No Deviation is a provider of patient-centric solutions for the pharmaceutical industry, and we are currently seeking individuals who are passionate about joining our team. Our areas of expertise include engineering consultancy, Commissioning Qualification Validation (CQV), as well as Quality, Compliance, and Regulatory services.

We strongly uphold our core values of Empathy, Integrity, and Transparency, and we strive to create a collaborative, innovative, and inclusive work environment that fosters personal growth and development.

No deviation is seeking a dedicated and detail-oriented QC IPC Chemist for a 1 year Night shift only (8pm-8am) contract role in a leading pharmaceutical company. The ideal candidate will play a key role in ensuring the quality and compliance of products by supporting chemical analysis and testing according to regulatory standards. This is an excellent opportunity for a junior-level professional looking to gain valuable experience in the pharmaceutical industry.

By joining our team, you will have the opportunity to make a meaningful impact in the pharmaceutical industry while advancing your career.

Key Responsibilities:

• The IPC Chemist is responsible for ensuring that the manufacturing process remains consistent and meets predefined quality standards throughout the various stages of production. They perform tests and checks on samples taken during production to ensure that the intermediate stages align with quality specifications before the final product is manufactured.
• Conducts analytical testing using methods like HPLC, GC, FTIR, UV-Vis spectrometry, titrations, and other chemical assays to analyze the potency, purity, and identity of drug substances.
• Performs stability studies to assess how the quality of a drug substance or product changes over time under various environmental conditions.
• Tests for impurities, residual solvents, and microbial content to ensure compliance with regulatory guidelines.
• Prepares and maintains lab documentation, such as test results, standard operating procedures (SOPs), and analytical reports.
• Works in a controlled laboratory environment, following Good Laboratory Practices (GLP) and regulatory standards such as those from the FDA or EMA.

Qualifications and Experience:

• Diploma in Chemistry, Pharmaceutical Science, or a related field.
• Basic knowledge of analytical techniques such as HPLC, GC, UV, and wet chemistry.
• Familiarity with GMP, GLP, and relevant regulatory guidelines.
• Strong attention to detail, problem-solving skills, and ability to work independently.
• Excellent organizational skills and ability to maintain accurate documentation.
• Effective communication skills and a team-oriented mindset.
• Preferred Experience:
• Prior experience in a pharmaceutical or chemical laboratory setting is advantageous, but fresh graduates are welcome to apply.
• Contract Duration: 1 year, with potential for extension based on performance and business needs.

OPERATIONAL

To design and perform detailed designing for machine electrical control systems.

To write Programmable Logic Control (PLC) program for automatic machine control & processes. Preferably, with Industrial PC (IPC) programming experiences too.

To collaborate and work together with the Design Team (comprising of both mechanical & electrical members) for the design concept arising from new projects proposal and confirmed projects.

To lead the in-house electrical staff and/or the company’s appointed electrical vendors on the respective machine control and electrical systems and operations of the projects.

To lead the assembly members & technicians during Machine set-up, Machine Assembly Process, Alignment, Testing & commissioning in the Company and/or customer site.

To spearhead meetings and review with the design team and the customers on control system requirements and specification.

SMART FACTORY TECHNOLOGIES & AI PLATFORM

To undertake robotics programming or programming as well as commissioning on the Industrial Robots, MIR and other collaborative robotics systems.

To Conduct 2D and 3D camera application evaluations.

To team up with cross-disciplinary teams of engineers & specialists focusing on smart factory technologies & projects.

To ideate and build robust data and digital technology driven solutions for advanced manufacturing / industrial processes.

To leverage AI and robotics-integration solutions to meet customers’ automation & real-time needs.

Responsibilities:

• Monitor and manage overdue accounts, ensuring timely collection of outstanding debts through phone calls and emails.
• Prepare and send monthly statement of account and reminder letters to customers.
• Generate monthly AR aging reports and provide updates on account collection status.
• Investigate and resolve balance discrepancies, performing account reconciliations as needed.
• Set up new customer accounts and maintain accurate, up-to-date customer account information in the System.
• Handle additional tasks and ad hoc duties as required.

Requirements:

• Diploma/Degree in Accounting/Finance/Business
• Prior experience in credit control and collections is advantageous
• Strong communication skills and confidence in engaging with customers
• Proficiency in MS Office applications
• Ability to work independently while being a strong team player

1. Perform analytical equipment lifecycle management as per current regulatory requirements / SOP.
2. Involve in equipment qualification, writing URS, reporting and implementing SOP’s for system operation and maintenance, monitoring performance of the equipment and decommissioning of equipment.
3. Ensure real time documentation, maintain data integrity and appropriate traceability.
4. Support and / or perform maintenance / calibration of laboratory equipment in compliance with established schedules.
5. Liaise with vendors/service providers for PM / Calibration in a timely manner.
6. Responsible for maintenance / calibration planning of equipment within QC Department.
7. Responsible for the accurate, timely and compliant execution of assigned projects and related documentation.
8. Assist / perform method validation and transfer as required.
9. Conduct QC Department equipment operation and maintenance training to QC staff as required.
10. Perform and / or support in maintaining the asset register for equipment in the QC Department.
11. Initiate CAPEX for equipment purchase.
12. Responsible for QC lab and equipment/instrument cleanliness.
13. Any other activities as and when assigned by the Superior.

