAD software (such as SolidWorks or AutoCAD).
• Strong knowledge of manufacturing processes and materials.

Interested candidates who wish to apply for the advertised position, please click 'APPLY' to send in your resume.

EA License No: 13C6305

Reg. No.: R1874608

For candidate who applied for the advertised position is deemed to have consented to us that we may collect, use or disclose your personal information for purpose in connection with the services provided by us.

Takeda's Singapore biologics manufacturing facility focuses on manufacturing potentially life-saving medicines for patients suffering from rare blood disorders such as Hemophilia A and B. As part of the company’s Biologics Operating Unit network, the site is Takeda’s only biologics drug substance manufacturing facility in Asia. The facility has two buildings, including manufacturing suites and laboratories, as well as Takeda’s first positive energy building certified by Singapore’s Building and Construction Authority’s Green Mark scheme in 2022.

Job Title: Senior Automation Engineer
Location: Woodlands, Singapore

About the role:

• Senior Automation Engineer is recognized within Takeda as SME personnel for the Singapore Biologics manufacturing facility with respect to most of the Automation and Control activities. In this role, he/she is delivering the Process and Facility Automation activities within the Site Engineering function.
• This position reports into the Automation Manager at the Singapore manufacturing site. Senior Automation Engineer is an integral member of the Automation Team whose results have a critical impact on Automation's objectives and goals. He / she also interacts closely and advice the options to the various functions within Singapore facility to ensure that all automation and control activities are delivered to support reliable and robust operations.
• Senior Automation Engineer ensures, supports and executes all automation activities result in fit for purpose assets which meet the business requirements (safety, functionality, capacity, capability, reliability) in a timely and cost-effective manner.

How you will contribute:

• Works on multiple highly complex major projects requiring innovative, original solutions.
• Represents Automation in working meetings to discuss the fulfillment of production targets and operational effectiveness.
• Represents Singapore Automation as SME for technical queries or alignment within Global Engineering
• Plans multiple projects simultaneously. Estimates, tracks & completes project on time and within budget.
• Implements complex changes or modifications. Providing guidance to the team on how the change can be implemented.
• Provides out-of-hours technical support to address and rectify technical issues and queries on a rotational basis.
• Provides systems training for groups and end-users.
• Leads and owns systemic issues.
• Understands and challenges the cost and effort per quotations.
• Represents Automation to present topics requested by Auditor with Guidance from Manager
• Develops and complies with quality related documents. (e.g. SOP´s, CAPAs, Change Controls, Specifications etc.
• Ensures the integrity of quality related electronic data within the systems.
• Develops and upkeeps spares management, routines, preventive and corrective maintenance plan in consideration of the production schedule.
• Provides guidance and support to junior automation engineers.
• Provides systems training for automation engineers and end-users.
• Leads investigation for systemic issues.
• Establishes and coordinates necessary preventive and corrective maintenance for automation systems, plant and terminal bus network, process electrics, field devices etc. in consideration of the production plan.
• Coordinate and execute validation work for Automation Systems
• Establish and manage spare parts for automation related items within the facility.
• Adhering to automation group´s budget and ongoing capital requirements
• Responsibility to adhere to any applicable EHS requirements.
• Commitment to a fair and respectful relationship to others and behavior in accordance with Takeda’s Code of Conduct.
• Any other duties as assigned by supervisor.

What you bring to Takeda:

Education and Experience Requirements

• Relevant degree for Engineering (Electrical, Computing, or Mechatronic)
• Min. 3 years of experience in biopharmaceutical industry.
• Min. 5 years of experience in good engineering practice, process automation and maintenance
• Experience in automation projects.
• Experience in establishing communication within different system.

Key Skills and Competencies

• Strong background in any of the listed: Interface with other system, Siemens PLC/ Step 7, Siemens PCS7/ Step7/ WinCC/ Batch/ Route Control, OSI PI system and architecture, Inmation, Hardware configuration and software coding, Process Knowledge, cGMP, GAMP, ISA 95, S88, FAT, IQ, OQ, PQ and Life Cycle management of computerized system, IT knowledge for Server/Client and Infrastructure, Electrical, instrumentations and control knowledge.
• Customer orientated.
• Analytical thinking
• Good communication skills for both written and spoken.
• Able to give effective presentations to general audiences and write convincing proposals and reports with all necessary backup material for Automation related topics.
• Ability to work productively with vendors.

More about us:

• At Takeda, we are transforming patient care through the development of novel specialty pharmaceuticals and best in class patient support programs. Takeda is a patient-focused company that will inspire and empower you to grow through life-changing work.
• Certified as a Global Top Employer, Takeda offers stimulating careers, encourages innovation, and strives for excellence in everything we do. We foster an inclusive, collaborative workplace, in which our teams are united by an unwavering commitment to deliver Better Health and a Brighter Future to people around the world.

Empowering our people to shine:

Takeda is proud in its commitment to creating a diverse workforce and providing equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, gender expression, parental status, national origin, age, disability, citizenship status, genetic information or characteristics, marital status, or any other characteristic protected by law.

Senior Machinist

• Working Days: Monday-Thursday
• Working Hours: 7.30am - 7.30pm // 7.30pm - 7.30am [Rotated shift]
• Location:Woodlands
• Salary: $3500 - $4000 + VB

Requirements:

• Possess at least 5 years of working experience in manufacturing and mechanical environment.
• NITEC in Precision Engineering or equivalent.
• Able to use basic measuring instruments, gauges and measuring techniques.
• Able to follow instructed job layouts and operate Lathe/Turn-Mill machines. Ability to operate 4½ and 5 axis is a plus.
• Able to calculate, set and modify machining parameters (speeds, feeds, depths of cuts tapers etc.)
• Demonstrate ability to interpret engineering drawings with multiple views and machining surface.
• Must be able to work 12 hours rotation shift.
• Able to manage a team of 5 machinists.

