Total 249 research associate job vacancies in Quality Assurance / Control category in The United States of America

About The Company

KGI Securities is a leading multi asset brokerage firm with presence across several countries in Asia and a pioneer member of the Securities & Derivatives, Trading and Clearing Member of Singapore Exchange, ICE Futures Singapore and ICE Clear Singapore.

We hold a Capital Markets Services License, is regulated by the Monetary Authority of Singapore (MAS) and is also an equal opportunity employer.

About The Job

The duties of Analyst/Associate - Compliance officer will include providing regulations guidance and training, consultation of securities and futures trading laws, as well as timely update of relevant laws and regulations. It is also responsible for supervising the periodic self-assessment of legal compliance among all units.

The duties of the staff will be mainly to assist the Compliance team in performing the compliance reviews and trade surveillance reviews in accordance with the work plan.

Job Responsibilities

• Conduct Compliance reviews and testing including trade surveillance, AML and BSC, and escalate any breaches of regulatory requirements or misconduct or company policies
• Review and process registration of trading representatives
• Carry out any compliance tasks as and when necessary as directed by the Head of Department
• Carry out awareness briefing and staff training on regulatory requirements, company policies and procedures

Requirements:

• Degree holder with minimum 1-2 years of relevant experience
• Familiarity with the relevant laws, regulations and exchange rules in the securities and/or futures market (SFA, FAA, SGX-ST Rules, Futures Trading Rules, AML) is a plus
• Meticulous, positive attitude and pro-active
• Strong communication, interpersonal, analytical and organizational skills
• Team player yet able to work independently and interact with people at all levels
• Relevant experience in exchanges (e.g. in market surveillance or supervision departments), public accounting firms, securities and futures brokerage firms and other financial institutions are encouraged to apply

Company:

Mercer

Description:

Mercer is seeking candidates for the following position based in Melbourne:

Quality and Care Associate (Aged Care) - Care & Living with Mercer

Care & Living with Mercer (CaLM) is a unique service helping ageing Australians and their carers understand and more easily access aged care and living options. The guidance and advice is made available to Australians through their employer or Superannuation fund as a benefit, via selected financial advisors or to consumers directly. CaLM has the goal of being the most widely used service of its kind in Australia.

As the Quality and Care Associate you will be primarily responsible for maintaining an up-to-date database of carefully vetted Aged Care providers. This is primarily achieved by building and maintaining connection with care providers, visiting aged care facilities, reaching out to provider contacts and systematically updating the database. The Quality and Care Associate supports a team of Care Consultants by assisting with Plan Reviews, reporting and generating provider information that is accurate and fit-for-purpose.

What is in it for you?

At Mercer, we recognise that our most important asset is our people. We offer benefits and programs that support career development such as professional development support, exam and study assistance and global rotation opportunities which will support and nurture you with every opportunity to reach your full potential.

We also recognise the value of healthy, happy colleagues and promote a culture of care and wellbeing, offering benefits such as flexible working and much more!

• Flexible work arrangements
• Leading training and development program
• Professional environment where your career path really matters and is supported in our global organisation
• Great team environment with energetic and supportive colleagues
• Genuine work life balance

Key Responsibilities:

• Perform due diligence of vetted aged care providers:
  • Manage and maintain the process for conducting due diligence of providers that Care & Living with Mercer will recommend to customers, including updating the due diligence spreadsheet and input fields as required
  • Manage and maintain the database of vetted providers and their associated status (recommend, do not recommend, on hold)
  • Work in partnership with the Care Consultant team to initiate provider due diligence when required for customers and update provider due diligence records when Care Consultants have new information, based on interaction with providers
  • Build relationships with providers’ contacts to build and develop the knowledge, brand and trust of Care & Living with Mercer with these contacts
• Information library: Maintain correct and up-to-date content of the Information Library with changes provided by DCM Media, as well as any changes requested by the Product & Operations Leader
• Customer Plan actions: Maintain the content of the Plan actions and related information based on changes requested by the Care Consultant Leader and Product & Operations Leader
• Periodic reporting: Collect required reporting data from Care Consultants and report in format required for other functions within Care & Living with Mercer, such as Client Growth Leader and Marketing Manager
• Periodically support completion of customer Plan reviews with Care Consultant team members
• Stay abreast on industry news and developments that may impact Care & Living with Mercer’s services