EDUCATION & EXPERIENCE:

EDUCATION: Degree / Diploma in science related discipline (e.g. Chemistry, Chemical Engineering, Biotechnology).

EXPERIENCE: Minimum 4 years of quality control experience in pharmaceutical manufacturing industry.

KNOWLEDGE & SKILLS:

1. Possess working knowledge of GMP in the pharmaceutical industry.
2. A good team player with positive learning attitude.
3. Working knowledge of validation, calibration and operation of laboratory equipment such as HPLC, GC, FTIR and Dissolution equipment.
4. Excellent interpersonal and analytical skills, good verbal and written communication skills.

Job Description:

• Ensure the machine is working correctly, and calibrating the machine to ensure proper measuring.
• Perform incoming, in-process and final inspection as per customer requirement.
• Maintain calibration record of measuring equipment.
• Document inspection results by completing reports and logs.
• Maintain safe and healthy working environment by following standards and procedures.
• Raise non-conformance report if necessary.

Job Requirements:

• NITEC/Higer NITEC in Precision Engineering.
• 2 -3 years of relevant QC experience in a manufacturing environment and knowledge.
• Able to interpret technical/mechanical drawings of geometrical dimensioning and tolerance.
• Able to perform CMM measurement; preferably with Wenzel or Zeiss.

Job Responsibilities:

• Support continuous improvement efforts in QMS.
• Support in root cause analysis and implementation of corrective/ preventive actions for process related concerns.
• Analyze and provide timely respond to customer complaints.
• Interface with Customer and Operations to ensure new product transfer to manufacturing are in accordance with approved requirements.
• Prepare Quality performance metrics and reports.

Requirements:

• Diploma in Mechanical Engineering, Quality, or equivalent.
• Minimum 2 years work experience in Quality Management System in manufacturing environment.
• Good knowledge of ISO 9001. Knowledge of API Q1 is preferred.
• Strong command of English language, both oral & writing.
• Knowledge of metal working industry is preferred.
• Knowledge of risk assessment principles and methods.
• Knowledge of SAP is preferred.
• Positive & proactive attitude.

Authorities and Responsibilities

1. Ensure all fabrication work is done with acceptable quality by daily monitoring include inspecting according to specification, procedure and applicable standards.
2. Understand all technical specification and standard compliance and ability to handle troubleshooting project correction.
3. Prepare welding methods, PQR assembly and other CWI duties.
4. Co-ordinate, communicate with member even carrying out inspection of all the welding and associated actions in accordance with the approved Welding Procedure Specification, drawings and Company Specification and requirements.
5. Co-ordinate and liaise with Production personnel to ensure that all inspection stages comply to inspection and test plans on material or structure.
6. Witness and verify all tests include reinstatement etc. and prepare reports after such tests are conducted.
7. Verify product identification through material verification inspection and periodical random checks on site.
8. Responsible in executing directives as set forth for the Quality Assurance Department in meeting management objectives in term of quality control/assurance of all production fabrication works/projects.
9. Implement and maintain a system of auditing the facility and periodic calibration of test, measuring equipment and tools include all documentation, procedure qualification records accordance to customer specification and code.
10. Manage and supervise a team of inspectors / technicians in meeting departmental quality goals and production schedule.
11. Manage customer complaints, corrective and preventive action programs and Administer and manage continuous improvement program for all QA processes.
12. Work closely with customers, production and suppliers to meet the quality requirements.
13. Review / prepare, administer and implement Quality Assurance Plans, Inspection Test Plans and other Operational procedures in accordance to the technical specifications, customer's surveillance requirements, and good manufacturing / engineering practices, and enforce the same on Operations in their execution.
14. Work closely among inter-department to ensure committed schedules are met in a timely and effectively manner.
15. Manage the implementation / schedule of calibration control.
16. Participate in the implementation of risk assessment and risk control of medical devices.
17. Any other tasks and responsibilities assigned from time to time.