Job Scope:

• Understands procedures, work orders, blueprints, and set-up sheets and receives verbal work instructions to plan the job layout with as few set-ups as possible.
• Sets-up machine as required using prescribed detail and operating procedures.
• Promptly reports any operational problems or safety issues with machinery, tools or equipment to Line Leader.
• Actively participate and stain high level of 5S.
• Safely performs all duties and keeps all employees aware of dangers in the work area.
• Practices good housekeeping in assigned areas and properly dispose of waste accordingly to safety and environmental policies.
• Able to set up tools with little guidance. Gathers required tooling and fixture or places order if necessary.
• Identifies the type of material being used and corrects or modifies tooling call-outs, offsets, speed and feeds to allow for variations in the material.
• Performs the majority of machining operations needed to complete the part. Consistently meets or exceeds manufacturing, safety and quality targets.

Lee Wan Ling | Reg No: R23116154

THE SUPREME HR ADVISORY PTE LTD | EA No: 14C7279

What if the work you did every day could impact the lives of people you know? Or all of humanity?

At Illumina, we are expanding access to genomic technology to realize health equity for billions of people around the world. Our efforts enable life-changing discoveries that are transforming human health through the early detection and diagnosis of diseases and new treatment options for patients.

Working at Illumina means being part of something bigger than yourself. Every person, in every role, has the opportunity to make a difference. Surrounded by extraordinary people, inspiring leaders, and world changing projects, you will do more and become more than you ever thought possible.

Reporting to the Assistant Director, Enterprise Information Security Engineering (EIS), this Sr. Staff Information Security Engineer plays an important tactical role at Illumina.   Member of an enterprise-wide and global Information Security team, this position participates in the deployment and support of controls and processes that protect the company’s data.  This key role interacts globally across all business units, performs technical reviews, technical security control testing, gap analysis, risk evaluation, and provides subject-matter expertise for solutions deployed and supported by the Information Security department.  Support of program controls and processes to ensure mitigation of risks and approved configuration certification of the entire Illumina environment.  This position requires extensive knowledge, experience, and proven skills in the areas of engineering, architecture, and design, especially within the SCADA, Operational Technology (OT) and Internet of Things (IoT) space.

Support includes understanding and enforcing of established processes, analysis of cloud and on-premises computing environment, coordination of project responsibilities, testing, documentation, technical diagraming, cybersecurity-based awareness and education, and participation in periodic audits.  Performs all duties in accordance with the company’s policies and procedures, all state, federal, and country laws and regulations, wherein the company operates.  Delivery of activity reporting, including metrics, environment impact, effectiveness progress, and performance indicators.  The role will also assist with ensuring discretionary and regulatory audits are aligned with Illumina’s current processes and procedures.

Duties & Responsibilities

• Assists in the execution of the Information Security Program, Data Governance practices, and Privacy assurance
• Analyzes risk of existing network and system architectures against correlating policies and risks, and provides technical input for appropriate remediation or action plans
• Participates in the following and enforcement of ongoing practices and procedures, technical documentation, and diagrams for appropriate security measure maturity and effectiveness
• Coordinates with team members and other technical departments, ensuring proper communication of the overall success of project tasks and dependencies
• Executes effective monitoring and actionable Information Security reporting across the InfoSec technical landscape
• Executes as a reliable second line-of-defense via documented processes, controls, templates, and rigors
• Practices applicable procedures and standards that meet existing and newly developed policy and regulatory requirements (i.e., PCI-DSS, SOX, GDPR, CCPA)
• Actively provides technical expertise for both Information Security and stakeholder teams for timely and effective delivery of enterprise-wide cybersecurity-based technology design, implementation, deployment, and support
• Provides consulting on best practices to internal customers to ensure processes are embedded at the correct time and frequency and to ensure compliance to security standards
• Provide technical control evidence for audits, evaluate existing tool effectiveness, and collaborates to deploy and support solutions to enhance the company’s security posture
• Build collaborative partnerships with manufacturing business unit departments and leaders to create alignment on security strategy advancement
• Demonstrate consistent goal deliverable performance, ability to embrace and accommodate business and technical challenges, maintain time-based commitments, and deliver results within reasonable expectations

Qualifications

• Minimum 5-8+ years’ experience implementing and supporting Information Security enterprise-level tools with track record of creating enterprise-wide scalable solutions based on industry standard security concepts, technical controls, and best practice frameworks
• Minimum 4+ years in a senior engineering role with experience identifying technical and procedural gaps across security focused solutions and processes
• Advanced degree in automation, robotics, mechatronics, electronic engineering, or manufacturing security disciplines
• OT/ICS system knowledge and experience (SCADA, DCS, PLC, EMS, etc.)
• Experience in evidence validation for OT frameworks (e.g., IEC ISA 99/62443, NIST SP 800-82, etc.)
• ICS protocols and technology hands-on expertise (Rockwell, Siemens, Schneider Electric, etc.)
• Expert-level knowledge and experience managing network and security devices (i.e., Firewalls, IDS/IPS, SIEMs, AV\Malware sandboxes, VPN's, vulnerability scanning tools, network taps, etc.)
• Ability to proactively collaborate by sharing information, managing knowledge across many technology domains, and championing solutions for broad adoption to improve security posture
• Strong oral and written communication skills, with a focus on technical document and diagrams
• Proven participation and advancement with team goals, projects, and work efficiency showing drive to achieve results
• A self-starter with a hands-on style, high level of energy, stamina, drive, and commendable organization and time management skills

Education

• Bachelor’s degree in Information Systems, Computer Science, Information Security, and/or related work experience
• Professional qualifications are preferred: CISSP, GISCP, GSEC, SANS, GIAC, or similar

#LI-HYBRID

#illuminacareers

Illumina believes that everyone has the ability to make an impact, and we are proud to be an equal opportunity employer committed to providing employment opportunity regardless of sex, race, creed, color, gender, religion, marital status, domestic partner status, age, national origin or ancestry, physical or mental disability, medical condition, sexual orientation, pregnancy, military or veteran status, citizenship status, and genetic information.

What if the work you did every day could impact the lives of people you know? Or all of humanity?