What you need to have: 

• Administration experience, ideally in Aged Care
• Ability to build strong relationships with providers through regular visits, phone interaction and emails
• Excellent verbal and written communication, particularly with negotiation and persuasion
• Outstanding customer service

What makes you stand out:

• Aged care industry experience
• Experience in Allied Health
• Sales experience

About us:

Mercer believes in building brighter futures by redefining the world of work, reshaping retirement and investment outcomes, and unlocking real health and well-being. Mercer’s approximately 25,000 employees are based in 43 countries and the firm operates in 130 countries. Mercer is a business of Marsh McLennan (NYSE: MMC), the world’s leading professional services firm in the areas of risk, strategy and people, with 85,000 colleagues and annual revenue of over $20 billion. Through its market-leading businesses including Marsh, Guy Carpenter and Oliver Wyman, Marsh McLennan helps clients navigate an increasingly dynamic and complex environment. For more information, visit mercer.com. Follow Mercer on LinkedIn and Twitter 

Marsh McLennan is committed to creating a diverse, inclusive and flexible work environment. We aim to attract and retain the best people and embrace diversity of age, background, disability, ethnic origin, family duties, gender orientation or expression, marital status, nationality, parental status, personal or social status, political affiliation, race, religion and beliefs, sex/gender, sexual orientation or expression, skin color, or any other characteristic protected by applicable law.

Marsh McLennan is committed to hybrid work, which includes the flexibility of working remotely and the collaboration, connections and professional development benefits of working together in the office. All Marsh McLennan colleagues are expected to be in their local office or working onsite with clients at least three days per week. Office-based teams will identify at least one “anchor day” per week on which their full team will be together in person. Note: the changes to our hybrid work policy do not apply to officially designated remote workers and are subject to any works council or local legal requirement.

Iedere werknemer binnen Pfizer is mede-verantwoordelijk voor de kwaliteit van de geproduceerde geneesmiddelen.  

Quality Operations (QO - Kwaliteitsafdeling binnen Puurs) heeft in het bij-zonder als rol om als onafhankelijke partij de kwaliteit te bewaken van alle aangekochte materialen, grondstoffen, alsook alle geproduceerde geneesmiddelen.

Deze functie situeert zich binnen onze kwaliteitsafdeling in het team dat de kwaliteitsaspecten behartigt binnen de projecten uitgevoerd in het Center voor Secondary Packaging (CSP).  Je voorziet alle betrokken teams binnen de verpakkingsafdeling van ondersteuning en expertise in het kader van kwaliteits- en GMP-compliancevereisten.  Met andere woorden, je waakt er – als onderdeel van een team – mee over dat alle verpakte en vervolgens getransporteerde presentaties van onze producten, alsook alle productielijnen en magazijnen aan de nodige kwaliteits- en compliancenormen voldoen.

“Binnen deze rol ben je het eerste aanspreekpunt omtrent kwaliteit in implementatie-, optimalisatie- en veranderingsprojectenbinnen het Center For Secondary Packaging (CSP)”

Takenpakket:

Binnen deze rol heb je de gelegenheid om als team player alle aspecten binnen de verpakkingsafdeling te leren kennen, waarbij je de “QA-stem” vertegenwoordigt.  Je komt in aanraking met een verscheidenheid aan productielijnen, met onze magazijnen, alsook met de specialiteiten rond het transporteren van onze finale verpakte goederen.