Competence Requirement

• Min. ITE-NTEC/Diploma/Degree level PE/ME or its related discipline.
• Fresh Degree or min 3 years in Quality Assurance in production/fabrication/welding environment or it relevant experience in QC/QA environment.
• Perform CMM programming, smart-scope and QC measuring tools/equipment.
• Certified with welding certification by American Welding Society, Certification Welding Inspector, AWS-CWI. - Optional
• Minimum 3 years of related experiences in welding capacity in structural fabrication.
• Able to interpret technical drawings and reading symbols.
• Understand the quality principles, standards, internal business systems and processes.
• Good interpersonal skills, ability to communicate and Works well with all levels of staff and technically competent.
• Good knowledge of International Codes and Standards (ASME, AWS, ASTM, API).
• Basic Knowledge and usage of Microsoft Office
• Sound Technical knowledge on steel structural and steel fabrication procedures and welding inspection.
• Basic knowledge of ISO 9001 and OHSAS 18001 Management system

Job Responsibilities:

• Support continuous improvement efforts in QMS.
• Support in root cause analysis and implementation of corrective/ preventive actions for process related concerns.
• Analyze and provide timely respond to customer complaints.
• Interface with Customer and Operations to ensure new product transfer to manufacturing are in accordance with approved requirements.
• Prepare Quality performance metrics and reports.

Requirements:

• Diploma in Mechanical Engineering, Quality, or equivalent.
• Minimum 2 years work experience in Quality Management System in manufacturing environment.
• Good knowledge of ISO 9001. Knowledge of API Q1 is preferred.
• Strong command of English language, both oral & writing.
• Knowledge of metal working industry is preferred.
• Knowledge of risk assessment principles and methods.
• Knowledge of SAP is preferred.
• Positive & proactive attitude.

Job Overview:

The QA Manager will be responsible for managing and overseeing all quality assurance activities within the organization, ensuring that products and services meet all quality standards. The ideal candidate will have in-depth knowledge of Quality Management Systems (QMS) and ISO certification processes, driving continuous improvement and compliance across the organization. This role plays a critical part in ensuring the company meets regulatory and customer expectations.

Key Responsibilities:

• Quality Management System (QMS):Develop, implement, and maintain the Quality Management System (QMS) in alignment with ISO standards (e.g., ISO 9001, ISO 14001, etc.).
  Regularly audit and review QMS processes to ensure continuous improvement and compliance.
  Ensure documentation, procedures, and processes align with QMS requirements.
  
• ISO Certification Management:Lead and manage the ISO certification process, including initial certification, recertification, and internal audits.
  Coordinate with external certification bodies and manage relationships to ensure the company's certification status is maintained.
  Provide guidance and training to staff regarding ISO requirements and their roles in maintaining certification.
  
• Quality Assurance Oversight:Oversee all quality assurance operations, including quality control procedures, testing protocols, and defect management.
  Implement and enforce QA standards and policies throughout the production and service delivery processes.
  Collaborate with cross-functional teams (production, engineering, procurement, etc.) to ensure product quality.
  
• Internal Audits & Continuous Improvement:Plan and conduct internal quality audits, identifying non-conformance and areas for improvement.
  Lead root cause analysis for quality-related issues and implement corrective and preventive actions (CAPA).
  Promote a culture of continuous improvement by developing and executing process optimization initiatives.
  
• Compliance & Risk Management:Ensure company compliance with applicable regulatory requirements, industry standards, and customer expectations.
  Identify and mitigate risks associated with product quality and process inefficiencies.
  Maintain an up-to-date understanding of changes in quality regulations and standards relevant to the industry.
  
• Team Leadership & Development:Manage and mentor the QA team, fostering a culture of accountability, professional development, and continuous improvement.
  Provide leadership in solving complex quality issues, both internally and with external stakeholders.
  
• Customer & Supplier Interface:Act as the primary point of contact for quality-related concerns from customers and suppliers.
  Ensure effective communication of quality standards and expectations to suppliers and collaborate to resolve quality issues.
  

Qualifications and Skills:

• Education:Bachelor’s degree in Engineering, Quality Management, or a related field.
  Advanced degrees or certifications in Quality Assurance or Management (preferred).
  
• Experience:Minimum of 8-10 years of experience in quality assurance, with at least 3-5 years in a management role.
  Proven experience in managing QMS and ISO certification processes in manufacturing, engineering, or production environments.
  
• Technical Skills:In-depth knowledge of ISO standards, especially ISO 9001 (Quality Management), ISO 14001 (Environmental Management), or related certifications.
  Proficiency in quality assurance methodologies such as Six Sigma, Lean, FMEA, and root cause analysis.
  Strong experience in conducting audits and leading CAPA processes.
  
• Soft Skills:Excellent leadership, communication, and team management abilities.
  Analytical mindset with problem-solving skills and attention to detail.
  Ability to work cross-functionally and manage multiple projects simultaneously.
  

Job Description:

1. Performing general inspection of parts and products at the Incoming/In-Process/Outgoing gate.
2. Generate Standard QA/QC inspection report.
3. Administrative tasks.
4. Logistics support.