At Illumina, we are expanding access to genomic technology to realize health equity for billions of people around the world. Our efforts enable life-changing discoveries that are transforming human health through the early detection and diagnosis of diseases and new treatment options for patients.

Working at Illumina means being part of something bigger than yourself. Every person, in every role, has the opportunity to make a difference. Surrounded by extraordinary people, inspiring leaders, and world changing projects, you will do more and become more than you ever thought possible.

Reporting to the Assistant Director, Enterprise Information Security Engineering (EIS), this Sr. Staff Information Security Engineer plays an important tactical role at Illumina.   Member of an enterprise-wide and global Information Security team, this position participates in the deployment and support of controls and processes that protect the company’s data.  This key role interacts globally across all business units, performs technical reviews, technical security control testing, gap analysis, risk evaluation, and provides subject-matter expertise for solutions deployed and supported by the Information Security department.  Support of program controls and processes to ensure mitigation of risks and approved configuration certification of the entire Illumina environment.  This position requires extensive knowledge, experience, and proven skills in the areas of engineering, architecture, and design, especially within the SCADA, Operational Technology (OT) and Internet of Things (IoT) space.

Support includes understanding and enforcing of established processes, analysis of cloud and on-premises computing environment, coordination of project responsibilities, testing, documentation, technical diagraming, cybersecurity-based awareness and education, and participation in periodic audits.  Performs all duties in accordance with the company’s policies and procedures, all state, federal, and country laws and regulations, wherein the company operates.  Delivery of activity reporting, including metrics, environment impact, effectiveness progress, and performance indicators.  The role will also assist with ensuring discretionary and regulatory audits are aligned with Illumina’s current processes and procedures.

Duties & Responsibilities

• Assists in the execution of the Information Security Program, Data Governance practices, and Privacy assurance
• Analyzes risk of existing network and system architectures against correlating policies and risks, and provides technical input for appropriate remediation or action plans
• Participates in the following and enforcement of ongoing practices and procedures, technical documentation, and diagrams for appropriate security measure maturity and effectiveness
• Coordinates with team members and other technical departments, ensuring proper communication of the overall success of project tasks and dependencies
• Executes effective monitoring and actionable Information Security reporting across the InfoSec technical landscape
• Executes as a reliable second line-of-defense via documented processes, controls, templates, and rigors
• Practices applicable procedures and standards that meet existing and newly developed policy and regulatory requirements (i.e., PCI-DSS, SOX, GDPR, CCPA)
• Actively provides technical expertise for both Information Security and stakeholder teams for timely and effective delivery of enterprise-wide cybersecurity-based technology design, implementation, deployment, and support
• Provides consulting on best practices to internal customers to ensure processes are embedded at the correct time and frequency and to ensure compliance to security standards
• Provide technical control evidence for audits, evaluate existing tool effectiveness, and collaborates to deploy and support solutions to enhance the company’s security posture
• Build collaborative partnerships with manufacturing business unit departments and leaders to create alignment on security strategy advancement
• Demonstrate consistent goal deliverable performance, ability to embrace and accommodate business and technical challenges, maintain time-based commitments, and deliver results within reasonable expectations

Qualifications

• Minimum 5-8+ years’ experience implementing and supporting Information Security enterprise-level tools with track record of creating enterprise-wide scalable solutions based on industry standard security concepts, technical controls, and best practice frameworks
• Minimum 4+ years in a senior engineering role with experience identifying technical and procedural gaps across security focused solutions and processes
• Advanced degree in automation, robotics, mechatronics, electronic engineering, or manufacturing security disciplines
• OT/ICS system knowledge and experience (SCADA, DCS, PLC, EMS, etc.)
• Experience in evidence validation for OT frameworks (e.g., IEC ISA 99/62443, NIST SP 800-82, etc.)
• ICS protocols and technology hands-on expertise (Rockwell, Siemens, Schneider Electric, etc.)
• Expert-level knowledge and experience managing network and security devices (i.e., Firewalls, IDS/IPS, SIEMs, AV\Malware sandboxes, VPN's, vulnerability scanning tools, network taps, etc.)
• Ability to proactively collaborate by sharing information, managing knowledge across many technology domains, and championing solutions for broad adoption to improve security posture
• Strong oral and written communication skills, with a focus on technical document and diagrams
• Proven participation and advancement with team goals, projects, and work efficiency showing drive to achieve results
• A self-starter with a hands-on style, high level of energy, stamina, drive, and commendable organization and time management skills

Education

• Bachelor’s degree in Information Systems, Computer Science, Information Security, and/or related work experience
• Professional qualifications are preferred: CISSP, GISCP, GSEC, SANS, GIAC, or similar

#LI-HYBRID

#illuminacareers

Illumina believes that everyone has the ability to make an impact, and we are proud to be an equal opportunity employer committed to providing employment opportunity regardless of sex, race, creed, color, gender, religion, marital status, domestic partner status, age, national origin or ancestry, physical or mental disability, medical condition, sexual orientation, pregnancy, military or veteran status, citizenship status, and genetic information.

Responsibilities

• Responsible for ensuring products produced meet the product and customers' quality requirement
• Responsible for developing and improving the processes to gain productivity, efficiency, quality and costs.
• Responsible for coordinating NPI/NPQ activities with details and meeting timeline.
• Responsible for supporting and resolving daily technical issues in operations
• Responsible for supporting analysis of failures from yield loss, reliability failures, new products, new materials.

Requirements

• Min Diploma in Electronic Engineering, Material Science or relevant
• Min 5 years of working experience in semicon assembly and test environment
• Experience in Assembly FOL of dicing, die attach, wire bond
• Experience in maintenance of assembly and test machines of dicing, die attach, wire bond encapsulation, testing

Please kindly email your resume in Ms Word to hr@xtalents.com.sg

We regret to inform that only shortlisted candidates would be notified.