Met betrekking tot projecten binnen verpakking:

• Ben je als onderdeel van de kwaliteitsafdeling het kwaliteitaanspreekpunt
• Werk je samen met alle betrokken teams, waaronder b.v. productie, engineering
• Bied je ondersteuning en expertise bij de creatie van de projectaanpak, waarbij je focus ligt op het waken over de kwaliteits- en compliancestrategie, die je borgt via contacten met het projectteam en de review van gecontroleerde documentatie.  Bij voorkeur zoek je hierbij onze klanten actief op om het te behandelen dossier of topic te bespreken aan b.v. de betrokken productielijn
• Ben je tevens de quality authority in de goedkeuring van SOP’s, validatiedocumenten, changes, risicoanalyses, enz.
• Evalueer je de impact van veranderingen en beslissingen op de gekozen of gevolgde aanpak en bestaande documentatie, processen en  procedures in analogie met bestaande regelgeving, standaarden en vereisten

Functieprofiel:

Kern

• Universitaire opleiding ingenieur, farmacie of wetenschappelijke richting
• Je bent een team player en houdt van face-to-face contact met je teamgenoten en collega’s
• Je hebt een probleemoplossende, pragmatische aanpak met veel zin voor initiatief
• Communicatief sterk en klantgericht
• Je werkt zelfstandig, georganiseerd en accuraat
• Perfecte beheersing van het Nederlands en het Engels

Zeker een voordeel

• Ervaring in een kwaliteitsomgeving
• Ervaring in een GMP-omgeving
• Ervaring in project management

Aanbod:

• Contract van onbepaalde duur met tal van extralegale voordelen
• Een cultuur van ondernemerschap en innovatie
• Een site met de grootste productie-en verpakkingssite van Europa binnen het Pfizernetwerk
• Hoog investeringsritme
• Hoogtechnologische omgeving
• Samenwerken met een team van gemotiveerde device- en combination productspecialisten, zowel binnen als buiten de Puurssite.

  
Work Location Assignment: Flexible

Quality Assurance and Control

#LI-PFE

CLA is a top 10 national professional services firm where our purpose is to create opportunities every day, for our clients, our people, and our communities through industry-focused wealth advisory, digital, audit, tax, consulting, and outsourcing services. Even with more than 8,500 people, 130 U.S. locations, and a global reach, we promise to know you and help you. 

CLA is dedicated to building a culture that invites different beliefs and perspectives to the table, so we can truly know and help our clients, communities, and each other.

Our Perks:
•    Flexible PTO (designed to offer flexible time away for you!)
•    Up to 12 weeks paid parental leave
•    Paid Volunteer Time Off
•    Mental health coverage
•    Quarterly Wellness stipend
•    Fertility benefits
•    Complete list of benefits here

CLA is looking to hire a Senior Assurance Associate to join growing team.

How you’ll create opportunities in this Senior Assurance Associate role:

• Become an industry professional and attend industry leading events and trainings.
• Develop and train team members to help them build inspired careers.
• Be given opportunities to lead client engagements.
• Get the opportunity to work with many great clients in exciting industries.
• Perform analytical reviews on financial accounts and identify trends.
• Foster and build opportunities for our clients, communities, and people through paid volunteer hours.

What you will need:

• You have a bachelor's degree in accounting, finance, or a related field.
• You have a CPA license or are eligible to sit for the CPA exams and meet the 150 credit hour requirement to obtain a CPA License.
• You have at least 2 years audit experience as an associate in public accounting.

Our approach to compensation emphasizes collaboration and career growth.  We pay competitive wages and view compensation as an investment in our people. Factors such as geography, experience, education, skills, and knowledge may impact position of pay within the range.  These same factors may cause starting pay to be below or above the posted range.

• For California, the posted range for this role is $77,000-$123,000.
• For Colorado, the posted range for this role is $75,000-$107,000.
• For Washington, the posted range for this role is $69,000-$111,000

#LI-NR1

Equal Opportunity Employer /AA Employer/Minorities/Women/Protected Veterans/Individuals with Disabilities.
 
Click here to learn about your hiring rights.