Competence Requirements

• Preferred Secondary, NTC certification holder from related CNC/Fabrication industry.
• Preferably with 2 years of related work experience in manufacturing environment for non-technical trained staff.
• Able to read part drawing, usage of measuring equipment are added advantage.
• Computer competency.

Job Description:

• Ensure the machine is working correctly, and calibrating the machine to ensure proper measuring.
• Perform incoming, in-process and final inspection as per customer requirement.
• Maintain calibration record of measuring equipment.
• Document inspection results by completing reports and logs.
• Maintain safe and healthy working environment by following standards and procedures.
• Raise non-conformance report if necessary.

Job Requirements:

• NITEC/Higer NITEC in Precision Engineering.
• 2 -3 years of relevant QC experience in a manufacturing environment and knowledge.
• Able to interpret technical/mechanical drawings of geometrical dimensioning and tolerance.
• Able to perform CMM measurement; preferably with Wenzel or Zeiss.

The incumbent is responsible for supervising/performing the steel works inspections on site as a third party in accordance with projects / consultant specifications with reference to International standards to support the achievement of the sales targets.

Job Description:

Inspection Preparation Works

• Plan the inspection jobs for the assigned project as per approved Inspection Test plans (ITP):
• Perform reviewing activities to ensure meeting the project requirements:

Inspection Works on Site

• Carry out the assigned inspection jobs as per client requirements:
• Resolve any inspection issues:

Completion of Inspection Reports

• Prepare inspection reports for submission to client:
• Submit inspection reports/certification for review and billing process:

Supporting Duties

• Prepare for new tests / certification as per organisation requirement
• Prepare /Update the calibration records and internal procedures for audits
• Recommend relevant testing services to clients
• Coach and guide staff on the job

Job Requirement:

• Diploma/Degree in Engineering
• 2 years experience in Building Structural Steel works inspection
• Experience in Oil & Gas shutdown projects
• Able to do punch list and Piping inspection
• 2 years in construction/marine construction and oil & gas.
• Certified with AWS CWI/SCWI or CSWIP 3.1/ 3.2 - WI

Ensure transactions are recorded accurately and promptly in the accounting system.

Prepare invoices and statements of accounts (SOA).

Process payments to suppliers.

Perform monthly reconciliations against vendors' statements of accounts and bank statements.

Manage full sets of accounts, including monthly financial statements and annual management accounting reports.

Coordinate and liaise with external parties such as auditors, tax agents, corporate secretarial agents, and local tax and government authorities, as required.

Submit GST returns.

Singaporean/Singapore Permanent Resident (SPR) only

Responsibilities:

● Perform FAI and sampling plan inspections as per AQL

● Conduct routine quality inspections throughout the production or manufacturing process, including in-process and final inspections

● Perform In-house equipment calibrations

● Maintain documentation of all inspections and potential issues

● Assist with problem resolution

● Handling customer complaints and Internal NCR

Job Requirements:

● Diploma in Mechanical Engineering or certificate / Nitec precision Engineering / GCE O level

● Manufacturing precision Engineering or machine shop experience preferred

● Ability to read technical drawings and knowledge in GDT

● Knowledge of CMM measuring equipment minimum 1year

● Ability to use a variety of precision measuring tools, including micrometres, calipers, Trimos height gauges, pin gauges , thread gauges

● Knowledge of Statical Process Control is ad added advantage

About Us

Established over a hundred years ago, Takasago is a global leading company in the flavour and fragrance industry, having developed flavours and fragrances for some of the world’s most successful manufacturers of foods, beverages, fine fragrances, home, and personal care products.

For over 35 years, we have been a leading industrial producer of L-Menthol, using our core technology, asymmetric synthesis.
This technology enables us to produce unique, novel, and nature-identical aroma ingredients, and in addition, to manufacture pharmaceutical intermediates, functional materials, and other fine chemicals.

Takasago Group maintains offices, production sites, and R&D centers in twenty-seven countries and regions.

Responsibilities:

• To assist senior for routine work involving sample management, registration.
• Involve in the preparation of sample for analysis and retrieving of reference sample.
• Maintain and house keep sample retain room
• Request sample from compounding lab as required
• Prepare reference samples/samples for affiliates as required
• Some basic knowledge of chemical and experiences in the chemical environment are preferred
• Maintain and ensure clean and safe working environment in FRQC Lab
• Clean lab equipment, glassware and apparatus after use
• Carry out any additional job-related duties that may be assigned from time to time

Requirements:

• Basic laboratory knowledge and experiences in chemical working environment required
• Able to read, speak, write basic English
• Minimum qualification with a Diploma in Chemical or relevant study
• Good communication and interpersonal skill
• Good organizing skill
• Basic knowledge of MS office

Centre for Advanced Robotics Technology Innovation (CARTIN) is looking for a candidate to join them as a Research Associate.