Registration Number: R1328870

EA License No. 22C1026

About Pierce, an Oshkosh company

At Pierce Manufacturing, we build trucks that protect people and communities around the world. To our team, there is no room for anything less than providing the absolute best. Since 1913, building truck bodies on Model T Ford chassis in an old converted church has evolved to creating highly customized, carefully designed and engineering pumpers, aerials, tankers and rescue units that have no equal. Today, you'll find more than 30,000 Pierce apparatuses on the road that are making a difference in people's lives, every day. To us, every step in the process of building our trucks is personal. From innovation and expertise, to the customization and service. Our trucks are designed to perform under the toughest conditions.

Senior Engineer - Electrical R25936

The Sr Engineer – Electrical designs functional, reliable and cost-effective heavy-duty vehicle high voltage electrical systems. Performs engineering analysis and electrical design or re-design, and development of electrical systems and subsystems into existing and new vehicles. Provides integration and execution support for vehicle control and embedded systems development.

YOUR IMPACT:  

• Responsible for design and integration of electrical components and circuitry into heavy duty vehicles.
• Responsible for a project or part of a project.
• Ensure design compliance to various regulations and standards across multiple regions and markets.
• Support more senior engineers in the preparation of accurate calculations, analysis and investigation according to Oshkosh as well as general industry engineering standards and processes.
• Support more senior engineers in the preparation of plans, designs, computation methods, and/or reporting.
• Collaborate as needed with other engineering or business support disciplines internally as well as suppliers externally.
• Provide guidance or mentorship to entry level engineers, designers, or technicians working on a common project.
• Provide technical assistance for prototype, pilot or production builds, including resolution of problems in manufacturing.
• Utilize multimeters / oscilloscopes, Controller Area Network (CAN) tools, and proprietary programming tools for design, validation, and interrogation.
• Work closely with controls / software engineers and communicate associated design implications and requirements involving electrical / electronic systems design.
• Other duties as assigned.
• Regular attendance is required.

MINIMUM QUALIFICATIONS:  

• Accredited Bachelor's degree in Engineering or related field with three (3) or more years of related experience.

STANDOUT QUALIFICATIONS: 

• Accredited Bachelor's degree in Electrical Engineering.                                    
• Familiarity with programming languages and controls software.
• Familiarity with Controller Area Network (CAN)/SAE J1939 protocol.
• Power Electronics and Machines familiarity.
• Energy Storage system familiarity.
• Diagnostic and troubleshooting experience.
• Zuken E3 Schematic Software.
• CATIA Modeling of Electrical Routings.

CORE COMPETENCIES:

• Internal Contacts: Contact with peers and others involving explanation of information (these contacts may be within or outside department or division), and the gathering of factual information; may include the communication of sensitive or confidential information.
• External Contacts:  Limited external contact to gather information, answer queries, or ask assistance.
• Communication Skills:  Read, write and comprehend simple instructions, short correspondence and memos; Read and interpret safety rules, operating/maintenance instructions and procedure manuals; Write routine reports, correspondence and speak effectively before both internal and external groups; Read, analyze and interpret business manuals, technical procedures and/or government regulations: Read, analyze and interpret scientific and technical journals, financial reports and legal documents.
• Decision-Making:  Regularly makes decisions of responsibility, involving evaluation of information. Decisions may require development or application of alternatives or precedents.
• Complexity, Judgment and Problem Solving:  Generally diversified and moderately difficult work. Requires judgment in the adaptation and interpretation of established practices and procedures to meet problems and situations to which the application is not clearly defined.
• Supervisory/Managerial:  General instructing, scheduling, and reviewing the work of others performing the same or directly related work. Acts as “lead worker”.

WORKING CONDITIONS:

• Physical Demands: Frequent: Standing, Walking/Running, Sitting, Reaching, Hearing, Talking, Visual, Typing; Occasional: Driving, Fine Dexterity, Manual Dexterity; Upper Extremity Repetitive Motion; Seldom: Lifting/Carrying 25lbs., Pushing/Pulling 25llbs.
• Non-Physical Demands: Frequent: Analysis/Reasoning, Communication/Interpretation, Math/Mental Computation, Reading, Sustained Mental Activity (i.e. auditing, problem solving, grant writing, composing reports), Writing.
• Environmental Demands: Frequent: Work Alone, Frequent Task Changes, Tedious/Exacting Work; Occasional: High Volume Public Contact.
• Work Schedule:  Routine shift hours. Infrequent overtime, weekend, or shift rotation.
• Demands/Deadlines: High volume and variable work demands and deadlines impose strain on routine basis or considerable stress intermittently; OR regular direct contacts with distressed individuals within the immediate work environment; and/or exposure to demands and pressures from persons other than immediate supervisor.

WHY PIERCE? 

Moving the future forward is our priority and this includes your future. We encourage professional development and champion our employees’ success through various skills and training opportunities. Named one of the World’s Most Ethical Companies™ by Ethisphere Institute for six consecutive years, everything we do at Oshkosh is guided by our core values and the 15k+ team members around the world who embody them.  

We put people first. We do the right thing. We persevere. We are better together. 

We offer our employees an outstanding range of benefits, including:

• Eligibility on Day 1 for medical, prescription, dental and vision insurance
• Up to $10,000 each year for tuition reimbursement to allow you to further your education in a degreed program (Associates, Bachelor’s or Master’s degree programs)
• 401k plan with company match, $.50 for every dollar up to 6%
• Competitive paid-time off plans
• Company bonus plan, free life, short and long-term disability plans
• Health Saving Account (HSA) with company contribution up to $1K per year
• Many, many more!

Visit our Glassdoor Profile
Keep up with us on LinkedIn

*OSH1917

#LI-BB1

Oshkosh is committed to working with and offering reasonable accommodations to job applicants with disabilities. If you need assistance or an accommodation due to a disability for any part of the recruitment process, please contact our reception desk by phone at +1 (920) 502.3009 or our talent acquisition team by email corporatetalentacquisition@oshkoshcorp.com.

Oshkosh Corporation is an Equal Opportunity and Affirmative Action Employer. This company will provide equal opportunity to all individuals without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status. Information collected regarding categories as provided by law will in no way affect the decision regarding an employment application.