Wellness at CLA

To support our CLA family members, we focus on their physical, financial, social, and emotional well-being and offer comprehensive benefit options that include health, dental, vision, 401k and much more.

To view a complete list of benefits click here.

The candidate should have computer system validation, Equipment. utility qualification. He should have adequate knowledge of protocol / report preparation and review.

Candidate should have experience on injectable quality system and validation activity.

Candidate should have exposure on Documentation and QMS activity.

 

Today, Lonza is a global leader in life sciences operating across three continents. While we work in science, there’s no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that’s the kind of work we want to be part of.

Manufacturing areas, incoming materials and utility supplies and products are all released and approved for use based on QC test results as generated by the QC Associate. QC Associate is responsible for planning and execution of daily quality assays and control activities while ensuring compliance with all existing GMP and safety standards in the area of responsibility.

Key responsibilities:

• Perform and review cell and/or micro based assays (e.g. qPCR, FLOW, ELISA, viability, endotoxin, cell count) defined per training program

• Writing or review of documentation (e.g. SOP’s, Quality Instructions, protocols…) related to quality control activities

• Ensure proper operations of laboratory equipment

• Be supportive for the performance of QC methods during the transfer of QC assays and stability testing

• Cross-departmental cooperation to ensure timely processing and reporting of results

• Responsible for reporting test results towards Team Leader Qc

• Initiation of Quality Events as NC’s, CRF’s and OOS’s

• Backup of Senior QC associate

• Main activities contain the performance of QC assays, mandatory for intermediate testing and the release of Drug Product.

• QC Associate will have the possibility to expand experience in several QC assays spread over several projects, which brings variation, and flexibility in the job.

Key requirements:

• The position requires a very precise and responsible working attitude.

• Intermediate or higher vocational education in chemistry/biotechnology.

• Preferably experience with GMP and basic knowledge of incoming materials, EM, microbiological (gram stain, sterility) or analytical (RT-qPCR, FACS, ELISA) techniques depending of the area of interest.

• Good communication skills in English.

• Accuracy, tidiness, self-organized, flexible, attention to detail.

• Team player.

• This role requires working in a shift pattern

Every day, Lonza’s products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically.

IPQA of Sterile Injectable Vial, PFS, Cartridge, IV bags etc.

Have knowledge of shop floor of sterile injectables, Media fill validation, cleaning validation.

At Baker Tilly Singapore, we welcome highly motivated and committed individuals who share our core values to join us. We are committed to our values of leading by example, delivering quality services with integrity, communicating openly, acting ethically, and fostering a community built around civic responsibility and teamwork.

We are looking for an Assurance (Financial Services) Associate, who will be involved in various sizes of financial services audit engagements which include planning, performing, and concluding the engagement. The Assurance Associate will be exposed to a broad range of capital markets entities and investment funds such as private equities, real estate, mutual funds, variable capital companies, etc.

In this role, you will:

• Involvement in a broad range of statutory and regulatory audit assignments for our financial services clients

• Assist in obtaining all necessary audit working papers and documentation including researching and documenting facts and findings

• Identify and communicate accounting and auditing matters to managers and partners

• Identify performance improvement opportunities

• Interact with clients to help ensure that the information flow from the client to the audit team is efficient

We are looking for people with the following:

• Graduates with an Accountancy degree or equivalent professional qualification in Accountancy

• Accountancy undergraduates in the final year of study are welcome to apply

• Graduates with non-accountancy degrees who are keen to pursue qualifications as Singapore Chartered Accountants are welcome to apply

• Good command of the English language

• Strong interpersonal and client relationship skills

• Experienced candidates will be considered for the Senior Associate position

Interested candidates, please email your updated CV to hr@bakertilly.sg.

We regret that only shortlisted candidates will be notified.