Key Responsibilities:

• Develop models, algorithms, and methods for multi-robot-human collaboration.
• Write the research results into project reports (and publication manuscripts if applicable).
• Contribute to project reporting and use case demonstration.

Job Requirements:

• Master in Electrical Engineering, or Automation, or Computer Science and Engineering, or related disciplines from a prestigious university
• Have research and/or academic achievements in related areas
• Knowledge in at least one of the following topics: human-robot collaboration, multi-robot cooperation, control and optimization, robot control, robotics
• Good simulation and programming skills
• Good interpersonal skills
• Good English verbal communication and writing skills

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

Responsibilities:

· Perform QC inspection at various stages of production and identify non-conformance quality issues.

· Perform QC inspections on incoming, WIP and outgoing parts in accordance with work instructions

· Liaise with relevant stakeholders for any material quality-related issues and closely follow-up effectiveness and closure of corrective actions.

· Collaborate with the Engineering team to define and implement quality control requirements.

· Prepare QC report and status update to relevant stakeholders.

· Maintain all QC document master list including including Mill Certificate / test report for all materials used in project.

· Maintain calibration status of Company’s equipment.

· Familiar with welding process such as SMAW, GTAW, SAW

· Any other ad-hoc duties as assigned.

Requirements: ·

· Minimum Diploma in Quality Engineering / Mechanical Engineering or equivalent

· Possess strong analytical skillsand meticulous individual

· Proficient in Microsoft Office

· Able to work both independently and as a team.

· Knowledge of ISO 9001, 14001, 13485 & 45001, FDA will be an advantage

· Preferable if able to commence work immediately

Job Summary:

Salary: Up to $4,500
Working Days: 5 day work week (Mon - Fri), 8.30am to 5.30pm
Location of work: Tuas (Transport allowance $100)

AWS & VB

Job Responsibilities:

• Lead and Drive First Article Submission for new and existing supplier
• Develop Quality plan such as Process Flow Diagram (PFD), Manufacturing Process Plan (MPP) & Inspection Test Plan (ITP) to new supplier.
• Perform supplier audits such as QMS, Process and HSE. This will involve visit/audit and assessing their capability and FAI.
• Work with Sourcing and Engineering, to engage and educate suppliers/sub - contractors.
• Lead quality performance review
• Worked closely with suppliers, to monitor conduct audit for vendor performance.
• Conduct in process audit and drive for closure of audit findings and continuous improvement and reduction of COPQ (Cost of Poor Quality). Lead the discussion with the suppliers and ensure timely response is executed to deliver result to our internal customers.
• Guide Procurement and team for supplier performance review process.
• Supplier Development.
• Drive for vendor development, identify and develop new special process to meet turnkey objective and reduce lead-time of supplier.
• Analyse supply market.
• Propose and execute creative ways to improve supplier process which creates financial value to the organization.
• Maintain good relationship with stake holders and customer/s
• Maintain good relationship with stakeholders such as Manufacturing, Procurement, Engineering and Quality.
• Work with cross functional teams in resolution of process and quality issues related to design, application and manufacturing process. Develop quality consciousness and impart application of quality tools such as FMEA, 8D.
• Customer /Third Party Inspection coordinator
• Manage Customer and Third-Party inspection of products/parts.
• Ensure that each Quality Control Plan activity which requires surveillance pointsare monitored and conducted accordingly.
• Perform any ad-hoc duties as and when assigned by the superior.
• Ensures 5S is implemented in the work area.
• Adheres company’s guidelines with regards to Safety and Quality.
• Complies to Company Code of Business Conduct.
• Support and participate in company-wide or departmental programs such as:
  · Total Quality Management, Lean Manufacturing
  · Social Activities

Requirements:
1. Minimum Degree in Technical/Engineering course preferably Mechanical Engineering
2. Experience: Minimum 3-5 years of working on the same field (Experience in Oil and Gas manufacturing is an advantage)

Applicants who possess relevant experience for the above responsibilities are most welcome to apply. If you do not possess the above experience, your application will still be considered on individual merits and you may be contacted for other opportunities.

Please submit your updated resume in MS Words format by using the APPLY NOW BUTTON

By submitting your personal data and/or resume, you give consent to collection, use and disclosure of your personal data and/or resume by the company (or its agent) for the purpose of the processing and administration by the company relating to this job application.

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

Gan Chen Yun
Registration Number: R23116696
EA Licence No.: 06C2859 (MCI Career Services Pte Ltd)

The Regional Trade Compliance Manager is responsible for ensuring the import or export of products and materials complies with the regulations within a region. This includes assisting in the deployment of regional and/or localized trade compliance procedures and guidelines that will assure compliance with import and export regulations, executing audit and risk assessment programs including corrective action plans and providing leadership in strategic projects that affect the supply chain to ensure proper/advantageous structuring of transactions. In addition to developing and ensuring process adherence, the role will act as a key knowledge point for all trade compliance issues and take a lead in the training and development of key stakeholders.