Oshkosh Corporation will not discharge or in any manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with Oshkosh Corporation's legal duty to furnish information.

Certain positions with Oshkosh Corporation require access to controlled goods and technologies subject to the International Traffic in Arms Regulations or the Export Administration Regulations. Applicants for these positions may need to be "U.S. Persons," as defined in these regulations. Generally, a "U.S. Person" is a U.S. citizen, lawful permanent resident, or an individual who has been admitted as a refugee or granted asylum.

Why Patients Need You

Whether you are involved in the design and development of manufacturing processes for products or supporting maintenance and reliability, engineering is vital to making sure customers and patients have the medicines they need, when they need them. Working with our innovative engineering team, you'll help bring medicines to the world even faster by imagining what’s possible and taking action.

What You Will Achieve

Working with Pfizer’s dynamic engineering team, you will play a critical role in the management of manufacturing information systems to improve manufacturing success rates and ensuring zero down time.
 

As a Senior Associate, your knowledge and skills will contribute towards the goals and objectives of the team.  Your focus and ability to meet team targets will help in completing critical deliverables. Your innovative use of communication tools and techniques will facilitate in explaining difficult issues and establishing consensus between teams.
 

It is your hard work and dedication that will make Pfizer ready to achieve new milestones and help patients across the globe.
 

How You Will Achieve It

• Contribute to the completion of projects, manage own time on agreed targets, develop plans for own projects and leads small project teams.

• Monitor, generate and complete the periodic review, validation master plan for the automation engineering program.

• Demonstrate good planning, organizing, time management and team participation skills.

• Responsible for routine and preventive maintenance work, ensure all the equipment and facilities work safely, efficiently and reliably.

• Generate and develop standard operating procedures and system support.

• Analyze operational process problems and recommend appropriate corrective and preventative actions.

• Manage change control authoring and execution.

• Participate in the site and network wide teams to provide cybersecurity alignment and direction.

• Provide 24x7x365 support of our automation systems and perform automation activities for capital and non-capital projects.

• Modify moderately complex to highly complex control logic that requires a degree of scientific and/or manufacturing process expertise.

• Mentor and guide junior staff and serve as a technical trainer, whenever necessary.

• Clearly communicate progress and issues to peers, customers, and project managers.

Qualifications

Must-Have

• Applicant must have a High School Diploma (or Equivalent) and 8 years of relevant experience.

• OR an Associate's degree with 6 years of experience.

• OR a Bachelor's with at least 3 years of experience.

• OR Master's with more than 1 year of experience.  

• 3+ years of demonstrated experience in Automation Engineering.

• Experience with writing software test plans, user requirements, and system design documents.

• Experience on Automation Compliance projects.

• Familiar with process controls equipment.

• Strong knowledge of Computerized Systems, Compliance regulations and standards.

• Understanding of programming, and proficiency in at least one language.

• Teamwork spirit, good communication skills and training abilities.

• Ability to learn new technologies and adapt to change.

Nice-to-Have

• Relevant pharmaceutical manufacturing experience

  
 

PHYSICAL/MENTAL REQUIREMENTS

• light lifting, sitting, standing, walking, bending.

NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS

• Travel less than 10% (typically training or equipment acceptance testing)

Work Location Assignment: On Premise

Other Job Details:

• Last Date to Apply for Job: March 31, 2024

• Eligible for Relocation Package

• Eligible for Employee Referral Bonus

The annual base salary for this position ranges from $78,000.00 to $130,000.00. In addition, this position is eligible for participation in Pfizer’s Global Performance Plan with a bonus target of 10.0% of the base salary. We offer comprehensive and generous benefits and programs to help our colleagues lead healthy lives and to support each of life’s moments. Benefits offered include a 401(k) plan with Pfizer Matching Contributions and an additional Pfizer Retirement Savings Contribution, paid vacation, holiday and personal days, paid caregiver/parental and medical leave, and health benefits to include medical, prescription drug, dental and vision coverage. Learn more at Pfizer Candidate Site – U.S. Benefits | (uscandidates.mypfizerbenefits.com). Pfizer compensation structures and benefit packages are aligned based on the location of hire. The United States salary range provided does not apply to Tampa, FL or any location outside of the United States.

Relocation assistance may be available based on business needs and/or eligibility.

Engineering

#LI-PFE

The Role:

Joining Moderna offers the unique opportunity to be part of a pioneering team that's revolutionizing medicine through mRNA technology with a diverse pipeline of development programs across various diseases. As an employee, you'll be part of a continually growing organization working alongside exceptional colleagues and strategic partners worldwide, contributing to global health initiatives. Moderna's commitment to advancing the technological frontier of mRNA medicines ensures a challenging and rewarding career experience with the potential to make a significant impact on patients' lives worldwide​​.

Moderna is solidifying its footprint in Basel, the vibrant hub of pharmaceutical innovation in Switzerland, to further our mission of delivering the greatest possible impact to people through mRNA medicines. As we grow our international operations and commercial activities in Basel, we invite global talents to join us in this exciting journey of transforming medicine and impacting lives worldwide​​.

Moderna is seeking a dedicated and innovative Senior Engineer I to join our Manufacturing Science and Technology (MS&T) department. This pivotal role is designed for a passionate individual who will be instrumental in supporting our Contract Manufacturing Organization (CMO) activities, primarily focusing on lipid nanoparticle manufacturing in Granada, Spain. As a key player in the external MS&T team, you will also extend your expertise to support plasmid and custom-made small molecule production at CMOs. The successful candidate will forge strong collaborative ties with CMOs and internal teams—including External Manufacturing, Supply Chain, Regulatory, and Quality—to ensure flawless execution of technology transfer and ongoing technical support. Your contributions will be critical in upholding Moderna's commitment to innovation and excellence in the biotechnology field.

Here’s What You’ll Do:

Your key responsibilities will be:

• Support technology transfer activities for commercial products into CMOs, ensuring seamless integration and operational excellence.