ESSENTIAL FUNCTIONS

• Undertake assigned internal audits and consultancy projects to ensure the clients meet their financial, operational and compliance objectives.
• Involvement in sustainability-related secondary research and analysis; developing and drafting sustainability disclosure documents; assisting with client relationship management; and supporting in organising seminars/workshops.
• Coordinate project kick-off meetings and other planning activities to support the planning reporting process.
• Report on control deficiencies and make recommendations to mitigate risk and add value.
• Support the internal audit projects by identifying opportunities for improvement and reducing business risk through effective implementation and monitoring of controls.
• Use of data analytics and visualisation tools to identify patterns/trends in data sets and evaluate exposure to business processes.
• Engage and communicate with a variety of internal and external stakeholders.

ESSENTIAL QUALITIES

• Possess a Bachelor’s degree from an accredited college/university in Accounting, Finance, or other relevant fields.
• Minimum 1 to 3 years of relevant working experience in external/internal audit in a public accounting firm or commercial environment will be preferred. Fresh graduates will also be considered.
• Candidates with industry-related certifications such as CIA, CISA, CA/CPA, and CRMA will be added advantage.
• Excellent attention to detail and exhibit organisational and time-keeping skills.
• Have an analytical mind that can assess and evaluate risk as well as recommend solutions.Be able to work both independently and as part of the team by establishing priorities and meeting deadlines.
• Excellent listening, written, and verbal communication skills.
• High level of interpersonal skills in handling sensitive and confidential documents.

WHAT SETS US APART

• Learn how to use Data Analytics and Visualisation Tools for our engagements.
• Sharing on industry best practices (i.e., internal controls/ sustainability) and adding value to clients.
• Monthly training sessions on required technical skills.

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 expanding its innovative reach in Harwell, UK, a leading center for scientific research and development. Our state-of-the-art manufacturing site here plays a critical role in advancing our mission of delivering mRNA medicines globally. We invite committed professionals to join our Harwell team and contribute to groundbreaking medical advancements.

A position of great responsibility and impact, the Associate Director for Quality Control at our Harwell manufacturing site is crucial in overseeing the commercial testing functions within the Quality Control department. This role supports raw materials and drug substances testing for mRNA products, encompassing Microbiological and Environmental Monitoring (EM) tests, and extends to method transfer, qualification, and validation activities.

Here's What You’ll Do:

Within 3 Months, You Will…

• Gain a comprehensive understanding of Moderna's Quality Control processes and standards, specifically focusing on the nuances of commercial testing functions for mRNA products. This includes familiarization with testing procedures for raw materials, drug substances, Microbiological and EM tests.

• Begin actively overseeing the daily operations of the Quality Control commercial program. This will involve directly managing functions related to stability testing, ensuring that all testing is conducted in line with Moderna’s high standards and regulatory compliance.

• Start leading the Quality Control laboratory team, getting to know each team member, their specific roles, and functions. This period will include establishing clear communication channels, understanding individual capabilities and areas of expertise, and setting preliminary objectives for the team.

Within 6 Months, You Will…

• Implement Lean methodologies within the Quality Control department. This will involve analyzing current processes, identifying areas for efficiency improvements, and suggesting changes that could enhance the overall productivity and effectiveness of testing functions.

• Take a lead role in the development and updating of Standard Operating Procedures (SOPs) and laboratory data collection & documentation systems, both paper and electronic. This task will be aimed at ensuring all procedures align with current cGMP compliance requirements.

• Begin extensive collaboration with other critical departments, including Analytical Sciences & Technology (AS&T), Global QC, External QC, Quality Assurance, and Regulatory Affairs. These collaborations will focus on supporting drug substance and product testing both internally and at Contract Manufacturing Organizations (CMOs), as well as other quality-related information for stability programs and Annual Product Quality Reviews (APQR).

Within 12 Months, You Will…

• Become fully integrated into your role, leading the Quality Control team with effectiveness and confidence. This will involve ongoing management and mentoring of laboratory personnel, fostering their career development and ensuring the team is meeting all performance and quality targets.