How You’ll Make an Impact:

• Maintains and evaluates the region’s compliance status with various regulatory bodies including customs, export control and applicable tax authorities. Ensuring proper documentation and procedures are maintained in accordance with regulations.
• Reviews internal controls, develops processes, administers the compliance audit program, and oversees corrective action plans for the region. Identifies compliance gaps and recommends process improvements.
• Assists in establishing and maintaining localized policies and procedures for compliance with import and export regulations as well as ensuring broad Company awareness of these requirements.
• Identifies and develops business processes to address compliance risks, with a focus on continuous process improvements to increase efficiency and improve performance to customers.
• Responsible for monitoring and reporting KPIs and metrics to senior management and daily reporting of import and export compliance for the region.
• Sets overall budget, operational strategy and priorities for assigned area of responsibility.
• Prioritizes and manages projects in the region for both import and export compliance which involves defining the project scope, budget, scheduling and execution of project risk.

What You Bring:

• Bachelor’s or advanced degree in International Business, Business Administration or Supply Chain management.
• Customs broker license.
• At least 10 years trade compliance experience, with minimum 5 years' of management experience and trade compliance for multiple countries or in a global environment.
• Expert working knowledge of import and export regulations across the region, including Import Licensing, Export Licensing, Free Trade Agreements, HTS and Export Control Classification, Country of Origin, Valuation, Transfer Pricing, Authorized Economic Operator, Customs Trade Partnership Against Terrorism, Approved Exporter.
• Knowledge and ability to handle other Government Agency requirements applicable to Bio-Rad products, such as, but not limited to health registration agencies, veterinary controls and other related Export and Impart regulations within the region and countries.
• Experience with global trade management software and systems, and with implementation and scaling of trade automation tools including but not limited to SAP-GTS.
• Experience writing and submitting binding rulings and a proven record of designing and implementing value added import/export policies and processes.
• Experience with audits and disclosure practices.
• Experience working in the Medical Device, Pharmaceutical, Life Sciences or Diagnostic industry highly preferred.
• Demonstrated strong leadership, communication, analytical and people management skills.
• Exceptional verbal and written communication skills and interpersonal skills at all levels in the organization.
• Results orientation and strong sense of accountability.

Who We Are: For 70 years, Bio-Rad has focused on advancing the discovery process and transforming the fields of science and healthcare. As one of the top five life science companies, we are a global leader in developing, manufacturing, and marketing a broad range of high-quality research and clinical diagnostic products. We help people everywhere live longer, healthier lives. Recently voted a Best Place to Work, Bio-Rad offers a unique employee experience with collaborative teams that span the globe. Here, you are supported by leadership to build your career and are empowered to drive change that makes an impact you can see.

Benefits: Bio-Rad's biggest asset is our people, and this is the reason why our Total Rewards deliver programs that provide value, quality, and inclusivity while satisfying the diverse needs of our evolving workforce. Our offerings serve to enrich the overall health, wealth, and wellbeing of our employees and their families through the various stages of an employee’s work and life cycle. We’re proud to offer comprehensive medical plans and insurance, wellness programs, extensive learning and development opportunities and more.

EEO Statement: Bio-Rad is an Equal Employment Opportunity/Affirmative Action employer, and we welcome candidates of all backgrounds. Veterans, people with disabilities, and people of all races, ethnicities, genders, ages, and orientations are encouraged to apply.

Agency Non-Solicitation: Bio-Rad does not accept agency resumes, unless the agency has been authorized by a Bio-Rad Recruiting Representative. Please do not submit resumes unless authorized to do so. Bio-Rad will not pay for any fees related to unsolicited resumes.

Job Summary:

Salary: Up to $4,500
Working Days: 5 day work week (Mon - Fri), 8.30am to 5.30pm
Location of work: Tuas (Transport allowance $100)

AWS & VB

Job Responsibilities:

• Lead and Drive First Article Submission for new and existing supplier
• Develop Quality plan such as Process Flow Diagram (PFD), Manufacturing Process Plan (MPP) & Inspection Test Plan (ITP) to new supplier.
• Perform supplier audits such as QMS, Process and HSE. This will involve visit/audit and assessing their capability and FAI.
• Work with Sourcing and Engineering, to engage and educate suppliers/sub - contractors.
• Lead quality performance review
• Worked closely with suppliers, to monitor conduct audit for vendor performance.
• Conduct in process audit and drive for closure of audit findings and continuous improvement and reduction of COPQ (Cost of Poor Quality). Lead the discussion with the suppliers and ensure timely response is executed to deliver result to our internal customers.
• Guide Procurement and team for supplier performance review process.
• Supplier Development.
• Drive for vendor development, identify and develop new special process to meet turnkey objective and reduce lead-time of supplier.
• Analyse supply market.
• Propose and execute creative ways to improve supplier process which creates financial value to the organization.
• Maintain good relationship with stake holders and customer/s
• Maintain good relationship with stakeholders such as Manufacturing, Procurement, Engineering and Quality.
• Work with cross functional teams in resolution of process and quality issues related to design, application and manufacturing process. Develop quality consciousness and impart application of quality tools such as FMEA, 8D.
• Customer /Third Party Inspection coordinator
• Manage Customer and Third-Party inspection of products/parts.
• Ensure that each Quality Control Plan activity which requires surveillance pointsare monitored and conducted accordingly.
• Perform any ad-hoc duties as and when assigned by the superior.
• Ensures 5S is implemented in the work area.
• Adheres company’s guidelines with regards to Safety and Quality.
• Complies to Company Code of Business Conduct.
• Support and participate in company-wide or departmental programs such as:
  · Total Quality Management, Lean Manufacturing
  · Social Activities

Requirements:
1. Minimum Degree in Technical/Engineering course preferably Mechanical Engineering
2. Experience: Minimum 3-5 years of working on the same field (Experience in Oil and Gas manufacturing is an advantage)

Applicants who possess relevant experience for the above responsibilities are most welcome to apply. If you do not possess the above experience, your application will still be considered on individual merits and you may be contacted for other opportunities.

Please submit your updated resume in MS Words format by using the APPLY NOW BUTTON

By submitting your personal data and/or resume, you give consent to collection, use and disclosure of your personal data and/or resume by the company (or its agent) for the purpose of the processing and administration by the company relating to this job application.

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

Gan Chen Yun
Registration Number: R23116696
EA Licence No.: 06C2859 (MCI Career Services Pte Ltd)

Job Summary:

Salary: Up to $4,500
Working Days: 5 day work week (Mon - Fri), 8.30am to 5.30pm
Location of work: Tuas (Transport allowance $100)

AWS & VB

Job Responsibilities:

• Lead and Drive First Article Submission for new and existing supplier
• Develop Quality plan such as Process Flow Diagram (PFD), Manufacturing Process Plan (MPP) & Inspection Test Plan (ITP) to new supplier.
• Perform supplier audits such as QMS, Process and HSE. This will involve visit/audit and assessing their capability and FAI.
• Work with Sourcing and Engineering, to engage and educate suppliers/sub - contractors.
• Lead quality performance review
• Worked closely with suppliers, to monitor conduct audit for vendor performance.
• Conduct in process audit and drive for closure of audit findings and continuous improvement and reduction of COPQ (Cost of Poor Quality). Lead the discussion with the suppliers and ensure timely response is executed to deliver result to our internal customers.
• Guide Procurement and team for supplier performance review process.
• Supplier Development.
• Drive for vendor development, identify and develop new special process to meet turnkey objective and reduce lead-time of supplier.
• Analyse supply market.
• Propose and execute creative ways to improve supplier process which creates financial value to the organization.
• Maintain good relationship with stake holders and customer/s
• Maintain good relationship with stakeholders such as Manufacturing, Procurement, Engineering and Quality.
• Work with cross functional teams in resolution of process and quality issues related to design, application and manufacturing process. Develop quality consciousness and impart application of quality tools such as FMEA, 8D.
• Customer /Third Party Inspection coordinator
• Manage Customer and Third-Party inspection of products/parts.
• Ensure that each Quality Control Plan activity which requires surveillance pointsare monitored and conducted accordingly.
• Perform any ad-hoc duties as and when assigned by the superior.
• Ensures 5S is implemented in the work area.
• Adheres company’s guidelines with regards to Safety and Quality.
• Complies to Company Code of Business Conduct.
• Support and participate in company-wide or departmental programs such as:
  · Total Quality Management, Lean Manufacturing
  · Social Activities

Requirements:
1. Minimum Degree in Technical/Engineering course preferably Mechanical Engineering
2. Experience: Minimum 3-5 years of working on the same field (Experience in Oil and Gas manufacturing is an advantage)

Applicants who possess relevant experience for the above responsibilities are most welcome to apply. If you do not possess the above experience, your application will still be considered on individual merits and you may be contacted for other opportunities.

Please submit your updated resume in MS Words format by using the APPLY NOW BUTTON

By submitting your personal data and/or resume, you give consent to collection, use and disclosure of your personal data and/or resume by the company (or its agent) for the purpose of the processing and administration by the company relating to this job application.