• Provide robust technical support for cGMP manufacturing processes at CMOs, including authoring technology transfer documents, addressing change controls, and assisting with manufacturing investigations, deviations, and leading process validation activities.

• Conduct thorough data reviews and analyses to evaluate manufacturing performance, authoring comprehensive summary reports.

• Lead cross-functional teams in troubleshooting, identifying, and implementing operational improvements for manufacturing processes and equipment.

• Maintain synergy with global manufacturing sites by sharing knowledge, data, and solutions to common manufacturing challenges.

Your responsibilities will also include:

• Demonstrating leadership in process development or operational experience in bioprocessing unit operations such as enzymatic reactions, chromatography, nanoparticle manufacturing, and tangential flow filtration.

• Familiarity with cGMP environments and single-use equipment is highly advantageous.

• Proficiency in English with excellent verbal and written communication skills; knowledge of Spanish is favorable.

The key Moderna Mindsets you’ll need to succeed in the role:

• We pursue options in parallel: Your role will demand managing multiple projects and priorities concurrently to ensure the best outcomes in technology transfer and manufacturing support.

• We pivot fearlessly: Given the dynamic nature of manufacturing processes and the need for constant innovation, a fearless approach to embracing and leading change is crucial.

Here’s What You’ll Need (Minimum Qualifications):

• M.S. or Ph.D. in Chemistry, Biochemistry, Chemical Engineering, Pharmaceutical Engineering, or a related technical discipline.

• A minimum of 5 years of related work experience in the pharmaceutical manufacturing industry.

• Demonstrable process development or operational experience in bioprocessing unit operations such as enzymatic reactions, chromatography, nanoparticle manufacturing and tangential flow filtration.

• Familiarity with cGMP environments and single-use equipment is highly advantageous.

• Proficiency in English with excellent verbal and written communication skills; knowledge of Spanish is favorable.

• Proven ability to manage complex projects in a dynamic, fast-paced environment.

• Capacity to effectively collaborate in a dynamic, cross-functional matrix environment.

• Flexibility and adaptability to meet the challenges of new and evolving technical opportunities in a rapidly changing environment.

Here’s What You’ll Bring to the Table (Preferred Qualifications)

• Demonstrated ability to drive projects to completion with minimal supervision.

• Proven track record of problem-solving and innovation in bioprocessing operations.

• Strong analytical skills with the ability to make data-driven decisions.

• Experience in a multinational organization with the ability to navigate cultural and operational complexities.

• A proactive, forward-thinking approach that anticipates and addresses challenges before they arise.

Moderna offers personalized benefit programs and well-being resources as unique as our global workforce so employees can do their best work.

We recognize and appreciate your diverse needs and interests and do our best to support you at work and at home with:

• Quality healthcare and insurance benefits
• Lifestyle Spending Accounts to create your own pathway to well-being
• Free premium access to fitness, nutrition, and mindfulness classes
• Family planning and adoption benefits
• Generous paid time off, including vacation, bank holidays, volunteer days, sabbatical, and a discretionary year-end shutdown
• Educational resources
• Savings and investments
• Location-specific perks and extras!

The benefits offered may vary depending on the nature of your employment with Moderna and the country where you work.

About Moderna

Since our founding in 2010, we have aspired to build the leading mRNA technology platform, the infrastructure to reimagine how medicines are created and delivered, and a world-class team. We believe in giving our people a platform to change medicine and an opportunity to change the world. 

By living our mission, values, and mindsets every day, our people are the driving force behind our scientific progress and our culture. Together, we are creating a culture of belonging and building an organization that cares deeply for our patients, our employees, the environment, and our communities.

We are proud to have been recognized as a Science Magazine Top Biopharma Employer, a Fast Company Best Workplace for Innovators, and a Great Place to Work in the U.S.

If you want to make a difference and join a team that is changing the future of medicine, we invite you to visit modernatx.com/careers to learn more about our current opportunities.

Moderna is a smoke-free, alcohol-free and drug-free work environment.

Moderna is a place where everyone can grow. If you meet the Basic Qualifications for the role and you would be excited to contribute to our mission every day, please apply!

Moderna is proud to be an equal opportunity workplace and is an affirmative action employer.

Moderna is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person's race, color, sex, gender identity or expression, age, religion, national origin, ancestry or citizenship, ethnicity, disability, military or protected veteran status, genetic information, sexual orientation, marital or familial status, or any other personal characteristic protected under applicable law. Moderna is an E-Verify Employer in the United States. We also consider qualified applicants regardless of criminal histories, consistent with legal requirements.

Belonging, Inclusion, and Diversity are critical to the success of our company and our impact on society. We’re focused on attracting, retaining, developing, and advancing our employees and believe that by cultivating diverse experiences, backgrounds, and ideas, we can provide an environment where every employee is able to contribute their best.

Moderna is committed to offering reasonable accommodations to qualified job applicants with disabilities. Any applicant requiring an accommodation in connection with the hiring process and/or to perform the essential functions of the position for which the applicant has applied should make a request to the Talent Acquisition Partner or contact the Accommodations team at leavesandaccommodations@modernatx.com.  (EEO/AAP Employer) 

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The Role:

Joining Moderna offers the unique opportunity to be part of a pioneering team that's revolutionizing medicine through mRNA technology with a diverse pipeline of development programs across various diseases. As an employee, you'll be part of a continually growing organization working alongside exceptional colleagues and strategic partners worldwide, contributing to global health initiatives. Moderna's commitment to advancing the technological frontier of mRNA medicines ensures a challenging and rewarding career experience with the potential to make a significant impact on patients' lives worldwide​​.

At the heart of Spain's Andalusia region, Moderna is solidifying its global presence by collaborating closely with a local CMO in Granada. This strategic partnership leverages Granada's rich history in science and innovation, focusing on the active substance manufacturing critical to our mRNA medicines. Our Granada team plays a pivotal role in our supply chain, ensuring the seamless production and global distribution of our transformative healthcare solutions. We are seeking dedicated professionals who are passionate about leveraging cutting-edge biotechnology to make a substantial impact on global health. Join us in Granada, where tradition meets innovation, to contribute to our mission of pioneering mRNA technology and improving lives worldwide​​.