• Play a pivotal role in overseeing and managing laboratory investigations, change controls, and Corrective and Preventative Actions (CAPAs) related to Quality Control operations. This includes ensuring all QC operations are compliant with relevant regulatory and company standards.

• Lead method transfer and qualification activities in close collaboration with AS&T and development groups. This will involve overseeing the transfer of new methods into the QC laboratory, ensuring all methods are robust, validated, and fit for purpose.

• Make significant contributions to the budget planning and resource allocation for the QC department, aligning with Moderna’s strategic goals and ensuring efficient use of resources.

• Provide essential support during health authority, internal/external, and vendor audits. This includes interfacing with health authorities during site and external inspections, ensuring that the QC department adheres to all relevant FDA, EU, ICH guidelines, and regulations, and demonstrating Moderna’s commitment to maintaining high-quality standards in all operations.

Here’s What You’ll Bring to the Table:

• Minimum education required: Bachelor’s Degree in a relevant scientific discipline.

• Minimum experience required: 10 + years in applied industry experience; 4-6 years of management/supervisory experience.

• Demonstrated proficiency with Quality System Records, Deviations, Change Controls and CAPAs.

• Previous supervisory experience is preferred, including testing scheduling and lab project management.

• Minimum knowledge required: general laboratory operations, method acquisition, qualification.

• Minimum skills required:

  • Technical writing.

  • Proficiency with Microsoft Office Programs.

  • Familiarity with electronic databases (e.g., LIMS, SAP, LMS).

  • Familiarity with QC operations including bioassay, chemistry, and microbiology.

  • HPLC Instrumentation/ Software experience is preferred.

  • Strong written and oral communication skills as well as organizational skills.

  • Knowledge of industry standards and guidelines, experience supporting compliance audits.

  • Demonstrated ability to work effectively under established guidelines and instructions.

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

  • Working knowledge of relevant and current FDA, EU, ICH guidelines and regulations.

  • Ability to efficiently prioritize and complete multiple projects and tasks in a fast-paced environment.

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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Join the team that is responsible for managing Controls Agenda in APAC.

Your new role will allow you to showcase your knowledge in driving Controls projects and assessments. You will also have many opportunities to leverage both your internal and external stakeholder skills.

As a Client Onboarding and Documentation (CO&D) Control manager, you will be responsible for managing the controls agenda in the APAC region whilst supporting global mandate including identifying and monitoring significant risks, ensuring compliance with operational policies, control procedures, and legal/regulatory requirements, and managing several engagements (e.g. Regulatory Exams, Regulatory Reporting, Internal/External Audits and Compliance Monitoring and Testing activities), special projects and risk assessments. The controls agenda support the end-to-end CO&D organization across Wholesale KYC Operations (WKO) and Digital Document Services (DDS) Operations by providing management with sufficient information to understand and monitor key operational risks and regulatory activities/concerns. CO&D control manager will partner with critical stakeholders including Operations, Cross-Regional control managers, Compliance, Technology, and Audit to ensure alignment to firm wide standards. CO&D is supported by Operations Control Management (OCM) team whose role is to develop and manage a Control Program in each region that identifies and monitors significant risks and ensures compliance with operational policies, control procedures and legal/regulatory requirements.

Job responsibilities

• Effectively manage a caseload of Engagements across CO&D remit including regulatory exams, internal audits, external audits, compliance tests and monitoring activities.

• Review requests for information from examiners, auditors, and testers, and in a timely and effective manner, prepare written responses, or coordinate with subject matter experts to collect, review, and submit responses.

• Develop and maintain strong knowledge of WKO/DDS Ops policies, procedures, and operating model as well as systems/platforms used to carry out these activities.

• Investigate and analyze emerging issues, perform root cause analysis, and work with Operations teams to define and execute plans to resolve the issue.

• Perform internal control reviews to document processes and validate the effectiveness of key controls in the CO&D operational processes.

• Advise on and continually reassess key risks and appropriateness of controls to ensure timely identification of significant risks and issues to support an evolving business & regulatory environment.