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

Gan Chen Yun
Registration Number: R23116696
EA Licence No.: 06C2859 (MCI Career Services Pte Ltd)

Job Summary:

Salary: Up to $4,500
Working Days: 5 day work week (Mon - Fri), 8.30am to 5.30pm
Location of work: Tuas (Transport allowance $100)

AWS & VB

Job Responsibilities:

• Lead and Drive First Article Submission for new and existing supplier
• Develop Quality plan such as Process Flow Diagram (PFD), Manufacturing Process Plan (MPP) & Inspection Test Plan (ITP) to new supplier.
• Perform supplier audits such as QMS, Process and HSE. This will involve visit/audit and assessing their capability and FAI.
• Work with Sourcing and Engineering, to engage and educate suppliers/sub - contractors.
• Lead quality performance review
• Worked closely with suppliers, to monitor conduct audit for vendor performance.
• Conduct in process audit and drive for closure of audit findings and continuous improvement and reduction of COPQ (Cost of Poor Quality). Lead the discussion with the suppliers and ensure timely response is executed to deliver result to our internal customers.
• Guide Procurement and team for supplier performance review process.
• Supplier Development.
• Drive for vendor development, identify and develop new special process to meet turnkey objective and reduce lead-time of supplier.
• Analyse supply market.
• Propose and execute creative ways to improve supplier process which creates financial value to the organization.
• Maintain good relationship with stake holders and customer/s
• Maintain good relationship with stakeholders such as Manufacturing, Procurement, Engineering and Quality.
• Work with cross functional teams in resolution of process and quality issues related to design, application and manufacturing process. Develop quality consciousness and impart application of quality tools such as FMEA, 8D.
• Customer /Third Party Inspection coordinator
• Manage Customer and Third-Party inspection of products/parts.
• Ensure that each Quality Control Plan activity which requires surveillance pointsare monitored and conducted accordingly.
• Perform any ad-hoc duties as and when assigned by the superior.
• Ensures 5S is implemented in the work area.
• Adheres company’s guidelines with regards to Safety and Quality.
• Complies to Company Code of Business Conduct.
• Support and participate in company-wide or departmental programs such as:
  · Total Quality Management, Lean Manufacturing
  · Social Activities

Requirements:
1. Minimum Degree in Technical/Engineering course preferably Mechanical Engineering
2. Experience: Minimum 3-5 years of working on the same field (Experience in Oil and Gas manufacturing is an advantage)

Applicants who possess relevant experience for the above responsibilities are most welcome to apply. If you do not possess the above experience, your application will still be considered on individual merits and you may be contacted for other opportunities.

Please submit your updated resume in MS Words format by using the APPLY NOW BUTTON

By submitting your personal data and/or resume, you give consent to collection, use and disclosure of your personal data and/or resume by the company (or its agent) for the purpose of the processing and administration by the company relating to this job application.

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

Gan Chen Yun
Registration Number: R23116696
EA Licence No.: 06C2859 (MCI Career Services Pte Ltd)

• planning and organising production schedules
• assessing project and resource requirements
• estimating, negotiating and agreeing to budgets and timeline with clients
• ensuring that health and safety regulations are met
• determining quality control standards
• overseeing production processes
• selecting, ordering and purchasing materials
• organising the repair and routine maintenance of production equipment
• liaising with buyers
• supervising and managing day-to-day work of junior staff and production workers in factory environment
• organising relevant training sessions
• ensure project goals are being met within approved budget.

REQUIREMENTS

• Min Diploma in management
• Min 2 years supervisory experience and 1 year experience in similar industry (manufactuing)
• PC literate
• Well organized & a team player
• Willing to work in West Area (Company transport from Joo Koon/Choa Chu Kang MRT)
• Extensive knowledge on safety processes

Job Description

1. Maintain, monitor the implementation & update of relevant audit programs
2. Provide technical advice & support various departments
3. Conduct compliance inspections in production floor & warehouse, identifying key areas for improvements and advice corrective actions
4. Perform QA inspections for incoming/outgoing cargoes based on compliance requirements
5. Coordinate with suppliers to resolve non-conformances
6. Provide in-house training on compliance etc for various departments

Job Requirement

• Diploma in Food Science/Food Technology or related disciplines
• Strong knowledge in food safety, well verse in GMP/GWP
• Strong analytical & problem solving skills
• Excellent interpersonal & communication skills

• Coordinate and Schedule Diabetic Foot Screening Services, Diabetic Retinal Photography and Nurse Counselling Services
• Assist in implementation and educating patients on Healthier SG and benefits.
• To work closely with the GPs to manage identified patients who need support and referral to community services and ensure that their changing needs are addressed
• Guide patients in achieving their target set as well as follow up on patient's progress where necessary. Escalate to GP when neccessary.
• To Track, Monitor and follow up on the quality of care provided by GPs and other Primary care professionals and to ensure the maintenance of good clinical care.
• Assist GPs in the Submission of data and other relevant administrative work
• Involve in the PCN planning team to ensure smooth coordination within PCN
• Perform any other task assigned by PCN leader or Supervisor