Moderna is seeking a dedicated and innovative Senior Engineer I to join our Manufacturing Science and Technology (MS&T) department. This pivotal role is designed for a passionate individual who will be instrumental in supporting our Contract Manufacturing Organization (CMO) activities, primarily focusing on lipid nanoparticle manufacturing in Granada, Spain. As a key player in the external MS&T team, you will also extend your expertise to support plasmid and custom-made small molecule production at CMOs. The successful candidate will forge strong collaborative ties with CMOs and internal teams—including External Manufacturing, Supply Chain, Regulatory, and Quality—to ensure flawless execution of technology transfer and ongoing technical support. Your contributions will be critical in upholding Moderna's commitment to innovation and excellence in the biotechnology field.

Here’s What You’ll Do:

Your key responsibilities will be:

• Support technology transfer activities for commercial products into CMOs, ensuring seamless integration and operational excellence.

• Provide robust technical support for cGMP manufacturing processes at CMOs, including authoring technology transfer documents, addressing change controls, and assisting with manufacturing investigations, deviations, and leading process validation activities.

• Conduct thorough data reviews and analyses to evaluate manufacturing performance, authoring comprehensive summary reports.

• Lead cross-functional teams in troubleshooting, identifying, and implementing operational improvements for manufacturing processes and equipment.

• Maintain synergy with global manufacturing sites by sharing knowledge, data, and solutions to common manufacturing challenges.

Your responsibilities will also include:

• Demonstrating leadership in process development or operational experience in bioprocessing unit operations such as enzymatic reactions, chromatography, nanoparticle manufacturing, and tangential flow filtration.

• Familiarity with cGMP environments and single-use equipment is highly advantageous.

• Proficiency in English with excellent verbal and written communication skills; knowledge of Spanish is favorable.

The key Moderna Mindsets you’ll need to succeed in the role:

• We pursue options in parallel: Your role will demand managing multiple projects and priorities concurrently to ensure the best outcomes in technology transfer and manufacturing support.

• We pivot fearlessly: Given the dynamic nature of manufacturing processes and the need for constant innovation, a fearless approach to embracing and leading change is crucial.

Here’s What You’ll Need (Minimum Qualifications):

• M.S. or Ph.D. in Chemistry, Biochemistry, Chemical Engineering, Pharmaceutical Engineering, or a related technical discipline.

• A minimum of 5 years of related work experience in the pharmaceutical manufacturing industry.

• Demonstrable process development or operational experience in bioprocessing unit operations such as enzymatic reactions, chromatography, nanoparticle manufacturing and tangential flow filtration.

• Familiarity with cGMP environments and single-use equipment is highly advantageous.

• Proficiency in English with excellent verbal and written communication skills; knowledge of Spanish is favorable.

• Proven ability to manage complex projects in a dynamic, fast-paced environment.

• Capacity to effectively collaborate in a dynamic, cross-functional matrix environment.

• Flexibility and adaptability to meet the challenges of new and evolving technical opportunities in a rapidly changing environment.

Here’s What You’ll Bring to the Table (Preferred Qualifications)

• Demonstrated ability to drive projects to completion with minimal supervision.

• Proven track record of problem-solving and innovation in bioprocessing operations.

• Strong analytical skills with the ability to make data-driven decisions.

• Experience in a multinational organization with the ability to navigate cultural and operational complexities.

• A proactive, forward-thinking approach that anticipates and addresses challenges before they arise.

Moderna offers personalized benefit programs and well-being resources as unique as our global workforce so employees can do their best work.

We recognize and appreciate your diverse needs and interests and do our best to support you at work and at home with:

• Quality healthcare and insurance benefits
• Lifestyle Spending Accounts to create your own pathway to well-being
• Free premium access to fitness, nutrition, and mindfulness classes
• Family planning and adoption benefits
• Generous paid time off, including vacation, bank holidays, volunteer days, sabbatical, and a discretionary year-end shutdown
• Educational resources
• Savings and investments
• Location-specific perks and extras!

The benefits offered may vary depending on the nature of your employment with Moderna and the country where you work.

About Moderna

Since our founding in 2010, we have aspired to build the leading mRNA technology platform, the infrastructure to reimagine how medicines are created and delivered, and a world-class team. We believe in giving our people a platform to change medicine and an opportunity to change the world. 

By living our mission, values, and mindsets every day, our people are the driving force behind our scientific progress and our culture. Together, we are creating a culture of belonging and building an organization that cares deeply for our patients, our employees, the environment, and our communities.

We are proud to have been recognized as a Science Magazine Top Biopharma Employer, a Fast Company Best Workplace for Innovators, and a Great Place to Work in the U.S.

If you want to make a difference and join a team that is changing the future of medicine, we invite you to visit modernatx.com/careers to learn more about our current opportunities.

Moderna is a smoke-free, alcohol-free and drug-free work environment.

Moderna is a place where everyone can grow. If you meet the Basic Qualifications for the role and you would be excited to contribute to our mission every day, please apply!

Moderna is proud to be an equal opportunity workplace and is an affirmative action employer.

Moderna is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person's race, color, sex, gender identity or expression, age, religion, national origin, ancestry or citizenship, ethnicity, disability, military or protected veteran status, genetic information, sexual orientation, marital or familial status, or any other personal characteristic protected under applicable law. Moderna is an E-Verify Employer in the United States. We also consider qualified applicants regardless of criminal histories, consistent with legal requirements.

Belonging, Inclusion, and Diversity are critical to the success of our company and our impact on society. We’re focused on attracting, retaining, developing, and advancing our employees and believe that by cultivating diverse experiences, backgrounds, and ideas, we can provide an environment where every employee is able to contribute their best.