• Perform record level testing across different client types to ensure alignment to procedures and quality expectations.

• Develop a cohesive and effective partnership with Senior Business leaders, Compliance teams, local and regional onboarding and banking teams, Oversight and Controls, Legal, Internal Audit and Operations.

• Understand and become familiar with the various data sources, platforms and tools including the flow of data from source systems.

• Provide strategic, clear, and regular updates and key messages to management regarding significant matters, including potential issues requiring timely escalation and resolution.

• Ensure all issues and concerns highlighted during the Engagement, including those not included on the final report, are reviewed, and addressed. Also partner with applicable Action Plan owners and Control Managers to develop and complete test steps to address root cause of the issue.

Required qualifications, capabilities, and skills:

• Minimum 6 years of relevant experience in either AML/KYC/ Compliance,/Risk/Controls within the banking industry is required.

• Develop positive relationships throughout the regions and at multiple levels of the organization.

• Prior exam management, audit or consulting experience is required.

• Self-starter and results-oriented individual who can deliver high-quality results under tight deadlines.

• Experience with Digital Tools / Dashboards (e.g. Alteryx, Pega, Tableau), Proficiency in MS Office (Outlook/ Word/ Excel/ PowerPoint)

• Bachelor’s degree or equivalent

To apply for this position, please use the following URL:

https://ars2.equest.com/?response_id=ae9d9e8b3590d2df926f674e9797433f

JOB DESCRIPTION:

• Responsible for day-to-day business data management and regular business report preparations, which includes SAP material master maintenance, data integrity checking and statistics.
• Daily monitoring of basic system health and to flag out any inconsistency in API/System functions when found/reported.
• Daily monitoring of system backend jobs and ensure transactional data are interfacing in healthy state with external/internal system.
• To support Business Analytics, extracting and reorganizing original data, dealing with data related issues with other departments.
• Responsible for data preparation, data mining, to create/identify opportunities through analytics, to optimize business objectives.
• Communicate findings and insights to relevant stakeholders in order to assist Manager in making data-driven decisions in KPI assessments.
• Drive continuous improvements /optimization of campaign performance tracking report with business while complying to A*STAR policies.

REQUIREMENTS:

• Bachelor's Degree or Diploma (with at least 5 years or more relevant experience), preferably Business Analytics, Information systems or Computer Science.
• Strong analytical skills, with experience solving problems using data and providing practical business insights.
• Self-Starter with a strong sense of urgency.
• Aptitude to challenge the status quo, think outside the box, and question what has been done.
• Comfortable with dealing with sets of data points from different sources.
• Qualities of matured thinking, dependable and requires minimum supervision.
• Excellent communication skills (oral and written).

The above eligibility criteria are not exhaustive. A*STAR may include additional selection criteria based on its prevailing recruitment policies. These policies may be amended from time to time without notice. We regret that only shortlisted candidates will be notified.

Key Job Accountabilities (Actual daily deliverables):

On line support to machine troubleshooting.

• Immediate machine failure troubleshooting and repair, handler conversion & setup capabilities, setup yield monitoring, machine UPH accountabilities.

Responsible for Housekeeping, spares and other logistical property control.

• Consistent maintain on a system to improve setup tidiness, cleanness, proper tools inventory and ownership practice.

Ensure handler performance optimization.

• To ensure maximization of plunger / index arm, pick & place arm, speed control to reach maximum utilization & handler UPH efficiency as well as setup performance.