Moderna is committed to offering reasonable accommodations to qualified job applicants with disabilities. Any applicant requiring an accommodation in connection with the hiring process and/or to perform the essential functions of the position for which the applicant has applied should make a request to the Talent Acquisition Partner or contact the Accommodations team at leavesandaccommodations@modernatx.com.  (EEO/AAP Employer) 

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At Alcon, we are driven by the meaningful work we do to help people see brilliantly. We innovate boldly, champion progress, and act with speed as the global leader in eye care. Here, you’ll be recognized for your commitment and contributions and see your career like never before. Together, we go above and beyond to make an impact in the lives of our patients and customers. We foster an inclusive culture and are looking for diverse, talented people to join Alcon.

As a Spare Parts Executive/ Engineer, you will be tasked to oversee inventory control under our Engineering Department. You will work closely with various Engineering and production team to ensure smooth day to day operations for manufacturing plant.

In this role, a typical day will include:

• Tracking of spares and consumables inventory min/max level and ordering to ensure availability to support operation
• Follow up on parts delivery, GR and invoices
• Plan and perform scheduled stock count to maintain inventory accuracy
• Tracking of monthly spending in system
• Maintain and sustain good housekeeping standards and practices
• Compliance to quality and HSE requirements
• Cost saving initiatives and continuous improvement plans i.e. Localization of parts and repairs, etc.
• Work with engineers (Engineer& production) new and obsoleted parts procurement

WHAT YOU’LL BRING TO ALCON:

• NITEC/ Diploma in Engineering or related field
• 3-5 years of relevant inventory control experience in manufacturing/ production setting
• Experience in using SAP/ Maximo is highly advantageous but not a must
• Office hours
• Comfortable to work at Tuas south (company transport provided at Outram Park/ Kranji/ Boon Lay MRT)

HOW YOU CAN THRIVE AT ALCON:

• Good team player
• Part of growing company
• Career development

Alcon Careers

See your impact at alcon.com/careers

Responsibilities

• Responsible for ensuring products produced meet the product and customers' quality requirement
• Responsible for developing and improving the processes to gain productivity, efficiency, quality and costs.
• Responsible for coordinating NPI/NPQ activities with details and meeting timeline.
• Responsible for supporting and resolving daily technical issues in operations
• Responsible for supporting analysis of failures from yield loss, reliability failures, new products, new materials.

Requirements

• Min Diploma in Electronic Engineering, Material Science or relevant
• Min 5 years of working experience in semicon assembly and test environment
• Experience in Assembly FOL of dicing, die attach, wire bond
• Experience in maintenance of assembly and test machines of dicing, die attach, wire bond encapsulation, testing

Please kindly email your resume in Ms Word to hr@xtalents.com.sg

We regret to inform that only shortlisted candidates would be notified.

Registration Number: R1328870

EA License No. 22C1026

Responsibilities

• Responsible for ensuring products produced meet the product and customers' quality requirement
• Responsible for developing and improving the processes to gain productivity, efficiency, quality and costs.
• Responsible for coordinating NPI/NPQ activities with details and meeting timeline.
• Responsible for supporting and resolving daily technical issues in operations
• Responsible for supporting analysis of failures from yield loss, reliability failures, new products, new materials.

Requirements

• Min Diploma in Electronic Engineering, Material Science or relevant
• Min 5 years of working experience in semicon assembly and test environment
• Experience in Assembly FOL of dicing, die attach, wire bond
• Experience in maintenance of assembly and test machines of dicing, die attach, wire bond encapsulation, testing

Please kindly email your resume in Ms Word to hr@xtalents.com.sg

We regret to inform that only shortlisted candidates would be notified.

Registration Number: R1328870

EA License No. 22C1026

SSMC (Systems on Silicon Manufacturing Company Pte. Ltd.), is a Joint Venture between NXP and TSMC. We offer flexible and cost effective semiconductor fabrication solutions by maintaining fully equipped SMIF cleanroom environment, 100% equipment automation and proven wafer-manufacturing processes.

At SSMC, every career journey is unique and rewarding. We're looking for innovative, passionate, and talented people like you to join our team.

We’re searching for a Senior Engineer to be part of our IT Department diverse team of talent. You will be responsible to Engineering Analytic Systems Software development, Design and Support.

What you will be working on:

• Responsible for system design, development and support of the application systems.
• Work closely with users, vendors and internal team for system requirement analysis, effort estimation, design, development, implementation and testing on IT application project.
• Responsible for core Software Development and deliver in timely manner
• Managing and develop of Engineering Data Analysis Systems
• Managing and develop Engineering data tracks
• Managing and develop DataMart and data warehouse applications
• Implement Service Request related to internal applications
• Provide support for Internal IT department and External customers

More About You:

• Candidate must possess at least a Diploma or Bachelor's Degree or Professional Degree in Computer Science/ Engineering/ Information Technology or equivalent
• Minimum 3 years of relevant experiences in Microsoft .Net Platform C#.Net and python.
• Minimum 3 years of relevant experiences in MS SQL Server, Oracle, Stored Procedure, Function, Trigger and etc.

SSMC is committed to equal employment opportunities and abides by the Tripartite Guidelines on Fair Employment Practices (TGFEP). All qualified applicants will receive non-discriminatory consideration for employment on the basis of merit and regardless of age, race, gender, religion, marital status and family responsibilities, or disability, or any other attributes as protected by the relevant laws.

Entry level Nitec / Diploma in Engineering X 5 Opening

Junior/Senior / No experience / Entry level welcome apply ( X5 Permanent Role Opening ) URGENT !!!

Good Pay + Good allowance + Good Bonus

Full training provided for Entry Level

The Job

• Assist Supervisor in day-to-day operation lines. Planning & Co-coordinating the workflow on production lines to achieve production targets. Trouble shooting production problems and assist in planning new project work.

Requirement

• Diploma / PSB Diploma / Higher Nitec / Nitec in Mechanical / Mechatronics Engineering or others Engineering related

Good Pay + Good allowance + Good Bonus

Interested candidates please send an updated Resume / CV in Ms Word format to lilian@recruitflash.com or WhatsApp’s your resume to 98332779 ( no Calls)

Consultant in-charge : Quah Li Lian (Lilian) ( Registration No: R1983286 )