Ensure effective OCAP execution to sustain setup performance

• Ability to perform effective line OCAP, apply systematically socket & load board ocap execution.
• Ensure do escalation on tester repair after load board ocap done but problem persisted
• Ensure do escalation on handler if jam rate occurrence more than 6 times/day
• Do Socket Monitoring Dashboard monitoring on socket insertion lifespan reached limit & replace socket immediately
• Ensure setup time & unscheduled downtimes meet KPI based on Mean time to repair (MTTR) & Waiting time (WT)
• Do shift handover & communication with incoming/outgoing for outstanding issue follow up continuation

Required Experience and Qualifications (Required knowledge, skills and experience---however acquired):

• Requires knowledge in electronics and mechanical principles and through understanding of Final Testing ATE machine & technology is an advantage.
• Requires through knowledge of practical applications of concepts, procedures and guidelines to solve extremely complex problems
• Meticulous, independent, analytical and possess good / positive interpersonal skill. Must be a team player and hard working.
• Diploma in Electrical / Electronics / Mechatronics Engineering or its equivalent (E3)
• Minimum Higher NITEC / NITEC in Electrical / Electronics / Mechatronics Engineering or its equivalent with minimum of 5 years experience in Final Test Line Support operation is an advantage.

We are seeking a dedicated and detail-oriented Quality Control Associate to join our team. This entry-level position is open to fresh graduates and individuals with up to 2 years of experience. The Quality Control Associate will play a vital role in ensuring the quality and compliance of our products through rigorous testing and inspection processes.

Key Responsibilities:

1. Product Inspection:Conduct thorough inspections of raw materials, components, and finished products to ensure compliance with quality standards.
   Identify and document any deviations from quality specifications.
   
2. Documentation:Maintain detailed and accurate records of all quality control activities.
   Record and report test results, deviations, and corrective actions taken.
   
3. Quality Assurance:Support the development and implementation of quality assurance processes.
   Collaborate with the quality control team to improve and streamline procedures.
   
4. Collaboration:Work closely with production and manufacturing teams to address quality concerns in real-time.
   Communicate effectively with cross-functional teams to achieve quality objectives.
   
5. Continuous Improvement:Contribute to the identification of areas for process improvement.
   Participate in discussions to enhance overall product quality.
   
6. Compliance:Ensure adherence to industry regulations and company quality standards.
   Stay updated on changes in quality control practices and regulations.
   

Requirements:

1. Experience: Fresh graduate to 2 years of experience in quality control or a related field.
2. Analytical Skills: Strong analytical and problem-solving abilities.
3. Attention to Detail: Exceptional attention to detail and accuracy in work.
4. Communication Skills: Effective verbal and written communication skills.
5. Team Player: Collaborative mindset and ability to work effectively within a team.
6. Adaptability: Willingness to learn and adapt to new testing methodologies and technologies.
7. Regulatory Awareness: Basic understanding of industry regulations related to quality control.

This is an excellent opportunity for an entry-level professional to gain valuable experience in quality control within a dynamic and growing organization. If you are passionate about ensuring product quality and compliance, we encourage you to apply for this position.

Job Description

We are looking for committed, passionate and resourceful individuals to drive and deliver the Centre’s service culture and quality objectives.

The successful candidate will be required to:

• Follow up on feedback from patients and stakeholders.
• Work with relevant stakeholders (e.g. Doctors, nurses, allied healthcare and ancillary staff) on conflicts resolution and ensure prompt service recoveries.
• Lead, participate or support improvement and transformation initiatives and be comfortable with using digital tools such as Zoom and teams to conduct training and execute patient oriented initiative.
• Assist with patient feedback systems maintenance, data collation, report preparation, service dashboard, customer analytics and insights.
• Assist to establish/coordinate Centre’s policies and procedures, as and when necessary, for continual improvement of service standards.
• Participate and support cluster initiatives such as the new CRM system and SingHealth Patient Advocacy Network.

Job Requirements

• Diploma with at least 3 years of relevant experience, preferably in healthcare or service-oriented industry.
• A self-driven and excellent team player who is positive, proactive and resourceful.
• Strong customer-centric mindset, interpersonal, communication (both verbal and written) and problem solving skills.
• Strong analytical, organizational and project management skills.
• Results-oriented with able to multi-task.
• Strong Microsoft Excel and PowerPoint skills; experience with digital media and data analytics software such as Tableau will be added advantage.